22 results on '"Purna A, Joshi"'
Search Results
2. RANK Signaling Amplifies WNT-Responsive Mammary Progenitors through R-SPONDIN1
- Author
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Purna A. Joshi, Paul D. Waterhouse, Nagarajan Kannan, Swami Narala, Hui Fang, Marco A. Di Grappa, Hartland W. Jackson, Josef M. Penninger, Connie Eaves, and Rama Khokha
- Subjects
Medicine (General) ,R5-920 ,Biology (General) ,QH301-705.5 - Abstract
Systemic and local signals must be integrated by mammary stem and progenitor cells to regulate their cyclic growth and turnover in the adult gland. Here, we show RANK-positive luminal progenitors exhibiting WNT pathway activation are selectively expanded in the human breast during the progesterone-high menstrual phase. To investigate underlying mechanisms, we examined mouse models and found that loss of RANK prevents the proliferation of hormone receptor-negative luminal mammary progenitors and basal cells, an accompanying loss of WNT activation, and, hence, a suppression of lobuloalveologenesis. We also show that R-spondin1 is depleted in RANK-null progenitors, and that its exogenous administration rescues key aspects of RANK deficiency by reinstating a WNT response and mammary cell expansion. Our findings point to a novel role of RANK in dictating WNT responsiveness to mediate hormone-induced changes in the growth dynamics of adult mammary cells.
- Published
- 2015
- Full Text
- View/download PDF
3. A Progesterone-CXCR4 Axis Controls Mammary Progenitor Cell Fate in the Adult Gland
- Author
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Yu-Jia Shiah, Pirashaanthy Tharmapalan, Alison E. Casey, Purna A. Joshi, Trevor D. McKee, Hartland W. Jackson, Alexander G. Beristain, Michelle A. Chan-Seng-Yue, Gary D. Bader, John P. Lydon, Paul D. Waterhouse, Paul C. Boutros, and Rama Khokha
- Subjects
Medicine (General) ,R5-920 ,Biology (General) ,QH301-705.5 - Abstract
Progesterone drives mammary stem and progenitor cell dynamics through paracrine mechanisms that are currently not well understood. Here, we demonstrate that CXCR4, the receptor for stromal-derived factor 1 (SDF-1; CXC12), is a crucial instructor of hormone-induced mammary stem and progenitor cell function. Progesterone elicits specific changes in the transcriptome of basal and luminal mammary epithelial populations, where CXCL12 and CXCR4 represent a putative ligand-receptor pair. In situ, CXCL12 localizes to progesterone-receptor-positive luminal cells, whereas CXCR4 is induced in both basal and luminal compartments in a progesterone-dependent manner. Pharmacological inhibition of CXCR4 signaling abrogates progesterone-directed expansion of basal (CD24+CD49fhi) and luminal (CD24+CD49flo) subsets. This is accompanied by a marked reduction in CD49b+SCA-1− luminal progenitors, their functional capacity, and lobuloalveologenesis. These findings uncover CXCL12 and CXCR4 as novel paracrine effectors of hormone signaling in the adult mammary gland, and present a new avenue for potentially targeting progenitor cell growth and malignant transformation in breast cancer.
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- 2015
- Full Text
- View/download PDF
4. PDGFRα+ stromal adipocyte progenitors transition into epithelial cells during lobulo-alveologenesis in the murine mammary gland
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Katayoon Kasaian, Rama Khokha, Paul Waterhouse, Hui Fang, Hei Sook Sul, Olga Gulyaeva, Purna A. Joshi, and Paul C. Boutros
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0301 basic medicine ,Stromal cell ,Cellular differentiation ,Science ,1.1 Normal biological development and functioning ,Population ,Morphogenesis ,General Physics and Astronomy ,Reproductive health and childbirth ,02 engineering and technology ,Biology ,Regenerative Medicine ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,Mice ,Underpinning research ,Breast Cancer ,Adipocytes ,Animals ,Humans ,2.1 Biological and endogenous factors ,Cell Lineage ,Aetiology ,Progenitor cell ,education ,lcsh:Science ,Cancer ,education.field_of_study ,Multidisciplinary ,Animal ,Mesenchymal stem cell ,Platelet-Derived Growth Factor alpha ,Cell migration ,Epithelial Cells ,Cell Differentiation ,General Chemistry ,021001 nanoscience & nanotechnology ,Stem Cell Research ,Mammary Glands ,Cell biology ,030104 developmental biology ,Stem Cell Research - Nonembryonic - Non-Human ,lcsh:Q ,Stem cell ,Stromal Cells ,0210 nano-technology ,Receptor - Abstract
The mammary gland experiences substantial remodeling and regeneration during development and reproductive life, facilitated by stem cells and progenitors that act in concert with physiological stimuli. While studies have focused on deciphering regenerative cells within the parenchymal epithelium, cell lineages in the stroma that may directly contribute to epithelial biology is unknown. Here we identify, in mouse, the transition of a PDGFRα+ mesenchymal cell population into mammary epithelial progenitors. In addition to being adipocyte progenitors, PDGFRα+ cells make a de novo contribution to luminal and basal epithelia during mammary morphogenesis. In the adult, this mesenchymal lineage primarily generates luminal progenitors within lobuloalveoli during sex hormone exposure or pregnancy. We identify cell migration as a key molecular event that is activated in mesenchymal progenitors in response to epithelium-derived chemoattractant. These findings demonstrate a stromal reservoir of epithelial progenitors and provide insight into cell origins and plasticity during mammary tissue growth.
- Published
- 2019
5. PDGFRα
- Author
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Purna A, Joshi, Paul D, Waterhouse, Katayoon, Kasaian, Hui, Fang, Olga, Gulyaeva, Hei Sook, Sul, Paul C, Boutros, and Rama, Khokha
- Subjects
Mice ,Mammary Glands, Animal ,Receptor, Platelet-Derived Growth Factor alpha ,Adipocytes ,Animals ,Humans ,Cell Differentiation ,Cell Lineage ,Epithelial Cells ,Stromal Cells ,Article - Abstract
The mammary gland experiences substantial remodeling and regeneration during development and reproductive life, facilitated by stem cells and progenitors that act in concert with physiological stimuli. While studies have focused on deciphering regenerative cells within the parenchymal epithelium, cell lineages in the stroma that may directly contribute to epithelial biology is unknown. Here we identify, in mouse, the transition of a PDGFRα+ mesenchymal cell population into mammary epithelial progenitors. In addition to being adipocyte progenitors, PDGFRα+ cells make a de novo contribution to luminal and basal epithelia during mammary morphogenesis. In the adult, this mesenchymal lineage primarily generates luminal progenitors within lobuloalveoli during sex hormone exposure or pregnancy. We identify cell migration as a key molecular event that is activated in mesenchymal progenitors in response to epithelium-derived chemoattractant. These findings demonstrate a stromal reservoir of epithelial progenitors and provide insight into cell origins and plasticity during mammary tissue growth., The origin and source of mammary gland progenitors and how they interact with the adipose‐rich stroma is unclear. Here, the authors identify PDGFRα+ adipocyte progenitors in the murine mammary stroma as a mesenchymal cell lineage recruited into the expanding epithelium during development, hormone exposure and pregnancy.
- Published
- 2019
6. RANKL/RANK control Brca1 mutation-driven mammary tumors
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Miguel Angel Pujana, Kwadwo Owusu-Boaitey, Georg Pfeiler, Shuan Rao, Luigi Tortola, Melita Ticevic, Eva Y.-H. P. Lee, Enrique Vidal, Purna A. Joshi, Anoop Kavirayani, Daniel Schramek, Gerald Wirnsberger, Josef M. Penninger, Ashley A Odai-Afotey, Eva González-Suárez, Renu Sarao, Verena Sigl, Maria Novatchkova, for Cimba, Aishia Sampson, Iris Uribesalgo, Nnamdi Edokobi, Helmuth Popper, Lukas Kenner, Rama Khokha, Yen Y. Tan, Jennifer Cruickshank, Conxi Lázaro, Christian F. Singer, Zsuzsanna Bago-Horvath, Ivona Kozieradzki, Jerome Hersl, Holger Heyn, Hal K. Berman, Laundette P. Jones, Targeted Gynaecologic Oncology (TARGON), and Damage and Repair in Cancer Development and Cancer Treatment (DARE)
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0301 basic medicine ,medicine.disease_cause ,RANK ,Prostate cancer ,Mice ,Mammary progenitor cells ,Genotype ,skin and connective tissue diseases ,biology ,Receptor Activator of Nuclear Factor-kappa B ,RANKL ,EPITHELIAL-CELLS ,3. Good health ,PROSTATE-CANCER ,inherited breast cancer ,DIFFERENTIATION ,Cell Transformation, Neoplastic ,POSTMENOPAUSAL WOMEN ,SUSCEPTIBILITY GENE BRCA1 ,Original Article ,Female ,Stem cell ,BONE-MINERAL DENSITY ,Signal Transduction ,mammary progenitor cells ,medicine.medical_specialty ,Breast Neoplasms ,MOUSE MAMMARY ,03 medical and health sciences ,Breast cancer ,Internal medicine ,medicine ,Animals ,Humans ,Progenitor cell ,Molecular Biology ,PROGESTERONE-RECEPTOR ,Inherited breast cancer ,RANK Ligand ,Cell Biology ,medicine.disease ,BRCA1 ,NEGATIVE BREAST-CANCER ,030104 developmental biology ,Endocrinology ,Mutation ,biology.protein ,Cancer research ,Carcinogenesis - Abstract
© 2016 IBCB, SIBS, CAS All rights reserved. Breast cancer is the most common female cancer, affecting approximately one in eight women during their life-time. Besides environmental triggers and hormones, inherited mutations in the breast cancer 1 (BRCA1) or BRCA2 genes markedly increase the risk for the development of breast cancer. Here, using two different mouse models, we show that genetic inactivation of the key osteoclast differentiation factor RANK in the mammary epithelium markedly delayed onset, reduced incidence, and attenuated progression of Brca1;p53 mutation-driven mammary cancer. Long-term pharmacological inhibition of the RANK ligand RANKL in mice abolished the occurrence of Brca1 mutation-driven pre-neoplastic lesions. Mechanistically, genetic inactivation of Rank or RANKL/RANK blockade impaired proliferation and expansion of both murine Brca1;p53 mutant mammary stem cells and mammary progenitors from human BRCA1 mutation carriers. In addition, genome variations within the RANK locus were significantly associated with risk of developing breast cancer in women with BRCA1 mutations. Thus, RANKL/RANK control progenitor cell expansion and tumorigenesis in inherited breast cancer. These results present a viable strategy for the possible prevention of breast cancer in BRCA1 mutant patients.
- Published
- 2016
7. BRCA1 interacts with Nrf2 to regulate antioxidant signaling and cell survival
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Peter Bouwman, Satoshi Inoue, Jennifer Cruickshank, Bernard Martin, Bryan E. Snow, Alan Tseng, Dirk Brenner, Pegah S. Baniasadi, David W. Cescon, Andrew J. Elia, Melinda A. Musgrave, Jos Jonkers, Andrew Wakeham, Sam D. Molyneux, Chiara Gorrini, Isaac S. Harris, Rama Khokha, Hal K. Berman, Jennifer Silvester, Mona L. Gauthier, Tak W. Mak, Zoe Winterton-Perks, and Purna A. Joshi
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Antioxidant ,endocrine system diseases ,medicine.medical_treatment ,Immunology ,Biology ,medicine.disease_cause ,environment and public health ,03 medical and health sciences ,0302 clinical medicine ,Ubiquitin ,medicine ,Immunology and Allergy ,skin and connective tissue diseases ,030304 developmental biology ,Regulation of gene expression ,chemistry.chemical_classification ,0303 health sciences ,Reactive oxygen species ,respiratory system ,3. Good health ,Cell biology ,chemistry ,Cell culture ,030220 oncology & carcinogenesis ,biology.protein ,Signal transduction ,Carcinogenesis ,Oxidative stress - Abstract
Oxidative stress plays an important role in cancer development and treatment. Recent data implicate the tumor suppressor BRCA1 in regulating oxidative stress, but the molecular mechanism and the impact in BRCA1-associated tumorigenesis remain unclear. Here, we show that BRCA1 regulates Nrf2-dependent antioxidant signaling by physically interacting with Nrf2 and promoting its stability and activation. BRCA1-deficient mouse primary mammary epithelial cells show low expression of Nrf2-regulated antioxidant enzymes and accumulate reactive oxygen species (ROS) that impair survival in vivo. Increased Nrf2 activation rescues survival and ROS levels in BRCA1-null cells. Interestingly, 53BP1 inactivation, which has been shown to alleviate several defects associated with BRCA1 loss, rescues survival of BRCA1-null cells without restoring ROS levels. We demonstrate that estrogen treatment partially restores Nrf2 levels in the absence of BRCA1. Our data suggest that Nrf2-regulated antioxidant response plays a crucial role in controlling survival downstream of BRCA1 loss. The ability of estrogen to induce Nrf2 posits an involvement of an estrogen-Nrf2 connection in BRCA1 tumor suppression. Lastly, BRCA1-mutated tumors retain a defective antioxidant response that increases the sensitivity to oxidative stress. In conclusion, the role of BRCA1 in regulating Nrf2 activity suggests important implications for both the etiology and treatment of BRCA1-related cancers.
- Published
- 2013
8. Progesterone and Synthetic Progestin Controversies--Reply
- Author
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Pamela J. Goodwin, Rama Khokha, and Purna A. Joshi
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Cancer Research ,medicine.medical_specialty ,Estrogens, Conjugated (USP) ,medicine.drug_class ,business.industry ,Estrogen Replacement Therapy ,Breast Neoplasms ,Medroxyprogesterone Acetate ,Bioinformatics ,Endocrinology ,Oncology ,Internal medicine ,medicine ,Medroxyprogesterone acetate ,Humans ,Female ,Estrogen replacement therapy ,business ,Progestin ,medicine.drug - Published
- 2015
9. Progesterone induces adult mammary stem cell expansion
- Author
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Rama Khokha, Alexander G. Beristain, Christine L. Clarke, Paul Waterhouse, Purna A. Joshi, Patricia A. Mote, Hartland W. Jackson, Marco A. Di Grappa, and John Stingl
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Aging ,medicine.medical_specialty ,Ovariectomy ,Cell ,Cell Count ,Estrous Cycle ,Integrin alpha6 ,Biology ,Luteal phase ,Mice ,Mammary Glands, Animal ,Wnt4 Protein ,Cancer stem cell ,Internal medicine ,Paracrine Communication ,WNT4 ,medicine ,Animals ,Homeostasis ,Stem Cell Niche ,Progesterone ,Multidisciplinary ,Stem Cells ,RANK Ligand ,Cancer ,Estrogens ,Cell cycle ,medicine.disease ,Wnt Proteins ,Cell Transformation, Neoplastic ,medicine.anatomical_structure ,Endocrinology ,Receptors, Estrogen ,RANKL ,Cancer research ,biology.protein ,Female ,Stem cell ,Receptors, Progesterone ,Cell Division - Abstract
Reproductive history is the strongest risk factor for breast cancer after age, genetics and breast density. Increased breast cancer risk is entwined with a greater number of ovarian hormone-dependent reproductive cycles, yet the basis for this predisposition is unknown. Mammary stem cells (MaSCs) are located within a specialized niche in the basal epithelial compartment that is under local and systemic regulation. The emerging role of MaSCs in cancer initiation warrants the study of ovarian hormones in MaSC homeostasis. Here we show that the MaSC pool increases 14-fold during maximal progesterone levels at the luteal dioestrus phase of the mouse. Stem-cell-enriched CD49fhi cells amplify at dioestrus, or with exogenous progesterone, demonstrating a key role for progesterone in propelling this expansion. In aged mice, CD49fhi cells display stasis upon cessation of the reproductive cycle. Progesterone drives a series of events where luminal cells probably provide Wnt4 and RANKL signals to basal cells which in turn respond by upregulating their cognate receptors, transcriptional targets and cell cycle markers. Our findings uncover a dynamic role for progesterone in activating adult MaSCs within the mammary stem cell niche during the reproductive cycle, where MaSCs are putative targets for cell transformation events leading to breast cancer.
- Published
- 2010
10. Osteoclast differentiation factor RANKL controls development of progestin-driven mammary cancer
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Lukas Kenner, Reiko Hanada, Andreas Leibbrandt, John A. Pospisilik, Purna A. Joshi, Martin Widschwendter, Daniel Schramek, Manolis Pasparakis, Antonios O. Aliprantis, Rama Khokha, Laurie H. Glimcher, Heather J. Lee, Georg Schett, Josef M. Penninger, Christopher J. Ormandy, and Verena Sigl
- Subjects
medicine.medical_specialty ,03 medical and health sciences ,0302 clinical medicine ,Breast cancer ,Osteoclast ,Internal medicine ,medicine ,Medroxyprogesterone acetate ,030304 developmental biology ,0303 health sciences ,Multidisciplinary ,biology ,business.industry ,Cancer ,RANK Ligand ,medicine.disease ,3. Good health ,medicine.anatomical_structure ,Denosumab ,Endocrinology ,RANKL ,030220 oncology & carcinogenesis ,biology.protein ,Breast disease ,business ,medicine.drug - Abstract
Progestins, used in contraceptives and hormone replacement therapy, have been linked to breast cancer. Two teams working independently have now found a mechanistic basis for this association. Schramek et al. show in a mouse model that synthetic progestins can promote mammary tumour formation by inducing the osteoclast differentiation factor RANKL, which acts on mammary epithelial cells through the RANKL receptor RANK. Gonzalez-Suarez et al. find that inhibition of RANKL reduces tumorigenesis in hormone-induced as well as in other mouse mammary gland tumour models, suggesting a new therapeutic approach. One RANKL inhibitor (denosumab) is in clinical trials as a treatment for bone loss in post-menopausal osteoporosis and for the treatment of skeletal-related symptoms in metastatic bone disease. Progestins, used in contraceptives and hormone replacement therapy, have been linked to breast cancer. These authors provide a mechanistic basis for this association. They show in a mouse model that synthetic progestins can promote mammary tumour formation by inducing RANKL (receptor activator of NF-KB ligand), which acts on mammary epithelial cells through the RANKL receptor RANK. Breast cancer is one of the most common cancers in humans and will on average affect up to one in eight women in their lifetime in the United States and Europe1. The Women’s Health Initiative and the Million Women Study have shown that hormone replacement therapy is associated with an increased risk of incident and fatal breast cancer2,3. In particular, synthetic progesterone derivatives (progestins) such as medroxyprogesterone acetate (MPA), used in millions of women for hormone replacement therapy and contraceptives, markedly increase the risk of developing breast cancer. Here we show that the in vivo administration of MPA triggers massive induction of the key osteoclast differentiation factor RANKL (receptor activator of NF-κB ligand) in mammary-gland epithelial cells. Genetic inactivation of the RANKL receptor RANK in mammary-gland epithelial cells prevents MPA-induced epithelial proliferation, impairs expansion of the CD49fhi stem-cell-enriched population, and sensitizes these cells to DNA-damage-induced cell death. Deletion of RANK from the mammary epithelium results in a markedly decreased incidence and delayed onset of MPA-driven mammary cancer. These data show that the RANKL/RANK system controls the incidence and onset of progestin-driven breast cancer.
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- 2010
- Full Text
- View/download PDF
11. Loss of Alx4, a stromally-restricted homeodomain protein, impairs mammary epithelial morphogenesis
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Purna A. Joshi, Paul A. Hamel, and Hong Chang
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medicine.medical_specialty ,Stromal cell ,Mammary gland ,Morphogenesis ,Mice, Transgenic ,Stroma ,Biology ,Fat pad ,Mice ,03 medical and health sciences ,Mammary Glands, Animal ,0302 clinical medicine ,Pregnancy ,Internal medicine ,Terminal end bud ,medicine ,Animals ,Estrogen receptor ,Molecular Biology ,030304 developmental biology ,Homeodomain Proteins ,Regulation of gene expression ,Alx4 ,0303 health sciences ,Estradiol ,Gene Expression Regulation, Developmental ,Epithelial Cells ,Cell Biology ,Null allele ,Cell biology ,Endocrinology ,medicine.anatomical_structure ,Animals, Newborn ,Organ Specificity ,Strong’s luxoid ,030220 oncology & carcinogenesis ,Pregnancy, Animal ,Homeobox ,Female ,Stromal Cells ,Developmental Biology - Abstract
Postnatal development of the mammary gland is determined by reciprocal interactions between the ductal epithelia and adjacent stroma. Alx4 is a mesenchymally restricted homeodomain transcription factor expressed in a number of developing tissues, including skin appendages such as hair follicles, whiskers and teeth. We show here that Alx4 is expressed in a subset of ERalpha-expressing mammary stromal cells adjacent to terminal end buds and alveoli during puberty and pregnancy, respectively. Alx4 expression is induced in mammary stromal cells at the onset of puberty and can be induced in prepubescent mice by administration of 17beta-estradiol. In order to determine the role of Alx4 during mammary gland development, we characterized mammary gland development of mice homozygous for the null allele of Alx4, lst(D). Mammary glands from animals lacking Alx4 activity exhibit profound alterations in ductal morphogenesis. Overall development is delayed, ducts being grossly distorted in size and structure. Terminal end buds are also disoriented, displaying aberrant architecture during bifurcation. Despite the developmental delay, the ductal network typically reaches the limits of the fat pad. However, during puberty and in the adult virgin mice, the frequency and density of branch points is significantly reduced. We show further that the defective ductal morphogenesis is due to defects in stromal cells. Specifically, when injected into the cleared fat pad of wild-type recipients, mixed populations of wild-type epithelial cells and Alx4-deficient stromal cells give rise to retarded ductal morphogenesis. Wild-type stromal cells mixed with Alx4-deficient epithelial cells result in normal progression of ductal development. Defective branching morphogenesis in Alx4-deficient females is not due to a loss in expression of HGF, since the level of HGF message in mammary stromal cells is similar in mutant and wild-type littermates. MMP3 is similarly expressed while a 40% increase in MMP2 and a 50% decrease in MMP9 message levels in Alx4-deficient mice relative to their wild-type littermates is observed. Thus, the activity of the stromally restricted homeodomain factor, Alx4, is required for normal branching morphogenesis of the ductal epithelia during pubescent mammary gland development.
- Published
- 2006
- Full Text
- View/download PDF
12. RANK Signaling Amplifies WNT-Responsive Mammary Progenitors through R-SPONDIN1
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Connie J. Eaves, Marco A. Di Grappa, Purna A. Joshi, Josef M. Penninger, Paul Waterhouse, Nagarajan Kannan, Hui Fang, Swami R. Narala, Rama Khokha, and Hartland W. Jackson
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medicine.medical_specialty ,R spondin1 ,Mammary cells ,Biology ,Biochemistry ,Article ,Basal (phylogenetics) ,Mice ,Mammary Glands, Animal ,Internal medicine ,Genetics ,medicine ,Animals ,Humans ,Progenitor cell ,lcsh:QH301-705.5 ,Wnt Signaling Pathway ,Cell Proliferation ,lcsh:R5-920 ,Receptor Activator of Nuclear Factor-kappa B ,Stem Cells ,Wnt signaling pathway ,Cell Biology ,Cell biology ,Endocrinology ,lcsh:Biology (General) ,Female ,lcsh:Medicine (General) ,Thrombospondins ,Human breast ,Developmental Biology ,Hormone - Abstract
Summary Systemic and local signals must be integrated by mammary stem and progenitor cells to regulate their cyclic growth and turnover in the adult gland. Here, we show RANK-positive luminal progenitors exhibiting WNT pathway activation are selectively expanded in the human breast during the progesterone-high menstrual phase. To investigate underlying mechanisms, we examined mouse models and found that loss of RANK prevents the proliferation of hormone receptor-negative luminal mammary progenitors and basal cells, an accompanying loss of WNT activation, and, hence, a suppression of lobuloalveologenesis. We also show that R-spondin1 is depleted in RANK-null progenitors, and that its exogenous administration rescues key aspects of RANK deficiency by reinstating a WNT response and mammary cell expansion. Our findings point to a novel role of RANK in dictating WNT responsiveness to mediate hormone-induced changes in the growth dynamics of adult mammary cells., Graphical Abstract, Highlights • Luminal progenitors are targets of progesterone in the adult human breast • Progesterone-induced expansion of mammary epithelial subsets requires RANK • RANK signaling targets WNT-responsive ER–PR– luminal progenitors and basal cells • RANK controls RSPO1, which rescues defective progenitor expansion in Rank-null state, Cellular signals governing the WNT response are largely unknown despite the widely recognized function of this pathway in the control of stem and progenitor cells in diverse tissues. Khoka and colleagues describe RANK signaling as a requisite step for the expansion of ER–PR– adult mammary epithelial progenitors and acquisition of WNT responsiveness through its regulation of the WNT agonist R-SPONDIN1.
- Published
- 2014
13. Begining open heart surgery in Nepal: Our experience and three years audit at Tribhuvan University Teaching Hospital
- Author
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Govinda Prasad Sharma, Sidhartha Pradhan, Paleswan Lakhey, Joytendra Sharma, Uttam Shrestha, Rabindra Timila, Mahendra Bhatta, Mod Nath Marahatta, Purna Raj Joshi, Bhagwan Koirala, and Bishow ManSingh Shrestha
- Subjects
medicine.medical_specialty ,business.industry ,General surgery ,Medicine ,Audit ,University teaching ,business - Abstract
The historic first open heart surgery by the all-Nepalese team was performed at Tribhuvan University Teaching Hospital (TUTH) on 20 February 1997. Since then with-in three years period 132 cases of Open Heart Surgeries were performed. Retrospective study of those cases and problems faced in continuing the service is presented here.
- Published
- 2000
14. PKA signaling drives mammary tumorigenesis through Src
- Author
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Lawrence S. Kirschner, Neil C. Pomroy, Alexander G. Beristain, M C Chang, Gilbert G. Privé, Purna A. Joshi, M A Di Grappa, Rama Khokha, Sam D. Molyneux, and Miguel Angel Pujana
- Subjects
Cancer Research ,medicine.medical_specialty ,Cyclic AMP-Dependent Protein Kinase RIalpha Subunit ,Dasatinib ,Biology ,Cell Line ,Mice ,Mammary Glands, Animal ,Internal medicine ,Genetics ,medicine ,Animals ,Humans ,Phosphorylation ,Protein kinase A ,Molecular Biology ,PRKAR1A ,Cell Proliferation ,Cell growth ,Cancer ,Mammary Neoplasms, Experimental ,Epithelial Cells ,medicine.disease ,Androstadienes ,Thiazoles ,Endocrinology ,Cell Transformation, Neoplastic ,Pyrimidines ,src-Family Kinases ,Cancer research ,Female ,Signal transduction ,Wortmannin ,medicine.drug ,Proto-oncogene tyrosine-protein kinase Src ,Signal Transduction - Abstract
Protein kinase A (PKA) hyperactivation causes hereditary endocrine neoplasias; however, its role in sporadic epithelial cancers is unknown. Here, we show that heightened PKA activity in the mammary epithelium generates tumors. Mammary-restricted biallelic ablation of Prkar1a, which encodes for the critical type-I PKA regulatory subunit, induced spontaneous breast tumors characterized by enhanced type-II PKA activity. Downstream of this, Src phosphorylation occurs at residues serine-17 and tyrosine-416 and mammary cell transformation is driven through a mechanism involving Src signaling. The phenotypic consequences of these alterations consisted of increased cell proliferation and, accordingly, expansion of both luminal and basal epithelial cell populations. In human breast cancer, low PRKAR1A/high SRC expression defines basal-like and HER2 breast tumors associated with poor clinical outcome. Together, the results of this study define a novel molecular mechanism altered in breast carcinogenesis and highlight the potential strategy of inhibiting SRC signaling in treating this cancer subtype in humans.
- Published
- 2013
15. Progesterone drives mammary secretory differentiation via RankL-mediated induction of Elf5 in luminal progenitor cells
- Author
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Anita Ledger, Daniel Schramek, Maria M. Szwarc, Christina Cho, Purna A. Joshi, Heather J. Lee, David Gallego-Ortega, Josef M. Penninger, Christopher J. Ormandy, John P. Lydon, and Rama Khokha
- Subjects
medicine.medical_specialty ,medicine.medical_treatment ,Mammary gland ,Mice, Transgenic ,Biology ,03 medical and health sciences ,Paracrine signalling ,Mice ,0302 clinical medicine ,Mammary Glands, Animal ,Internal medicine ,Progesterone receptor ,medicine ,Animals ,Progenitor cell ,Molecular Biology ,Progesterone ,030304 developmental biology ,0303 health sciences ,Stem Cells ,RANK Ligand ,Gene Expression Regulation, Developmental ,Epithelial Cells ,Cell biology ,Up-Regulation ,DNA-Binding Proteins ,Steroid hormone ,medicine.anatomical_structure ,Endocrinology ,RANKL ,030220 oncology & carcinogenesis ,biology.protein ,06 Biological Sciences, 11 Medical and Health Sciences ,Female ,Stem cell ,Receptors, Progesterone ,Developmental Biology ,Hormone ,Transcription Factors - Abstract
Progesterone-RankL paracrine signaling has been proposed as a driver of stem cell expansion in the mammary gland, and Elf5 is essential for the differentiation of mammary epithelial progenitor cells. We demonstrate that Elf5 expression is induced by progesterone and that Elf5 and progesterone cooperate to promote alveolar development. The progesterone receptor and Elf5 are expressed in a mutually exclusive pattern, and we identify RankL as the paracrine mediator of the effects of progesterone on Elf5 expression in CD61+ progenitor cells and their consequent differentiation. Blockade of RankL action prevented progesterone-induced side branching and the expansion of Elf5+ mature luminal cells. These findings describe a mechanism by which steroid hormones can produce the expansion of steroid hormone receptor-negative mammary epithelial cells.
- Published
- 2013
16. The mammary stem cell conundrum: is it unipotent or multipotent?
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Rama Khokha and Purna A. Joshi
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Pathology ,medicine.medical_specialty ,Multipotent Stem Cells ,Mammary gland ,Biology ,medicine.disease ,Embryonic stem cell ,Mammary Glands, Animal ,Viewpoint ,Breast cancer ,medicine.anatomical_structure ,Multipotent Stem Cell ,Surgical oncology ,Cancer stem cell ,medicine ,Cancer research ,Animals ,Humans ,Cell Lineage ,Female ,Stem cell ,Mammary Glands, Human ,Adult stem cell - Abstract
Exploring the normal biology and regulation of stem cells has the promise to yield insights into the etiological roots and survival of breast cancer cells. Many studies have supported the existence of a multipotent mammary stem cell that regenerates all aspects of glandular development. However, Van Keymeulen and colleagues (2011) illustrated the presence of lineage-restricted unipotent stem cells that self-renew and collaborate in postnatal mammary development, whereas multipotent stem cells were found only during embryonic mammogenesis. This prompts a re-evaluation of currently accepted mammary stem cell dynamics and conceivably its impact on the evolution of different breast cancer subtypes.
- Published
- 2012
17. Active allies: hormones, stem cells and the niche in adult mammopoiesis
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Purna A. Joshi, Rama Khokha, and Marco A. Di Grappa
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Endocrinology, Diabetes and Metabolism ,Cellular differentiation ,Stem Cells ,Niche ,Clinical uses of mesenchymal stem cells ,Breast Neoplasms ,Cell Differentiation ,Biology ,Cell biology ,Endothelial stem cell ,Endocrinology ,Mammary Glands, Animal ,Risk Factors ,Immunology ,Models, Animal ,Animals ,Humans ,Female ,Stem cell ,Progenitor cell ,Stem Cell Niche ,Gonadal Steroid Hormones ,Mammary Glands, Human ,Adult stem cell ,Hormone - Abstract
Adult stem cells are recruited in response to specific physiological demands to regenerate, repair or maintain essential cellular components of tissues, while preserving self-renewal capacity. Signals that activate adult stem cells are not simply cell autonomous and stem cells are part of a larger dynamic framework, the stem cell 'niche', which integrates systemic and local cues to sustain stem cell functionality. The mammary stem cell niche responds readily to hormonal stimuli, generating pertinent signals that activate stem cells, culminating in stem cell expansion and tissue growth. We review here current knowledge of the mammary stem cell niche with attention to the potent stimulation rendered by ovarian hormones, relevant cellular and molecular players, and the implication of a deregulated niche, for breast cancer risk.
- Published
- 2012
18. Superior Vena Cava Syndrome Due to Metastatic Transitional Cell Carcinoma
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B R Joshi, Bishwo Man Singh Shrestha, Mahendra Bhatta, Govind Prasad Sharma, Purna Raj Joshi, Gita Sayami, Laxmi Rajbhandari, Mod Nath Marhatha, Bhagawan Koirala, and Ramesh Koirala
- Subjects
Pulmonary and Respiratory Medicine ,Right atrial wall ,medicine.medical_specialty ,Metastatic Transitional Cell Carcinoma ,Superior vena cava syndrome ,business.industry ,General Medicine ,030204 cardiovascular system & hematology ,medicine.disease ,Surgery ,Resection ,Metastasis ,03 medical and health sciences ,0302 clinical medicine ,Transitional cell carcinoma ,030228 respiratory system ,cardiovascular system ,medicine ,Bladder tumor ,cardiovascular diseases ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business - Abstract
Superior vena cava syndrome due to infradiaphragmatic tumor metastasis was detected in a 70-year-old man. A tumor attached to the right atrial wall was excised and subsequent transurethral resection of a bladder tumor revealed high-grade transitional cell carcinoma. The disease progressed and the patient died 6 months later.
- Published
- 2000
19. Progesterone Exposure and Breast Cancer Risk
- Author
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Pamela J. Goodwin, Rama Khokha, and Purna A. Joshi
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Oncology ,Cancer Research ,medicine.medical_specialty ,business.industry ,medicine.drug_class ,Women's Health Initiative ,medicine.medical_treatment ,Endocrine therapy ,Hormone replacement therapy (menopause) ,medicine.disease ,Breast cancer ,Estrogen ,Internal medicine ,Medicine ,business - Published
- 2015
20. A Progesterone-CXCR4 Axis Controls Mammary Progenitor Cell Fate in the Adult Gland
- Author
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Rama Khokha, John P. Lydon, Trevor D. McKee, Yu Jia Shiah, Pirashaanthy Tharmapalan, Purna A. Joshi, Paul Waterhouse, Michelle Chan-Seng-Yue, Paul C. Boutros, Hartland W. Jackson, Alison E. Casey, Alexander G. Beristain, and Gary D. Bader
- Subjects
lcsh:R5-920 ,Clinical Sciences ,Mammary gland ,Correction ,Cell Biology ,Biology ,Biochemistry ,CXCR4 ,Cell biology ,Malignant transformation ,Transcriptome ,Paracrine signalling ,Basal (phylogenetics) ,medicine.anatomical_structure ,lcsh:Biology (General) ,Report ,Immunology ,Genetics ,medicine ,Biochemistry and Cell Biology ,Progenitor cell ,lcsh:Medicine (General) ,Receptor ,lcsh:QH301-705.5 ,Developmental Biology - Abstract
Summary Progesterone drives mammary stem and progenitor cell dynamics through paracrine mechanisms that are currently not well understood. Here, we demonstrate that CXCR4, the receptor for stromal-derived factor 1 (SDF-1; CXC12), is a crucial instructor of hormone-induced mammary stem and progenitor cell function. Progesterone elicits specific changes in the transcriptome of basal and luminal mammary epithelial populations, where CXCL12 and CXCR4 represent a putative ligand-receptor pair. In situ, CXCL12 localizes to progesterone-receptor-positive luminal cells, whereas CXCR4 is induced in both basal and luminal compartments in a progesterone-dependent manner. Pharmacological inhibition of CXCR4 signaling abrogates progesterone-directed expansion of basal (CD24+CD49fhi) and luminal (CD24+CD49flo) subsets. This is accompanied by a marked reduction in CD49b+SCA-1− luminal progenitors, their functional capacity, and lobuloalveologenesis. These findings uncover CXCL12 and CXCR4 as novel paracrine effectors of hormone signaling in the adult mammary gland, and present a new avenue for potentially targeting progenitor cell growth and malignant transformation in breast cancer., Graphical Abstract, Highlights • Progesterone induces distinct molecular programs in mammary cell compartments • CXCR4 induction occurs in lobuloalveoli and is progesterone dependent • CXCR4 inhibition abrogates luminal progenitor expansion and mammopoiesis • Targeting of the CXCL12-CXCR4 axis may limit mammary progenitor cell transformation, In this article, Khokha and colleagues use expression profiling and functional assays to identify CXCR4, the receptor for stromal-derived factor 1 (SDF-1; CXC12), as a crucial instructor of hormone-induced mammary stem and progenitor cell function. Pharmacological inhibition of CXCR4 signaling abrogates progesterone-directed expansion of basal and luminal subsets, resulting in a marked reduction in CD49b+SCA-1− luminal progenitors and their functional capacity, and lobuloalveologenesis.
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- 2015
21. Abstract B023: Identifying molecular programs of progesterone-driven mammary stem cell expansion
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Michelle Chan-Seng-Yue, Yu-Jia Shiah, Rama Khokha, Purna A. Joshi, Paul C. Boutros, and Alexander G. Beristain
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Cancer Research ,education.field_of_study ,medicine.drug_class ,Receptor expression ,Population ,Mammary gland ,Cancer ,Biology ,medicine.disease ,Paracrine signalling ,medicine.anatomical_structure ,Oncology ,Estrogen ,medicine ,Cancer research ,Stem cell ,Progenitor cell ,education ,Molecular Biology - Abstract
Lifetime exposure to ovarian hormones plays a crucial role in determining a woman's risk for breast cancer: the risk of developing breast cancer is positively correlated with the number of ovarian-hormone-dependent menstrual cycles. Progesterone is an ovarian steroid hormone that peaks during the luteal phase of the female menstrual cycle. Recent research has revealed that progesterone is a key mediator of cellular changes in the mammary gland that likely underlies the correlation between ovarian hormones and breast cancer risk. These studies have shown that progesterone can exert mitogenic effects through paracrine signaling between specific mammary epithelial populations and control mammary stem cell (MaSC) expansion. Such findings provide new insights into MaSC dynamics and underscore the involvement of ovarian hormones in regulating fundamental mammary epithelial changes. Given the differentiation potential of luminal progenitors and MaSCs, they are the proposed cellular targets of transformation in breast cancer. Although it is known that progesterone can induce luminal and basal cell expansion, the underlying mechanisms driving hormone action within the different cellular compartments (basal, luminal and stromal) of the mammary gland are yet to be defined. Therefore, I hypothesize that the transcriptional response to progesterone will reveal important paracrine signaling pathways involved in MaSC changes. To test my hypothesis, mRNA expression profiles were generated from the different mammary cellular compartments under defined hormone treatments. More specifically, basal, luminal and stromal cells were FACS purified after 2 weeks of hormone stimulation with progesterone, estrogen, progesterone plus estrogen, or vehicle control and subjected to microarray analyses using the Agilent platform. To analyze this microarray data, an optimal pre-processing method was generated before any downstream analysis. After pre-processing, significantly altered genes under each hormone treatment were investigated and cross compared within different cellular compartments. Our lab is interested in examining progesterone-mediated ligand and receptor expression changes in the different epithelial compartments that may play a paracrine role in altering the MaSC population. Once significantly altered ligand-receptor pairs are identified, I will validate specific pathways through both in vivo and in vitro experiments utilizing knockout mice to test their functional significance and investigate the effects of aberrant signaling in these pathways in cell culture assays. Progesterone is believed to play a crucial role in MaSC regulation and this might in part explain why a greater number of reproductive cycles and hormone replacement therapy using progestins contribute to a higher risk of developing breast cancer. MaSCs are postulated to be involved in breast cancer initiation, hence elucidating the mechanisms that induce MaSC expansion will allow us to identify putative targets that can be harnessed to control stem/progenitor cells and limit cellular transformation. Citation Format: Yu-Jia Shiah, Purna A. Joshi, Alexander G. Beristain, Michelle Chan-Seng-Yue, Paul C. Boutros, Rama Khokha. Identifying molecular programs of progesterone-driven mammary stem cell expansion. [abstract]. In: Proceedings of the AACR Special Conference on Advances in Breast Cancer Research: Genetics, Biology, and Clinical Applications; Oct 3-6, 2013; San Diego, CA. Philadelphia (PA): AACR; Mol Cancer Res 2013;11(10 Suppl):Abstract nr B023.
- Published
- 2013
22. Fully Interlocking: A Story of Teamwork among Breast Epithelial Cells
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Rama Khokha, Caroline M. Alexander, and Purna A. Joshi
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medicine.medical_specialty ,Neuregulin-1 ,Biology ,Article ,General Biochemistry, Genetics and Molecular Biology ,Basal (phylogenetics) ,Pregnancy ,Internal medicine ,Lactation ,medicine ,Animals ,Humans ,Molecular Biology ,book ,Myoepithelial cell ,Developmental cell ,Epithelial Cells ,Cell Biology ,Phosphoproteins ,Milk production ,Cell biology ,Adult Stem Cells ,Endocrinology ,medicine.anatomical_structure ,Luminal epithelium ,Trans-Activators ,book.journal ,Female ,Developmental Biology ,Adult stem cell - Abstract
The mammary epithelium is organized as a bi-layer of luminal and basal/myoepithelial cells. During pregnancy the luminal compartment expands for milk production, while basal cells are thought to provide structural and contractile support. Here we reveal an unanticipated, pregnancy-specific role of basal epithelia as a central coordinator of lactogenesis. We demonstrate that genetic deletion of the transcription factor p63 (Trp63) gene exclusively within basal cells of the adult gland during pregnancy leads to dramatic defects in luminal cell proliferation and differentiation, resulting in lactation failure. This phenotype is explained by direct transcriptional activation of the EGF-family ligand gene Nrg1 by p63 selectively in basal cells, which is required for luminal ERBB4/STAT5A activation and consequent luminal progenitor cell maturation. Thus, paracrine basal-to-luminal cell signaling, controlled by p63 via NRG1, orchestrates the entire lactation program. Collectively, these findings redefine the paradigm for cellular interactions specifying the functional maturation of the mammary gland.
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