23 results on '"Špaková, Ivana"'
Search Results
2. An In Vivo Model of Estrogen Supplementation Concerning the Expression of Ca 2+ -Dependent Exchangers and Mortality, Vitality and Survival After Myocardial Infarction in Ovariectomized Rats.
- Author
-
Toporcer, Tomáš, Grendel, Tomáš, Špaková, Ivana, Blichárová, Alžbeta, Verbóová, Ľudmila, Benetinová, Zuzana, Čižmárová, Beata, Rabajdová, Miroslava, and Toporcerová, Silvia
- Published
- 2024
- Full Text
- View/download PDF
3. Zinc(II) niflumato complex with neocuproine: Synthesis, crystal structure, characterization and cytotoxic effects on human endometrial cell lines
- Author
-
Smolko, Lukáš, Špaková, Ivana, Klepcová, Zuzana, Dubayová, Katarína, Samoľová, Erika, Rabajdová, Miroslava, and Mareková, Mária
- Published
- 2021
- Full Text
- View/download PDF
4. The Pivotal Role of the Key Angiogenic Factors in the Development of Endometrioid Pathologies of the Uterus and Ovary.
- Author
-
Sabolová, Gabriela, Špaková, Ivana, Artimovič, Peter, Bohuš, Peter, Rabajdová, Miroslava, and Mareková, Mária
- Subjects
- *
VASCULAR endothelial growth factors , *ADENOCARCINOMA , *WOUND healing , *CELL communication , *GENOMICS , *DATA analysis , *RESEARCH funding , *OVARIAN tumors , *CELL motility , *DESCRIPTIVE statistics , *ENDOMETRIOSIS , *ENDOMETRIAL tumors , *CELL lines , *RNA , *ONE-way analysis of variance , *STATISTICS , *CONFIDENCE intervals , *DATA analysis software , *NEOVASCULARIZATION , *TRANSFORMING growth factors-beta - Abstract
Simple Summary: Angiogenesis is a synchronous mechanism of new blood vessel formation that is controlled by pro- and anti-angiogenic factors. Angiogenesis differs from tissue to tissue, especially in pathological conditions. The exact nature of the co-operation between angiogenic markers is still unknown. Herein, we describe the possible critical changes in VEGF-A, TGF-β1, ANG1, ANG2, and HIF-1α in ectopic endometriosis (with elevated pro-angiogenic factors in all studied fields), in ovarian endometrioid adenocarcinoma (showing typical upregulation on the TGF-β1 axis), and two different types of endometrial carcinoma (with an extreme pathological ANG2/ANG1 axis for mixed mesodermal tumors). Understanding the angiogenic mechanism within pathological tissues could help to improve angiogenic treatment strategies and lead to better prognoses. A characteristic feature of uterine pathologies is a specific change in cell metabolism, which predominantly manifests as a shift in the need for nutrients, thereby directing cells to engage in different angiogenic marker activities. Angiogenesis is one of the main signals supporting the survival and development of cells and tissues not only under physiological conditions. Therefore, it is necessary that we understand pathological hyperactivation in all uterine diseases, from endometriosis through ovarian endometrioid adenocarcinoma to malignant transformed cells of the uterine epithelium and body. This work presents the gene expression results of selected angiogenesis targets (VEGF-A, TGF-β1, ANG1/2, and HIF-1α), cell migration, and cell–cell interaction determined in vitro. Our results suggest that angiogenesis varies in the tested pathological conditions (ectopic endometriosis—12Z; ovarian endometrioid adenocarcinoma—A2780; tumors—SK-UT-1 and RL-95-2) compared to physiological angiogenesis (HME1). The differential expression of angiogenic factors may contribute (or is a contributing factor) to the observed differences to acknowledge an inherent variability in angiogenesis among cell lines. Determining the genomic phenomena responsible for processes associated with inadequate angiogenesis in the pelvic region could help us to develop individual treatment strategies and explain resistance to treatment. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
5. Development of novel parameter for monitoring of malignant melanoma progression
- Author
-
Špaková, Ivana, Rabajdová, Miroslava, Dubayová, Katarína, Nagyová, Vladimíra, Pilátová, Martina Bago, and Mareková, Mária
- Published
- 2020
- Full Text
- View/download PDF
6. Fluorescence biomarkers of malignant melanoma detectable in urine
- Author
-
Špaková Ivana, Dubayová Katarína, Nagyová Vladimíra, and Mareková Mária
- Subjects
nad(p)h ,lipofuscin ,hif-1α ,mitf-m ,igf1 ,Chemistry ,QD1-999 - Abstract
Malignant melanoma (MM) is a cancerous transformation of melanocytes. It is a disease with the worst response to therapy and, compared to other malignancies, presents much earlier with metastases. MM still belongs to relatively late-detected malignant diseases. Even so, the MM mortality rate is up to 96% for a relatively small incidence (5%). The gold standard for MM diagnosis is a histopathological examination that requires invasive surgery. An invasive sampling method of a biological material can be a stressful factor for the patient, which is often the reason why patients do not seek medical assistance as soon as possible. Our goal was to find a link between metabolites in urine and the stage of MM. Two excitation peaks at 360–370 nm and 450 nm were characterised in spectra of urine samples. The emission spectra have shown one significant peak at 410–460 nm. After addition of glutathione reductase to the samples, fluorescence dropped down only in patient samples and hidden fluorophores appeared. Malignant diseases are associated with the presence of specific metabolites that can be detected fluorescently in biological material such as urine, which can be a suitable alternative for an early detection of cancer or for tracking changes during and after treatment.
- Published
- 2020
- Full Text
- View/download PDF
7. Zinc(II) niflumato complex effects on MMP activity and gene expression in human endometrial cell lines
- Author
-
Rabajdová, Miroslava, Špaková, Ivana, Klepcová, Zuzana, Smolko, Lukáš, Abrahamovská, Michaela, Urdzík, Peter, and Mareková, Mária
- Published
- 2021
- Full Text
- View/download PDF
8. Effect of hypoxia factors gene silencing on ROS production and metabolic status of A375 malignant melanoma cells
- Author
-
Špaková, Ivana, Rabajdová, Miroslava, Mičková, Helena, Graier, Wolfgang F., and Mareková, Mária
- Published
- 2021
- Full Text
- View/download PDF
9. Oxidative Stress and the Nrf2/PPARγ Axis in the Endometrium: Insights into Female Fertility.
- Author
-
Artimovič, Peter, Badovská, Zuzana, Toporcerová, Silvia, Špaková, Ivana, Smolko, Lukáš, Sabolová, Gabriela, Kriváková, Eva, and Rabajdová, Miroslava
- Subjects
OXIDATIVE stress ,CELL communication ,NEOVASCULARIZATION ,FERTILITY ,PHYSIOLOGY - Abstract
Successful pregnancy depends on precise molecular regulation of uterine physiology, especially during the menstrual cycle. Deregulated oxidative stress (OS), often influenced by inflammatory changes but also by environmental factors, represents a constant threat to this delicate balance. Oxidative stress induces a reciprocally regulated nuclear factor erythroid 2-related factor 2/peroxisome proliferator-activated receptor-gamma (Nrf2/PPARγ) pathway. However, increased PPARγ activity appears to be a double-edged sword in endometrial physiology. Activated PPARγ attenuates inflammation and attenuates OS to restore redox homeostasis. However, it also interferes with physiological processes during the menstrual cycle, such as hormonal signaling and angiogenesis. This review provides an elucidation of the molecular mechanisms that support the interplay between PPARγ and OS. Additionally, it offers fresh perspectives on the Nrf2/PPARγ pathway concerning endometrial receptivity and its potential implications for infertility. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
10. Serum trace element levels and activity of enzymes associated with oxidative stress in endometriosis and endometrial cancer
- Author
-
Rabajdová, Miroslava, primary, Špaková, Ivana, additional, Smolko, Lukáš, additional, Abrahamovská, Michaela, additional, Baranovičová, Barbora, additional, Birková, Anna, additional, Vašková, Janka, additional, and Mareková, Mária, additional
- Published
- 2023
- Full Text
- View/download PDF
11. Serum trace element levels and activity of enzymes associated with oxidative stress in endometriosis and endometrial cancer.
- Author
-
Rabajdová, Miroslava, Špaková, Ivana, Smolko, Lukáš, Abrahamovská, Michaela, Baranovičová, Barbora, Birková, Anna, Vašková, Janka, and Mareková, Mária
- Subjects
ENDOMETRIAL cancer ,ENDOMETRIOSIS ,OXIDATIVE stress ,GLUTATHIONE transferase ,TRACE elements ,INTRACELLULAR space ,GLUTATHIONE reductase - Abstract
Endometriosis and endometrial cancer are closely related to oxidative stress. However, the direct relationship between copper and zinc levels and oxidative stress in the extracellular and intracellular space remains unclear. The presented study is focused on the determination of serum Zn and Cu levels, glutathione concentration and enzyme activity in three groups: patients diagnosed with endometrial cancer (EC), patients diagnosed with endometriosis (EM), and a healthy control group. Spectrophotometric determination of trace elements revealed that levels of zinc and copper were lower in blood plasma of patients with endometriosis as compared with the other groups; however, there were no significant differences in the Cu/Zn ratio. Furthermore, significantly increased blood serum glutathione levels were detected in both EM and EC groups compared with the control group. While the activity of superoxide dismutase (SOD) was similar across the studied groups, we observed differences in the activity of other enzymes associated with oxidative stress, including glutathione peroxidase (GPx), glutathione reductase (GR) and glutathione S‐transferase (GST), between the control group and the EM and EC patients. Additionally, analysis of gene expression based on free circulating mRNA indicated significant differences in the expression of SOD isoenzymes between the patient groups and the control group; expression of GPx isoenzymes was also altered. Obtained results may have potential application in diagnostics as well as monitoring of endometriosis and endometrial cancer. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
12. The Importance of Natural Antioxidants in Female Reproduction
- Author
-
Vašková, Janka, primary, Klepcová, Zuzana, additional, Špaková, Ivana, additional, Urdzík, Peter, additional, Štofilová, Jana, additional, Bertková, Izabela, additional, Kľoc, Marek, additional, and Rabajdová, Miroslava, additional
- Published
- 2023
- Full Text
- View/download PDF
13. Small Non-Coding RNAs as New Biomarkers to Evaluate the Quality of the Embryo in the IVF Process
- Author
-
Toporcerová, Silvia, primary, Špaková, Ivana, additional, Šoltys, Katarína, additional, Klepcová, Zuzana, additional, Kľoc, Marek, additional, Bohošová, Júlia, additional, Trachtová, Karolína, additional, Peterová, Lucia, additional, Mičková, Helena, additional, Urdzík, Peter, additional, Mareková, Mária, additional, Slabý, Ondřej, additional, and Rabajdová, Miroslava, additional
- Published
- 2022
- Full Text
- View/download PDF
14. Investigation of novel Mn(II) fenamato complexes with neocuproine and their effects on endometrial cell lines.
- Author
-
Klepcová, Zuzana, Špaková, Ivana, Madreiter-Sokolowski, Corina T., Graier, Wolfgang, Kalinová, Katarína, Samoová, Erika, Smolková, Romana, Smolko, Lukáš, and Rabajdová, Miroslava
- Subjects
- *
CELL lines , *MOLECULAR structure , *LIGANDS (Chemistry) , *BENZOIC acid , *ENDOMETRIAL cancer , *INFLAMMATION , *X-ray diffraction , *SCHIFF bases - Abstract
Two novel Mn(II) complexes with non-steroidal anti-inflammatory drugs, fenamic (Hfen = 2-(phenylamino)benzoic acid) and flufenamic acid (Hflu = N-(3-trifluoromethylphenyl)-2-aminobenzoic acid) and neocuproine (neo) as a supporting ligand were designed, synthesized and characterized. Their molecular structure was determined by the single-crystal X-ray diffraction method, which revealed that the complexes are isostructural and form analogous molecules [Mn(neo)(fen)2] and [Mn(neo)(flu)2]. Both complexes create an interesting structural motif resembling molecular tweezers, with an open cavity between the fenamato and flufenamato ligands, and exhibit moderate radical scavenging activity, with the fenamato complex being more active. The cytotoxic effects of the complexes were studied on three selected cell lines, including epithelial hTERT HME1 used as a healthy control, endometriotic 12Z and endometrial cancer SK-UT-1. The complexes were most active against the 12Z among the studied cell lines, while the flufenamato complex, which showed an IC50 value around 2 μM, was able to effectively trigger apoptosis through the caspase pathway. The impact of the complexes on the expression of selected genes in the tested cell lines was further investigated by qRT-PCR methods and their DNA binding properties towards the isolated genomic DNA samples were evaluated by competitive binding studies with ethidium bromide. Although some differences in the biological activity of the complexes were found, it can be concluded that both complexes target the inflammatory processes on a cellular level. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
15. Biotechnology in the process of assisted reproduction
- Author
-
Toporcerová Silvia, Špaková Ivana, Mareková Mária, and Rabajdová Mirka
- Published
- 2022
- Full Text
- View/download PDF
16. Omics applications in reproductive medicine
- Author
-
Rabajdová Miroslava, Šoltýs Katarína, Špaková Ivana, and Urdzík Peter
- Published
- 2022
- Full Text
- View/download PDF
17. List of contributors
- Author
-
Ruchika Agrawal, Pallavi Bhat Ajakkala, Amjad Ali, Qinza Ali, Gautam Anand, Faryal Mehwish Awan, Hayeqa Shahwar Awan, Amina Basheer, Maloyjo Joyraj Bhattacharjee, Isabel S. Carvalho, James Chapman, Daniel Cozzolino, Vijaya Kumar Deekshit, Salah ud Din, Shailendra Dwivedi, Shruti Dwivedi, Supriya Gupta, Mubashir Hassan, Zhixia He, Shanmugam Hemaiswarya, Chia-Hsien Hsu, Aqsa Ikram, Špaková Ivana, Yusuf Izci, Sabariswaran Kandasamy, Šoltýs Katarína, Surekha Kishore, Ballamoole Krishna Kumar, Manish Kumar, Kenneth Lundstrom, Kľoc Marek, Mareková Mária, Rabajdová Miroslava, Radhieka Misra, Sanjeev Misra, Juliet Roshini Mohan Raj, Sawaira Naqvi, Mathiyazhagan Narayanan, Anam Naz, Urdzík Peter, Purvi Purohit, Praveen Rai, Rathinam Raja, Neelam Sangwan, Fatima Shahid, Saba Shahzadi, Nishat Ahmed Sheikh, Ammara Siddique, Aiman Tanveer, Tugba Tezcan, Basant K. Tiwary, Vi Khanh Truong, Abhimanyu Vasudeva, Maaz Waseem, Dinesh Yadav, Kanchan Yadav, Nisha Yadav, Pramod K. Yadav, Zainab Yaseen, and Tahreem Zaheer
- Published
- 2022
- Full Text
- View/download PDF
18. Contributors
- Author
-
Shah Rukh Abbas, Richa Agarwal, Ruchika Agrawal, Saba Anjum, Jaspreet Singh Arora, Debmalya Barh, Siddhivinayak Barve, Muhammad Talha Basir, Attya Bhatti, Gülay Büyükköroğlu, Bilgen Çalışkan, Rekha Chawla, Mauricio Corredor, Pranjali Dhawal, Shailendra Dwivedi, Ota Fuchs, Edward Giniger, Naureen Ehsan Ilahi, Sana Ilahi, Muhammad Imran, Špaková Ivana, Zeenath Jehan, Peter John, Hari Shanker Joshi, Surekha Kishore, Birendra Kumar, Sudhir Shyam Kushwaha, Kenneth Lundstrom, Rabbiah Manzoor Malik, Sahar Malik, Rabajdová Mirka, Radhieka Misra, Sanjeev Misra, Mareková Mária, Amalia Muñoz-Gómez, Bela Nabar, Fakhira Nazir, Rasika Pawar, Abdur Rahman, Ayesha Rehman, Neelam S. Sangwan, Gençay Sevim, Anurag Sharma, Vipin Kumar Sharma, Vikas Shrivastava, Arvind Kumar Shukla, Abubakar Siddique, Toporcerová Silvia, Emine Şalva, Tahira Tayyaba, Behiye Şenel, Alka Tripathi, Abhimanyu Vasudeva, Nitin Wakchaure, Andrew P.K. Wodrich, and Vasudeo Zambare
- Published
- 2022
- Full Text
- View/download PDF
19. Detekcia expresie miRNA v IVF procese – možnosť využitia v diagnostike neplodnosti
- Author
-
Kalinová, Katarína, Remešová, Dominika, Špaková, Ivana, Toporcerová, Silvia, and Rabajdová, Miroslava
- Subjects
miREIA ,RT-PCR ,neplodnosť / infertility ,miRNA - Abstract
SÚHRN Neplodnosť v súčasnosti postihuje približne 10% populácie a na základe vysokej prevalencie je zaraďovaná Svetovou zdravotníckou organizáciou medzi populačné ochorenia. Za fyziologických okolností sú v reprodukcii kľúčovými procesmi okno implantácie a receptivita endometria, ktoré podliehajú regulácii na génovej úrovni. Narušením tejto regulácie, môže následne dôjsť k patologickým zmenám, ktoré prispievajú k poruchám plodnosti. Hlavnými faktormi, ktoré ovplyvňujú reguláciu génovej expresie sú nekódujúce RNA, ktoré modifikujú génovú expresiu najmä na posttranskripčnej úrovni. Posttranskripčná úroveň regulácie sa považuje za kľúčovú pri vzniku rôznych deregulácií. Ich naakumulovaním môže dôjsť k vzniku rôznych patologických procesov. Objasnením mechanizmu pôsobenia konkrétnych nekódujúcich RNA v rámci infertility sa ukazuje ako možnosť ich využitia v diagnostike. Využitím detekcie citlivých miRNA markerov sa celý proces diagnostiky môže významne urýchliť a tiež prispieť k zlepšeniu výsledku liečby neplodnosti. ABSTRACT Infertility affects about 10% of the population currently and, due to its high prevalence, is classified by the World Health Organization as a population disease. Under physiological circumstances, the key processes in reproduction are implantation window and endometrial receptivity, which are regulated at the gene level. By disrupting this regulation, pathological changes can subsequently occur, which contribute to fertility disorders. The main factors that influence the regulation of gene expression are non-coding RNAs that modify gene expression, especially at the post-transcriptional level. The post-transcriptional level of regulation is considered to be key in the emergence of various dysregulations. Accumulation of this dysregulations can lead to various pathological processes. By elucidating the mechanism of action of specific non-coding RNAs in the context of infertility, is possible to use them in diagnostic process. By using the detection of sensitive miRNA markers, the whole diagnostic process can be significantly accelerated and also contribute to improving the outcome of infertility treatment., Práca vznikla na základe grantovej podpory: VEGA 1/0873/18 a VEGA 1/0620/19. Tieto projekty sú realizované v spolupráci s Gynekologicko-pôrodníckou klinikou UPJŠ LF a UNLP v Košiciach a Centrom pre asistovanú reprodukciu Gyncare v Košiciach., {"references":["BioVendor (2021a): miRNA-RT-qPCR. Dostupné na: https:// www.biovendor.com/mirna-rt-qpcr (Accessed: 7 March 2021).","BioVendor (2021b): Two-Tailed RT-qPCR. Dostupné na: https://www.biovendor.com/two-tailed-rt-qpcr (Accessed: 7 March 2021).","Buh Gašparič, M. et al. (2010): Comparison of nine different real-time PCR chemistries for qualitative and quantitative applications in GMO detection. Analytical and Bioanalytical Chemistry, 396(6), pp. 2023–2029. doi: 10.1007/s00216-009- 3418-0.","Butler, A. E. et al. (2020): Increased MicroRNA Levels in Women With Polycystic Ovarian Syndrome but Without Insulin Resistance: A Pilot Prospective Study. Frontiers in Endocrinology, 11. doi: 10.3389/fendo.2020.571357.","Benes, V., Castoldi, M. (2010): Expression profiling of microRNA using real-time quantitative PCR, how to use it and what is available. Methods. Methods, pp. 244–249. doi: 10. 1016/j.ymeth.2010.01.026.","Chen, Y. H. et al. (2013): miRNA-93 inhibits GLUT4 and is overexpressed in adipose tissue of polycystic ovary syndrome patients and women with insulin resistance. Diabetes, 62(7), pp. 2278–2286. doi: 10.2337/db12-0963.","Cho, S. et al. (2015): Circulating microRNAs as potential biomarkers for endometriosis. Fertility and Sterility, 103(5), pp. 1252–1260.e1. doi: 10.1016/j.fertnstert.2015.02.013.","Dehghan, Z., Mohammadi-Yeganeh, S. and Salehi, M. (2020): miRNA-155 regulates cumulus cells function, oocyte maturation, and blastocyst formation. Biology of Reproduction, 103(3), pp. 548–559. doi: 10.1093/biolre/ioaa098.","Devesa-Peiró, A., Sánchez-Reyes, J. M. and Díaz-Gimeno, P. (2020): Molecular biology approaches utilized in preimplantation genetics: real-time PCR, microarrays, next-generation sequencing, karyomapping, and others. in Human Reproductive Genetics. Elsevier, pp. 49–67. doi: 10.1016/ b978-0-12-816561-4.00004-1.","Ding, C. F. et al. (2015): Circulating microRNAs in patients with polycystic ovary syndrome. Human Fertility, 18(1), pp. 22–29. doi: 10.3109/14647273.2014.956811.","Ha, M. and Kim, V. N. (2014): Regulation of microRNA biogenesis. Nature Reviews Molecular Cell Biology. Nature Publishing Group, pp. 509–524. doi: 10.1038/nrm3838.","Hale, B. J. et al. (2015): Small RNAs: Their possible roles in reproductive failure. In Advances in Experimental Medicine and Biology. Springer New York LLC, pp. 49–79. doi: 10.1007/ 978-3-319-18881-2_3.","Hosseini, A. H. et al. (2017): Association of miR-146a rs2910164 and miR-222 rs2858060 polymorphisms with the risk of polycystic ovary syndrome in Iranian women: A case– control study. Taiwanese Journal of Obstetrics and Gynecology, 56(5), pp. 652–656. doi: 10.1016/j.tjog.2017.08.014.","Huang, J. et al. (2020): Endometrium Gene Expression and Epigenetic Regulation in Reproductive Failure. In Endometrial Gene Expression. Springer International Publishing, pp. 103–116. doi: 10.1007/978-3-030-28584-5_7","Izakova, J. (2018): miREIA—microRNA Enzyme Immunoassay (Technical note). Available at: https://www.biovendor.com/mireia--microrna-enzyme-immunoassay-technical-note?utm_source=google&utm_medium=organic (Accessed: 31 January 2021).","Jia, S. Z. et al. (2013): Plasma miR-17-5p, miR-20a and miR22 are down-regulated in women with endometriosis. Human Reproduction, 28(2), pp. 322–330. doi: 10.1093/humrep/ des413.","Kamalidehghan, B. et al. (2020): The importance of small non-coding RNAs in human reproduction: A review article. Application of Clinical Genetics. Dove Medical Press Ltd., pp. 1–11. doi: 10.2147/TACG.S207491.","Kappel, A. et al. (2015): MicroRNA in vitro diagnostics using immunoassay analyzers. Clinical Chemistry, 61(4), pp. 600–607. doi: 10.1373/clinchem.2014.232165.","Klepcová, Z. et al. (2020): MikroRNA a triple negatívny karcinóm prsníka. Lekársky Obzor, 69(4), pp. 134–139.","Krepelkova, I. et al. (2019): Evaluation of miRNA detection methods for the analytical characteristics necessary for clinical utilization. BioTechniques, 66(6), pp. 277–284. doi: 10. 2144/btn-2019-0021.","Kurita, T., Terakawa, J. (2020): Endometrial Development and Its Fine Structure. In Endometrial Gene Expression. Springer International Publishing, pp. 1–32. doi: 10.1007/978- 3-030-28584-5_1.","Lam, E. W. F., Shah, K. and Brosens, J. J. (2012): The diversity of sex steroid action: The role of micro-RNAs and FOXO transcription factors in cycling endometrium and cancer. J. Endocrinol., pp. 13–25. doi: 10.1530/JOE-10-0480","MacFarlane, L.-A., R. Murphy, P. (2010): MicroRNA: Biogenesis, Function and Role in Cancer. Current Genomics, 11(7), pp. 537–561. doi: 10.2174/138920210793175895.","Matsuyama, H. and Suzuki, H. I. (2020): Systems and synthetic microRNA biology: From biogenesis to disease pathogenesis. International Journal of Molecular Sciences. MDPI AG. doi: 10.3390/ijms21010132.","Mcallister, J. M. et al. (2019): miRNA Profiling Reveals miRNA-130b-3p Mediates DENND1A Variant 2 Expression and Androgen Biosynthesis. Endocrinology, 160(8), pp. 1964– 1981. doi: 10.1210/en.2019-00013.","Murphy, C. R. (2004): Uterine receptivity and the plasma membrane transformation. Cell Research, pp. 259–267. doi: 10.1038/sj.cr.7290227.","Ohlsson Teague, E. M. C., Print, C. G., Hull, M. L. (2009): The role of microRNAs in endometriosis and associated reproductive conditions. Hum Reprod Update, pp. 142–165. doi: 10.1093/humupd/dmp034.","Öner, Ç. (2019): Two different mechanisms of two different non-coding RNAs—MicroRNAs and PIWI-interacting RNAs: From origin to cancer. In AGO-Driven Non-Coding RNAs. Elsevier, pp. 3–34. doi: 10.1016/b978-0-12-815669-8. 00001-4.","Pan, Q. et al. (2007): The expression profile of micro-RNA in endometrium and endometriosis and the influence of ovarian steroids on their expression. Molecular Human Reproduction, 13(11), pp. 797–806. doi: 10.1093/molehr/gam063.","Pateisky, P. et al. (2018): hsa-miRNA-154-5p expression in plasma of endometriosis patients is a potential diagnostic marker for the disease. Reproductive BioMedicine Online, 37(4), pp. 449–466. doi: 10.1016/j.rbmo.2018.05.007.","Petracco, R. et al. (2011): MicroRNA 135 regulates HOXA10 expression in endometriosis. Journal of Clinical Endocrinology and Metabolism, 96(12). doi: 10.1210/jc.2011-1231.","Rabajdová, M. et al. (2017): Analysis of transcriptional activities of angiogenic biomarkers during intrauterine complications leading to preterm birth. European review for medical and pharmacological sciences, 21(7), pp. 1433–1442.","Rekker, K. et al. (2015): Circulating miR-200-family micro-RNAs have altered plasma levels in patients with endometriosis and vary with blood collection time. Fertility and Sterility, 104(4), pp. 938–946.e2. doi: 10.1016/j.fertnstert. 2015.06.029.","Ruiz-Alonso, M., Blesa, D., Simón, C. (2012): The genomics of the human endometrium. Biochimica et Biophysica Acta (BBA)—Molecular Basis of Disease, 1822(12), pp. 1931–1942. doi: 10.1016/j.bbadis.2012.05.004.","Sathyapalan, T. et al. (2015): Increased expression of circulating miRNA-93 in women with polycystic ovary syndrome may represent a novel, non-invasive biomarker for diagnosis. Endocrine Abstracts. doi: 10.1530/endoabs.38.p354.","Sirotkin, A. V. et al. (2009): Identification of microRNAs controlling human ovarian cell steroidogenesis via a genome-scale screen. Journal of Cellular Physiology, 219(2), pp. 415–420. doi: 10.1002/jcp.21689.","Song, J., Luo, S., Li, S. W. (2015): miRNA-592 is downregulated and may target LHCGR in polycystic ovary syndrome patients. Reproductive Biology, 15(4), pp. 229–237. doi: 10. 1016/j.repbio.2015.10.005.","Song, Y. et al. (2019): Altered miR-186 and miR-135a contribute to granulosa cell dysfunction by targeting ESR2: A possible role in polycystic ovary syndrome. Molecular and Cellular Endocrinology, 494, p. 110478. doi: 10.1016/j.mce. 2019.110478.","Sørensen, A. E. et al. (2014): MicroRNAs related to polycystic ovary syndrome (PCOS). Genes. MDPI AG, pp. 684–708. doi: 10.3390/genes5030684.","Stejskal, D. et al. (2019): Comparison of a new immunoassay and PCR-based method for quantification of microRNAs in whole blood. A pilot methodical study. Biomedical Papers, 163(1), pp. 39–44. doi: 10.5507/bp.2018.080.","Tabrizi, Z. P. F. et al. (2020): Plasma Levels of miR-27a, miR-130b, and miR-301a in Polycystic Ovary Syndrome. International Journal of Molecular and Cellular Medicine, 9(3), pp. 198–206. doi: 10.22088/IJMCM.BUMS.9.3.198.","Wang, Q. et al. (2021): Association of miRNA-145 with the occurrence and prognosis of hydrosalpinx-induced defective endometrial receptivity. Bosnian Journal of Basic Medical Sciences, 21(1), pp. 81–92. doi: 10.17305/bjbms.2020.4538.","Zeka, F., Mestdagh, P., Vandesompele, J. (2015): RT-qPCRbased quantification of small non-coding RNAs. Methods in Molecular Biology, 1296, pp. 85–102. doi: 10.1007/978-1- 4939-2547-6_9."]}
- Published
- 2021
- Full Text
- View/download PDF
20. Is There a Role for the IGF System and Epidermal Growth Factor (EGF) in the Pathogenesis of Adrenocortical Adenomas? A Preliminary Case-Control Study.
- Author
-
LAZÚROVÁ, Ivica, JOCHMANOVÁ, Ivana, SOTAK, Štefan, ŠPAKOVÁ, Ivana, and MAREKOVÁ, Mária
- Subjects
EPIDERMAL growth factor ,METABOLIC syndrome ,GROWTH factors ,CASE-control method ,INSULIN resistance ,INTERLEUKIN-23 ,SOMATOTROPIN - Abstract
Adrenal incidentalomas (AI) are very common and mostly they are non-functioning adenomas (NFA). NFAs are often associated with insulin resistance and metabolic syndrome. Several biomarkers, including certain growth factors, may participate in the pathogenesis of metabolic changes in patients with adrenal adenomas. Patients with NFA and age-matched control subjects were enrolled in the study. Data on age, gender, presence of metabolic syndrome or its components were obtained for each subject. Blood samples were obtained and glycemia, insulinemia, lipid profile, and selected growth factor levels were measured. Forty-three patients with NFA and 40 controls were included in the study. Differences were not found in the metabolic syndrome and its components prevalence or in the biochemical profile between patients and the control group. Significant differences were noticed in the levels of IGF1, IGF2, and IGFBP3 (p=0.016, p=0.005, p=0.004, respectively), but there were no differences in VEGF or EGF concentrations. In NFA patients, an association between glycemia and EGF levels was present (p=0.026). No significant correlations between tumor size and insulin or growth factor concentrations were present in AI patients. Significantly higher serum IGF1, IGF2, and IGFBP3 concentrations in NFA patients may support the role of the IGF axis in the pathogenesis of adrenocortical lesions. No correlation between IGFs or IGFBP3 and parameters of glucose or lipid metabolism was found. Present results may support the role of the growth hormone axis rather than hyperinsulinemia and insulin resistance in the pathogenesis of adrenocortical adenomas. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
21. Detection of Pathological Changes in the Aorta during Thoracic Aortic Aneurysm Progression on Molecular Level
- Author
-
Rabajdová, Miroslava, primary, Urban, Peter, additional, Špaková, Ivana, additional, Panagiotis, Artemiou, additional, Ferenčáková, Michaela, additional, Rybár, Dušan, additional, Bobrov, Nikita, additional, Sabol, František, additional, and Mareková, Mária, additional
- Published
- 2017
- Full Text
- View/download PDF
22. The Importance of MITF Signaling Pathway in the Regulation of Proliferation and Invasiveness of Malignant Melanoma
- Author
-
Urban, Peter, primary, Rabajdová, Miroslava, additional, Veliká, Beáta, additional, Špaková, Ivana, additional, Bolerázska, Beáta, additional, and Mareková, Mária, additional
- Published
- 2016
- Full Text
- View/download PDF
23. Effect of Vitamin D Receptor Polymorphisms on the Development and Progression of Malignant Melanoma
- Author
-
Špaková, Ivana, primary, Bilecová-Rabajdová, Miroslava, additional, Zábavníková, Marianna, additional, Urban, Peter, additional, and Mereková, Mária, additional
- Published
- 2014
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.