25 results on '"James R Cochrane"'
Search Results
2. Methylglyoxal, a glycolysis side-product, induces Hsp90 glycation and YAP-mediated tumor growth and metastasis
- Author
-
Marie-Julie Nokin, Florence Durieux, Paul Peixoto, Barbara Chiavarina, Olivier Peulen, Arnaud Blomme, Andrei Turtoi, Brunella Costanza, Nicolas Smargiasso, Dominique Baiwir, Jean L Scheijen, Casper G Schalkwijk, Justine Leenders, Pascal De Tullio, Elettra Bianchi, Marc Thiry, Koji Uchida, David A Spiegel, James R Cochrane, Craig A Hutton, Edwin De Pauw, Philippe Delvenne, Dominique Belpomme, Vincent Castronovo, and Akeila Bellahcène
- Subjects
carbonyl stress ,glyoxalase 1 ,LATS1 ,breast cancer ,methylglyoxal ,YAP ,Medicine ,Science ,Biology (General) ,QH301-705.5 - Abstract
Metabolic reprogramming toward aerobic glycolysis unavoidably induces methylglyoxal (MG) formation in cancer cells. MG mediates the glycation of proteins to form advanced glycation end products (AGEs). We have recently demonstrated that MG-induced AGEs are a common feature of breast cancer. Little is known regarding the impact of MG-mediated carbonyl stress on tumor progression. Breast tumors with MG stress presented with high nuclear YAP, a key transcriptional co-activator regulating tumor growth and invasion. Elevated MG levels resulted in sustained YAP nuclear localization/activity that could be reverted using Carnosine, a scavenger for MG. MG treatment affected Hsp90 chaperone activity and decreased its binding to LATS1, a key kinase of the Hippo pathway. Cancer cells with high MG stress showed enhanced growth and metastatic potential in vivo. These findings reinforce the cumulative evidence pointing to hyperglycemia as a risk factor for cancer incidence and bring renewed interest in MG scavengers for cancer treatment.
- Published
- 2016
- Full Text
- View/download PDF
3. 'Spiritual Capacities' in Psychological Research: Confronting the Appearances
- Author
-
James R. Cochrane, Naiema Taliep, Sandy Lazarus, Douglas McGaughey, Dan Christie, Mohamed Seedat, Teresa Cutts, and Gary Gunderson
- Abstract
Researching phenomena associated with religion or spirituality faces a triple conundrum not easily resolved: What counts as religion or spirituality, are they independent or derivative phenomena, and can they be empirically determined at all? Appropriately, therefore, a recent special issue of the journal Psychology of Religion and Spirituality asks: What is its object of study? We argue that this cannot be resolved merely by considering diverse religious or spiritual phenomena. It requires a turn instead to what grounds religious and spiritual experience. Illustrating this claim from field research on “spiritual capacities and religious assets for health” in the face of interpersonal violence in two local communities, we argue that a set of supersensible, non-material, and therefore “spiritual” but nonetheless real human capacities that we must assume human beings possess, ground the sensible, empirical phenomena or “appearances” we call religion or spirituality. The notion of supersensible spiritual capacities, by definition incapable of empirical proof or disproof, places strict limits on phenomenal claims about religion or spirituality, particularly ontological ones. Although studying the phenomena or appearances remains important, paying attention to spiritual capacities enables us better to grasp the contingent nature of such phenomena while grounding them in that innate and general disposition of the human being—which we tentatively define as the C-factor.
- Published
- 2022
- Full Text
- View/download PDF
4. Handbook on Religion and Health : Pathways for a Turbulent Future
- Author
-
James R. Cochrane, Gary R. Gunderson, Teresa Cutts, James R. Cochrane, Gary R. Gunderson, and Teresa Cutts
- Subjects
- Medicine--Religious aspects--Handbooks, manuals, etc, Health--Religious aspects--Handbooks, manuals, etc, Public health--Religious aspects--Handbooks, manuals, etc
- Abstract
This revelatory Handbook explores the relationship between religion and health, emphasising the effects of organised religion and spirituality on community, population, and public health. While comprehensively summarising the current state of the field, it focusses on pursuing new pathways vital for human health in a turbulent world.Bringing together an impressive array of internationally recognised experts, the Handbook on Religion and Health outlines a number of conceptual and theoretical frameworks for the field. Chapters examine religion and health on the micro, macro, and meso levels, before analysing wider, more holistic understandings of religion and health, through ecological, de-colonial, and sociological perspectives. Chapter authors also assess religion and health from the grassroots, and the centrality of the community to experiences of disease and spirituality.Expertly traversing an interdisciplinary area which is constantly expanding, this Handbook is a fascinating resource for students and scholars of health policy, religious studies, and cultural sociology. It will also appeal to practitioners and policy makers in global organisations operating in the public health sector.
- Published
- 2024
5. GOD IN CONTEXT: THE SYMBOLIC CONSTRUCTION OF A RELIGIOUS UNIVERSE IN A BASE CHRISTIAN COMMUNITY
- Author
-
James R Cochrane
- Subjects
Latin Americans ,Active listening ,Context (language use) ,The Symbolic ,Gender studies ,Sociology ,Settlement (litigation) ,Metropolitan area ,Universe (mathematics) - Abstract
‘We have depended,’ says Teresa Okure, ‘either on expatriates … or on African men to speak for us theologically and otherwise. Has the time now come to speak for ourselves? Okure’s question is asked as an African woman, but in South Africa at least, it can also be asked for marginalized and oppressed black groups as a whole. The concern of this essay is to reflect on the speaking of a small base Christian community in a large informal peri-urban settlement, similar to the favellas of Latin America, outside the Durban metropolitan area. The first step is ‘listening to’ what they have to say.
- Published
- 2020
- Full Text
- View/download PDF
6. African theology
- Author
-
James R. Cochrane
- Subjects
Social order ,Politics ,Political theology ,Christian theology ,Kairos ,Criticism ,Africanization ,Sociology ,Religious studies ,Black theology - Abstract
Christian theology, whether African or not, for most of its history and even in its most introspective moments, has either explicitly or implicitly always had something to do with the political or the public. Public or political theology is implicit when it happily coexists with the dominant political order but its impact is indirect, a side effect of what theology says to its primary addressee, the Christian community itself. Africa is not short of public or political theologies that express either resistance to, or strong criticism of, a dominant social order, laying bare its contradictions and/or the harm it may do. They include theologies of inculturation or Africanization, black theology and Kairos theology in South Africa, African women’s theology, theologies concerned with issues of sexual orientation, and postcolonial theology. African Christian theology lives alongside Islamic theologies and African indigenous thought.
- Published
- 2020
- Full Text
- View/download PDF
7. Religion, Health, and Wellbeing
- Author
-
Gary R. Gunderson, Heather Wood Ion, and James R. Cochrane
- Subjects
medicine.medical_specialty ,Public health ,Agency (sociology) ,medicine ,Sociology ,Public administration ,Vitality - Published
- 2018
- Full Text
- View/download PDF
8. Hormetic potential of methylglyoxal, a side-product of glycolysis, in switching tumours from growth to death
- Author
-
David Spiegel, Koji Uchida, Craig A. Hutton, Justine Bellier, Akeila Bellahcene, Florence Durieux, Olivier Peulen, Marie-Julie Nokin, Vincenzo Castronovo, and James R. Cochrane
- Subjects
Glycation End Products, Advanced ,0301 basic medicine ,NF-E2-Related Factor 2 ,lcsh:Medicine ,Article ,03 medical and health sciences ,chemistry.chemical_compound ,Lactoylglutathione lyase ,Hormesis ,0302 clinical medicine ,Glycation ,Cell Line, Tumor ,Neoplasms ,Humans ,Glycolysis ,lcsh:Science ,Cell Proliferation ,Multidisciplinary ,Cell Death ,biology ,Cell growth ,Methylglyoxal ,lcsh:R ,Lactoylglutathione Lyase ,Pyruvaldehyde ,030104 developmental biology ,chemistry ,Biochemistry ,Anaerobic glycolysis ,030220 oncology & carcinogenesis ,Cancer cell ,biology.protein ,Cancer research ,lcsh:Q ,Glyoxalase system - Abstract
Metabolic reprogramming toward aerobic glycolysis unavoidably favours methylglyoxal (MG) and advanced glycation end products (AGEs) formation in cancer cells. MG was initially considered a highly cytotoxic molecule with potential anti-cancer value. However, we have recently demonstrated that MG enhanced tumour growth and metastasis. In an attempt to understand this dual role, we explored MG-mediated dicarbonyl stress status in four breast and glioblastoma cancer cell lines in relation with their glycolytic phenotype and MG detoxifying capacity. In glycolytic cancer cells cultured in high glucose, we observed a significant increase of the conversion of MG to D-lactate through the glyoxalase system. Moreover, upon exogenous MG challenge, glycolytic cells showed elevated amounts of intracellular MG and induced de novo GLO1 detoxifying enzyme and Nrf2 expression. Thus, supporting the adaptive nature of glycolytic cancer cells to MG dicarbonyl stress when compared to non-glycolytic ones. Finally and consistent with the pro-tumoural role of MG, we showed that low doses of MG induced AGEs formation and tumour growth in vivo, both of which can be reversed using a MG scavenger. Our study represents the first demonstration of a hormetic effect of MG defined by a low-dose stimulation and a high-dose inhibition of tumour growth.
- Published
- 2017
- Full Text
- View/download PDF
9. The role of religious leaders in anti-Apartheid mobilisation: implications for violence prevention in contemporary South Africa
- Author
-
Naiema Taliep, Sandy Lazarus, James R. Cochrane, and Mohamed Seedat
- Subjects
Sociology and Political Science ,media_common.quotation_subject ,05 social sciences ,Religious studies ,050109 social psychology ,Gender studies ,Structural violence ,0506 political science ,State (polity) ,050602 political science & public administration ,0501 psychology and cognitive sciences ,Sociology ,Anti apartheid ,media_common - Abstract
This study examines how South African religious leaders mobilised spiritual capacity and religious assets to resist and fight against state and structural violence during the 1970s and 1980s. Docum...
- Published
- 2016
- Full Text
- View/download PDF
10. ReligioninSustainable Development
- Author
-
James R. Cochrane
- Subjects
Sustainable development ,060303 religions & theology ,Economic growth ,Sociology and Political Science ,05 social sciences ,World War II ,Religious studies ,050109 social psychology ,06 humanities and the arts ,0603 philosophy, ethics and religion ,World health ,Development policy ,Political science ,Sustainability ,0501 psychology and cognitive sciences - Abstract
After World War II religion was effectively rejected or sidelined in development policy and practice. Newly emerging international agencies—like the United Nations (UN), the World Health Organizati...
- Published
- 2016
- Full Text
- View/download PDF
11. The International Encyclopedia of Anthropology
- Author
-
Sharyn Graham Davies, Claire Lowrie, Karenleigh Anne Overmann, Justin Lane, Caroline Schuster, James R. Cochrane, and Alana Jelinek
- Subjects
Firth ,media_common.quotation_subject ,Art ,Archaeology ,media_common - Published
- 2018
- Full Text
- View/download PDF
12. On freedom
- Author
-
James R. Cochrane
- Published
- 2018
- Full Text
- View/download PDF
13. Total Synthesis and Reassignment of the Structures of the Antimicrobial Lipodepsipeptides Circulocin γ and δ
- Author
-
Katrina A. Jolliffe, James R. Cochrane, and Claudia J. Exner
- Subjects
chemistry.chemical_classification ,Molecular Structure ,Chemistry ,Stereochemistry ,Organic Chemistry ,Absolute configuration ,Fatty acid ,Total synthesis ,Coupling reaction ,chemistry.chemical_compound ,Anti-Infective Agents ,Depsipeptides ,Side chain ,Molecule ,Epimer ,Methylene ,Antimicrobial Cationic Peptides - Abstract
The structures of the naturally occurring antimicrobial lipodepsipeptides circulocin γ and circulocin δ have been reported to comprise a common cyclic depsipeptide core attached to 3-hydroxy,ω-guanidino fatty acid chains differing in length by two methylene units, but analysis of the reported data suggested that the originally reported structures had incorrect side chain lengths. The total synthesis of both side chain epimers of the originally reported structure of circulocin γ bearing a 19-guanidino-3-hydroxynonadecanoyl (GHND) side chain has been accomplished using a modular approach involving synthesis of the cyclic depsipeptide and side chain fragments followed by a late stage coupling reaction. This revealed that the originally reported structure for circulocin γ bearing the GHND side chain is incorrect and that this structure is actually that of circulocin δ. It has also enabled the absolute configuration of the side chain hydroxy group of the natural product to be assigned as (R). Subsequent synthesis of the analogue bearing a 17-guanidino-3-(R)-hydroxyheptadecanoyl (GHHD) side chain provided confirmation that this revised structure is that of circulocin γ.
- Published
- 2015
- Full Text
- View/download PDF
14. 'Breathing' Motion of a Modulable Molecular Cavity
- Author
-
Sebastiano Di Pietro, Alexandre Martinez, James R. Cochrane, Dawei Zhang, Jean-Pierre Dutasta, Heinz Gornitzka, Laure Guy, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, East China Normal University [Shangaï] (ECNU), Laboratoire de Chimie - UMR5182 (LC), École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT), Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-École normale supérieure - Lyon (ENS Lyon)-Institut de Chimie du CNRS (INC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Université Fédérale Toulouse Midi-Pyrénées
- Subjects
molecular cages ,Solid-state ,Motion (geometry) ,Vanadium ,chemistry.chemical_element ,chirality ,010402 general chemistry ,01 natural sciences ,Catalysis ,hemicryptophane ,Metal ,Computational chemistry ,[CHIM]Chemical Sciences ,Quantitative Biology::Biomolecules ,010405 organic chemistry ,Chemistry ,Ligand ,Folded structure ,Organic Chemistry ,Chemistry (all) ,General Chemistry ,Nuclear magnetic resonance spectroscopy ,imploded conformation ,molecular switch ,0104 chemical sciences ,Chemical physics ,visual_art ,visual_art.visual_art_medium - Abstract
International audience; A class of hemicryptophane cages that adopt imploded conformations in solution and in the solid state has been described and studied by NMR spectroscopy and X-ray crystallography. It is reported that the degree of collapse of the molecular cavity can be controlled by changing the stereochemistry of the chiral elements of the hemicryptophanes, leading to a modulation of their physical and chemical properties. Upon the binding of an oxidovanadium unit, the collapsed molecular cavity can inflate to give an expanded conformation. Removal of the vanadium core by an ancillary complexing ligand restores the initial folded structure. Thus, coordination/de-coordination of the metal ion controls the dynamic motions of the cage, leading to a reversible nanomechanical process. This controlled motion between a collapsed and expanded cavity can be seen as that of a breathable molecular cage. There is an increased interest in the synthesis and development of systems able to perform a defined function at the molecular level. [1] For instance, molecular machines can produce quasi-mechanical movements (output) in response to specific stimuli (input). Currently, synthetic systems mimicking the ability of brakes, [2a]
- Published
- 2017
- Full Text
- View/download PDF
15. Community asset mapping as an action research strategy for developing an interpersonal violence prevention programme in South Africa
- Author
-
Hazel Swanepoel, Anna-Marie James, Jill Olivier, Naiema Taliep, Mohamed Seedat, Sandy Lazarus, Samed Bulbulia, and James R. Cochrane
- Subjects
Organizational Behavior and Human Resource Management ,Sociology and Political Science ,business.industry ,Strategy and Management ,05 social sciences ,050401 social sciences methods ,Community-based participatory research ,Public relations ,Interpersonal violence ,0504 sociology ,0502 economics and business ,Asset (economics) ,Sociology ,Action research ,business ,050203 business & management - Abstract
The aim of this article was to report and critically reflect on community asset mapping processes used to develop a contextually valid interpersonal violence prevention programme in South Africa to...
- Published
- 2020
- Full Text
- View/download PDF
16. Identifying and Mobilising Factors That Promote Community Peace
- Author
-
Candice Simmons, Naiema Taliep, Sandy Lazarus, James R. Cochrane, and Mohamed Seedat
- Subjects
business.industry ,Values education ,Peace psychology ,Political science ,Community health ,Economic security ,Peacebuilding ,Community-based participatory research ,Participatory action research ,Public relations ,business ,Qualitative research - Abstract
The identification and mobilisation of factors that promote peace is central to peace promotion. Through a community-based participatory research project, SCRATCHMAPS (Spiritual Capacity and Religious Assets for Transforming Community Health through mobilising Males for Peace and Safety), a grounded-theoretical study in a low-income community in South Africa, including both quantitative and qualitative methods and forms of analysis, was conducted to explore community members’ perceptions of factors that promote peace. The findings presented in this chapter reveal a major emphasis on ‘intangible’ factors, many of them linked to a new concept of ‘spiritual capacity’, that the community believe play a central role in promoting peace. In line with initiatives that combine research and action in efforts to promote peace, the authors briefly describe how these findings were used to direct a community intervention aimed at mobilising religious assets and enabling spiritual capacity to promote peace. Structural factors such as employment and economic security are centrally important in any attempts to promote peace, but the authors argue that more attention should be focused on understanding and mobilising factors such as compassion, respect, and hope, at different levels of the social system. This raises a number of challenges to those involved in peace psychology.
- Published
- 2016
- Full Text
- View/download PDF
17. Methylglyoxal, a glycolysis side-product, induces Hsp90 glycation and YAP-mediated tumor growth and metastasis
- Author
-
Barbara Chiavarina, Brunella Costanza, Justine Leenders, Philippe Delvenne, Elettra Bianchi, James R. Cochrane, Koji Uchida, Pascal de Tullio, Paul Peixoto, Akeila Bellahcene, Craig A. Hutton, Olivier Peulen, Dominique Baiwir, Marc Thiry, Casper G. Schalkwijk, Vincent Castronovo, Andrei Turtoi, Dominique Belpomme, Arnaud Blomme, Florence Durieux, Jean L.J.M. Scheijen, Nicolas Smargiasso, Marie-Julie Nokin, Edwin De Pauw, David Spiegel, Promovendi CD, Interne Geneeskunde, MUMC+: MA Alg Interne Geneeskunde (9), RS: CARIM - R3.01 - Vascular complications of diabetes and the metabolic syndrome, Université de Liège, Institut de Recherche en Cancérologie de Montpellier (IRCM - U1194 Inserm - UM), CRLCC Val d'Aurelle - Paul Lamarque-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Maastricht University [Maastricht], Cardiovascular Research Institute Maastricht (CARIM), Centre Hospitalier Universitaire de Liège (CHU-Liège), Nagoya University, Yale University [New Haven], University of Melbourne, and Association for Research and Treatments Against Cancer (ARTAC)
- Subjects
Glycation End Products, Advanced ,0301 basic medicine ,Glycosylation ,Metastasis ,chemistry.chemical_compound ,Lactoylglutathione lyase ,Glycation ,cell biology ,methylglyoxal ,Neoplasm Metastasis ,Biology (General) ,cancer biology ,General Neuroscience ,MESH: Glycation End Products, Advanced ,Methylglyoxal ,General Medicine ,Pyruvaldehyde ,MESH: Glycosylation ,Aerobiosis ,LATS1 ,3. Good health ,carbonyl stress ,MESH: Glycolysis ,Medicine ,YAP ,Glycolysis ,Research Article ,medicine.medical_specialty ,MESH: Pyruvaldehyde ,MESH: Cell Line, Tumor ,QH301-705.5 ,Science ,chicken ,Breast Neoplasms ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Biology ,MESH: Phosphoproteins ,glyoxalase 1 ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,breast cancer ,Cell Line, Tumor ,MESH: Aerobiosis ,MESH: Cell Proliferation ,Internal medicine ,MESH: HSP90 Heat-Shock Proteins ,medicine ,Humans ,HSP90 Heat-Shock Proteins ,human ,[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM] ,mouse ,Adaptor Proteins, Signal Transducing ,Cell Proliferation ,MESH: Adaptor Proteins, Signal Transducing ,Hippo signaling pathway ,MESH: Humans ,General Immunology and Microbiology ,YAP-Signaling Proteins ,Phosphoproteins ,medicine.disease ,MESH: Neoplasm Metastasis ,030104 developmental biology ,Endocrinology ,chemistry ,Tumor progression ,Anaerobic glycolysis ,MESH: Protein Processing, Post-Translational ,Cancer cell ,biology.protein ,Cancer research ,Protein Processing, Post-Translational ,MESH: Breast Neoplasms ,Transcription Factors - Abstract
Metabolic reprogramming toward aerobic glycolysis unavoidably induces methylglyoxal (MG) formation in cancer cells. MG mediates the glycation of proteins to form advanced glycation end products (AGEs). We have recently demonstrated that MG-induced AGEs are a common feature of breast cancer. Little is known regarding the impact of MG-mediated carbonyl stress on tumor progression. Breast tumors with MG stress presented with high nuclear YAP, a key transcriptional co-activator regulating tumor growth and invasion. Elevated MG levels resulted in sustained YAP nuclear localization/activity that could be reverted using Carnosine, a scavenger for MG. MG treatment affected Hsp90 chaperone activity and decreased its binding to LATS1, a key kinase of the Hippo pathway. Cancer cells with high MG stress showed enhanced growth and metastatic potential in vivo. These findings reinforce the cumulative evidence pointing to hyperglycemia as a risk factor for cancer incidence and bring renewed interest in MG scavengers for cancer treatment. DOI: http://dx.doi.org/10.7554/eLife.19375.001
- Published
- 2016
- Full Text
- View/download PDF
18. Author response: Methylglyoxal, a glycolysis side-product, induces Hsp90 glycation and YAP-mediated tumor growth and metastasis
- Author
-
Jean L.J.M. Scheijen, Andrei Turtoi, James R. Cochrane, Florence Durieux, Dominique Baiwir, Paul Peixoto, Marie-Julie Nokin, Dominique Belpomme, Akeila Bellahcene, Pascal De Tullio, Edwin De Pauw, David Spiegel, Elettra Bianchi, Vincent Castronovo, Marc Thiry, Nicolas Smargiasso, Arnaud Blomme, Brunella Costanza, Craig A. Hutton, Olivier Peulen, Philippe Delvenne, Koji Uchida, Barbara Chiavarina, Casper G. Schalkwijk, and Justine Leenders
- Subjects
0301 basic medicine ,biology ,Methylglyoxal ,medicine.disease ,Hsp90 ,Metastasis ,03 medical and health sciences ,chemistry.chemical_compound ,030104 developmental biology ,0302 clinical medicine ,chemistry ,Glycation ,030220 oncology & carcinogenesis ,Side product ,Cancer research ,biology.protein ,medicine ,Glycolysis ,Tumor growth - Published
- 2016
- Full Text
- View/download PDF
19. CLOSE ENCOUNTERS OF THE FOREIGN KIND: ALIENS AND OTHERS*
- Author
-
James R Cochrane
- Subjects
Literature ,New Testament ,business.industry ,Xenophobia ,media_common.quotation_subject ,Philosophy ,Religious studies ,business ,media_common - Published
- 2016
- Full Text
- View/download PDF
20. ChemInform Abstract: Helical, Axial, and Central Chirality Combined in a Single Cage: Synthesis, Absolute Configuration, and Recognition Properties
- Author
-
Dawei Zhang, Laure Guy, Jean-Christophe Mulatier, Jean-Pierre Dutasta, James R. Cochrane, Guohua Gao, and Alexandre Martinez
- Subjects
chemistry.chemical_compound ,Enantiopure drug ,chemistry ,Asymmetric carbon ,Stereochemistry ,Diastereomer ,Absolute configuration ,Stereoselectivity ,Cyclotriveratrylene ,General Medicine ,Enantiomer ,Chirality (chemistry) - Abstract
The synthesis of eight enantiopure molecular cages (four diastereomeric pairs of enantiomers) comprising a helically chiral cyclotriveratrylene (CTV) unit, three axially chiral binaphthol linkages, and three centrally asymmetric carbon atoms of a trialkanolamine core, is described. These new cages constitute a novel family of hemicryptophanes, which combine three classes of chirality. Their absolute configuration was successfully assigned by a chemical correlation method to overcome the signals overlap in the ECD spectra of the binaphtol and CTV units. Stereoselective recognition of glucose and mannose derivatives was investigated with these new chiral cages. Excellent enantio-and diastereoselectivity were reached, since in some cases, both exclusive enantio-and diastereo-discrimination have been observed. In addition, compared with the most relevant hemicryptophanes, these new cages also exhibit improved binding affinities.
- Published
- 2016
- Full Text
- View/download PDF
21. Helical, Axial, and Central Chirality Combined in a Single Cage: Synthesis, Absolute Configuration, and Recognition Properties
- Author
-
Alexandre Martinez, Laure Guy, Guohua Gao, Dawei Zhang, Jean-Pierre Dutasta, Jean-Christophe Mulatier, James R. Cochrane, Laboratoire de Chimie - UMR5182 (LC), École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Shanghai Key Laboratory of Green Chemistry and Chemical Processes, East China Normal University [Shangaï] (ECNU), Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-École normale supérieure - Lyon (ENS Lyon)-Institut de Chimie du CNRS (INC), and Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)
- Subjects
010405 organic chemistry ,Stereochemistry ,Organic Chemistry ,Supramolecular chemistry ,Diastereomer ,Absolute configuration ,Cyclotriveratrylene ,General Chemistry ,010402 general chemistry ,01 natural sciences ,Catalysis ,0104 chemical sciences ,chemistry.chemical_compound ,Enantiopure drug ,chemistry ,Asymmetric carbon ,[CHIM]Chemical Sciences ,Enantiomer ,Chirality (chemistry) - Abstract
International audience; The synthesis of eight enantiopure molecular cages (four diastereomeric pairs of enantiomers) comprising a helically chiral cyclotriveratrylene (CTV) unit, three axially chiral binaphthol linkages, and three centrally asymmetric carbon atoms of a trialkanolamine core, is described. These new cages constitute a novel family of hemicryptophanes, which combine three classes of chirality. Their absolute configuration was successfully assigned by a chemical correlation method to overcome the signals overlap in the ECD spectra of the binaphtol and CTV units. Stereoselective recognition of glucose and mannose derivatives was investigated with these new chiral cages. Excellent enantio-and diastereoselectivity were reached, since in some cases, both exclusive enantio-and diastereo-discrimination have been observed. In addition, compared with the most relevant hemicryptophanes, these new cages also exhibit improved binding affinities.
- Published
- 2016
- Full Text
- View/download PDF
22. Fundamental Evaluation Criteria in the Medicine of the Twenty-First Century
- Author
-
James R. Cochrane
- Subjects
Palliative care ,Conceptual framework ,business.industry ,Agency (sociology) ,Health care ,Accountability ,Medicine ,Context (language use) ,Public relations ,Rational choice theory (criminology) ,business ,Common good - Abstract
Based on ongoing research and analysis by a transdisciplinary, international collaboration of non-formal health services in the context of health challenges such as HIV and AIDS, congestive heart failure, diabetes, palliative care, and interpersonal violence, this paper addresses the question of evaluation criteria for medicine in the twenty-first century. It offers no detailed discussion of specific legal frameworks, medical choices, or standard financial challenges. Rather, it suggests that crucial to their resolution may be a different way of looking at them. This is expressed via four interrelated but discrete notions: health assets, healthworlds, causes of life, and deep accountability. To contextualize these notions, two themes that are central to questions of prioritization in medicine and health care are first considered: the lure and allure of science and aspects of rational choice theory and the question of the common good. Health assets are then explained and their relevance illustrated with reference to research conducted in Zambia and Lesotho for the World Health Organization. From this research arises the idea of healthworlds, which articulates the crucial agency of the health seeker in most, if not all, medical or health interventions. Healthworlds reflect ways of understanding health and healing that exceed clinical perspectives but that nonetheless have clinical relevance. The significance of these concepts is illustrated with reference to an innovative, community-based partnership established by a major health system in Memphis, Tennessee, that has attracted national interest and that offers insights into the question of criteria for evaluating medicine in formal health systems. Finally, this leads to the suggestion that we would be well served to grasp the crucial health and health care in terms of what we might call “leading causes of life.” This conceptual framework emphasizes that which is generative of health; it seeks to balance the overwhelming stress on pathology which is taken as normative but which might be precisely where we are failing. The paper ends by calling for a “deep accountability” that surpasses, without setting aside, financial and operational accountability, placing the question of prioritization in medicine within a larger framework of criteria for evaluating medicine in the twenty-first century.
- Published
- 2016
- Full Text
- View/download PDF
23. The Health of Complex Human Populations
- Author
-
James R. Cochrane, Teresa Cutts, and Gary R. Gunderson
- Subjects
Political science - Published
- 2015
- Full Text
- View/download PDF
24. ChemInform Abstract: Total Synthesis and Reassignment of the Structures of the Antimicrobial Lipodepsipeptides Circulocin γ and δ
- Author
-
James R. Cochrane, Claudia J. Exner, and Katrina A. Jolliffe
- Subjects
chemistry.chemical_classification ,chemistry.chemical_compound ,Natural product ,chemistry ,Stereochemistry ,Side chain ,Absolute configuration ,Total synthesis ,Fatty acid ,Epimer ,General Medicine ,Methylene ,Coupling reaction - Abstract
The structures of the naturally occurring antimicrobial lipodepsipeptides circulocin γ and circulocin δ have been reported to comprise a common cyclic depsipeptide core attached to 3-hydroxy,ω-guanidino fatty acid chains differing in length by two methylene units, but analysis of the reported data suggested that the originally reported structures had incorrect side chain lengths. The total synthesis of both side chain epimers of the originally reported structure of circulocin γ bearing a 19-guanidino-3-hydroxynonadecanoyl (GHND) side chain has been accomplished using a modular approach involving synthesis of the cyclic depsipeptide and side chain fragments followed by a late stage coupling reaction. This revealed that the originally reported structure for circulocin γ bearing the GHND side chain is incorrect and that this structure is actually that of circulocin δ. It has also enabled the absolute configuration of the side chain hydroxy group of the natural product to be assigned as (R). Subsequent synthe...
- Published
- 2015
- Full Text
- View/download PDF
25. ChemInform Abstract: A New Method for Peptide Synthesis in the N→C Direction: Amide Assembly Through Silver-Promoted Reaction of Thioamides
- Author
-
James R. Cochrane, Aysa Pourvali, and Craig A. Hutton
- Subjects
Coupling (electronics) ,chemistry.chemical_classification ,chemistry.chemical_compound ,chemistry ,Stereochemistry ,Amide ,Yield (chemistry) ,Peptide synthesis ,Epimer ,General Medicine ,Amino acid - Abstract
N-Protected amino acids (I) undergo an interesting Ag2CO3-promoted coupling with amino ester thioamides to yield N-acetylated dipeptides (III) without epimerization.
- Published
- 2015
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.