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Leptin and cancer: Pathogenesis and modulation

Leptin, a product of Ob gene from adipocytes regulates appetite, energy expenditure and body mass composition by decreasing orexigenic and increasing anorexigenic neuropeptide release from hypothalamus. Research over the past few years have suggested leptin/leptin receptor dysregulation to have a ro...

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Autores principales: Dutta, Deep, Ghosh, Sujoy, Pandit, Kaushik, Mukhopadhyay, Pradip, Chowdhury, Subhankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602989/
https://www.ncbi.nlm.nih.gov/pubmed/23565495
http://dx.doi.org/10.4103/2230-8210.105577
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author Dutta, Deep
Ghosh, Sujoy
Pandit, Kaushik
Mukhopadhyay, Pradip
Chowdhury, Subhankar
author_facet Dutta, Deep
Ghosh, Sujoy
Pandit, Kaushik
Mukhopadhyay, Pradip
Chowdhury, Subhankar
author_sort Dutta, Deep
collection PubMed
description Leptin, a product of Ob gene from adipocytes regulates appetite, energy expenditure and body mass composition by decreasing orexigenic and increasing anorexigenic neuropeptide release from hypothalamus. Research over the past few years have suggested leptin/leptin receptor dysregulation to have a role in the development of a large variety of malignancies like breast ca, thyroid ca, endometrial ca and gastrointestinal malignancies, predominantly through JAK/STAT pathway which modulates PI3K/AKT3 signaling, ERK1/2 signaling, expression of antiapoptotic proteins (like XIAP), systemic inflammation (TNF-α, IL6), angiogenic factors (VEGF) and hypoxia inducible factor-1a (HIF-1a) expression. In this review, the current understanding of leptin's role in carcinogenesis has been elaborated. Also a few agents modulating leptin signaling to inhibit cancer cell growth has been described.
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spelling pubmed-36029892013-04-05 Leptin and cancer: Pathogenesis and modulation Dutta, Deep Ghosh, Sujoy Pandit, Kaushik Mukhopadhyay, Pradip Chowdhury, Subhankar Indian J Endocrinol Metab Review Article Leptin, a product of Ob gene from adipocytes regulates appetite, energy expenditure and body mass composition by decreasing orexigenic and increasing anorexigenic neuropeptide release from hypothalamus. Research over the past few years have suggested leptin/leptin receptor dysregulation to have a role in the development of a large variety of malignancies like breast ca, thyroid ca, endometrial ca and gastrointestinal malignancies, predominantly through JAK/STAT pathway which modulates PI3K/AKT3 signaling, ERK1/2 signaling, expression of antiapoptotic proteins (like XIAP), systemic inflammation (TNF-α, IL6), angiogenic factors (VEGF) and hypoxia inducible factor-1a (HIF-1a) expression. In this review, the current understanding of leptin's role in carcinogenesis has been elaborated. Also a few agents modulating leptin signaling to inhibit cancer cell growth has been described. Medknow Publications & Media Pvt Ltd 2012-12 /pmc/articles/PMC3602989/ /pubmed/23565495 http://dx.doi.org/10.4103/2230-8210.105577 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Dutta, Deep
Ghosh, Sujoy
Pandit, Kaushik
Mukhopadhyay, Pradip
Chowdhury, Subhankar
Leptin and cancer: Pathogenesis and modulation
title Leptin and cancer: Pathogenesis and modulation
title_full Leptin and cancer: Pathogenesis and modulation
title_fullStr Leptin and cancer: Pathogenesis and modulation
title_full_unstemmed Leptin and cancer: Pathogenesis and modulation
title_short Leptin and cancer: Pathogenesis and modulation
title_sort leptin and cancer: pathogenesis and modulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602989/
https://www.ncbi.nlm.nih.gov/pubmed/23565495
http://dx.doi.org/10.4103/2230-8210.105577
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