Cargando…

Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells

Hyperinsulinemia is a major complication associated with the development of insulin resistance. In addition to its normal spectrum of metabolic effects, insulin can act as a growth factor and has the ability to promote mitogenic activity. Thus, hyperinsulinemia is regarded as a potentially important...

Descripción completa

Detalles Bibliográficos
Autores principales: Weinstein, Doron, Sarfstein, Rive, Laron, Zvi, Werner, Haim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938039/
https://www.ncbi.nlm.nih.gov/pubmed/24434591
http://dx.doi.org/10.1530/EC-13-0086
_version_ 1782305561376718848
author Weinstein, Doron
Sarfstein, Rive
Laron, Zvi
Werner, Haim
author_facet Weinstein, Doron
Sarfstein, Rive
Laron, Zvi
Werner, Haim
author_sort Weinstein, Doron
collection PubMed
description Hyperinsulinemia is a major complication associated with the development of insulin resistance. In addition to its normal spectrum of metabolic effects, insulin can act as a growth factor and has the ability to promote mitogenic activity. Thus, hyperinsulinemia is regarded as a potentially important cancer risk factor among diabetic patients. However, the mechanisms of action of insulin in the specific context of prostate cancer (PCa) and, in particular, the specific receptor that mediates its actions have not been elucidated yet. The aims of this study were to investigate whether insulin can directly induce mitogenic activities in PCa-derived cell lines and to examine the mechanisms responsible for these actions. To this end, we used several PCa-derived cell lines, representing early and advanced stages of the disease. Our results indicated that insulin induces cell proliferation in a dose-dependent fashion in the LNCaP, C4-2, and P69 cell lines. We also demonstrated that insulin enabled LNCaP and C4-2 cells to progress through the cell cycle. Immunoprecipitation assays revealed that insulin activated the insulin receptor (INSR), but not the IGF1 receptor (IGF1R). In addition, INSR was able to compensate for and mediate IGF1 mitogenic signals following IGF1R inhibition. In conclusion, insulin exhibits direct mitogenic activities in PCa cells, which are mediated exclusively through the INSR. Further research is needed to fully dissect the molecular mechanisms underlying the biological actions of insulin in PCa.
format Online
Article
Text
id pubmed-3938039
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Bioscientifica Ltd
record_format MEDLINE/PubMed
spelling pubmed-39380392014-03-05 Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells Weinstein, Doron Sarfstein, Rive Laron, Zvi Werner, Haim Endocr Connect Research Hyperinsulinemia is a major complication associated with the development of insulin resistance. In addition to its normal spectrum of metabolic effects, insulin can act as a growth factor and has the ability to promote mitogenic activity. Thus, hyperinsulinemia is regarded as a potentially important cancer risk factor among diabetic patients. However, the mechanisms of action of insulin in the specific context of prostate cancer (PCa) and, in particular, the specific receptor that mediates its actions have not been elucidated yet. The aims of this study were to investigate whether insulin can directly induce mitogenic activities in PCa-derived cell lines and to examine the mechanisms responsible for these actions. To this end, we used several PCa-derived cell lines, representing early and advanced stages of the disease. Our results indicated that insulin induces cell proliferation in a dose-dependent fashion in the LNCaP, C4-2, and P69 cell lines. We also demonstrated that insulin enabled LNCaP and C4-2 cells to progress through the cell cycle. Immunoprecipitation assays revealed that insulin activated the insulin receptor (INSR), but not the IGF1 receptor (IGF1R). In addition, INSR was able to compensate for and mediate IGF1 mitogenic signals following IGF1R inhibition. In conclusion, insulin exhibits direct mitogenic activities in PCa cells, which are mediated exclusively through the INSR. Further research is needed to fully dissect the molecular mechanisms underlying the biological actions of insulin in PCa. Bioscientifica Ltd 2014-02-28 /pmc/articles/PMC3938039/ /pubmed/24434591 http://dx.doi.org/10.1530/EC-13-0086 Text en © 2014 The authors http://creativecommons.org/licenses/by/3.0/deed.en_GB This work is licensed under a Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/deed.en_GB)
spellingShingle Research
Weinstein, Doron
Sarfstein, Rive
Laron, Zvi
Werner, Haim
Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells
title Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells
title_full Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells
title_fullStr Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells
title_full_unstemmed Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells
title_short Insulin receptor compensates for IGF1R inhibition and directly induces mitogenic activity in prostate cancer cells
title_sort insulin receptor compensates for igf1r inhibition and directly induces mitogenic activity in prostate cancer cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938039/
https://www.ncbi.nlm.nih.gov/pubmed/24434591
http://dx.doi.org/10.1530/EC-13-0086
work_keys_str_mv AT weinsteindoron insulinreceptorcompensatesforigf1rinhibitionanddirectlyinducesmitogenicactivityinprostatecancercells
AT sarfsteinrive insulinreceptorcompensatesforigf1rinhibitionanddirectlyinducesmitogenicactivityinprostatecancercells
AT laronzvi insulinreceptorcompensatesforigf1rinhibitionanddirectlyinducesmitogenicactivityinprostatecancercells
AT wernerhaim insulinreceptorcompensatesforigf1rinhibitionanddirectlyinducesmitogenicactivityinprostatecancercells