Cargando…
Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer
BACKGROUND: A positive association between diabetes and breast cancer has been identified by various epidemiological and clinical studies. However, the possible molecular interactions between the two heterogeneous diseases have not been fully determined yet. There are several underlying mechanisms w...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265603/ https://www.ncbi.nlm.nih.gov/pubmed/30515357 http://dx.doi.org/10.7717/peerj.5917 |
_version_ | 1783375661201620992 |
---|---|
author | Rehman, Sammia Obaid, Ayesha Naz, Anam Ali, Amjad Kanwal, Shahzina Ahmad, Jamil |
author_facet | Rehman, Sammia Obaid, Ayesha Naz, Anam Ali, Amjad Kanwal, Shahzina Ahmad, Jamil |
author_sort | Rehman, Sammia |
collection | PubMed |
description | BACKGROUND: A positive association between diabetes and breast cancer has been identified by various epidemiological and clinical studies. However, the possible molecular interactions between the two heterogeneous diseases have not been fully determined yet. There are several underlying mechanisms which may increase the risk of breast cancer in diabetic patients. INTRODUCTION: In this study, we focused on the role of O-GlcNAc transferase (OGT) enzyme in the regulation of phosphatidylinositol-3 kinase (PI3K) pathway through activation/deactivation of Akt protein. The efficiency of insulin signaling in adipocytes is reduced as a result of OGT overexpression which further attenuates Akt signaling; as a result, the efficiency of insulin signaling is reduced by downregulation of insulin-responsive genes. On the other hand, increased expression of OGT results in Akt activation in breast cancer cells, leading to enhanced cell proliferation and inhibition of the apoptosis. However, the interplay amongst these signaling pathways is still under investigation. METHODS: In this study, we used Petri nets (PNs) to model and investigate the role of PI3K and OGT pathways, acting as key players in crosstalk between diabetes and breast cancer, resulting in progression of these chronic diseases. Moreover, in silico perturbation experiments were applied on the model to analyze the effects of anti-cancer agents (shRNA and BZX) and anti-diabetic drug (Metformin) on the system. RESULTS: Our PN model reflects the alterations in protein expression and behavior and the correlation between breast cancer and diabetes. The analysis proposed two combination therapies to combat breast cancer progression in diabetic patients including combination of OGTmRNA silencing and OGT inhibitor (BZX) as first combination and BZX and Metformin as the second. CONCLUSION: The PN model verified that alterations in O-GlcNAc signaling affect both insulin resistance and breast cancer. Moreover, the combination therapy for breast cancer patients consisting of anti-diabetic drugs such as Metformin along with OGT inhibitors, for example BZX, can produce better treatment regimens. |
format | Online Article Text |
id | pubmed-6265603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62656032018-12-04 Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer Rehman, Sammia Obaid, Ayesha Naz, Anam Ali, Amjad Kanwal, Shahzina Ahmad, Jamil PeerJ Bioinformatics BACKGROUND: A positive association between diabetes and breast cancer has been identified by various epidemiological and clinical studies. However, the possible molecular interactions between the two heterogeneous diseases have not been fully determined yet. There are several underlying mechanisms which may increase the risk of breast cancer in diabetic patients. INTRODUCTION: In this study, we focused on the role of O-GlcNAc transferase (OGT) enzyme in the regulation of phosphatidylinositol-3 kinase (PI3K) pathway through activation/deactivation of Akt protein. The efficiency of insulin signaling in adipocytes is reduced as a result of OGT overexpression which further attenuates Akt signaling; as a result, the efficiency of insulin signaling is reduced by downregulation of insulin-responsive genes. On the other hand, increased expression of OGT results in Akt activation in breast cancer cells, leading to enhanced cell proliferation and inhibition of the apoptosis. However, the interplay amongst these signaling pathways is still under investigation. METHODS: In this study, we used Petri nets (PNs) to model and investigate the role of PI3K and OGT pathways, acting as key players in crosstalk between diabetes and breast cancer, resulting in progression of these chronic diseases. Moreover, in silico perturbation experiments were applied on the model to analyze the effects of anti-cancer agents (shRNA and BZX) and anti-diabetic drug (Metformin) on the system. RESULTS: Our PN model reflects the alterations in protein expression and behavior and the correlation between breast cancer and diabetes. The analysis proposed two combination therapies to combat breast cancer progression in diabetic patients including combination of OGTmRNA silencing and OGT inhibitor (BZX) as first combination and BZX and Metformin as the second. CONCLUSION: The PN model verified that alterations in O-GlcNAc signaling affect both insulin resistance and breast cancer. Moreover, the combination therapy for breast cancer patients consisting of anti-diabetic drugs such as Metformin along with OGT inhibitors, for example BZX, can produce better treatment regimens. PeerJ Inc. 2018-11-09 /pmc/articles/PMC6265603/ /pubmed/30515357 http://dx.doi.org/10.7717/peerj.5917 Text en © 2018 Rehman et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Rehman, Sammia Obaid, Ayesha Naz, Anam Ali, Amjad Kanwal, Shahzina Ahmad, Jamil Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
title | Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
title_full | Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
title_fullStr | Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
title_full_unstemmed | Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
title_short | Model-based in silico analysis of the PI3K/Akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
title_sort | model-based in silico analysis of the pi3k/akt pathway: the elucidation of cross-talk between diabetes and breast cancer |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265603/ https://www.ncbi.nlm.nih.gov/pubmed/30515357 http://dx.doi.org/10.7717/peerj.5917 |
work_keys_str_mv | AT rehmansammia modelbasedinsilicoanalysisofthepi3kaktpathwaytheelucidationofcrosstalkbetweendiabetesandbreastcancer AT obaidayesha modelbasedinsilicoanalysisofthepi3kaktpathwaytheelucidationofcrosstalkbetweendiabetesandbreastcancer AT nazanam modelbasedinsilicoanalysisofthepi3kaktpathwaytheelucidationofcrosstalkbetweendiabetesandbreastcancer AT aliamjad modelbasedinsilicoanalysisofthepi3kaktpathwaytheelucidationofcrosstalkbetweendiabetesandbreastcancer AT kanwalshahzina modelbasedinsilicoanalysisofthepi3kaktpathwaytheelucidationofcrosstalkbetweendiabetesandbreastcancer AT ahmadjamil modelbasedinsilicoanalysisofthepi3kaktpathwaytheelucidationofcrosstalkbetweendiabetesandbreastcancer |