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Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer

SIMPLE SUMMARY: Protein kinases, which are molecules involved in cell growth and signaling, can go haywire in cancer cells, causing them to multiply uncontrollably. Using drugs to target these kinases shows promise for cancer treatment, but we still have a lot to learn about effectively targeting th...

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Autores principales: Singha, Manali, Pu, Limeng, Srivastava, Gopal, Ni, Xialong, Stanfield, Brent A., Uche, Ifeanyi K., Rider, Paul J. F., Kousoulas, Konstantin G., Ramanujam, J., Brylinski, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452340/
https://www.ncbi.nlm.nih.gov/pubmed/37627077
http://dx.doi.org/10.3390/cancers15164050
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author Singha, Manali
Pu, Limeng
Srivastava, Gopal
Ni, Xialong
Stanfield, Brent A.
Uche, Ifeanyi K.
Rider, Paul J. F.
Kousoulas, Konstantin G.
Ramanujam, J.
Brylinski, Michal
author_facet Singha, Manali
Pu, Limeng
Srivastava, Gopal
Ni, Xialong
Stanfield, Brent A.
Uche, Ifeanyi K.
Rider, Paul J. F.
Kousoulas, Konstantin G.
Ramanujam, J.
Brylinski, Michal
author_sort Singha, Manali
collection PubMed
description SIMPLE SUMMARY: Protein kinases, which are molecules involved in cell growth and signaling, can go haywire in cancer cells, causing them to multiply uncontrollably. Using drugs to target these kinases shows promise for cancer treatment, but we still have a lot to learn about effectively targeting them. To prioritize kinases to focus on, we developed CancerOmicsNet, an artificial intelligence model that predicts the response of cancer cells to kinase inhibitor treatment. We tested the model extensively and validated its predictions in real experiments with different types of cancer. To understand how the model makes its decisions and the role of each kinase, we used a special tool called a saliency map. This map helps identify the most important kinases driving tumor growth. By examining a wide range of biomedical literature, CancerOmicsNet indeed has shown promise in selecting potential targets for further investigation in various types of cancer. ABSTRACT: Deregulated protein kinases are crucial in promoting cancer cell proliferation and driving malignant cell signaling. Although these kinases are essential targets for cancer therapy due to their involvement in cell development and proliferation, only a small part of the human kinome has been targeted by drugs. A comprehensive scoring system is needed to evaluate and prioritize clinically relevant kinases. We recently developed CancerOmicsNet, an artificial intelligence model employing graph-based algorithms to predict the cancer cell response to treatment with kinase inhibitors. The performance of this approach has been evaluated in large-scale benchmarking calculations, followed by the experimental validation of selected predictions against several cancer types. To shed light on the decision-making process of CancerOmicsNet and to better understand the role of each kinase in the model, we employed a customized saliency map with adjustable channel weights. The saliency map, functioning as an explainable AI tool, allows for the analysis of input contributions to the output of a trained deep-learning model and facilitates the identification of essential kinases involved in tumor progression. The comprehensive survey of biomedical literature for essential kinases selected by CancerOmicsNet demonstrated that it could help pinpoint potential druggable targets for further investigation in diverse cancer types.
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spelling pubmed-104523402023-08-26 Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer Singha, Manali Pu, Limeng Srivastava, Gopal Ni, Xialong Stanfield, Brent A. Uche, Ifeanyi K. Rider, Paul J. F. Kousoulas, Konstantin G. Ramanujam, J. Brylinski, Michal Cancers (Basel) Article SIMPLE SUMMARY: Protein kinases, which are molecules involved in cell growth and signaling, can go haywire in cancer cells, causing them to multiply uncontrollably. Using drugs to target these kinases shows promise for cancer treatment, but we still have a lot to learn about effectively targeting them. To prioritize kinases to focus on, we developed CancerOmicsNet, an artificial intelligence model that predicts the response of cancer cells to kinase inhibitor treatment. We tested the model extensively and validated its predictions in real experiments with different types of cancer. To understand how the model makes its decisions and the role of each kinase, we used a special tool called a saliency map. This map helps identify the most important kinases driving tumor growth. By examining a wide range of biomedical literature, CancerOmicsNet indeed has shown promise in selecting potential targets for further investigation in various types of cancer. ABSTRACT: Deregulated protein kinases are crucial in promoting cancer cell proliferation and driving malignant cell signaling. Although these kinases are essential targets for cancer therapy due to their involvement in cell development and proliferation, only a small part of the human kinome has been targeted by drugs. A comprehensive scoring system is needed to evaluate and prioritize clinically relevant kinases. We recently developed CancerOmicsNet, an artificial intelligence model employing graph-based algorithms to predict the cancer cell response to treatment with kinase inhibitors. The performance of this approach has been evaluated in large-scale benchmarking calculations, followed by the experimental validation of selected predictions against several cancer types. To shed light on the decision-making process of CancerOmicsNet and to better understand the role of each kinase in the model, we employed a customized saliency map with adjustable channel weights. The saliency map, functioning as an explainable AI tool, allows for the analysis of input contributions to the output of a trained deep-learning model and facilitates the identification of essential kinases involved in tumor progression. The comprehensive survey of biomedical literature for essential kinases selected by CancerOmicsNet demonstrated that it could help pinpoint potential druggable targets for further investigation in diverse cancer types. MDPI 2023-08-10 /pmc/articles/PMC10452340/ /pubmed/37627077 http://dx.doi.org/10.3390/cancers15164050 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Singha, Manali
Pu, Limeng
Srivastava, Gopal
Ni, Xialong
Stanfield, Brent A.
Uche, Ifeanyi K.
Rider, Paul J. F.
Kousoulas, Konstantin G.
Ramanujam, J.
Brylinski, Michal
Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer
title Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer
title_full Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer
title_fullStr Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer
title_full_unstemmed Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer
title_short Unlocking the Potential of Kinase Targets in Cancer: Insights from CancerOmicsNet, an AI-Driven Approach to Drug Response Prediction in Cancer
title_sort unlocking the potential of kinase targets in cancer: insights from canceromicsnet, an ai-driven approach to drug response prediction in cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452340/
https://www.ncbi.nlm.nih.gov/pubmed/37627077
http://dx.doi.org/10.3390/cancers15164050
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