Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma

Summary: Phenotypic (i.e. non-genetic) heterogeneity in melanoma drives dedifferentiation, recalcitrance to targeted therapy and immunotherapy, and consequent tumor relapse and metastasis. Various markers or regulators associated with distinct phenotypes in melanoma have been identified, but, how do...

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Main Authors: Maalavika Pillai, Mohit Kumar Jolly
Format: Article
Language:English
Published: Elsevier 2021-10-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004221010798
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spelling doaj-779ec1ac4d9c4b76b15c18f8ddc039862021-09-25T05:10:47ZengElsevieriScience2589-00422021-10-012410103111Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanomaMaalavika Pillai0Mohit Kumar Jolly1Centre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore, India; Undergraduate Programme, Indian Institute of Science, Bangalore, IndiaCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore, India; Corresponding authorSummary: Phenotypic (i.e. non-genetic) heterogeneity in melanoma drives dedifferentiation, recalcitrance to targeted therapy and immunotherapy, and consequent tumor relapse and metastasis. Various markers or regulators associated with distinct phenotypes in melanoma have been identified, but, how does a network of interactions among these regulators give rise to multiple “attractor” states and phenotypic switching remains elusive. Here, we inferred a network of transcription factors (TFs) that act as master regulators for gene signatures of diverse cell-states in melanoma. Dynamical simulations of this network predicted how this network can settle into different “attractors” (TF expression patterns), suggesting that TF network dynamics drives the emergence of phenotypic heterogeneity. These simulations can recapitulate major phenotypes observed in melanoma and explain de-differentiation trajectory observed upon BRAF inhibition. Our systems-level modeling framework offers a platform to understand trajectories of phenotypic transitions in the landscape of a regulatory TF network and identify novel therapeutic strategies targeting melanoma plasticity.http://www.sciencedirect.com/science/article/pii/S2589004221010798Cell biologyCancer systems biologyTranscriptomicsNetwork modeling
collection DOAJ
language English
format Article
sources DOAJ
author Maalavika Pillai
Mohit Kumar Jolly
spellingShingle Maalavika Pillai
Mohit Kumar Jolly
Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
iScience
Cell biology
Cancer systems biology
Transcriptomics
Network modeling
author_facet Maalavika Pillai
Mohit Kumar Jolly
author_sort Maalavika Pillai
title Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
title_short Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
title_full Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
title_fullStr Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
title_full_unstemmed Systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
title_sort systems-level network modeling deciphers the master regulators of phenotypic plasticity and heterogeneity in melanoma
publisher Elsevier
series iScience
issn 2589-0042
publishDate 2021-10-01
description Summary: Phenotypic (i.e. non-genetic) heterogeneity in melanoma drives dedifferentiation, recalcitrance to targeted therapy and immunotherapy, and consequent tumor relapse and metastasis. Various markers or regulators associated with distinct phenotypes in melanoma have been identified, but, how does a network of interactions among these regulators give rise to multiple “attractor” states and phenotypic switching remains elusive. Here, we inferred a network of transcription factors (TFs) that act as master regulators for gene signatures of diverse cell-states in melanoma. Dynamical simulations of this network predicted how this network can settle into different “attractors” (TF expression patterns), suggesting that TF network dynamics drives the emergence of phenotypic heterogeneity. These simulations can recapitulate major phenotypes observed in melanoma and explain de-differentiation trajectory observed upon BRAF inhibition. Our systems-level modeling framework offers a platform to understand trajectories of phenotypic transitions in the landscape of a regulatory TF network and identify novel therapeutic strategies targeting melanoma plasticity.
topic Cell biology
Cancer systems biology
Transcriptomics
Network modeling
url http://www.sciencedirect.com/science/article/pii/S2589004221010798
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AT mohitkumarjolly systemslevelnetworkmodelingdeciphersthemasterregulatorsofphenotypicplasticityandheterogeneityinmelanoma
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