Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors

Adaptive drug resistance is a major obstacle to successful treatment of colorectal cancers. Physiologic tumor models of drug resistance are crucial to understand mechanisms of treatment failure and improve therapy by developing new therapeutics and treatment strategies. Using our aqueous two-phase s...

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Main Authors: Pradip Shahi Thakuri, Gary D. Luker, Hossein Tavana
Format: Article
Language:English
Published: Elsevier 2019-03-01
Series:Translational Oncology
Online Access:http://www.sciencedirect.com/science/article/pii/S1936523318305862
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author Pradip Shahi Thakuri
Gary D. Luker
Hossein Tavana
author_facet Pradip Shahi Thakuri
Gary D. Luker
Hossein Tavana
author_sort Pradip Shahi Thakuri
collection DOAJ
description Adaptive drug resistance is a major obstacle to successful treatment of colorectal cancers. Physiologic tumor models of drug resistance are crucial to understand mechanisms of treatment failure and improve therapy by developing new therapeutics and treatment strategies. Using our aqueous two-phase system microtechnology, we developed colorectal tumor spheroids and periodically treated them with sub-lethal concentrations of three Mitogen Activated Kinase inhibitors (MEKi) used in clinical trials. We used long-term, periodic treatment and recovery of spheroids to mimic cycles of clinical chemotherapy and implemented a growth rate metric to quantitatively assess efficacy of the MEKi during treatment. Our results showed that efficacy of the MEKi significantly reduced with increased treatment cycles. Using a comprehensive molecular analysis, we established that resistance of colorectal tumor spheroids to the MEKi developed through activation of the PI3K/AKT/mTOR pathway. We also showed that other potential feedback mechanisms, such as STAT3 activation or amplified B-RAF, did not account for resistance to the MEKi. We combined each of the three MEKi with a PI3K/mTOR inhibitor and showed that the combination treatments synergistically blocked resistance to the MEKi. Importantly, and unlike the individual inhibitors, we demonstrated that synergistic concentrations of combinations of MEK and PI3K/mTOR inhibitors effectively inhibited growth of colorectal tumor spheroids in long-term treatments. This proof-of-concept study to model treatment-induced drug resistance of cancer cells using 3D cultures offers a unique approach to identify underlying molecular mechanisms and develop effective treatments.
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spelling doaj.art-8e6e1ceb35a54a25ad6843712549be9b2022-12-22T00:47:30ZengElsevierTranslational Oncology1936-52332019-03-01123404416Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK InhibitorsPradip Shahi Thakuri0Gary D. Luker1Hossein Tavana2Department of Biomedical Engineering, The University of Akron, Akron, OH 44325, USADepartment of Radiology, University of Michigan, Ann Arbor, MI 48105, USA; Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI 48105, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48105, USADepartment of Biomedical Engineering, The University of Akron, Akron, OH 44325, USA; Address all correspondence to: Hossein Tavana, Ph.D., P. Eng., 260 S. Forge St., Akron, OH 44325.Adaptive drug resistance is a major obstacle to successful treatment of colorectal cancers. Physiologic tumor models of drug resistance are crucial to understand mechanisms of treatment failure and improve therapy by developing new therapeutics and treatment strategies. Using our aqueous two-phase system microtechnology, we developed colorectal tumor spheroids and periodically treated them with sub-lethal concentrations of three Mitogen Activated Kinase inhibitors (MEKi) used in clinical trials. We used long-term, periodic treatment and recovery of spheroids to mimic cycles of clinical chemotherapy and implemented a growth rate metric to quantitatively assess efficacy of the MEKi during treatment. Our results showed that efficacy of the MEKi significantly reduced with increased treatment cycles. Using a comprehensive molecular analysis, we established that resistance of colorectal tumor spheroids to the MEKi developed through activation of the PI3K/AKT/mTOR pathway. We also showed that other potential feedback mechanisms, such as STAT3 activation or amplified B-RAF, did not account for resistance to the MEKi. We combined each of the three MEKi with a PI3K/mTOR inhibitor and showed that the combination treatments synergistically blocked resistance to the MEKi. Importantly, and unlike the individual inhibitors, we demonstrated that synergistic concentrations of combinations of MEK and PI3K/mTOR inhibitors effectively inhibited growth of colorectal tumor spheroids in long-term treatments. This proof-of-concept study to model treatment-induced drug resistance of cancer cells using 3D cultures offers a unique approach to identify underlying molecular mechanisms and develop effective treatments.http://www.sciencedirect.com/science/article/pii/S1936523318305862
spellingShingle Pradip Shahi Thakuri
Gary D. Luker
Hossein Tavana
Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors
Translational Oncology
title Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors
title_full Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors
title_fullStr Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors
title_full_unstemmed Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors
title_short Cyclical Treatment of Colorectal Tumor Spheroids Induces Resistance to MEK Inhibitors
title_sort cyclical treatment of colorectal tumor spheroids induces resistance to mek inhibitors
url http://www.sciencedirect.com/science/article/pii/S1936523318305862
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AT garydluker cyclicaltreatmentofcolorectaltumorspheroidsinducesresistancetomekinhibitors
AT hosseintavana cyclicaltreatmentofcolorectaltumorspheroidsinducesresistancetomekinhibitors