Precision Oncology-Based Therapeutic Targeting in Mesothelioma

Abstract

Purpose: Given that mesothelioma nearly universally exhibits cell cycle abnormalities and the cell cycle interacts with multiple pathways important to the growth of mesothelioma, disruption of the cell cycle presents as a likely effective approach (or will contribute to a multiple pathway-targeted combination approach) to treating mesothelioma clinically. Our hypothesis is that combined inhibition of 1) multiple cell cycle proteins, and 2) one of 3 separate and alternative molecular pathways will serve as an effective therapy against multiple molecular subtypes of mesothelioma. Scope: We are utilizing in vitro and in vivo studies to evaluate how to best target molecular subtypes of mesothelioma. Major Findings: We have determined in multiple cell lines that cell cycle inhibitors (dinaciclib, abemaciclib, palbociclib) and inhibitors of antioxidant defense (gentian violet and auranofin) have significant activity against mesothelioma in vitro.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2020
Accession Number
AD1118320

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  • Mark Klein

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  • Biomedical

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  • Abstracts
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  • Cell Line
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  • Medicine

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