| Literature DB >> 36110381 |
Astha Lamichhane1, Pradip Shahi Thakuri1, Sunil Singh1, Pouria Rafsanjani Nejad1, Jacob Heiss1, Gary D Luker2, Hossein Tavana1.
Abstract
Drug resistance is a leading cause for the failure of cancer treatments. Plasticity of cancer cells to acquire stem cell-like properties enables them to escape drug toxicity through different adaptive mechanisms. Eliminating cancer stem cells (CSCs) can potentially improve treatment outcomes for patients. To determine the role of CSCs in resistance of colorectal cancer cells to targeted therapies and identify treatment strategies, we treated spheroids of BRAFmut and KRASmut colorectal cancer cells with inhibitors of the mitogen-activated protein kinase pathway and studied resistance mechanisms through gene and protein expression analyses. We found that treatments activated several oncogenic pathways and expression of CSC markers CD166 and ALDH1A3. We identified a specific combination treatment using trametinib and mithramycin A to simultaneously inhibit the CSC phenotype and activities of several pathways in cancer cells. This study demonstrates the feasibility of therapeutic targeting of CSCs as a strategy to block tumorigenic activities of cancer cells.Entities:
Year: 2022 PMID: 36110381 PMCID: PMC9469186 DOI: 10.1021/acsptsci.1c00257
Source DB: PubMed Journal: ACS Pharmacol Transl Sci ISSN: 2575-9108