Colon cancer stemness as a reversible epigenetic state: Implications for anticancer therapies.

World J Stem Cells

Lille University, Institut National de la Santé et de la Recherche Médicale, CHU Lille, UMR-S 1172-Jean-Pierre Aubert Research Center, Lille F-59000, France.

Published: November 2019

AI Article Synopsis

  • The discovery of cancer cell plasticity reveals that cancer cells can transform into cancer stem cells (CSCs), complicating treatment strategies involving chemotherapy and radiotherapy.
  • Researchers suggest that targeting the epigenetic factors that regulate CSCs could offer new therapeutic options, although current methods with certain inhibitors may not be the most effective for treating advanced solid tumors like colorectal cancer.
  • The review highlights challenges in isolating CSCs and evaluating existing epigenetic inhibitors, proposing that analyzing associations between CSC markers and chromatin modifier expression may help identify more effective treatment candidates.

Article Abstract

The recent discovery of cancer cell plasticity, . their ability to reprogram into cancer stem cells (CSCs) either naturally or under chemotherapy and/or radiotherapy, has changed, once again, the way we consider cancer treatment. If cancer stemness is a reversible epigenetic state rather than a genetic identity, opportunities will arise for therapeutic strategies that remodel epigenetic landscapes of CSCs. However, the systematic use of DNA methyltransferase and histone deacetylase inhibitors, alone or in combination, in advanced solid tumors including colorectal cancers, regardless of their molecular subtypes, does not seem to be the best strategy. In this review, we first summarize the knowledge researchers have gathered on the epigenetic signatures of CSCs with the difficulty of isolating rare populations of cells. We raise questions about the relevant use of currently available epigenetic inhibitors (epidrugs) while the expression of numerous cancer stem cell markers are often repressed by epigenetic mechanisms. These markers include the three cluster of differentiation CD133, CD44 and CD166 that have been extensively used for the isolation of colon CSCs.and . Finally, we describe current treatment strategies using epidrugs, and we hypothesize that, using correlation tools comparing associations of relevant CSC markers with chromatin modifier expression, we could identify better candidates for epienzyme targeting.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851010PMC
http://dx.doi.org/10.4252/wjsc.v11.i11.920DOI Listing

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