Published June 16, 2021 | Version v1

Personalized medicine: Stem cells in colorectal cancer treatment

  • 1. Department of Oncology, University of Oxford, ORCRB, Roosevelt Drive, OX3 7DQ Oxford, United Kingdom
  • 2. Department of Molecular Oncology, Cancer Research Institute, Biomedical Research Center, University Science Park for Biomedicine, Slovak Academy of Sciences, Dubravska cesta 9, 845 05 Bratislava, Slovakia; Correspondence to: Department of Molecular Oncology, Cancer Research Institute of Biomedical Research Center SAS, Dubravska cesta 9, 845 05 Bratislava, Slovakia. E-mail addresses: athanasios.patsalias@oncology.ox.ac.uk (A. Patsalias), zuzana.kozovska@savba.sk (Z. Kozovska).

Description

Treatment failure in primary as well as metastatic cancer patients, caused by chemo and radioresistance, has reinforced the research for the applicability of personalized medicine. The use of stem cells (SCs) and cancer stem cells (CSCs) in such a treatment approach will be reviewed in this study. Colorectal cancer (CRC) SCs prove to be a promising asset for CRC treatment optimization both by serving as biomarkers for the current therapy modalities, by means of treatment personalization and patient/tumor stratification, as well as in the development of targeted therapies, selective for the stem cell population. Similar conclusions are drawn, regarding mesenchymal stromal cells (MSCs) and their effect in CRC therapy; while resident stromal cells (RSCs) of tumor microenvironment (TME) seem to promote the tumorigenic and metastatic processes in addition to conferring to the chemo- and radioresistance, under certain conditions they are able to improve the treatment outcome of CRC chemotherapy, e.g. by targeted enzyme/prodrug treatment of CRC cells. This review, points out the dynamic potential of CSCs and other SCs types in CRC treatment personalization as well as, in the improvement of current treatment approaches, opting to a higher therapeutic rate, improved prognosis, survival and quality of life for CRC patients.

Notes

The studies and experiments mentioned in this study were performed with the kind support provided by Slovak Cancer Research Foundation; VEGA grant No 2/0178/21 and by funding from the European Union's Horizon 2020 Research and Innovation Strategies to Programme under grant agreement no. 857381 (project VISION).

Files

doi_org101016jbiopha2021111821.pdf

Files (2.5 MB)

Name Size Download all
md5:f671048d9a0617ce4753edb854b4a7fc
2.5 MB Preview Download

Additional details

Funding

European Commission
VISION - Strategies to strengthen scientific excellence and innoVation capacIty for early diagnoSIs of gastrOintestinal caNcers 857381