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Cell Therapy as Target Therapy against Colon Cancer Stem Cells

  • Elsa N. Garza Treviño
    ,
  • Adriana G. Quiroz Reyes
    ,
  • Antonio Rojas-Murillo
    ,
  • David A de la Garza Kalife
    ,
  • Paulina Delgado Gonzalez
    ,
  • Jose Francisco Islas
Research Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Publication metrics

Metrics

SciVal
Citations
23
Scopus
Citations
SciVal
FWCI
0.66
SciVal
Author count
8
SciVal
Paper percentile
59

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Captures
27
Mentions
2
Citations
23

Abstract

Cancer stem cells (CSCs) are a small subpopulation of cells within tumors with properties, such as self-renewal, differentiation, and tumorigenicity. CSCs have been proposed as a plausible therapeutic target as they are responsible for tumor recurrence, metastasis, and conventional therapy resistance. Selectively targeting CSCs is a promising strategy to eliminate the propagation of tumor cells and impair overall tumor development. Recent research shows that several immune cells play a crucial role in regulating tumor cell proliferation by regulating different CSC maintenance or proliferation pathways. There have been great advances in cellular immunotherapy using T cells, natural killer (NK) cells, macrophages, or stem cells for the selective targeting of tumor cells or CSCs in colorectal cancer (CRC). This review summarizes the CRC molecular profiles that may benefit from said therapy and the main vehicles used in cell therapy against CSCs. We also discuss the challenges, limitations, and advantages of combining conventional and/or current targeted treatments in the late stages of CRC.

Publication Information

Output type

Research Output:
Contribution to journal
Review article
Peer-review

Original language

English

Article number

8163

Journal (Volume, Issue Number)

International Journal of Molecular Sciences (Volume 24, Issue 9)

Publication milestones

  • Published - 01/2023

Publication status

Published - 01/2023

ISSN

1661-6596

Publication IDs

  • ORCID: /0000-0002-0301-9394/work/150179194
  • Scopus: 85159279839
  • PubMed: 37175871