Human-derived normal mesenchymal stem/stromal cells in anticancer therapies

Cheng Zhang1, Shi-Jie Yang1, Qin Wen1

  • 1Department of Hematology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, People's Republic of China.; Division of Periodontology, Diagnostic Sciences & Dental Hygiene, and Division of Biomedical Sciences, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, 90033, USA.; Norris Cancer Center, University of Southern California, Los Angeles, CA, 90033, USA.

Journal of Cancer
|January 27, 2017
PubMed

Insights

Mesenchymal stem/stromal cells (MSCs) show potential in cancer therapy, but their efficacy depends on various factors. This review explores human MSCs

Area of Science:

  • Oncology
  • Cell Biology
  • Immunology

Background:

  • The tumor microenvironment (TME) significantly influences cancer progression, metastasis, and treatment response.
  • Stromal cells within the TME are emerging as critical targets for anticancer therapeutics.
  • Mesenchymal stem/stromal cells (MSCs) present a complex role in cancer, with their therapeutic application debated due to context-dependent effects.

Purpose of the Study:

  • To review the multifaceted role of human-derived normal MSCs in anticancer therapies.
  • To discuss the application of different MSC subtypes in treating various cancers.
  • To elucidate the anticancer mechanisms and clinical potential of MSCs.

Main Methods:

  • Literature review focusing on human MSCs and their interactions within the TME.
  • Analysis of studies investigating MSCs in different cancer types and conditions (in vitro/in vivo).
  • Examination of MSC-secreted factors and their impact on cancer cells and host immune cells.

Main Results:

  • The efficacy of MSCs as anticancer agents is highly variable, influenced by MSC subtype, experimental conditions, secreted factors, cancer type, and cellular interactions.
  • Human MSCs exhibit diverse roles, potentially promoting or inhibiting tumor growth depending on the specific context.
  • Understanding these complex interactions is crucial for harnessing MSCs effectively in cancer treatment.

Conclusions:

  • Human MSCs hold promise for anticancer therapies, but careful consideration of their context-specific functions is essential.
  • Further research into MSC mechanisms and clinical applications is needed to optimize their use in oncology.
  • Tailoring MSC-based strategies to specific cancer types and patient profiles may enhance therapeutic outcomes.

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