Applications of Modified Mesenchymal Stem Cells as Targeted Systems against Tumor Cells

Elsa N Garza Treviño1, Adriana G Quiroz Reyes1, Paulina Delgado Gonzalez1

  • 1Laboratorio de Terapia Celular, Departamento de Bioquímica y Medicina Molecular, Facultad de Medicina, Universidad Autónoma de Nuevo León, Av. Dr. José Eleuterio González 235, Monterrey 64460, Nuevo León, Mexico.

Insights

Mesenchymal stem cells (MSCs) offer dual roles in cancer therapy. This review explores engineered MSCs for solid tumor treatment, detailing methods, objectives, and challenges for improved cancer gene and cell therapy.

Area of Science:

  • Oncology
  • Immunology
  • Biotechnology

Background:

  • Mesenchymal stem cells (MSCs) exhibit complex immune-modulatory effects, presenting both antitumor and protumor potential in cancer treatment.
  • MSCs are explored as delivery vehicles for gene and cell therapy, with genetic modification aiming to enhance their tumor-targeting and cancer-eliminating capabilities.
  • Despite advancements, the efficacy of engineered MSCs in solid tumors remains constrained by factors including cell source, transgene choice, and tumor microenvironment interactions.

Purpose of the Study:

  • To review the progress of gene and cell therapy utilizing mesenchymal stem cells (MSCs) as a core strategy against solid tumors.
  • To address various MSC engineering methods developed over decades of research.
  • To summarize the therapeutic objectives of engineered MSCs for common cancers and discuss associated challenges and benefits.

Main Methods:

  • Review of existing literature on mesenchymal stem cell (MSC) based gene and cell therapy for solid tumors.
  • Analysis of different MSC engineering techniques and their outcomes.
  • Discussion of challenges, limitations, risks, and advantages of engineered MSCs in combination with conventional cancer therapies.

Main Results:

  • Mesenchymal stem cells (MSCs) can be engineered to enhance their antitumor effects, acting as targeted delivery systems for gene and cell therapies.
  • Various genetic modification strategies have been employed to improve MSC efficacy against solid tumors.
  • The effectiveness of engineered MSCs is influenced by the specific cancer type, the genetic modifications, and the tumor microenvironment.

Conclusions:

  • Engineered mesenchymal stem cells (MSCs) represent a promising frontier in combined gene and cell therapy for solid tumors.
  • Further research into MSC engineering methods and understanding tumor-specific interactions is crucial for optimizing therapeutic outcomes.
  • Addressing the challenges and risks associated with engineered MSCs is essential for their successful clinical translation in cancer treatment.

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