The tumour microenvironment (TME) is composed of various
cellular and non-cellular elements, including immune cells, fibroblasts,
endothelial cells, mesenchymal stem cells (MSCs), extracellular matrix (ECM)
components, and soluble factors such as cytokines, chemokines, and growth
factors. The dynamic interaction between cancer stem cells (CSCs) and the TME
is now recognised as a critical driver of tumour progression, metastasis, and
therapeutic resistance. Targeting this molecular crosstalk presents a promising
avenue for improving cancer treatment outcomes. This review explores the
therapeutic implications of the interactions between cancer stem cells and the
tumour microenvironment. CSC-derived exosomes serve as key mediators of
communication with the TME, fostering tumour growth by sustaining CSC stemness,
promoting angiogenesis, facilitating metastatic spread, and shaping an
immunosuppressive milieu through immune modulation. Emerging evidence
underscores the therapeutic potential of disrupting this supportive CSC niche,
reprogramming immune responses, and blocking exosome-mediated signalling to
eliminate CSCs and counteract resistance. Novel strategies such as precision
stem cell therapies, personalised approaches tailored to TME characteristics,
and advanced 3D tumour models or organoids are driving the development of more
effective, individualised interventions. Moreover, 3D tumour models and
organoids are evolving in response to treatment, identifying biomarkers of
resistance, and testing new drugs designed to overcome the therapeutic
barriers. MSCs in combination with immune checkpoint inhibitors have reported
encouraging outcomes, including increased tumour response rates and prolonged
survival in patients with certain cancers like melanoma and non-small cell lung
cancer. Furthermore, combining immunotherapy with CSC-directed treatments holds
promise for enhancing clinical efficacy. Sustained research into CSC–TME
interactions remains essential for translating these mechanistic insights into
transformative cancer therapies.
Author(s) Details
Sharmy Saimon Mano
Department of Biotechnology, Hindusthan College of Arts and Science,
Avinashi Road, Behind Nava, Coimbatore, Tamil Nadu-641 028, India.
Please see the book here :- https://doi.org/10.9734/bpi/msup/v1/6475
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