Cancer-Associated Fibroblasts: Tumorigenicity and Targeting for Cancer Therapy.
Raisa A GlabmanPeter C BlackNoriko SatoPublished in: Cancers (2022)
Cancer-associated fibroblasts (CAFs) are a heterogenous group of activated fibroblasts and a major component of the tumor stroma. CAFs may be derived from fibroblasts, epithelial cells, endothelial cells, cancer stem cells, adipocytes, pericytes, or stellate cells. These complex origins may underlie their functional diversity, which includes pro-tumorigenic roles in extracellular matrix remodeling, the suppression of anti-tumor immunity, and resistance to cancer therapy. Several methods for targeting CAFs to inhibit tumor progression and enhance anti-tumor immunity have recently been reported. While preclinical studies have shown promise, to date they have been unsuccessful in human clinical trials against melanoma, breast cancer, pancreas cancer, and colorectal cancers. This review summarizes recent and major advances in CAF-targeting therapies, including DNA-based vaccines, anti-CAF CAR-T cells, and modifying and reprogramming CAF functions. The challenges in developing effective anti-CAF treatment are highlighted, which include CAF heterogeneity and plasticity, the lack of specific target markers for CAFs, the limitations in animal models recapitulating the human cancer microenvironment, and the undesirable off-target and systemic side effects. Overcoming these challenges and expanding our understanding of the basic biology of CAFs is necessary for making progress towards safe and effective therapeutic strategies against cancers in human patients.
Keyphrases
- cancer therapy
- endothelial cells
- extracellular matrix
- drug delivery
- clinical trial
- end stage renal disease
- induced pluripotent stem cells
- papillary thyroid
- pluripotent stem cells
- cancer stem cells
- stem cells
- newly diagnosed
- chronic kidney disease
- high glucose
- induced apoptosis
- squamous cell
- oxidative stress
- single cell
- peritoneal dialysis
- circulating tumor
- big data
- insulin resistance
- young adults
- vascular endothelial growth factor
- poor prognosis
- anti inflammatory
- single molecule
- bone marrow
- cell free
- artificial intelligence
- open label
- replacement therapy