Cancer-associated fibroblast cell surface markers as potential biomarkers or therapeutic targets in lung cancer

被引:0
|
作者
Tokhanbigli, Samaneh [1 ,2 ]
Haghi, Mehra [3 ]
Dua, Kamal [3 ,4 ]
Oliver, Brian Gregory George [1 ,2 ]
机构
[1] Univ Technol Sydney, Sch Life Sci, Bldg 4-745 Harris St, Sydney, NSW 2007, Australia
[2] Woolcock Inst Med Res, Resp Cellular & Mol Biol Grp, Sydney, NSW 2037, Australia
[3] Univ Technol Sydney, Grad Sch Hlth, Discipline Pharm, Sydney, NSW 2008, Australia
[4] Univ Technol Sydney, Fac Hlth, Australian Res Ctr Complementary & Integrat Med, Sydney, NSW 2008, Australia
关键词
Fibroblasts; lung cancer; inflammation; targeted therapy; therapeutic markers; EPITHELIAL-MESENCHYMAL TRANSITION; CARCINOMA-ASSOCIATED FIBROBLASTS; ACTIVATION PROTEIN-ALPHA; PREDICTS POOR-PROGNOSIS; GROWTH-FACTOR RECEPTOR; TENASCIN-C; STROMAL FIBROBLASTS; TUMOR MICROENVIRONMENT; BREAST-CANCER; T-CELLS;
D O I
10.20517/cdr.2024.55
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer-associated fibroblasts (CAFs) are the vital constituent of the tumor microenvironment, and in communication with other cells, they contribute to tumor progression and metastasis. Fibroblasts are the proposed origin of CAFs, which are mediated by pro-inflammatory cytokines and the recruitment of immune cells akin to wound healing. Although various studies have identified different subpopulations of CAFs in lung cancer, the heterogeneity of CAFs, particularly in lung cancer, and their potential as a therapeutic target remain largely unknown. Notwithstanding CAFs were previously thought to have predominantly tumor-promoting features, their pro- or anti-tumorigenic properties may depend on various conditions and cell origins. The absence of distinct markers to identify CAF subpopulations presents obstacles to the successful therapeutic targeting and treatment of CAFs in cancer. Human clinical and animal studies targeting CAFs have shown that targeting CAFs exacerbates the disease progression, suggesting that subpopulations of CAFs may exert opposing functions in cancer progression. Therefore, it is essential to pinpoint specific markers capable of characterizing these subpopulations and revealing their mechanisms of function. The cell-specific surface markers of CAFs will serve as an initial step in investigating precise CAF subpopulations and their role in diagnosing and targeting therapy against cancer- promoting CAF subsets in lung cancer.
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页数:23
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