Cancer‐associated fibroblasts in renal cell carcinoma: implication in prognosis and resistance to anti‐angiogenic therapy

医学 肾透明细胞癌 癌相关成纤维细胞 淋巴管新生 肾细胞癌 癌症研究 肿瘤科 内科学 肿瘤微环境 血管生成 转移 癌症
作者
Damien Ambrosetti,Michael Coutts,Charlotte Paoli,M. Durand,Delphine Borchiellini,Christopher Montemagno,Olivia Rastoin,Arnaud Borderie,Renaud Grépin,Nathalie Rioux‐Leclercq,Jean‐Christophe Bernhard,Gilles Pagès,Maeva Dufies
出处
期刊:BJUI [Wiley]
卷期号:129 (1): 80-92 被引量:36
标识
DOI:10.1111/bju.15506
摘要

To investigate the role of cancer-associated fibroblasts (CAFs) in clear cell renal cell carcinoma (ccRCC) with respect to tumour aggressiveness, metastasis development, and resistance to anti-angiogenic therapy (vascular endothelial growth factor receptor-tyrosine kinase inhibitors [VEGFR-TKI]).Our study involved tissue samples from three distinct and independent cohorts of patients with ccRCC. The presence of CAFs and tumour lymphangiogenesis was investigated, respectively, by transcriptional signatures and then correlated with tumour development and prognosis. The effect of these CAFs on tumour cell migration and VEGFR-TKI resistance was analysed on co-cultures of ccRCC cells with CAFs.Results from our cohorts and from in silico investigations showed that VEGFR-TKI significantly increase the number of CAFs in tumours. In the same populations of patients with ccRCC, the proportion of intra-tumoral CAFs correlated to shorter disease-free and overall survival. The presence of CAFs was also correlated with lymphangiogenesis and lymph node metastasis. CAFs increased the migration and decreased the VEGFR-TKI-dependent cytotoxic effect of tumour cells.Our results show that VEGFR-TKI promote the development of CAFs, and CAFs favour tumour aggressiveness, metastatic dissemination, and resistance to treatment in ccRCC. CAFs could represent a new therapeutic target to fight resistance to treatment of ccRCC. Targeting CAF and immunotherapies combination are emerging as efficient treatments in many types of solid tumours. Our results highlight their relevance in ccRCC.
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