Medical Research Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Henan International Joint Laboratory of Tumor Immune Microenvironment, Zhengzhou, China.
J Cell Mol Med. 2021 Jun;25(12):5457-5469. doi: 10.1111/jcmm.16556. Epub 2021 May 4.
Cancer-associated fibroblasts (CAFs) activation is crucial for the establishment of a tumour promoting microenvironment, but our understanding of CAFs activation is still limited. In this study, we found that hypoxia-inducible factor-1α (HIF-1α) was highly expressed in CAFs of human lung cancer tissues and mouse spontaneous lung tumour. Accordingly, enhancing the expression of HIF-1α in fibroblasts via hypoxia induced the conversion of normal fibroblasts into CAFs. HIF-1α-specific inhibitor or HIF-1α knockout (KO) significantly attenuated CAFs activation, which was manifested by the decreased expression of COL1A2 and α-SMA. In vivo, during tumour formation, the expression of Ki-67 and proliferating cell nuclear antigen (PCNA) in the tumour tissue with HIF-1α KO fibroblasts was significantly lower than that of normal fibroblasts. Moreover, HIF-1α in fibroblasts could activate the NF-κB signalling pathway and enhance a subsequent secretion of CCL5, thus promoting the tumour growth. In conclusion, our results suggest that HIF-1α is essential for the activation and tumour-promotion function of CAFs in lung cancer (LC). And targeting HIF-1α expression on CAFs may be a promising strategy for LC therapy.
癌症相关成纤维细胞(CAFs)的激活对于建立肿瘤促进微环境至关重要,但我们对 CAFs 激活的理解仍然有限。在本研究中,我们发现缺氧诱导因子-1α(HIF-1α)在人肺癌组织和小鼠自发性肺肿瘤的 CAFs 中高度表达。因此,通过缺氧增强成纤维细胞中 HIF-1α的表达可将正常成纤维细胞转化为 CAFs。HIF-1α特异性抑制剂或 HIF-1α 敲除(KO)显著减弱 CAFs 的激活,其表现为 COL1A2 和 α-SMA 的表达减少。在体内,在肿瘤形成过程中,HIF-1α KO 成纤维细胞肿瘤组织中 Ki-67 和增殖细胞核抗原(PCNA)的表达明显低于正常成纤维细胞。此外,成纤维细胞中的 HIF-1α 可激活 NF-κB 信号通路,并增强随后的 CCL5 分泌,从而促进肿瘤生长。总之,我们的研究结果表明,HIF-1α对于肺癌(LC)中 CAFs 的激活和促肿瘤功能至关重要。靶向 CAFs 上的 HIF-1α 表达可能是 LC 治疗的一种有前途的策略。