1. Academic Validation
  2. HIF-1α is necessary for activation and tumour-promotion effect of cancer-associated fibroblasts in lung cancer

HIF-1α is necessary for activation and tumour-promotion effect of cancer-associated fibroblasts in lung cancer

  • J Cell Mol Med. 2021 Jun;25(12):5457-5469. doi: 10.1111/jcmm.16556.
Yana Zhang 1 2 Yangyang Bian 1 2 Yuan Wang 1 2 Yuanyuan Wang 1 2 Xixi Duan 1 2 Yuning Han 3 Lijing Zhang 1 2 Fei Wang 1 2 Zhuoyu Gu 1 2 Zhihai Qin 1 2 4
Affiliations

Affiliations

  • 1 Medical Research Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • 2 Henan International Joint Laboratory of Tumor Immune Microenvironment, Zhengzhou, China.
  • 3 General Hospital of Ningxia Medical University, Ningxia, China.
  • 4 Key Laboratory of Protein and Peptide Pharmaceuticals, CAS-University of Tokyo Joint Laboratory of Structural Virology and Immunology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Abstract

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.

Keywords

CAFs; CCL5; HIF-1α; fibroblasts; lung cancer.

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