HIF-1α is necessary for activation and tumour-promotion effect of cancer-associated fibroblasts in lung cancer.
Yana ZhangYangyang BianYuan WangYuanyuan WangXixi DuanYuning HanLijing ZhangFei WangZhuoyu GuZhihai QinPublished in: Journal of cellular and molecular medicine (2021)
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.
Keyphrases
- endothelial cells
- poor prognosis
- extracellular matrix
- stem cells
- squamous cell carcinoma
- signaling pathway
- binding protein
- radiation therapy
- mesenchymal stem cells
- neoadjuvant chemotherapy
- bone marrow
- lps induced
- cell therapy
- drug delivery
- toll like receptor
- induced pluripotent stem cells
- nuclear factor
- locally advanced
- rectal cancer
- solid phase extraction
- high resolution mass spectrometry