Chang Wei-An, Tsai Ming-Ju, Hung Jen-Yu, Wu Kuan-Li, Tsai Ying-Ming, Huang Yung-Chi, Chang Chao-Yuan, Tsai Pei-Hsun, Hsu Ya-Ling
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Cancers (Basel). 2021 Dec 13;13(24):6252. doi: 10.3390/cancers13246252.
Natural killer (NKs) cells are cytotoxic effector cells, which can modulate tumor metastasis according to their function; however, the role of NK cells in lung cancer has not been extensively investigated. In this study, we determined the functional profiles of NK cells in a hypoxic tumor microenvironment (TME) of lung cancer. We revealed CD226 downregulation and functional repression of NK cells after hypoxic lung cancer priming and we then investigated their interaction with extracellular vesicles (EVs) and miR-150-5p. We also found that NK cells from lung cancer patients had lower expression of CD226 on their surface and exhibited a pro-inflammatory, pro-angiogenic and tumorigenesis phenotype by expressing VEGF, CXCL1, CXCL8, S100A8 and MMPs. Moreover, inhibition of miR-150 improved tumor surveillance by reversing CD226 expression and subsequently reinstating cytotoxic NK cell activity in an animal model. Our study introduces a new scenario for the pro-inflammatory and pro-angiogenic activities of NK cells in the hypoxic TME in lung cancer.
自然杀伤(NK)细胞是细胞毒性效应细胞,可根据其功能调节肿瘤转移;然而,NK细胞在肺癌中的作用尚未得到广泛研究。在本研究中,我们确定了肺癌缺氧肿瘤微环境(TME)中NK细胞的功能特征。我们发现缺氧肺癌预处理后NK细胞的CD226下调和功能抑制,然后研究了它们与细胞外囊泡(EVs)和miR-150-5p的相互作用。我们还发现肺癌患者的NK细胞表面CD226表达较低,并通过表达VEGF、CXCL1、CXCL8、S100A8和MMPs表现出促炎、促血管生成和肿瘤发生表型。此外,在动物模型中,抑制miR-150可通过逆转CD226表达并随后恢复细胞毒性NK细胞活性来改善肿瘤监测。我们的研究为肺癌缺氧TME中NK细胞的促炎和促血管生成活性引入了一种新情况。