Lin Aifen, Yan Wei-Hua
Medical Research Center, Taizhou Hospital of Zhejiang Province, Wenzhou Medical University, Linhai, Zhejiang, People's Republic of China.
Mol Med. 2015 Nov;21(1):782-791. doi: 10.2119/molmed.2015.00083. Epub 2015 Aug 24.
Aberrant induction of human leukocyte antigen-G (HLA-G) expression has been observed in various malignancies and is strongly associated with tumor immune escape, metastasis and poor prognosis. To date, great achievements have been made in understanding the underlying mechanisms of HLA-G involved in tumor progression. HLA-G could lead to tumor evasion by inhibition of immune cell cytolysis, differentiation and proliferation and inhibition of cytokine production, induction of immune cell apoptosis, generation of regulatory cells and expansion of myeloid-derived suppressive cells and by impairment of chemotaxis. Moreover, HLA-G could arm tumor cells with a higher invasive and metastatic potential with the upregulation of tumor-promoting factor expression such as matrix metalloproteinases (MMPs), indicating that ectopic HLA-G expression could render multiple effects during the progression of malignancies. In this review, we summarized the mechanisms of HLA-G involved in promoting tumor cell immune escaping, metastasis and disease progression. Special attention will be paid to its significance as an attractive therapeutic target in cancers.
在各种恶性肿瘤中均观察到人类白细胞抗原-G(HLA-G)表达异常,且其与肿瘤免疫逃逸、转移及预后不良密切相关。迄今为止,在理解HLA-G参与肿瘤进展的潜在机制方面已取得了重大进展。HLA-G可通过抑制免疫细胞溶解、分化和增殖、抑制细胞因子产生、诱导免疫细胞凋亡、产生调节性细胞以及髓源性抑制细胞的扩增和趋化性受损来导致肿瘤逃逸。此外,HLA-G可通过上调肿瘤促进因子如基质金属蛋白酶(MMPs)的表达,赋予肿瘤细胞更高的侵袭和转移潜能,这表明异位HLA-G表达在恶性肿瘤进展过程中可产生多种影响。在本综述中,我们总结了HLA-G参与促进肿瘤细胞免疫逃逸、转移和疾病进展的机制。将特别关注其作为癌症中有吸引力的治疗靶点的意义。