Cancer-associated Molecular Abnormalities in Human NK cells

G. Zakiryanova, M. Shurin
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引用次数: 1

Abstract

Natural Killer (NK) cells play a key role in the immune responses against infection and cancer as powerful cytotoxic effector cells and regulators of both innate and adaptive immunity [1,2]. Therefore, defects in NK cell functions are important mechanisms for immune evasion of malignant cells [3]. For instance, the ability of tumor cells and tumor-associated stromal/infiltrating cells to inhibit NK cell activity, which results in preventing NK cells from recognizing and killing tumor cells, has been reported for melanoma, neuroblastoma, gastrointestinal sarcoma, hepatocellular cancer (HCC), pancreatic cancer, colorectal carcinoma and other types of cancer [4-9]. A potential loss of NK cell numbers and function at preneoplastic stages of tumorigenesis as a possible mechanism for cancer induction and progression has been also recently proposed [5,10]. However, molecular mechanisms regulating NK cell dysfunction and exhaustion in cancer are largely unclear.
人类NK细胞中与癌症相关的分子异常
自然杀伤细胞(NK)作为强大的细胞毒性效应细胞和先天免疫和适应性免疫的调节剂,在抗感染和癌症的免疫应答中发挥着关键作用[1,2]。因此,NK细胞功能缺陷是恶性细胞免疫逃避的重要机制[3]。例如,在黑色素瘤、神经母细胞瘤、胃肠道肉瘤、肝细胞癌(HCC)、胰腺癌、结直肠癌等类型的癌症中,肿瘤细胞和肿瘤相关的基质/浸润细胞抑制NK细胞活性的能力,从而阻止NK细胞识别和杀伤肿瘤细胞[4-9]。最近也有人提出,在肿瘤发生的癌前阶段,NK细胞数量和功能的潜在丧失可能是癌症诱导和进展的一种机制[5,10]。然而,在癌症中调节NK细胞功能障碍和衰竭的分子机制在很大程度上是不清楚的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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