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热休克和电离辐射导致肿瘤细胞NKG2D配体增加及对NK细胞介导的细胞毒性敏感性增强。

Increase of NKG2D ligands and sensitivity to NK cell-mediated cytotoxicity of tumor cells by heat shock and ionizing radiation.

作者信息

Kim Joo-Young, Son Young-Ok, Park Soon-Won, Bae Jae-Ho, Chung Joo Seop, Kim Hyung Hoi, Chung Byung-Seon, Kim Sun-Hee, Kang Chi-Dug

机构信息

Department of Biochemistry, Pusan National University School of Medicine, Busan 602-739, Korea.

出版信息

Exp Mol Med. 2006 Oct 31;38(5):474-84. doi: 10.1038/emm.2006.56.

Abstract

In this study, we have investigated if current cancer therapeutic modalities including hyperthermia and ionizing radiation can increase the expression of NKG2D ligands in human cancer cell lines. The expressions of NKG2D ligands were induced by both heat shock and ionizing radiation in various cell lines including KM12, NCI-H23, HeLa and A375 cells with peaks at 2 h and 9 h after treatment, respectively, although inducibility of each NKG2D ligand was various depending on cell lines. During the induction of NKG2D ligands, heat shock protein 70 was induced by heat shock but not by ionizing radiation. These results were followed by increased susceptibilities to NK cell-mediated cytolysis after treatment with heat shock and ionizing radiation. These results suggest that heat shock and ionizing radiation induce NKG2D ligands and consequently might lead to increased NK cell-mediated cytotoxicity in various cancer cells.

摘要

在本研究中,我们探究了包括热疗和电离辐射在内的当前癌症治疗方式是否能增加人癌细胞系中NKG2D配体的表达。在包括KM12、NCI-H23、HeLa和A375细胞在内的多种细胞系中,热休克和电离辐射均能诱导NKG2D配体的表达,处理后分别在2小时和9小时达到峰值,不过每种NKG2D配体的诱导能力因细胞系而异。在诱导NKG2D配体的过程中,热休克蛋白70由热休克诱导产生,而非电离辐射。热休克和电离辐射处理后,这些细胞对NK细胞介导的细胞溶解的敏感性增加。这些结果表明,热休克和电离辐射诱导NKG2D配体,因此可能导致各种癌细胞中NK细胞介导的细胞毒性增加。

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