Quy Linh Nguyen, Choi Yong Won, Kim Yeong Hwa, Chwae Yong-Joon, Park Tae Jun, Lim In Kyoung
Department of Biochemistry and Molecular Biology, Ajou University, School of Medicine, Suwon 443-721, Republic of Korea.
Cell Signal. 2013 Dec;25(12):2391-9. doi: 10.1016/j.cellsig.2013.07.024. Epub 2013 Aug 1.
Cancer cell growth was increased when co-cultured with fibroblasts, however, no effect was observed when co-cultured with TIS21-overexpressed fibroblast. Therefore, the role of TIS21 played in cancer microenvironment was investigated. TIS21 decreased interleukin-6 (IL-6) expression in human dermal fibroblast (HDF). Adenoviral transduction of TIS21 gene to HDF decreased the secretion of IL-6, whereas knockdown of the gene increased IL-6 expression. Furthermore, TIS21 overexpression inhibited STAT3 binding to IL-6 promoter region as well as JAK2-STAT3 signaling by inhibiting reactive oxygen species (ROS) generation by being localized in mitochondria. Mitochondria-target TIS21 (MT-TIS21) also inhibited IL-6 expression by downregulating STAT3 phosphorylation, whereas NF-κB pathway was not influenced by TIS21 expression. These results indicate that TIS21 negatively regulated cancer cell growth by inhibiting IL-6 expression through downregulation of STAT3 activation.
与成纤维细胞共培养时癌细胞生长增加,然而,与过表达TIS21的成纤维细胞共培养时未观察到影响。因此,研究了TIS21在癌症微环境中的作用。TIS21降低了人皮肤成纤维细胞(HDF)中白细胞介素-6(IL-6)的表达。将TIS21基因腺病毒转导至HDF可降低IL-6的分泌,而该基因的敲低则增加IL-6的表达。此外,TIS21的过表达通过定位于线粒体抑制活性氧(ROS)的产生,从而抑制STAT3与IL-6启动子区域的结合以及JAK2-STAT3信号传导。线粒体靶向TIS21(MT-TIS21)也通过下调STAT3磷酸化来抑制IL-6表达,而NF-κB途径不受TIS21表达的影响。这些结果表明,TIS21通过下调STAT3激活来抑制IL-6表达,从而对癌细胞生长产生负调控作用。