Zhang Yan, Howell Ronald D, Alfonso Daniel T, Yu Jin, Kong Li, Wittig James C, Liu Chuan-ju
Department of Orthopaedic Surgery, New York University School of Medicine, New York, New York 10003, USA.
Front Biosci. 2007 Sep 1;12:4855-63. doi: 10.2741/2433.
IFI16 is a member of the interferon-inducible p200-protein family, capable of modulating cell proliferation, and cellular senescence. In this study, these effects of IFI16 were studied in tumor cells derived from bone and cartilage. The level of IFI16 was markedly lower in human osteosarcomas as compared with its level in normal bone. Overexpression of functional IFI16 in human osteosarcoma and chondrosarcoma cell lines markedly inhibited colony formation, and significantly inhibited cell growth, an effect that could be reversed by introduction of gene specific siRNA into tumor cells. These inhibitory effects of IFI16 were associated with upregulation of p21 and inhibition of cyclin E, cyclin D1, c-Myc and Ras. In addition, ectopic expression of IFI16 in tumor cells increased senescence-associated beta-galactosidase and induced a senescence-like phenotype. In view of such effects, IFI16 might be a suitable target for therapeutic intervention in osteosarcoma and chondrosarcoma.
IFI16是干扰素诱导的p200蛋白家族成员,能够调节细胞增殖和细胞衰老。在本研究中,在源自骨和软骨的肿瘤细胞中研究了IFI16的这些作用。与正常骨中的水平相比,人骨肉瘤中IFI16的水平明显较低。在人骨肉瘤和软骨肉瘤细胞系中功能性IFI16的过表达显著抑制集落形成,并显著抑制细胞生长,将基因特异性小干扰RNA导入肿瘤细胞可逆转这一效应。IFI16的这些抑制作用与p21的上调以及细胞周期蛋白E、细胞周期蛋白D1、c-Myc和Ras的抑制有关。此外,肿瘤细胞中IFI16的异位表达增加了衰老相关的β-半乳糖苷酶并诱导了衰老样表型。鉴于这些作用,IFI16可能是骨肉瘤和软骨肉瘤治疗干预的合适靶点。