Huang Li-Qiong, Zheng Bo, He Yi
Department of Obstetrics and Gynecology, Xianning Central Hospital, The First Affiliated Hospital of Hubei University of Science and Technology, 228 Jingui Road, Xianning 437100, China.
Open Life Sci. 2019 Dec 31;14:528-536. doi: 10.1515/biol-2019-0059. eCollection 2019 Jan.
Tumor necrosis factor (TNF)-α-induced protein-8-like 2, or TIPE2, is a newly found immune negative regulatory molecule. This study further investigated the role of TIPE2 on proliferation and invasion of cervical squamous cancer cells. Expression of TIPE2 was compared in cervical squamous cancer tissues and adjacent normal tissues by Western blot and immunohistochemistry (IHC). Cervical squamous cancer cell lines, SiHa and C33A, were transfected with recombinant plasmid encoding TIPE2 and tested for cytologic characteristics. The impact of TIPE2 on phosphorylation of extracellular signal-regulated kinase (Erk) signaling pathway was also tested by Western blot analysis of key factors. TIPE2 expression was higher in cervical cancer tissues than that in normal tissue. IHC score of tumor tissue was negatively associated with lymphatic metastasis. Over expression of TIPE2 effectively inhibited the proliferation of cervical cancer cells. Wound healing and transwell assay showed that over expression of TIPE2 suppressed cell migration and invasion in vitro. Meanwhile, phosphorylation of Erk1/2 and upstream mitogen-activated protein kinase kinase (MEK) 1/2 was reduced by TIPE2. TIPE2 is negatively related with development of cervical squamous cancer. TIPE2 is an inhibitory factor of proliferation and invasion of cervical squamous cancer cells, probably through inhibiting Erk signaling pathway.
肿瘤坏死因子(TNF)-α诱导蛋白8样2(TIPE2)是一种新发现的免疫负调控分子。本研究进一步探讨了TIPE2在宫颈鳞状癌细胞增殖和侵袭中的作用。通过蛋白质免疫印迹法(Western blot)和免疫组织化学(IHC)比较了TIPE2在宫颈鳞状癌组织和癌旁正常组织中的表达情况。将编码TIPE2的重组质粒转染至宫颈鳞状癌细胞系SiHa和C33A中,并检测其细胞学特征。同时通过对关键因子进行蛋白质免疫印迹分析,检测TIPE2对细胞外信号调节激酶(Erk)信号通路磷酸化的影响。结果显示,TIPE2在宫颈癌组织中的表达高于正常组织。肿瘤组织的免疫组织化学评分与淋巴转移呈负相关。TIPE2过表达可有效抑制宫颈癌细胞的增殖。划痕实验和Transwell实验表明,TIPE2过表达可抑制宫颈癌细胞的体外迁移和侵袭。同时,TIPE2可降低Erk1/2及其上游丝裂原活化蛋白激酶激酶(MEK)1/2的磷酸化水平。TIPE2与宫颈鳞状癌的发生发展呈负相关。TIPE2可能通过抑制Erk信号通路,从而成为宫颈鳞状癌细胞增殖和侵袭的抑制因子。