Zhao Shuang, Sun Hong-Zhi, Zhu Shi-Tu, Lu Hang, Niu Zhe-Feng, Guo Wen-Feng, Takano Yasuo, Zheng Hua-Chuan
Cancer Research Center, The First Affiliated Hospital of Liaoning Medical University, JinZhou, China. zheng_huachuan @hotmail.com
Asian Pac J Cancer Prev. 2013;14(7):4249-54. doi: 10.7314/apjcp.2013.14.7.4249.
Parafibromin is a protein encoded by the HRPT2 (hyperparathyroidism 2) oncosuppressor gene and its down-regulated expression is involved in pathogenesis of parathyroid, breast, gastric and colorectal carcinomas. This study aimed to clarify the effects of parafibromin expression on the phenotypes and relevant mechanisms of DLD-1 colon carcinoma cells.
DLD-1 cells transfected with a parafibromin-expressing plasmid were subjected to examination of phenotype, including proliferation, differentiation, apoptosis, migration and invasion. Phenotype-related proteins were measured by Western blot. Parafibromin and ki-67 expression was detected by immunohistochemistry on tissue microarrays.
The transfectants showed higher proliferation by CCK-8, better differentiation by electron microscopy and ALP activity and more apoptotic resistance to cisplatin by DNA fragmentation than controls. There was no difference in early apoptosis by annexin V, capase-3 activity, migration and invasion between DLD-1 cells and their transfectants. Ectopic parafibromin expression resulted in down-regulated expression of smad4, MEKK, GRP94, GRP78, GSK3β-ser9, and Caspase-9. However, no difference was detectable in caspase-12 and -8 expression. A positive relationship was noted between parafibromin and ki-67 expression in colorectal carcinoma.
Parafibromin overexpression could promote cell proliferation, apoptotic resistance, and differentiation of DLD-1 cells.
副纤维蛋白是由抑癌基因HRPT2(甲状旁腺功能亢进2)编码的一种蛋白质,其表达下调与甲状旁腺癌、乳腺癌、胃癌和结直肠癌的发病机制有关。本研究旨在阐明副纤维蛋白表达对DLD-1结肠癌细胞表型及相关机制的影响。
对转染了副纤维蛋白表达质粒的DLD-1细胞进行表型检测,包括增殖、分化、凋亡、迁移和侵袭。通过蛋白质免疫印迹法检测与表型相关的蛋白质。在组织芯片上通过免疫组织化学检测副纤维蛋白和ki-67的表达。
与对照组相比,转染细胞通过CCK-8检测显示出更高的增殖能力,通过电子显微镜和碱性磷酸酶活性检测显示出更好的分化能力,通过DNA片段化检测显示出对顺铂诱导的凋亡具有更强的抗性。在膜联蛋白V检测的早期凋亡、caspase-3活性、迁移和侵袭方面,DLD-1细胞与其转染细胞之间没有差异。异位表达副纤维蛋白导致smad4、MEKK、GRP94、GRP78、GSK3β-ser9和Caspase-9的表达下调。然而,在caspase-12和-8表达方面未检测到差异。在结直肠癌中,副纤维蛋白与ki-67表达之间呈正相关。
副纤维蛋白过表达可促进DLD-1细胞的增殖、抗凋亡能力和分化。