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抑制微管相关蛋白18可抑制Chk1蛋白表达,并降低宫颈癌细胞的侵袭和致瘤性。

Suppressing stathmin-l can inhibit chkl protein expression and reduce the invasion and tumorigenicity of cervical cancer cells.

作者信息

Kong Sh F, Lv T, Sun X, Yuan H, Zhong J Y, Li X R, Dai S Zh

出版信息

Eur J Gynaecol Oncol. 2017;38(2):271-276.

Abstract

The purpose of this study was to evaluate the effects of stathmin-l on chkl protein expression in cervical cancer cells and the influ- ences on the cells' invasion and tumorigenicity. Suppressed stathmin-l expression in Hela cells and C33A cells by lentiviral vector were utilized. Real time PCR and Western blot were used to examine the expression of chkl. Cell proliferation and invasion were stud- ied using MTT assays and transwell migration assays.The differences of tumorigenicity in vivo were explored using xenograft experi- ments. In addition, stathmin-l expressions in 24 cervical cancer patients were studied without regional lymph nodes metastasis and 16 metastatic patients by immunohistochemistry assays and real time PCR. This study found downregulating stathmin-l reduced chkl ex- pressions and the proliferation and invasion in cervical cancer cells and reduced the tumorigenicity of tumor cells.

摘要

本研究旨在评估stathmin-1对宫颈癌细胞中chk1蛋白表达的影响以及对细胞侵袭和致瘤性的影响。利用慢病毒载体抑制Hela细胞和C33A细胞中stathmin-1的表达。采用实时PCR和蛋白质印迹法检测chk1的表达。使用MTT法和transwell迁移试验研究细胞增殖和侵袭。通过异种移植实验探讨体内致瘤性差异。此外,通过免疫组织化学检测和实时PCR研究了24例无区域淋巴结转移的宫颈癌患者和16例转移患者中stathmin-1的表达。本研究发现,下调stathmin-1可降低宫颈癌细胞中chk1的表达、细胞增殖和侵袭,并降低肿瘤细胞的致瘤性。

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