基础医学与临床 ›› 2016, Vol. 36 ›› Issue (3): 301-306.

• 研究论文 • 上一篇    下一篇

稳定表达可诱导型CKS2 shRNA的卵巢癌OVCAR3细胞系的建立与鉴定

董梦梦,孙倩玲,张灵芝,黄梦庭,卢红艳,张佳乐,袁成福   

  1. 三峡大学
  • 收稿日期:2015-08-24 修回日期:2015-11-04 出版日期:2016-03-05 发布日期:2016-02-22
  • 通讯作者: 袁成福 E-mail:yuancf46@ctgu.edu.cn
  • 基金资助:
    国家自然科学基金;湖北省自然科学基金;校人才启动基金

Establishment and identification of OVCAR3 cell line stably expressing inducible shRNA targeting CKS2

  • Received:2015-08-24 Revised:2015-11-04 Online:2016-03-05 Published:2016-02-22
  • Contact: Cheng-Fu YUAN E-mail:yuancf46@ctgu.edu.cn
  • Supported by:
    National Natural Science Foundation of China

摘要: 目的 建立稳定表达可诱导型CKS2 shRNA的卵巢癌OVCAR3细胞系并研究CKS2 knockdown对卵巢癌OVCAR3细胞增殖的影响。方法 根据siRNA的原理设计2对靶向CKS2的shRNA序列,构建慢病毒表达质粒(pLVTHM/CKS2 shRNA重组质粒);先用pLV-tTR/KRAB-Red空载体制备慢病毒并感染OVCAR3细胞;在此基础上再用pLVTHM/CKS2 shRNA重组质粒制备慢病毒并感染上述OVCAR3细胞;对上述两次慢病毒感染的OVCAR3细胞,用强力霉素(DOX)处理72 h后,用real time PCR及Western blot检测CKS2 mRNA及蛋白的表达;用MTT法检测细胞增殖。结果 构建靶向CKS2的shRNA慢病毒表达质粒,包装出慢病毒并感染OVCAR3细胞;建立稳定表达可诱导型CKS2 shRNA的OVCAR3细胞系,通过DOX诱导,可明显抑制该细胞系中CKS2在mRNA及蛋白水平的表达(P < 0.05,P < 0.01);CKS2 knockdown可明显抑制OVCAR3细胞的增殖。结论 建立稳定表达可诱导型CKS2 shRNA的OVCAR3细胞系,DOX诱导的CKS2 knockdown可明显抑制OVCAR3细胞增殖。

关键词: CKS2, 可诱导型shRNA, 卵巢癌

Abstract: Objective To establish a OVCAR3 cell line stably expressing inducible shRNA targeting CKS2 and explore the effects of CKS2 knockdown on cell proliferation of OVCAR3. Methods Two oligonucleotides targeting CKS2 gene were synthesized and cloned into lentivirus expression plasmid pLVTHM, thus, pLVTHM/CKS2 shRNA recombinant plasmids were constructed. OVCAR3 cells were firstly infected with lentivirus made from pLV-tTR/KRAB-Red empty vector, followed by infecting with another kind of lentivirus prepared from pLVTHM/CKS2 shRNA recombinant plasmid. The expression of CKS2 mRNA and protein were determined by real time PCR and Western blot in OVCAR3 cells infected with lentivirus and treated with doxycycline (DOX) for 72h, respectively. The effects of cell proliferation were determined by MTT. Results The lentivirus expression plasmids containing CKS2 shRNA were constructed successfully, the lentivirus were produced and OVCAR3 cells were infected by these lentivirus. A OVCAR3 cell line stably expressing inducible shRNA targeting CKS2 was established successfully and the CKS2 expression levels were decreased obviously after induction by DOX(P < 0.05,P < 0.01). CKS2 knockdown could inhibit OVCAR3 cell proliferation. Conclusions A OVCAR3 cell line stably expressing inducible shRNA targeting CKS2 was established successfully, CKS2 expression suppression induced by DOX could inhibit OVCAR3 cell proliferation.

Key words: CKS2, Inducible shRNA, Ovarian cancer