期刊文献+

抑癌基因Fhit重组腺病毒的构建表达及其在结肠癌细胞中的生物学功能 被引量:5

Construction and Expression of Recombinant Adenovirus Encoding Tumor Suppressor Fhit and Its Biological Function in Colon Cancer Cells
原文传递
导出
摘要 目的:构建携带抑癌基因Fhit的重组腺病毒并通过其研究Fhit蛋白对结直肠癌细胞增殖能力的影响。方法:利用PCR方法从人胎肝文库中克隆Fhit基因片段,Fhit基因PCR产物连入T载体构建重组质粒pMD18T-Fhit。测序正确后,将基因片段导入ptrack-CMV穿梭质粒中,构建重组穿梭载体ptrack-CMV-Fhit。将经PmeⅠ单酶切线性化的ptrack-CMV-Fhit和骨架腺病毒质粒pAdEasy-1共转BJ5183大肠杆菌,使ptrack-CMV-Fhit和pAdEasy-1发生同源重组。经PacI酶切鉴定正确后,将重组腺病毒质粒转染293A细胞获得表达Fhit蛋白的重组腺病毒rAd-Fhit,将获得的重组腺病毒感染结肠癌细胞,采用蛋白印迹法检测外源Fhit蛋白的表达,并进一步观察其对细胞增殖能力的影响。结果:成功构建了携带有Fhit基因的重组腺病毒,且能够在结肠癌细胞中成功表达Fhit蛋白。在结肠癌细胞中,Fhit蛋白明显减弱了结肠癌细胞的增殖能力。结论:在结肠癌细胞中,Fhit基因可能扮演抑癌基因的角色,而表达Fhit的重组腺病毒很可能成为一种结肠癌生物治疗的新策略。 AIM:To construct a recombinant adenovirus carrying Fhit gene,a tumor suppressor in many types of cancer,and to observe its biological function on the proliferation of colon cancer cells.METHODS:Fhit gene was cloned from the fetal liver cDNA library using the PCR method.The PCR product was inserted into the T vector to construct the plasmid pMD18T-Fhit.The Fhit fragment from the pMD18T-Fhit was inserted into the vector ptrack-CMV to construct a shuttle plasmid ptrack-CMV-Fhit.After PmeI digested and linearized process,ptrack-CMV-Fhit was co-transformed into Escherichia coli strain BJ5183 together with the adenovirus backbone vector pAdEasy-1 to generate a recombinant adenovirus plasmid by homologous recombination.The adenovirus plasmid was identified by PacI digestion and transfected into 293A cells to package a recombinant adenovirus which expressed the Fhit protein.Furthermore,the adenovirus rAd-Fhit was infected into colon cancer cells,and the expression of the ectogenic protein was detected by Western blotting.Finally,the proliferation of colon cancer cells was observed in adenovirus-infected cells by the MTT assay.RESULTS:Constructed the recombinant adenovirus encoding Fhit gene and expressed it in colon cancer cells successfully.Detected that the proliferation of colon cancer cells was inhibited obviously in rAd-Fhit-infected cells with comparison to the control groups.CONCLUSION:Fhit may function as a tumor suppressor in colon cancer cells,and the adenovirus-mediated Fhit can be a novel strategy for the colon cancer therapeutics.
出处 《中国生物工程杂志》 CAS CSCD 北大核心 2010年第1期7-11,共5页 China Biotechnology
基金 国家自然科学基金(30873006 30901771) 第四军医大学"青年英才支持计划"(2009) 第四军医大学学员课外科研课题(2008)资助项目
关键词 FHIT 重组腺病毒 结肠癌 细胞增殖 Fhit Adenovirus Colon cancer Proliferation
  • 相关文献

参考文献10

  • 1Smith D I, Mcavoy S, Zhu Y, et al. Large common fragile site genes and cancer. Semin Cancer Biol, 2007, 17( 1 ) : 31-41.
  • 2Mady H H, Melhem M F. FHIT protein expression and its relation to apoptosis, tumor histologic grade and prognosis in colorectal adenocarcinoma: an immunohistochemical and image analysis study. Clin Exp Metastasis, 2002, 19(4) : 351-358.
  • 3Barnes L D, Garrison P N, Siprashvili Z, et al. Fhit, a putative tumor suppressor in humans, is a dinucleoside 5 ' , 5'' -P1, P3- triphosphate hydrolase. Biochemistry, 1996, 35 (36) : 11529- 11535.
  • 4Nishizaki M, Sasaki J, Fang B, et al. Synergistic tumor suppression by coexpression of FHIT and p53 coincides with FHIT-mediated MDM2 inactivation and p53 stabilization in human non-small cell lung cancer cells. Cancer Res, 2004, 64 ( 16 ) : 5745-5752.
  • 5Gopalakrishnan V K, Banerjee A G, Vishwanatha J K. Effect of FH1T gene replacement on growth, cell cycle and apoptosis in pancreatic cancer cells. Pancreatology, 2003, 3(4) : 293-302.
  • 6Trapasso F, Pichiorri F, Gaspari M, et al. Fhit interaction with ferredoxin reductase triggers generation of reactive oxygen species and apoptosis of cancer cells. J Biol Chem, 2008, 283 ( 20 ) : 13736-13744.
  • 7Weiske J, Albring K F, Huber O. The tumor suppressor Fhit acts as a repressor of beta-catenin transcriptional activity. Proc Natl Acad Sci U S A, 2007, 104(51 ) : 20344-20349.
  • 8Morin P J. beta-catenin signaling and cancer. Bioessays, 1999, 21 (12) : 1021-1030.
  • 9Bienz M, Clevers H. Linking colorectal cancer to Wnt signaling. Cell, 2000, 103(2) : 311-320.
  • 10Mosimann C, Hausmann G, Basler K. Beta-catenin hits chromatin: regulation of Wnt target gene activation. Nat Rev Mol Cell Biol, 2009, 10(4) : 276-286.

同被引文献41

引证文献5

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部