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大肠癌细胞的原代培养方法 被引量:3

The Study on the Primary Culture Methods of Human Colorectal Cancer Cells
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摘要 目的:探讨大肠癌细胞体外分离培养方法,建立合理、高效、稳定的短期大肠癌细胞原代培养模式。方法:取60例大肠癌(T3或T4,且CT示肿瘤直径>2.0 cm)的新鲜肿瘤组织,随机分为黏膜层取材组与浆膜层取材租,分别采用组织块法、机械分离法、胰酶消化法、胶原酶消化法进行体外培养大肠癌细胞,对不同方法及培养条件进行比较并加以改进。结果:黏膜层取材组优于浆膜层取材组(P<0.05),胶原酶消化法优于胰酶消化法(P<0.05),胰酶消化法优于机械分离法(P<0.05),胶原酶消化法是最优的人类大肠癌细胞原代培养方法,细胞培养成功率达到66.7%。结论:通过黏膜层取材的胶原酶消化法可成功建立较为合理、高效、稳定的短期大肠癌细胞原代培养模式。 Objective To investigate the human colorectal cancer cells how to be cultured in vitro methods, then establish a rational, efficient and stable short-term primary culture model of colorectal cancer cells. Methods 60 cases of colorectal cancer (T3 or T4, and CT showed: tumor size〉2.0 cm) of fresh tumor tissue which were diagnosed in the hospital were randomly divided into 2 groups,namely the mucous layer and serosal layer derived group. Tissue were divided in these vitro methods to cultivate human colorectal cancer cells ,then culture conditions on the different methods were compared and improved.These methods include tis sue nubbles cultivation, mechanical separation, trypsin digestion, collagenase digestion and cultured. Results The success rate of the mucous layer derived group was better than the mucosal serosal layer derived group (P 〈 0.05). Col- lagenase digestion method was superior to trypsin digestion method (P 〈 0.05). Trypsin digestion method was bet- ter than mechanical separation method to achieve the target (P 〈 0.05).Among these methods, collagenase diges- tion method in which human colorectal cancer cells is the best method for primary culture.The success rate of cell cultivation could be 66.7%. Conclusion The more rational, efficient and stable short-term primary cul- ture model of colorectal cancer cells has been established,which is to draw through the mucous layer,in opti- mized collagenase digestion method.
出处 《中国中西医结合外科杂志》 CAS 2012年第4期341-345,共5页 Chinese Journal of Surgery of Integrated Traditional and Western Medicine
基金 浙江省医学会临床科研基金项目(2009ZYC50) 台州市科技计划项目(2010-26-48)
关键词 大肠癌细胞 原代培养 鉴定 黏膜层 胶原酶消化法 Colorectal cancer cell,primary culture,identification, mucous layer, collagenase digestion
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参考文献4

  • 1Saunders M, Iveson T. Management of advanced colorectal cancer:state of the art [J]. Br J Cancer,2006,95(2):131-138.
  • 2Dangles-Marie V, Pocard M, Richon S,et al. Establishment of human colon cancer cell lines from fresh tumors versus xenografts: comparison of success rate and cell line features [J]. Cancer Res, 2007,67(1):398-407.
  • 3Alessandra Faillil,Rita Consolinil.The challenge of culturing human colorectal tumor cells: establishment of a cell culture model by the comparison of different methodological approaches [J]. Tumori,2009,95(3):343 -347.
  • 4Simon P. Cancer cell culture:methods and protocols [M]. New Jersey Humana Press,2004:79-93.

同被引文献43

  • 1朱学泰,谢溱,马瑞君.单克隆抗体制备技术研究进展[J].甘肃科技,2005,21(3):108-109. 被引量:16
  • 2鄢开胜,罗凌惠,付勇,陈广理,龚树生.鼠尾胶原在原代培养耳蜗血管纹边缘细胞中的应用[J].临床耳鼻咽喉科杂志,2006,20(10):463-465. 被引量:4
  • 3吕会增,魏波,陈图峰.奥沙利铂对人结肠癌细胞LoVo和SW480/M5作用的实验研究[J].消化肿瘤杂志,2012,34(1):34-39.
  • 4Alessandra Faillil,Rita Consolinil. The challenge of cul- turing human colorectal tumor cells: establishment of a cell culture model by the comparison of different method- ological approaches[J]. Tumori, 2009,95 (3) :343 -347.
  • 5Durocher Y,Butler M. Expression systems for therapeutic glycoprotein production [J].Curr Opin Biotechnol, 2009, 20(6):700-707.
  • 6Ko K,Ahn MH,Song M,et al. Glyco-engineering of bio- therapeutic proteins in plants[J]. Mol Cells, 2008,25 (4) : 494-503.
  • 7焦保庭,杨伟明,贺子彪,宋辉.原代大肠癌细胞分离培养中的影响因素[J].贵州医药,2007,31(10):870-872. 被引量:3
  • 8SAUNDERS M, IVESON T. Management of advanced col- orectal cancer: state of the art [J]. Br J Cancer,2006,95 (2): 131-138.
  • 9LANGDON S P. Basic principles of cancer cell culture[J]. Methods Mol Med, 2004,88( 1 ) : 3- 15.
  • 10ARUL M, ROSLANI A C, NG C L,et al. Culture of low passage colorectal cancer cells and demonstration of varia- tion in selected turnout marker expression [ J ]. Cytotechnol- ogy, 2014,66( 1 ) :481 -491.

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