中国组织工程研究 ›› 2012, Vol. 16 ›› Issue (11): 1959-1962.doi: 10.3969/j.issn.1673-8225.2012.11.014

• 组织构建细胞学实验 cytology experiments in tissue construction • 上一篇    下一篇

人宫颈癌细胞的体外培养及鉴定*★

马秀萍,程静新,张  瑜,袁  敏   

  1. 新疆医科大学附属肿瘤医院妇科,新疆维吾尔自治区乌鲁木齐市 830000
  • 收稿日期:2011-10-14 修回日期:2011-12-24 出版日期:2012-03-11
  • 通讯作者: 程静新,硕士,主任医师,教授,新疆肿瘤医院妇科,新疆维吾尔自治区乌鲁木齐市 830000 13899899061@139.com
  • 作者简介:马秀萍★,女,回族,1980年生,新疆维吾尔自治区吉木萨尔县人,新疆医科大学在读硕士,主要从事妇科肿瘤方面的研究。 mxp8080@163.com
  • 基金资助:

    新疆维吾尔自治区自然科学基金资助项目(项目编号:2010211A31),课题名称:局部晚期子宫颈癌个体化新辅助化疗模式探讨。

Culture in vitro and identification of human cervical carcinoma cells

Ma Xiu-ping, Cheng Jing-xin, Zhang Yu, Yuan Min   

  1. Department of Gynecology, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi  830000, Xinjiang Uygur Autonomous Region, China
  • Received:2011-10-14 Revised:2011-12-24 Online:2012-03-11
  • Contact: author: Cheng Jing-xin, Master, Chief physician, Professor, Department of Gynecology, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi 830000, Xinjiang Uygur Autonomous Region, China 13899899061@139.com
  • About author:Ma Xiu-ping★, Studying for master’s degree, Department of Gynecology, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi 830000, Xinjiang Uygur Autonomous Region, China mxp8080@163.com
  • Supported by:

    Natural Science Foundation of Xinjiang Uygur Autonomous Region, No. 2010211A31*

摘要:

背景:由于肿瘤存在个体差异,对癌株的研究不能准确反映个体之间的差异,原代细胞培养则与体内状态更相近。
目的:体外培养建立宫颈癌细胞原代培养方法。
方法:采用胰蛋白酶及Ⅰ型胶原酶联合消化法从23例新鲜宫颈癌组织获取宫颈癌细胞,测定其细胞生长曲线,并用免疫荧光染色检测细胞表面标记物CD44、CK17进行鉴定。
结果与结论:23例中有21例成功从宫颈癌组织中获取宫颈癌细胞并能连续传代,稳定增殖,免疫荧光染色显示宫颈癌细胞表面标记物CD44、CK17表达呈阳性。说明胰蛋白酶及Ⅰ型胶原酶联合消化法能成功分离原代宫颈癌细胞。
关键词:原代培养;鳞状上皮细胞;宫颈癌;增殖;胰蛋白酶
doi:10.3969/j.issn.1673-8225.2012.11.014

关键词: 原代培养, 鳞状上皮细胞, 宫颈癌, 增殖, 胰蛋白酶

Abstract:

BACKGROUND: There are individual differences in the patients suffered tumor. Therefore the research on the cancer line can not show accurate differences between individuals, while primary cell culture can show more similar characteristics to in vivo state.
OBJECTIVE: To establish a method in vitro for primary culture of cervical carcinoma cells.
METHODS: Cervical cancer cells were obtained from 23 fresh cervical cancer tissues using the trypsin and collagenase type Ⅰdigestion, and their growth curve was detected. Cell surface markers of CK17and CD44 were identified with immunofluorescence staining.
RESULTS AND CONCLUSION: Cervical cancer cells were obtained from 21 of 23 cases, and the cells had the continuous passage and steady proliferation. Immunofluorescence staining showed that the cells positively expressed CK17 and CD44. It is indicated that primary cervical carcinoma cells can be obtained by trypsin and collagenase type Ⅰdigestion.
 

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