首都医科大学学报 ›› 2016, Vol. 37 ›› Issue (1): 12-16.doi: 10.3969/j.issn.1006-7795.2016.01.003

• 消化系统重大疾病的全链条研究 • 上一篇    下一篇

PHF8基因对食管鳞状细胞癌裸鼠移植瘤生长的影响

朱圣韬1,2,3, 孙秀静2,3,4, 李鹏1,2,3, 郭庆东1,2,3, 朱圣泉1,2,3, 张澍田1,2,3   

  1. 1. 首都医科大学附属北京友谊医院消化内科, 北京 100050;
    2. 国家消化系统疾病临床医学研究中心, 北京 100050;
    3. 首都医科大学消化病学系, 北京 100050;
    4. 首都医科大学附属北京天坛医院消化内科, 北京 100050
  • 收稿日期:2015-12-25 出版日期:2016-02-21 发布日期:2016-02-01
  • 通讯作者: 张澍田 E-mail:zhangshutian@ccmu.edu.cn
  • 基金资助:
    国家自然科学基金(81302160, 81272447), 国家消化系统疾病临床医学研究中心基金(2015BAI13B09)。

Effect of PHF8 gene on the growth of transplanted tumor of esophageal squamous-cell carcinoma in nude mice

Zhu Shengtao1,2,3, Sun Xiujing2,3,4, Li Peng1,2,3, Guo Qingdong1,2,3, Zhu Shengquan1,2,3, Zhang Shutian1,2,3   

  1. 1. Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China;
    2. National Clinical Research Center for Digestive Diseases, Beijing 100050, China;
    3. Faculty of Gastroenterology, Capital Medical University, Beijing 100050, China;
    4. Department of Gastroenterology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China
  • Received:2015-12-25 Online:2016-02-21 Published:2016-02-01
  • Supported by:
    This study was supported by National Natural Science Foundation of China (81302160, 81272447), National Clinical Research Center for Digestive Diseases (2015BAI13B09).

摘要: 目的 利用慢病毒(lentivirus)介导的短发卡RNA(short hairpin RNA,shRNA)建立人食管鳞状细胞癌(esophageal squamous-cell carcinoma,ESCC,以下简称食管鳞癌)裸鼠移植瘤模型,观察锌指蛋白8(plant homeodomain finger protein 8,PHF8)对移植瘤生长的影响。方法 分别将未感染慢病毒(空白对照组)、感染Nonsilencing-shRNA慢病毒(阴性对照shRNA组)和PHF8 shRNA慢病毒(PHF8 shRNA组)的人食管鳞癌细胞系TE-1接种于裸鼠背部皮下,建立食管鳞癌裸鼠移植瘤模型。定期测量肿瘤体积,绘制肿瘤生长曲线。4周后处死裸鼠,定量PCR及Western blotting法检测肿瘤组织中PHF8的表达。结果 PHF8 shRNA组较阴性对照shRNA组、空白对照组的裸鼠致瘤能力明显减弱,PHF8 mRNA和蛋白的表达水平显著降低。结论 慢病毒介导的shRNA干扰能有效减少食管鳞癌裸鼠移植瘤中PHF8的表达,而降低PHF8的表达能抑制食管鳞癌移植瘤的生长。

关键词: PHD锌指蛋白8, 慢病毒, 食管鳞状细胞癌, 裸鼠移植瘤

Abstract: Objective To establish nude mice models with implanted tumor of esophageal squamous-cell carcinoma cells, and to observe the effects of PHF8 gene on the growth of implanted tumor. Methods Nude mice were injected subcutaneously into their right posterior flank with human TE-1 esophageal squamous-cell carcinoma cells (control group), lentivirus mediated Non-silencing shRNA TE-1 cells (Non-silencing shRNA group), or lentivirus mediated PHF8 shRNA TE-1 cells (PHF8 shRNA group), respectively. The size of implanted tumor was measured at regular intervals and the growth curve of tumor was portrayed. Animals were sacrificed at 4 weeks, and the silencing of PHF8 in tumor tissues was confirmed by real-time PCR and Western blotting.Results The tumorigenic effect on nude mice was weaker and lower in PHF8 shRNA group, as compared to those in Non-silencing shRNA group and control group. The expression of PHF8 mRNA and protein in PHF8 shRNA group was significantly decreased. Conclusion Lentivirus mediated shRNA effectively inhibited the expression of PHF8 in transplanted tumor of nude mice with human esophageal squamous-cell carcinoma cell lines, and the tumorigenic ability was significantly reduced.

Key words: PHD finger protein 8, lentivirus, esophageal squamous cell carcinoma, transplanted tumor in nude mice

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