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中国临床药理学与治疗学 ›› 2007, Vol. 12 ›› Issue (5): 512-515.

• 基础研究 • 上一篇    下一篇

胃泌素释放肽DNA疫苗抑制EMT6乳腺癌生长的实验研究

欧阳可栋1, 过为1, 吴国君1, 张舒亚2, 刘景晶1   

  1. 1中国药科大学生命科学与技术学院,南京 210009,江苏;
    2上海出入境检验检疫局,上海 200135
  • 收稿日期:2007-03-06 修回日期:2007-04-27 发布日期:2020-10-29
  • 通讯作者: 刘景晶,男,博导,研究方向:基因工程药学。Tel:025-83271242 E-mail:minigene1@yahoo.com.cn
  • 作者简介:欧阳可栋,男,博士,研究方向:肿瘤免疫。Tel:13818725338 E-mail:ouyangkedong@yahoo.com.cn
  • 基金资助:
    国家自然科学基金资助( 30270298)

Suppressing effect of gastrin-releasing peptide DNA vaccine on EMT6 breast cancer growth

OUYANG Ke-dong1, GUO Wei1, WU Guo-jun1, ZHANG Shu-ya2, LIU Jing-jing1   

  1. 1School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, Jiangsu, China;
    2Shanghai Entry-Exit Inspection and Quarantine Bureau, Shanghai 200135, China
  • Received:2007-03-06 Revised:2007-04-27 Published:2020-10-29

摘要: 目的: 观察胃泌素释放肽(GRP)DNA 疫苗对EMT6 小鼠乳腺癌生长的抑制作用。方法: 将构建的GRP DNA疫苗pCR3.1-VS-HSP65-TP-GRP6-M2 肌肉注射免疫BALB/c 雌性小鼠,2 周1 次,共5 次。采用ELISA 法对小鼠的血清中抗GRP-IgG 类抗体进行检测。最后一次免疫后第2 周,接种EMT6小鼠乳腺癌细胞。于肿瘤细胞接种后d 14,处死全部动物,称量肿瘤的质量和测量肿瘤的体积。并对瘤组织进行常规HE 染色。结果: pCR3.1-VS-HSP65-TPGRP6-M2 免疫BALB/c 小鼠,可诱导抗GRP-IgG 类抗体的产生。并对随后的EMT6 肿瘤细胞攻击有显著的抑制作用(P<0.01),抑瘤率为46.53 %。病理学检查结果显示,GRP DNA 疫苗成功地激发了宿主的抗肿瘤免疫反应;与pCR3.1-VS-HSP65-TP 对照组相比,GRP DNA疫苗免疫组小鼠EMT6肿瘤组织浸润性下降。结论: GRP DNA 疫苗显著抑制EMT6 乳腺癌生长, 为此类疫苗应用研究奠定了基础。

关键词: 胃泌素释放肽, DNA疫苗, 乳腺癌, 抑瘤率

Abstract: AIM: To observe the inhibiting effect of the GRP DNA vaccine on EMT6 breast cancer tissue. METHODS: Female BALB c mice were immunized intramuscularly with GRP DNA vaccine pCR3. 1-VS-HSP65- TP-GRP6-M2 5 times at 2-weekly intervals. The specific anti-GRP antibody was detected by ELISA method. Two weeks after the last immunization, tumor challenge experiments were performed by using EMT6. After 14 d of challenge experiments, all mice were killed and tumors were weighted. Histological analysis of tumor tissue was carried out with HE staining. RESULTS: The specific anti-GRP antibodies were detected in the antiserum of the female BALB c mice immunized with pCR3. 1-VS-HSP65-TPGRP6- M2 DNA vaccine. It showed that EMT6 tumor growth in mice of GRP DNA vaccine group was obviously suppressed (P<0.01) compared with that in pCR3. 1- VS-HSP65-TP or saline control group, with tumor inhibitory rate of 46. 53 %. Histological analysis showed that GRP DNA vaccine successfully induced anti-tumor immune responses in vivo, and, the invasiveness of EMT6 tumor tissues was markedly decreased in mice of GRP DNA vaccine group compared with that in pCR3. 1-VSHSP65- TP control group. CONCLUSION: GRP DNA vaccine can significantly suppress the growth of EMT6 breast cancer in vivo, which lays a basis for further research.

Key words: gastrin-releasing peptide, DNA vaccine, breast cancer, tumor inhibitory rate

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