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胃泌素及其受体拮抗剂丙谷胺与胃癌BGC-823细胞系P16、P21蛋白的表达研究 被引量:4

Research of the relationship of gastrin and gastrin receptor antagonist proglumide and the expression of protein P16 as well as P21 in BGC-823 gastric cancer cell line
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摘要 目的:探讨丙谷胺(PGM)抑制胃癌BGC-823细胞增殖及胃泌素的促增殖作用,通过P16及P21蛋白表达的变化,为内分泌途径治疗胃癌提供理论依据,并提供内分泌途径治疗癌症疗效的指标。方法:通过体外细胞培养及对癌细胞进行分组实验研究,应用免疫荧光技术及Northern blot方法测定癌细胞内P16及P21蛋白的表达情况。结果:P16蛋白的表达量随PGM的抑癌作用而升高,两者呈负相关;P21蛋白的表达量与PGM的抑癌作用无明显相关。结论:丙谷胺作为胃癌的一种内分泌治疗手段,可采用P16的表达情况作为其疗效的一个指标。 Objective: To explore the effect of proglumide (PGM) on inhibiting the multiplication of stomach cancer cell line BGC-823 and the effect of gastrin on multiplication of BGC-823, and provide theoretical basis for curing stomach cancer for endocrine pathway by the expression change of P16 and P21, and provide indicators for the cure effect of endocrine pathway. Methods: Stomach cancer cells were cultured in vitro and divided into different groups for experiment, then immunofluorescent technique and Northern blot were used to detect the expression of P16 and P21. Results: The expression of P16 protein increased with the inhibitory effect of PGM, and they showed negative correlation; the expression of P21 protein showed no obvious correlation with the inhibitory effect of PGM. Conclusion: As one of the endocrine cure methods for stomach cancer, the expression of P16 can be one indicator for the curative effect.
出处 《中国医药导报》 CAS 2009年第32期5-7,共3页 China Medical Herald
关键词 胃泌素 丙谷胺 P16 P21 细胞周期 Gastrin Proglumide P16 P21 Cell cycle
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  • 1He SW,Shen KQ,He YJ,Xie B,Zhao YM.Regulatory effect and mechanism of gastrin and its antagonists on colorectal carcinoma[J].World Journal of Gastroenterology,1999,5(5):408-416. 被引量:20
  • 2孙为豪,曹大中,俞谦,欧希龙,沈洪,俞婷,朱峰,孙运良,傅熙玲.胃泌素对大鼠胃粘膜环氧合酶及生长因子表达的影响[J].中国病理生理杂志,2005,21(2):271-275. 被引量:4
  • 3黄广建,王和明,张延龄.胃泌素受体拮抗剂抑制胃癌细胞生长的可行性研究[J].中国胃肠外科杂志,1999,2(4):228-231. 被引量:6
  • 4金正均.合并用药中的相加[J].中国药理学报,1980,1:70-73.
  • 5Aly A, Shulkes A, Baldwin GS. Gastrins, cholecystokinins and gastrointestinal cancer. Biochim Biophys Acta, 2004, 1704: 1-10.
  • 6Szabo I, Rumi G, Bodis B, et al. Gastrin and pentagastrin enhance the tumour proliferation of human stable cultured gastric adenocarcinoma cells. J Physiol Paris, 2000, 94: 71-74.
  • 7Martinsen TC, Kawase S, Hakanson R, et al. Spontaneous ECL cell carcinomas in cotton rats: natural course and prevention by a gastrin receptor antagonist. Carcinogenesis, 2003, 24 : 1887-1896.
  • 8Sawaoka H, Kawano S, Tsuji S, et al. Cyclooxygenase-2 inhibitors suppress the growth of gastric cancer xenografts via induction of apoptosis in nude mice. Am J Physiol, 1998, 274 : G1061-1067.
  • 9Konturek PC, Kania J, Kukharsky V, et al. Influence of gastrin on the expression of cyclooxygenase-2, hepatocyte growth factor and apoptosis-related proteins in gastric epithelial cells. J Physiol Pharmacol, 2003, 54: 17-32.
  • 10Yao M, Song DH, Rana B, et al. COX-2 selective inhibition reverses the trophic properties of gastrin in colorectal cancer. Br J Cancer, 2002, 87: 574-579.

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