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人内皮抑素基因导入对裸鼠舌鳞癌移植瘤的抑制影响 被引量:2

Intra-tumoral and intra-muscular administration of human endostatin gene inhibits Tca8113 cell growth
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摘要 目的:探讨经体内注入人内皮抑素(humanendostatin,hES)基因治疗口腔鳞癌的可行性。方法:荷瘤人舌鳞癌Tca8113细胞裸鼠瘤体内和肌内分别注射含hES的基因质粒,观察转入hES基因对舌鳞癌移植瘤生长的影响,免疫组织化学检测肿瘤组织中hES及血管内皮细胞生长因子(vascularvesselendotheliacellgrowthfactor,VEGF)的表达,Weidern法行肿瘤微血管密度(microvesseldensity,MVD)计数,流式细胞仪检测肿瘤细胞凋亡率,采用精确概率法和单因素方差分析进行统计学处理。结果:荷瘤注射hES后第16天,瘤体注射组抑瘤率为75.0%,肌内注射组抑瘤率为66.1%(P<0.01)。免疫组织化学检测结果显示,hES在瘤体注射组和肌内注射组肿瘤中的表达率分别为90.0%和85.0%,均高于对照组的20.0%(P<0.01)。2实验组肿瘤MVD值分别为18.60±3.44和16.70±2.63,均低于对照组的22.40±3.41(P<0.01)。流式细胞仪检测发现,瘤体注射和肌内注射hES基因质粒后,肿瘤细胞凋亡率分别为11.36%±3.20%和8.08%±2.00%,均高于对照组的1.80%±0.50%(P<0.01)。结论:注射hES基因具有抑制舌鳞癌Tca8113细胞移植瘤生长的效应。 PURPOSE: To investigate the inhibitory effect of Lipofectatmin-mediated p^BLST-hES on Tca8113 cell implantation tumor growth in rivo. METHODS: To observe tumor growth, the nude mice bearing Tca8113 tumors received injection of lipofectamin-plasmid complexes, then the tumors were measured once in every three days. 16 days after injection, S-P immunohistochemistry was used to detect the expression of hES and VEGF in the tumors, FCM was used to detect the apoptosis of tumor cell. With CD34 staining, the MVD in tumors was counted. Fisher's exact test and the analysis of variance were adopted for statistical analysis of count data and measurement data. RESULTS: Compared with the control group, the reduction of tumor volume was about 75.0% in the group of intratumoral administration hES gene and 66.1% in the group of intramuscular injection of hES gene. The volume reduction obtained in both groups was statistically significant when compared with controls (P〈0.01). The expression of hES was 90.0% and 85.0% respectively, both significantly higher than that in the control group (20.0%,P〈0.01). Otherwise, the expression of VEGF in the experimental groups was lower than that in the controls (P〈0.01). The MVD was 18.60±3.44 in tumors received injection of hES gene intratumorally and 16.70±2.63 in tumors received injection of hES gene intramuscully, both showed statistically significant when compared with that in the control group (P〈0.01), The apoptosis rate was 11.36%±3.20% and 8.08%±2.00% respectively, both higher than that of the control group (1.80%±0.50% ,P〈0.01). CONCLUSION: The results suggested that intratumoral and intramuscular injection of hES gene can inhibit the growth of Tca8113 cell tumor effectively.
出处 《中国口腔颌面外科杂志》 CAS 2005年第3期218-222,共5页 China Journal of Oral and Maxillofacial Surgery
基金 广东省自然科学基金(04300248) 广东省医学科学技术基金(2003A025)
关键词 内皮抑素 基因治疗 抗血管生成 舌鳞癌细胞Tca8113 Endostain Gene therapy Anti-angiogenesis Tea8113
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参考文献12

  • 1[1]O'Reilly MS, Boehm T, Shing Y, et al. Endostatin: an endogenous inhibitor of angiogenesis and tumor growth [J]. Cell, 1997, 88(2):277-285. 被引量:1
  • 2[2]Nguyen JT, WU P, Clouse ME, et al. Adeno-associated virusmediated delivery of anti angiogenic factors as an antitumor strategy [J]. Cancer Res, 1998, 58(24): 5673-5677. 被引量:1
  • 3潘朝斌,黄洪章,王建广,侯劲松,李海刚.人内皮抑素基因转染对舌鳞癌Tca8113细胞生长的影响[J].中华口腔医学杂志,2004,39(4):273-276. 被引量:4
  • 4潘朝斌,黄洪章,王建广,侯劲松.脂质体介导hES基因转染人舌鳞癌Tca8113细胞及其蛋白表达[J].华西口腔医学杂志,2004,22(2):96-99. 被引量:1
  • 5[5]Weidner N. Current pathologic methods for measuring intratumoral microvessel density within breast carcinoma and other solid tumors [J]. Breast Cancer Res Treat, 1995, 36(2): 169-180. 被引量:1
  • 6[6]Blezinger P, Wang J, Gondo M, et al. Systemic inhibition of tumor growth and tumor metastases by intramuscular administration of the endostatin gene [J]. Nat Biotechnol, 1999, 17(4): 343-348. 被引量:1
  • 7[7]Boehn T, Folkman J, Browder T, et al. Antiangiogenesis therapy of experimental cancer dose not induce acquired drug resistance [J].Nature, 1997, 390(6658): 404-407. 被引量:1
  • 8[8]Folkman J. Antiangiogenic gene therapy [J]. Proc Natl Acad Sci 1998, 95(16): 9064-9066. 被引量:1
  • 9[9]Chen QR, Kumar D, Stass SA, et al. Liposomes complexed to plasmids encoding angiostatin and endostatin inhibit breast cancer in nude mice [J]. Cancer Res, 1999, 59(14): 3308-3312. 被引量:1
  • 10[10]Szary J, Szala S. Intra-tumoral administration of naked plasmid and encoding mouse endostatin inhibits renal carcinoma growth [J]. Int J Cancer, 2001, 91(6): 835-839. 被引量:1

二级参考文献14

  • 1李晓明.血管内皮细胞生长因子及其受体与肿瘤血管形成[J].国外医学(肿瘤学分册),1997,24(1):11-13. 被引量:54
  • 2Olkman J. Clinical applications of research on angiogenesis . N Engl Med, 1995,333: 1757-1763. 被引量:1
  • 3Weidner N. Current pathologic methods for measuring intratumoral microvessel density within breast carcinoma and other solid tumors . Breast Cancer Res Treat, 1995, 36: 169-180. 被引量:1
  • 4Yamaguchi N, Anand- Apte B, Lee M, et al. Endostatin inhibits VEGF-induced endothelial cell migration and tumor growth independently of zinc binding . EMBO J, 1999, 18: 4414-4423. 被引量:1
  • 5Yoon SS, Eto H, Lin CM, et al. Mouse endostatin inhibits the formation of lung and liver metastases. Cancer Res, 1999, 59: 6251-6256. 被引量:1
  • 6Dixelius J, Larsson H, Sasaki T, et al. Endostatin- induced tyrosine kinase signaling through the Shb adaptor protein regulates endothelial cell apoptosis . Blood, 2000, 95: 3403-3411. 被引量:1
  • 7Dhanabal M, Ramchandran R, Waterman MJ, et al. Endostatin induce enthothelial cell apoptosis. J Biol Chem, 1999, 274: 11721-11726. 被引量:1
  • 8Taddei L, Chiarugi P, Brogelli L, et al. Inhibitory effect of full length human endostatin on in vitro angiogenesis. Biochem Biophys Res Commun, 1999, 263: 340-345. 被引量:1
  • 9Redlitz A, Daum G, Sage EH. Angiostatin diminishes activation of the mitogen- activated protein kinases ERK-1 and ERK-2 in human dermal microvascular endothelial cells . J Vasc Res, 1999, 36: 28-34. 被引量:1
  • 10O′Reilly MS, Boehm T, Shing Y, et al. Endostatin: an endogenous inhibitor of angiogenesis and tumor growth. Cell, 1997, 88: 277-285. 被引量:1

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