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Midkine和Caspase-3在胰腺癌中的表达与细胞凋亡的关系 被引量:8

Expression of Midkine and Caspase-3 and their relationship with apoptosis in pancreatic cancer
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摘要 目的:研究人胰腺癌组织中Midkine(MK)和Caspase-3蛋白的表达特点,探讨其表达与胰腺癌细胞凋亡的关系.方法:收集人胰腺癌组织标本49例,免疫组织化学SP法检测MK和Caspase-3蛋白的表达,原位凋亡检测试剂盒辣根过氧化物酶(TUNEL)检测细胞凋亡指数.以同期15例正常胰腺组织标本为对照.结果:MK蛋白、Caspase-3蛋白在胰腺癌组织中的阳性表达率高于正常胰腺组织(71.4%vs0,P<0.01;77.6%vs46.7%,P<0.05),MK蛋白表达与胰腺癌组织学分化、临床分期和淋巴转移相关(P<0.05),Caspase-3蛋白表达仅与组织学分化有关;胰腺癌组织标本中,MK阳性表达组凋亡指数显著低于MK阴性表达组(5.13±2.69vs7.93±6.65,P<0.05);胰腺癌组织中MK与Caspase-3蛋白的表达呈负相关(r=-0.34,P<0.05).结论:MK和Caspase-3参与了胰腺癌的发生发展,MK在胰腺癌组织中的高表达具有抑制细胞凋亡的生物学功能,其作用机制可能是通过抑制Caspase-3的活性. AIM: To study the expression of Midkine (MK) protein and Caspase-3 protein in human pancreatic cancer and to investigate their association with cell apoptosis. METHODS: The immunohistochemical staining (SP) method was used to detect the expression of MK protein and Caspase-3 in 49 cases of pancreatic cancer tissues and 15 cases of normal pancreatic tissues. The TUNEL method was used to detect apoptotic index in pancreatic cancer tissues. RESULTS: The positive rates of MK protein and Caspase-3 protein were significantly higher in pancreatic cancer tissue than in normal pancreatic tissue (71.4% vs 0, P 〈 0.01; 77.6% vs 46.7%, P 〈 0.05). Expression of MK protein was correlated with tumor's histological grading, clinical stages and lymph node metastasis (P 〈 0.05) while expression of Caspase-3 protein was only correlated with tumor's histological grading (P 〈 0.05). The mean apoptotic index was significantly lower in MK positive expression group than in MK negative expression group (5.13 ± 2.69 vs 7.93 ± 6.65, P 〈 0.05). The expression level of MK protein had a negative correlation with Caspase-3 (r = -0.34, P 〈 0.05). CONCLUSION: The gene of Midkine and Caspase-3 participate in development of pancreatic cancer, and high express of Midkine has a biological function of inhibiting cell apoptosis possibly through suppressing cell activity of Caspase-3 protein.
出处 《世界华人消化杂志》 CAS 北大核心 2008年第35期4015-4019,共5页 World Chinese Journal of Digestology
基金 武汉科技大学附属天佑医院中青年科研基金资助项目 No.zq2008006~~
关键词 胰腺癌 MIDKINE CASPASE-3 细胞凋亡 Pancreatic cancer Midkine Caspase-3 Apoptosis
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  • 1刘剑波,连涛,高学岗,赵爱志,李开宗.原发性肝癌患者血清高水平VEGF的意义[J].肿瘤防治杂志,2005,12(9):682-685. 被引量:8
  • 2Ying-Jia Ren,Qing-Yun Zhang.Expression of midkine and its clinical significance in esophageal squamous cell carcinoma[J].World Journal of Gastroenterology,2006,12(13):2006-2010. 被引量:14
  • 3Lieberman SM, Horig H, Kaufman HL. Innovative treatments for pancreatic cancer[J]. Surg Clin North Am,2001,81(3) :715-739.
  • 4Rosenberg L, Lipsett M.Biotherapeutic approaches to pancreatic cancer[J]. Expert Opin Biol Ther, 2003,3(2): 319-337.
  • 5Mulvihill S, Warren R, Venook A, et al. Safety and feasibility of injection with an E1B-55 kDa gene-deleted, replication-selective adenovirus (ONYX-015) into primary carcinomas of the pancreas: a phase I trial[J]. Gene Ther,2001,8(4) :308-315.
  • 6Tango Y, Fujiwara T, Itoshim T, et al. Adenovirus-mediated pl4ARF gene transfer cooperates with Ad5CMV-p53 to induce apoptosis in human cancer cells[J]. Hum Gene Ther, 2002, 13(11):1373-1382.
  • 7Hecht JR, Bedford R, Abbmzzese JL, et al. A Phase I/Ⅱ Trial of Intratumoral Endoscopic Ultrasound Injection of ONYX-015 with Intravenous Gemcitabine in Unresectable Pancreatic Carcinoma [J].Clin Cancer Res, 2003,9(2): 555-561.
  • 8Wesseling JG, Yamamoto M, Adachi Y, et al. Midkine and cyclooxygenase-2 promoters are promising for adenoviral vector gene delivery of pancreatic carcinoma [J]. Cancer Gene Ther, 2001,8 (12): 990-996.
  • 9Ohashi M, Kanai F, Tanaka T, et al. In vivo adenovirus-mediated prodrug gene therapy for carcinoernbryonic antigen-producing pancreatic cancer[J]. Jpn J Cancer Res, 1998,89 (4): 457-462.
  • 10Miki K, Xu M, Gupta A, et al. Methioninase cancer gene therapy with selenomethionine as suicide prodrug substrate [J]. Cancer Res,2001,61(18) :6805-6810.

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