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胰腺癌组织存活素和极光B表达的相关性[J]. 肿瘤防治研究, 2010, 37(02): 185-188. DOI: 10.3971/j.issn.1000-8578.2010.02.016
引用本文: 胰腺癌组织存活素和极光B表达的相关性[J]. 肿瘤防治研究, 2010, 37(02): 185-188. DOI: 10.3971/j.issn.1000-8578.2010.02.016
Investigation of Expression and Correlation of survivin and AURORA_B in Pancreatic Denocarcinoma Tissues[J]. Cancer Research on Prevention and Treatment, 2010, 37(02): 185-188. DOI: 10.3971/j.issn.1000-8578.2010.02.016
Citation: Investigation of Expression and Correlation of survivin and AURORA_B in Pancreatic Denocarcinoma Tissues[J]. Cancer Research on Prevention and Treatment, 2010, 37(02): 185-188. DOI: 10.3971/j.issn.1000-8578.2010.02.016

胰腺癌组织存活素和极光B表达的相关性

Investigation of Expression and Correlation of survivin and AURORA_B in Pancreatic Denocarcinoma Tissues

  • 摘要: 目的 探讨凋亡抑制蛋白存活素(survivin)和极光B(AURORA_B)在胰腺癌组织中的表达与生物学行为之间的关系及两者的相关性。 方法 用免疫组织化学SP法检测45例胰腺癌和8例慢性胰腺炎及7例正常胰腺组织切片的survivin和AURORA_B的表达。 结果 45例胰腺癌中survivin和AURORA_B蛋白的阳性表达率分别为75.55%和53.33%;两者在7例正常胰腺组织中均未发现阳性表达;两者在8例慢性胰腺炎组织中的阳性表达率分别为25%和0。survivin的表达与组织学分级有关(P<0.05),而与临床分期和淋巴结转移关系不大(P>0.05),AURORA_B的表达与临床分期和淋巴结转移有关(P<0.05),而与组织学分级关系不大(P>0.05);survivin与AURORA_B的表达密切相关(P<0.05)。两者的表达与患者的性别、年龄、肿瘤的大小及部位均无关。 结论 survivin和AURORA_B密切相关,可能在胰腺癌的发生、发展过程中起关键作用,可能为胰腺癌的治疗和预防提供了新的靶点。

     

    Abstract: Objective To investigate the correlation between the expression of survivin and AURORA_B protein and their clinical biological behavior in human pancreatic carcinoma tissues. Methods SP immunohistochemical method was used to detect expression of survivin and AURORA_B in 45 cases of human pancreatic carcinoma tissues,8 cases of chronic pancreatitis tissues and 7 normal pancreas tissues. Results The positive expression rates of survivin and AURORA_B in 45 cases of pancreatic carcinoma tissues were 75.55% and 53.33%, respectively, and no expression of survivin and AURORA_B was found in the 7 cases of normal pancreas tissues. In addition, the expression rates of survivin and AURORA_B in 8 cases of chronic pancreatitis tissues were 25% and 0, respectively. The survivin expression was significantly correlated with the histological grade (P<0.05), but not with the clinical stages and lymph node metastasis (P>0.05). The AURORA_B expression was significantly correlated with the clinical stages and lymph node metastasis (P<0.05), but not with the histological grades(P>0.05). The expressions of survivin and AURORA_B had no correlation with age, gender, tumor size and location, however, the expression of survivin was closely correlated with that of AURORA_B (P<0.05). Conclusion survivin and AURORA_B were intimately related to pancreatic carcinoma. They may play an important role in the tumorigenesis and tumor progression in pancreatic cancer and provide some new targets for the therapy and prevention of pancreatic cancer.

     

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