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STK15、P53蛋白在结肠癌中的表达及其临床意义 被引量:5

Expressions and clinical significance of STK15 and P53 in colon cancer
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摘要 目的探讨结肠癌组织中丝氨酸/苏氨酸激酶15(Serine/threonine kinase15,STK15)、P53蛋白的表达及其临床意义。方法采用免疫组织化学法检测72例结肠癌组织和36例癌旁正常组织中STK15、P53蛋白的表达情况,分析两者在结肠癌发生发展中相关性,及与结肠癌患者临床病理特征之间的关系。结果 STK15、P53蛋白在结肠癌组织中的阳性表达率分别为65.3%(47/72)、69.4%(50/72),明显高于癌旁正常组织中的表达,两者在结肠癌的发生发展中比较差异有统计学意义(r=0.615,P<0.05)。STK15在结肠癌中表达与肿瘤TNM分期、浸润深度密切相关(P<0.05),与患者年龄、性别、肿瘤大小、分化状态无关(P>0.05)。结论 STK15、P53在结肠癌中高表达,且两者在结肠癌中呈正相关,提示STK15、P53可能共同参与了结肠癌发生发展的过程,二者的表达可能与结肠癌的不良预后有密切关系。 Objective To investigate expression and clinical significance of STK15 and P53 in colon cancer. Methods The immunohistochemieal method was used to determine the expressions of STK15 and P53 in the colon cancer tissues of 72 patients and adjacent normal tissues of 36 patients to explore the correlation of the two protein in colon carcinogenesis process, and analyze the relationship between these two proteins and pathological features of colon cancer. Results The expressions of STK15 ( 65.7%, 47/72) and P53 ( 69.4%, 50/72), in colon cancer tissue were significantly higher than that in adjacent normal tissue (5.6%, 2.8% respectively) (P 〈0.001),these proteins were positively correlated in colon adenocarcinoma (r=0.615, P 〈0.001 ). The expression of these two kinds of protein were related with the TNM staging of tumor, depth of invasion (P 〈 0.05 ), no association with patients age, gender, tumor size and histological grading was observed (P 〉0.05). Conclusion STK15, p53 showed high expression in colon cancer, and a positive correlation between the two proteins, suggesting that STK15, p53 might be involved in the process of developing colon cancer. And the expression of the two proteins might be closely associated with poor prognosis in colon cancer treatment.
出处 《中国热带医学》 CAS 2015年第1期104-106,共3页 China Tropical Medicine
关键词 丝氨酸/苏氨酸激酶15 P53蛋白 结肠癌 免疫组化 中心体 STK15 P53 Colon cancer Centrosome Immunohistochemical
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  • 1蔡扬,李秉琦,陈谦明.口腔黏膜癌变过程中中心体的扩增及其意义[J].华西口腔医学杂志,2004,22(3):238-241. 被引量:17
  • 2赵旭,李福才,李英慧,富伟能,黄带发,叶燕,徐振明,孙开来.p53基因突变和STK15基因过表达与喉癌发生的关系[J].中华肿瘤杂志,2005,27(3):134-137. 被引量:4
  • 3蔡扬.中心体异常与肿瘤发生关系的研究进展[J].中国药物与临床,2005,5(6):412-414. 被引量:1
  • 4蔡扬,柳咏发,李世灵,潘玉霞,朱炎,于燕妮.口腔鳞状细胞癌细胞周期蛋白E表达与中心体扩增相关性[J].中华病理学杂志,2007,36(6):375-378. 被引量:3
  • 5Zhou H, KuangJ, Zhong L, et al. Tumour amplified khaase STK15/ BTAK induces centrosome amplification,aneuploidy and transfor- mation[J]. Nat Genet, 1998 20(2):189-193.
  • 6Miyoshi Y, Iwao K, Eqawa C, et al. Association of centrosomal ki- nase STK15/BTAK mRNA expression with chromosomal instabili- ty in human breast cancers[J]. IntJ Cancer, 2001, 92(3):370-373.
  • 7Kramer A, Neben K, Ho AD. Centrosome replication,genomic in- stability and cancer[J]. Leukemia, 2002, 16(5):767-775.
  • 8Andrews PD. Aurora kinases: Shining lights on the therapeutic hori- zon[J]. Oixcogene, 2005,24(32) :5005-5010.
  • 9Tanaka E, Hashimoto Y, Ito T, et al. Tile clinical significance of Au-rora-A/STK15/BTAK expression in human esophageal squamous cell carcinoma0]. Clin Cancer Res, 2005, 11 (5):1827-1834.
  • 10Chen SS, Chang PC, Cheng YW, et al. Suppression of the STK15 oncogenic activity requires a transactivation-independent p53 func- tion[J]. EMBOJ, 2002, 21(17):4491-4499.

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