Expression of serine threonine kinase 15 is associated with poor differentiation in lung squamous cell carcinoma and adenocarcinoma

被引:27
作者
Xu, Hong-Tao
Ma, Lin
Qi, Feng-Jie
Liu, Yang
Yu, Juan-Han
Dai, Shun-Dong
Zhu, Ji-Jiang
Wang, En-Hua [1 ]
机构
[1] China Med Univ, Coll Basic Med Sci, Dept Pathol, Shenyang 110001, Peoples R China
[2] Univ Texas, MD Anderson Canc Ctr, Dept GI Med Oncol, Houston, TX 77030 USA
关键词
adenocarcinoma; lung; STK15; expression; squamous cell carcinoma;
D O I
10.1111/j.1440-1827.2006.01974.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Serine threonine kinase 15 (STK15, also named BTAK, Aurora-A, aurora-2, or AIKI) is a type of mitotic kinase. The overexpression of STK15 is significantly associated with carcinogenesis in many tumors. The purpose of the present study was to investigate the expression of STK15 in lung squamous cell carcinoma and adenocarcinoma and analyze the correlation between STK15 expression and clinicopathological factors. The expression patterns of STK15 were examined by immunohistochemistry in 80 lung squamous cell carcinomas and adenocarcinomas and 20 normal lung tissues. The protein and mRNA expression of STK15 were evaluated by western blot and reverse transcription-polymerase chain reaction (RT-PCR) in 40 lung cancer samples and corresponding normal lung tissues. Immunohistochemically, the positivity of STK15 expression was 68.75% (55/80). The STK15 expression was significantly higher in poorly differentiated lung cancers than in well-differentiated or moderately differentiated lung cancers (P = 0.011). Western blot and RT-PCR showed that the protein and mRNA expression of STK15 were correlated (P = 0.044) and significantly higher in tumors than in corresponding normal lung tissues (P < 0.05). These results indicate that the overexpression of STK15 contributes to the carcinogenesis and de-differentiation of lung cancers.
引用
收藏
页码:375 / 380
页数:6
相关论文
共 30 条
  • [21] pEg2 aurora-A kinase, histone H3 phosphorylation, and chromosome assembly in Xenopus egg extract
    Scrittori, L
    Hans, F
    Angelov, D
    Charra, M
    Prigent, C
    Dimitrov, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (32) : 30002 - 30010
  • [22] Sen S, 2002, JNCI-J NATL CANCER I, V94, P1320
  • [23] A putative serine/threonine kinase encoding gene BTAK on chromosome 20q13 is amplified and overexpressed in human breast cancer cell lines
    Sen, S
    Zhou, HY
    White, RA
    [J]. ONCOGENE, 1997, 14 (18) : 2195 - 2200
  • [24] The clinical significance of Aurora-A/STK15/BTAK expression in human esophageal squamous cell carcinoma
    Tanaka, E
    Hashimoto, Y
    Ito, T
    Okumura, T
    Kan, T
    Watanabe, G
    Imamura, M
    Inazawa, J
    Shimada, Y
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (05) : 1827 - 1834
  • [25] Tanaka T, 1999, CANCER RES, V59, P2041
  • [26] Overexpression of aurora-A contributes to malignant development of human esophageal squamous cell carcinoma
    Tong, T
    Zhong, YL
    Kong, JP
    Dong, LJ
    Song, YM
    Fu, M
    Liu, ZH
    Wang, MR
    Guo, LP
    Lu, SX
    Wu, M
    Zhan, QM
    [J]. CLINICAL CANCER RESEARCH, 2004, 10 (21) : 7304 - 7310
  • [27] Travis W., 2004, WHO CLASSIFICATION T
  • [28] Watanabe Yoh, 2003, Ann Thorac Cardiovasc Surg, V9, P343
  • [29] Functional implication of human serine/threonine kinase, hAlK, in cell cycle progression
    Yang, SC
    Huang, CH
    Chen, NJ
    Chou, CK
    Lin, CH
    [J]. JOURNAL OF BIOMEDICAL SCIENCE, 2000, 7 (06) : 484 - 493
  • [30] AURKA amplification, chromosome instability, and centrosome abnormality in human pancreatic carcinoma cells
    Zhu, JJ
    Abbruzzese, JL
    Izzo, J
    Hittelman, WN
    Li, DH
    [J]. CANCER GENETICS AND CYTOGENETICS, 2005, 159 (01) : 10 - 17