Expression and prognostic significance of cyclin B1 and cyclin A in non-small cell lung cancer

被引:52
|
作者
Cooper, Wendy A. [1 ]
Kohonen-Corish, Maija R. J. [2 ,3 ]
McCaughan, Brian [4 ]
Kennedy, Catherine [5 ]
Sutherland, Robert L. [2 ,3 ]
Lee, Cheok Soon [1 ,6 ,7 ,8 ]
机构
[1] Royal Prince Alfred Hosp, Dept Anat Pathol, Sydney, NSW 2050, Australia
[2] Univ NSW, Canc Res Program, Garvan Inst Med Res, Fac Med, Sydney, NSW, Australia
[3] Univ NSW, St Vincents Clin Sch, Fac Med, Sydney, NSW, Australia
[4] Royal Prince Alfred Hosp, Dept Cardiothorac Surg, Sydney, NSW 2050, Australia
[5] Strathfield Private Hosp, Sydney, NSW, Australia
[6] Univ Sydney, Discipline Pathol, Fac Med, Sydney, NSW 2006, Australia
[7] Univ Sydney, Bosch Inst, Sydney, NSW 2006, Australia
[8] Univ Sydney, Cent Clin Sch, Sydney, NSW 2006, Australia
基金
英国医学研究理事会;
关键词
cyclin A; cyclin B1; immunohistochemistry; lung neoplasm; non-small cell lung cancer; prognosis; NEGATIVE BREAST-CANCER; LYMPH-NODE METASTASIS; COLORECTAL-CANCER; GASTRIC-CANCER; CLINICAL-SIGNIFICANCE; PROTEIN EXPRESSION; PATIENT SURVIVAL; OVEREXPRESSION; CARCINOMA; P53;
D O I
10.1111/j.1365-2559.2009.03331.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: Aberrant expression of cell cycle regulators has been implicated in the pathogenesis of many neoplasms, including non-small cell lung cancer (NSCLC). The aim was to examine the expression and prognostic value of cyclin B1 and cyclin A, key regulators of the G(2)/M checkpoint of the cell cycle, in NSCLC and bronchial precursor lesions. Methods and results: Immunohistochemical expression of cyclin B1 and A was examined in 90 cases of stage I-II primary NSCLC and bronchial precursor lesions using tissue microarrays. Increased cyclin B1 and A expression was found in 40.9 and 58.9% of NSCLC cases, respectively, and was significantly higher in primary NSCLC, lymph node metastases and some bronchial precursor lesions compared with normal bronchial epithelium. Increased expression of cyclin A and cyclin B1 correlated with tumour type, poorly differentiated tumours and male gender. A significant association was found between increased cyclin B1 expression and reduced survival using Kaplan-Meier survival analysis. On multivariate analysis, cyclin B1 was not an independent prognostic factor (P = 0.067). Cyclin A expression was not associated with survival. Conclusions: Cyclin B1 and cyclin A are aberrantly expressed in NSCLC and some precursor lesions. Cyclin B1, but not cyclin A, shows some promise as a potential prognostic marker in NSCLC.
引用
收藏
页码:28 / 36
页数:9
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