Prognostic significance of DNA repair proteins MLH1, MSH2 and MGMT expression in non-small-cell lung cancer and precursor lesions

被引:46
作者
Cooper, W. A. [1 ]
Kohonen-Corish, M. R. J. [2 ,3 ]
Chan, C. [4 ]
Kwun, S. Y. [4 ]
McCaughan, B. [5 ]
Kennedy, C. [6 ]
Sutherland, R. L. [2 ,3 ]
Lee, C-S [1 ,7 ]
机构
[1] Royal Prince Alfred Hosp, Dept Anat Pathol, Camperdown, NSW 2050, Australia
[2] Univ New S Wales, Garvan Inst Med Res, Canc Res Program, Sydney, NSW, Australia
[3] Univ New S Wales, Fac Med, St Vincents Clin Sch, Sydney, NSW, Australia
[4] Concord Hosp, Dept Anat Pathol, Sydney, NSW, Australia
[5] Royal Prince Alfred Hosp, Dept Cardiothorac Surg, Sydney, NSW, Australia
[6] Strathfield Private Hosp, Sydney, NSW, Australia
[7] Univ Sydney, Bosch Inst & Discipline Pathol, Canc Pathol Lab, Sydney, NSW 2006, Australia
关键词
DNA mismatch repair proteins; immunohistochemistry; MGMT; MLH1; MSH2; non-small-cell lung cancer; prognosis;
D O I
10.1111/j.1365-2559.2008.02999.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To investigate the role of DNA repair proteins and their prognostic significance in non-small-cell lung cancer (NSCLC). Methods and results: A retrospective analysis of 108 cases of stage I-II NSCLC was undertaken. Immunohistochemical expression of DNA repair proteins MLH1, MSH2 and MGMT was assessed using tissue microarrays of paraffin-embedded samples of invasive carcinoma and precursor lesions. Results were analysed in relation to clinicopathological parameters and patient survival. Reduced expression of MLH1 was found in 58.5% of tumours and occurred less frequently in poorly differentiated tumours (P = 0.044) and large cell carcinomas (P = 0.004). MSH2 and MGMT expression was reduced in 18.1% and 77.8% of cases, respectively. There was an inverse relationship between MLH1 and MSH2 expression (P = 0.012). Normal expression of MLH1, MSH2 and MGMT was found in all cases of squamous metaplasia and squamous dysplasia. Only a single case of carcinoma in situ (12.5%) showed reduced MLH1, none showed reduced MSH2 and 25% showed reduced MGMT. Survival analyses showed no prognostic significance based on expression of MLH1 (P = 0.92), MSH2 (P = 0.78) or MGMT (P = 0.57). Conclusions: Reduction in expression of DNA repair proteins MLH1, MSH2 and MGMT is relatively common in NSCLC, appears to be a late event in the development of invasive malignancy and does not influence survival in this patient cohort.
引用
收藏
页码:613 / 622
页数:10
相关论文
共 29 条
[1]  
Aubry MC, 2001, CANCER-AM CANCER SOC, V92, P2898, DOI 10.1002/1097-0142(20011201)92:11<2898::AID-CNCR10104>3.0.CO
[2]  
2-Q
[3]   Functional interactions and signaling properties of mammalian DNA mismatch repair proteins [J].
Bellacosa, A .
CELL DEATH AND DIFFERENTIATION, 2001, 8 (11) :1076-1092
[4]  
Benachenhou N, 1998, INT J CANCER, V77, P173, DOI 10.1002/(SICI)1097-0215(19980717)77:2<173::AID-IJC1>3.0.CO
[5]  
2-N
[6]  
Bocker T, 1996, J PATHOL, V179, P15
[7]  
Brabender J, 2003, CLIN CANCER RES, V9, P223
[8]   Choice of management strategy for colorectal cancer based on a diagnostic immunohistochemical test for defective mismatch repair [J].
Cawkwell, L ;
Gray, S ;
Murgatroyd, H ;
Sutherland, F ;
Haine, L ;
Longfellow, M ;
O'Loughlin, S ;
Cross, D ;
Kronborg, O ;
Fenger, C ;
Mapstone, N ;
Dixon, M ;
Quirke, P .
GUT, 1999, 45 (03) :409-415
[9]  
Chang JW, 2000, CLIN CANCER RES, V6, P1639
[10]  
Chaves P, 2000, J PATHOL, V191, P355