Nuclear localization of survivin is a positive prognostic factor for survival in advanced non-small-cell lung cancer

被引:78
作者
Vischioni, B
van der Valk, P
Span, SW
Kruyt, FAE
Rodriguez, JA
Giaccone, G
机构
[1] Free Univ Amsterdam, Med Ctr, Dept Med Oncol, Amsterdam, Netherlands
[2] Free Univ Amsterdam, Med Ctr, Dept Pathol, Amsterdam, Netherlands
关键词
inhibitors of apoptosis; non-small-cell lung cancer; nuclear localization; survivin;
D O I
10.1093/annonc/mdh436
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Expression of survivin, a member of the inhibitor of apoptosis protein family, is commonly detected in cancers but not in normal differentiated tissues. Survivin is usually localized in the cytoplasm of cancer cells, but nuclear localization has also been described, and we recently reported that survivin is a nuclear-cytoplasmic shuttling protein. Patients and methods: Fifty-three tumor specimens from patients with inoperable non-small-cell lung cancer (NSCLC) (55% stage IIIA, 17% stage IIIB and 28% stage IV) who underwent chemotherapy treatment were evaluated with immunohistochemistry for survivin expression and localization. These two sets of data were processed and tested for correlation with major patient characteristics, response to chemotherapy, and overall and relapse-free survival. Results: Survivin was present only in malignant tissues, and 47/53 (89%) of the specimens were positive. The overall median expression of tumor cells was 40%, and this value was used as a cut-off point for statistical analysis. By dichotomizing the specimens as expressing low or high levels of survivin, a significant association was seen between the expression of survivin and the histology of the tumors (P=0.020), squamous cell carcinoma being the histotype with lower levels of survivin expression. Three patterns of localization were observed: 42% of cases (22/53) showed reactivity confined to the nucleus, 17% (nine of 53) only in the cytoplasm and 30% (16/53) in both the nucleus and the cytoplasm. Interestingly, nuclear survivin levels predicted longer overall and relapse-free survival, in univariate and multivariate analyses. Expression and localization of survivin did not correlate with response to chemotherapy. Conclusions: Our results indicate that differential localization of survivin may be a prognostic factor. for NSCLC. Further studies are warranted.
引用
收藏
页码:1654 / 1660
页数:7
相关论文
共 34 条
[1]   Anti-apoptosis gene, survivin, and prognosis of neuroblastoma [J].
Adida, C ;
Berrebi, D ;
Peuchmaur, M ;
Reyes-Mugica, M ;
Altieri, DC .
LANCET, 1998, 351 (9106) :882-883
[2]   Survivin, versatile modulation of cell division and apoptosis in cancer [J].
Altieri, DC .
ONCOGENE, 2003, 22 (53) :8581-8589
[3]   The molecular basis and potential role of survivin in cancer diagnosis and therapy [J].
Altieri, DC .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (12) :542-547
[4]   DANGERS OF USING OPTIMAL CUTPOINTS IN THE EVALUATION OF PROGNOSTIC FACTORS [J].
ALTMAN, DG ;
LAUSEN, B ;
SAUERBREI, W ;
SCHUMACHER, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (11) :829-835
[5]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[6]   Survivin as a radioresistance factor in pancreatic cancer [J].
Asanuma, K ;
Moriai, R ;
Yajima, T ;
Yagihashi, A ;
Yamada, M ;
Kobayashi, D ;
Watanabe, N .
JAPANESE JOURNAL OF CANCER RESEARCH, 2000, 91 (11) :1204-1209
[7]   IAP family proteins - suppressors of apoptosis [J].
Deveraux, QL ;
Reed, TC .
GENES & DEVELOPMENT, 1999, 13 (03) :239-252
[8]   Survivin gene expression in early-stage non-small cell lung cancer [J].
Falleni, M ;
Pellegrini, C ;
Marchetti, A ;
Oprandi, B ;
Buttitta, F ;
Barassi, F ;
Santambrogio, L ;
Coggi, G ;
Bosari, S .
JOURNAL OF PATHOLOGY, 2003, 200 (05) :620-626
[9]   Assessment of IAP (inhibitor of apoptosis) proteins as predictors of response to chemotherapy in advanced non-small-cell lung cancer patients [J].
Ferreira, CG ;
van der Valk, P ;
Span, SW ;
Jonker, JM ;
Postmus, PE ;
Kruyt, FAE ;
Giaccone, G .
ANNALS OF ONCOLOGY, 2001, 12 (06) :799-805
[10]  
Ferreira CG, 2001, CLIN CANCER RES, V7, P2468