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Prognostic role of CIP2A expression in serous ovarian cancer
被引:86
作者:
Bockelman, C.
[1
,2
,3
,4
]
Lassus, H.
[5
]
Hemmes, A.
[1
,2
,3
]
Leminen, A.
[5
]
Westermarck, J.
[6
,7
,8
]
Haglund, C.
[4
]
Butzow, R.
[3
]
Ristimaki, A.
[1
,2
,3
]
机构:
[1] Univ Helsinki, Dept Pathol, HUSLAB, Cent Hosp, FIN-00014 Helsinki 00014, Finland
[2] Univ Helsinki, Haartman Inst, Cent Hosp, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Res Program Unit, FIN-00014 Helsinki, Finland
[4] Univ Helsinki, Dept Surg, Cent Hosp, FIN-00014 Helsinki 00014, Finland
[5] Univ Helsinki, Dept Obstet & Gynaecol, Cent Hosp, FIN-00014 Helsinki 00014, Finland
[6] Univ Turku, Ctr Biotechnol, Turku, Finland
[7] Abo Akad Univ, Turku, Finland
[8] Univ Turku, Dept Pathol, Turku, Finland
基金:
芬兰科学院;
关键词:
ovarian cancer;
CIP2A;
survival;
prognosis;
grade;
PROTEIN EXPRESSION;
TISSUE MICROARRAYS;
BORDERLINE TUMORS;
BREAST-CANCER;
AMPLIFICATION;
PATHOGENESIS;
CARCINOMA;
P53;
STATISTICS;
MUTATIONS;
D O I:
10.1038/bjc.2011.346
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BACKGROUND: Cancerous inhibitor of protein phosphatase 2A (CIP2A) is an oncoprotein expressed in several solid cancers. Our purpose was to study its role in serous ovarian cancer patients, and the association to clinicopathological variables and molecular markers. METHODS: We collected retrospectively 562 consecutive serous ovarian cancer patients treated at the Helsinki University Central Hospital. We stained tumour tissue microarrays for CIP2A by immunohistochemistry and constructed survival curves according to the Kaplan-Meier method. Associations to clinicopathological and molecular markers were assessed by the chi(2)-test. RESULTS: We found strong cytoplasmic CIP2A immunoreactivity in 212 (40.4%) specimens, weak positivity in 222 (42.4%) specimens, and negative in 90 (17.2%). Immunopositive CIP2A expression was associated with high grade (P<0.0001), advanced stage (P = 0.0005), and aneuploidy (P = 0.001, chi(2)-test). Cancerous inhibitor of protein phosphatase 2A overexpression was also associated with EGFR protein expression (P = 0.006) and EGFR amplification (P = 0.043). Strong cytoplasmic CIP2A immunopositivity predicted poor outcome in ovarian cancer patients (P<0.0001, log-rank test). CONCLUSION: Our results show that CIP2A associates with reduced survival and parameters associated with high grade in ovarian cancer patients, and may thus be one of the factors that identify aggressive subtype (type II) of this disease. British Journal of Cancer (2011) 105, 989-995. doi:10.1038/bjc.2011.346 www.bjcancer.com Published online 6 September 2011 (C) 2011 Cancer Research UK
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页码:989 / 995
页数:7
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