Gene expression profile association with poor prognosis in epithelial ovarian cancer patients

被引:15
|
作者
Oliveira, Douglas V. N. P. [1 ]
Prahm, Kira P. [1 ]
Christensen, Ib J. [1 ]
Hansen, Anker [3 ]
Hogdall, Claus K. [2 ]
Hogdall, Estrid V. [1 ]
机构
[1] Univ Copenhagen, Herlev Hosp, Dept Pathol, Herlev, Denmark
[2] Univ Copenhagen, Dept Gynaecol, Juliane Marie Ctr, Rigshosp, Copenhagen, Denmark
[3] Oncol Venture, Horsholm, Denmark
关键词
HEAT-SHOCK PROTEINS; STEROID CELL TUMOR; LOW-GRADE; CARCINOMA; CD99; CHEMOSENSITIVITY; CLASSIFICATION; PATTERNS; SURVIVAL; SUBTYPES;
D O I
10.1038/s41598-021-84953-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ovarian cancer (OC) is the eighth most common type of cancer for women worldwide. The current diagnostic and prognostic routine available for OC management either lack specificity or are very costly. Gene expression profiling has shown to be a very effective tool in exploring new molecular markers for patients with OC, although association of such markers with patient survival and clinical outcome is still elusive. Here, we performed gene expression profiling of different subtypes of OC to evaluate its association with patient overall survival (OS) and aggressive forms of the disease. By global mRNA microarray profiling in a total of 196 epithelial OC patients (161 serous, 15 endometrioid, 11 mucinous, and 9 clear cell carcinomas), we found four candidates-HSPA1A, CD99, RAB3A and POM121L9P, which associated with OS and poor clinicopathological features. The overexpression of all combined was correlated with shorter OS and progression-free survival (PFS). Furthermore, the combination of at least two markers were further associated with advanced grade, chemotherapy resistance, and progressive disease. These results indicate that a panel comprised of a few predictors that associates with a more aggressive form of OC may be clinically relevant, presenting a better performance than one marker alone.
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页数:10
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