CCNE1 expression in high grade serous carcinoma does not correlate with chemoresistance

被引:15
|
作者
Sapoznik, Stav [1 ]
Aviel-Ronen, Sarit [2 ,3 ,4 ]
Bahar-Shany, Keren [1 ]
Zadok, Oranit [2 ]
Levanon, Keren [1 ,3 ,4 ]
机构
[1] Chaim Sheba Med Ctr, Sheba Canc Res Ctr, IL-52621 Ramat Gan, Israel
[2] Chaim Sheba Med Ctr, Dept Pathol, IL-52621 Ramat Gan, Israel
[3] Chaim Sheba Med Ctr, Talpiot Med Leadership Program, IL-52621 Ramat Gan, Israel
[4] Tel Aviv Univ, Sackler Fac Med, IL-69978 Ramat Aviv, Israel
关键词
CCNE1; ovarian cancer; predictive biomarker; chemoresistance; neoadjuvant chemotherapy; DEPENDENT KINASE 2; NEOADJUVANT CHEMOTHERAPY; OVARIAN-CANCER; CYCLIN-E; AMPLIFICATION; DINACICLIB; INHIBITOR; TARGET;
D O I
10.18632/oncotarget.19272
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Delayed diagnosis of ovarian cancer, as well as high recurrence rates and lack of personalized therapy options, are among the causes for poor survival figures. Much effort is made towards developing new therapeutic possibilities, however predictive biomarkers are still unavailable. CCNE1 amplification, occurring in similar to 20% of the high grade serous ovarian tumors, was previously proposed as a marker for platinum resistance and poor prognosis as well as for CDK2 inhibition. The current study aimed to examine the role of CCNE1 positive-immunostain as a predictor of first-line taxane-platinum chemoresistance. We evaluated matched pre- vs. postneoadjuvant chemotherapy tumor samples and correlated the degree of pathological response to treatment with CCNE1 expression levels. Our results indicate that CCNE1 immunohistochemistry does not predict taxane-platinum chemoresistance in ovarian cancer patients. Further research is required in order to enable personalized adjuvant treatment, in cases where poor pathological response is achieved after the neoadjuvant phase.
引用
收藏
页码:62240 / 62247
页数:8
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