ABCC2 (MRP2, cMOAT) can be localized in the nuclear membrane of ovarian carcinomas and correlates with resistance to cisplatin and clinical outcome

被引:86
作者
Surowiak, Pawel
Materna, Verena
Kaplenko, Irina
Spaczynski, Marek
Dolinska-Krajewska, Barbara
Gebarowska, Elzbieta
Dietel, Manfred
Zabel, Maciej
Lage, Hermann
机构
[1] Univ Hosp Charite, Inst Pathol, D-10117 Berlin, Germany
[2] Univ Wroclaw, Sch Med, Dept Histol & Embryol, PL-50138 Wroclaw, Poland
[3] Univ Sch Med, Dept Obstet & Gynecol, Poznan, Poland
[4] Univ Sch Med, Dept Histol & Embryol, Poznan, Poland
关键词
D O I
10.1158/1078-0432.CCR-06-0564
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Cisplatin resistance is a major obstacle in the treatment of ovarian carcinoma. ABCC2 is commonly localized in apical cell membranes and could confer cisplatin resistance. Here, we show that ABCC2 can be localized in the cytoplasmic membrane as well as in the nuclear membrane of various human tissues including ovarian carcinoma cells. Experimental Design: For the subcellular detection of ABCC2, immunohistochemistry was done using 41 Federation Internationale des Gynaecologistes et Obstetristes stage III ovarian carcinoma specimens prepared before treatment with cisplatin-based schemes and 35 specimens from the same group after chemotherapy. Furthermore, 11 ovarian carcinoma cell lines as well as tissue microarrays consisting of various human tissues were analyzed. Results: Nuclear membranous localization of ABCC2 was associated with response to first-line chemotherapy at primary (P = 0.0013) and secondary surgery (P = 0.0060). Cases with relapse showed higher nuclear membrane expression at primary (P = 0.0003) and secondary surgery (P = 0.0024). Kaplan-Meter analyses showed that weak nuclear membrane ABCC2 expression before treatment was associated with significantly longer overall (P = 0.04) and progression-free survival (P = 0.001); following chemotherapy, it correlated with significantly longer progression-free survival (P = 0.038). Tissue microarrays confirmed nuclear membranous localization of ABCC2, in particular, in poorly differentiated cells. In ovarian carcinoma cells, it correlated with resistance against cisplatin, whereas localization in the cytoplasmic membrane did not. Conclusions: ABCC2 confers resistance to cisplatin of ovarian carcinoma in cell culture systems and in clinics when expressed in the nuclear membrane. Thus, ABCC2 localization can predict platinum therapy outcome. Furthermore, expression of ABCC2 in nuclear membranes in human tissues is specific for poorly differentiated cells including stem cells.
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页码:7149 / 7158
页数:10
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