Elsnerova Katerina, Mohelnikova-Duchonova Beatrice, Cerovska Ela, Ehrlichova Marie, Gut Ivan, Rob Lukas, Skapa Petr, Hruda Martin, Bartakova Alena, Bouda Jiri, Vodicka Pavel, Soucek Pavel, Vaclavikova Radka
Toxicogenomics Unit, National Institute of Public Health, Prague, Czech Republic.
Department of Gynecology and Obstetrics, Second Faculty of Medicine and Motol University Hospital, Charles University in Prague, Prague, Czech Republic.
Oncol Rep. 2016 Apr;35(4):2159-70. doi: 10.3892/or.2016.4599. Epub 2016 Jan 28.
Membrane transporters (such as ABCs, SLCs and ATPases) act in carcinogenesis and chemoresistance development, but their relevance for prognosis of epithelial ovarian cancer (EOC) remains poorly understood. We evaluated the gene expression profile of 39 ABC and 12 SLC transporters and three ATPases in EOC tissues and addressed their putative role in prognosis and clinical course of EOC patients. Relative gene expression in a set of primary EOC (n=57) and in control ovarian tissues (n=14) was estimated and compared with clinical data and survival of patients. Obtained data were validated in an independent set of patients (n=60). Six ABCs and SLC22A18 gene were significantly overexpressed in carcinomas when compared with controls, while expression of 12 ABCs, five SLCs, ATP7A and ATP11B was decreased. Expression of ABCA12, ABCC3, ABCC6, ABCD3, ABCG1 and SLC22A5 was higher in high grade serous carcinoma compared with other subtypes. ABCA2 gene expression significantly associated with EOC grade in both sets of patients. Notably, expression level of ABCA9, ABCA10, ABCC9 and SLC16A14 significantly associated with progression-free survival (PFS) of the disease in either pilot or validation sets. ABCG2 level associated with PFS in the pooled set of patients. In conclusion, ABCA2, ABCA9, ABCA10, ABCC9, ABCG2 and SLC16A14 present novel putative markers of EOC progression and together with the revealed relationship between ABCA12, ABCC3, ABCC6, ABCD3, ABCG1 and SLC22A5 expression, and high grade serous type of EOC should be further examined by larger follow-up study.
膜转运蛋白(如ABC转运蛋白、溶质载体家族蛋白和ATP酶)在肿瘤发生和化疗耐药性发展中发挥作用,但其对上皮性卵巢癌(EOC)预后的相关性仍知之甚少。我们评估了39种ABC转运蛋白、12种溶质载体家族蛋白转运蛋白和3种ATP酶在EOC组织中的基因表达谱,并探讨了它们在EOC患者预后和临床病程中的潜在作用。估计了一组原发性EOC(n = 57)和对照卵巢组织(n = 14)中的相对基因表达,并与患者的临床数据和生存率进行比较。所获得的数据在另一组独立患者(n = 60)中得到验证。与对照组相比,6种ABC转运蛋白和溶质载体家族蛋白22成员A18(SLC22A18)基因在癌组织中显著过表达,而12种ABC转运蛋白、5种溶质载体家族蛋白、ATP7A和ATP11B的表达则降低。与其他亚型相比,ABCA12、ABCC3、ABCC6、ABCD3、ABCG1和SLC22A5在高级别浆液性癌中的表达更高。在两组患者中,ABCA2基因表达均与EOC分级显著相关。值得注意的是,在试验组或验证组中,ABCA9、ABCA10、ABCC9和溶质载体家族蛋白16成员A14(SLC16A14)的表达水平均与疾病的无进展生存期(PFS)显著相关。在合并的患者组中,ABCG2水平与PFS相关。总之,ABCA2、ABCA9、ABCA10、ABCC9、ABCG2和SLC16A14是EOC进展的新型潜在标志物,并且鉴于所揭示的ABCA12、ABCC3、ABCC6、ABCD3、ABCG1和SLC22A5表达与高级别浆液性EOC类型之间的关系,应通过更大规模的随访研究进一步检查。