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SLC7A2 serves as a potential biomarker and therapeutic target for ovarian cancer

机译:SLC7A2用作卵巢癌的潜在生物标志物和治疗靶标

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摘要

The solute carrier (SLC) family is the largest group of membrane transporters, but their functions in ovarian cancer (OV) remain unclear. We analyzed SLC family members with amino acids-transporting functions in OV. The mRNA expression levels and prognostic values of SLCs in OV were analyzed in the Gene Expression Profiling Interactive Analysis and Kaplan–Meier Plotter database. Solute carrier family 7 member 2 (SLC7A2), which showed differential expression and the most significant prognostic value, was selected for further analyses. The cBioPortal database, Gene Set Enrichment Analysis and Weighted Correlation Network Analysis were used to explore the potential functions and molecular mechanisms of SLC7A2 in OV. Validations in our own samples and in Gene Expression Omnibus datasets were conducted. Functional validation in OV cell lines was carried out. In total, 73 SLC family members were analyzed. Seven members were upregulated while 11 members were downregulated in OV and 15 members were protective factors for prognosis while 12 members were risk factors. SLC7A2 was downregulated in OV, and it was positively associated with prognosis. Knockdown of SLC7A2 promoted viability, invasion and migration of OV cells. These SLC family members and in particular SLC7A2 represented novel biomarkers for diagnosis and treatment for OV.
机译:溶质载体(SLC)家族是最大的膜转运蛋白组,但它们在卵巢癌(OV)中的功能仍然尚不清楚。我们分析了SLC系列成员,在OV中具有氨基酸转运功能。在基因表达分析互动分析和Kaplan-Meier绘图仪数据库中分析了OV中SLCS的mRNA表达水平和预后值。选择溶质载体家族7构成表2(SLC7A2),其显示出差异表达和最显着的预后值,以进一步分析。 CBIoPortal数据库,基因集富集分析和加权相关网络分析用于探讨SLC7A2在OV中的潜在功能和分子机制。进行了我们自己的样本和基因表达的验证综合数据集。进行OV细胞系的功能验证。共有73个SLC家族成员分析。上调七名成员,而11名成员在OV和15名成员中下调,则为预后的保护因素,而12名成员是危险因素。 SLC7A2在OV中下调,它与预后正相关。 SLC7A2的敲低促进了OV细胞的活力,侵袭和迁移。这些SLC家族成员和特别是SLC7A2代表了用于ov的新型生物标志物,用于ov的诊断和治疗。

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