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Sphingosine kinase 2 promotes colorectal cancer cell proliferation and invasion by enhancing MYC expression

机译:鞘氨醇激酶2通过增强MYC表达来促进结直肠癌细胞的增殖和侵袭

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Colorectal cancer (CRC) is one of the most commonly diagnosed cancers and causes of cancer death in developed countries. SphK2 is overexpressed in a number of aggressive human carcinomas; however, the expression profile and potential function of SphK2 in CRC are still unknown. In this study, we investigated the SphK2 expression in tumoral tissue and the matched normal mucosae using quantitative real-time PCR (qRT-PCR), Western blot, and immunohistochemistry. We also evaluated the impact of SphK2 knockdown on CRC cell proliferation and metastasis in vitro. SphK2 was significantly upregulated in CRC tissue as compared to the matched normal mucosae, and significant overexpression was found in the LoVo CRC cell line. SphK2 depletion by specific small interfering RNA (siRNA) in the CRC cell line was found to affect cell proliferation and cell migration. Our data suggest that the pathogenesis of CRC maybe mediated by SphK2, and SphK2 could represent a selective target for the molecularly targeted treatments of CRC.
机译:结肠直肠癌(CRC)是发达国家中最常见的癌症之一,也是导致癌症死亡的原因。 SphK2在许多侵略性人类癌中过表达;然而,SphK2在CRC中的表达谱和潜在功能仍然未知。在这项研究中,我们使用定量实时荧光定量PCR(qRT-PCR),蛋白质印迹和免疫组化研究了SphK2在肿瘤组织和匹配的正常黏膜中的表达。我们还评估了SphK2敲除对体外CRC细胞增殖和转移的影响。与匹配的正常粘膜相比,SphK2在CRC组织中显着上调,并且在LoVo CRC细胞系中发现了明显的过表达。发现CRC细胞系中特定小分子干扰RNA(siRNA)对SphK2的消耗会影响细胞增殖和细胞迁移。我们的数据表明,CRC的发病机制可能由SphK2介导,而SphK2可能代表CRC分子靶向治疗的选择性靶标。

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