首页> 外文期刊>Oncology reports >Altered mRNA expression levels of the major components of sphingolipid metabolism, ceramide synthases and their clinical implication in colorectal cancer
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Altered mRNA expression levels of the major components of sphingolipid metabolism, ceramide synthases and their clinical implication in colorectal cancer

机译:改变了鞘脂代谢,神经酰胺合成酶的主要成分的mRNA表达水平及其在结肠直肠癌中的临床意义

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摘要

Ceramide synthases (CerSs) synthesize various ceramides of different acyl chain lengths and serve important roles in the proliferation and death of cancer cells by regulating sphingolipid metabolism-related signaling pathways. The present study investigated the mRNA expression levels of various CerS genes using mRNA expression data from six independent colorectal cancer (CRC) cohorts and a Korean CRC dataset. Expression levels of CERS2, CERS5 and CERS6 mRNA were significantly increased in the majority of the studied groups. However, CERS4 expression was only significantly altered in two groups. Additionally, a positive correlation was observed between altered CERS4 and CERS5 mRNA levels in The Cancer Genome Atlas Colon and Rectal Cancer dataset. Notably, CERS2 and CERS4, as well as CERS5 and CERS6 levels, were positively correlated with each other in Korean patients with CRC. However, the mRNA expression levels of these four CerS genes were not associated with any clinicopathological characteristics in Korean patients with CRC. Finally, overexpressing CERS2 or CERS6 inhibited the in vitro viability of various CRC cells. Taken together, these findings indicated that CERS2, CERS4, CERS5, and CERS6 are significantly dysregulated in CRC, suggesting they may serve important roles in the pathophysiology of this malignancy.
机译:神经酰胺合成酶(CERSS)通过调节鞘脂代谢相关的信号通路,合成不同酰基链长度的各种酰基链长度的酰胺,并在癌细胞的增殖和死亡中发挥重要作用。本研究研究了使用来自六种独立结肠直肠癌(CRC)群组和韩国CRC数据集的mRNA表达数据的各种CER基因的mRNA表达水平。在大多数研究组中,CERS2,CERS5和CERS6 mRNA的表达水平显着增加。然而,CERS4表达仅在两组中显着改变。另外,在癌症基因组阿麻结肠和直肠癌数据集中,在改变的CERS4和CERS5 mRNA水平之间观察到阳性相关性。值得注意的是,CERS2和CERS4以及CERS5和CERS6水平在韩国CRC患者中彼此正相关。然而,这四个CER基因的mRNA表达水平与CRC患者的任何临床病理特征无关。最后,过表达CERS2或CERS6抑制了各种CRC细胞的体外活力。这些研究结果表明,CERS2,CERS4,CERS5和CERS6在CRC中显着讨论,表明它们可能在这种恶性肿瘤的病理生理学中提供重要作用。

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