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Exosomal lncRNA 91H is associated with poor development in colorectal cancer by modifying HNRNPK expression

机译:外泌体lncRNA 91H通过修饰HNRNPK表达与大肠癌的不良发展有关

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Exosomes mediated transfer of lncRNA 91H may play a critical role in the development of CRC. However, few studies have proved the mechanism. So we performed this study to deeply explore the biological functions of exosomal 91H in the development and progression of CRC. The association between lncRNA 91H and exosomes was detected in vitro and vivo. Then RNA pulldown and RIP were used to detect how lncRNA 91H affect CRC IGF2 express. At last, clinic pathological significance of exosomal 91H was evaluated by Cox proportional hazards model. We found that serum lncRNA 91H expression was closely related to cancer exosomes in vitro and vivo which may enhance tumor-cell migration and invasion in tumor development by modifying HNRNPK expression. Then the clinic pathological significance of exosomal 91H was evaluated which demonstrated that CRC patients with high lncRNA 91H expression usually showed a higher risk in tumor recurrence and metastasis than patients with low lncRNA 91H expression (P?
机译:外泌体介导的lncRNA 91H转移可能在CRC的发生中起关键作用。但是,很少有研究证明其机理。因此,我们进行了这项研究,以深入探索外泌体91H在CRC发生和发展中的生物学功能。在体外和体内检测到lncRNA 91H和外泌体之间的关联。然后使用RNA pulldown和RIP检测lncRNA 91H如何影响CRC IGF2表达。最后,通过Cox比例风险模型评估了外泌体91H的临床病理学意义。我们发现血清lncRNA 91H表达在体外和体内与癌症外泌体密切相关,这可能通过修饰HNRNPK表达来增强肿瘤细胞的迁移和侵袭。然后评估了外泌体91H的临床病理学意义,证明了高lncRNA 91H表达的CRC患者通常比低lncRNA 91H表达的患者具有更高的肿瘤复发和转移风险(P <0.05)。所有这些数据表明,通过修饰HNRNPK表达,外泌体lncRNA 91H增强CRC转移可能是CRC复发或转移的早期基于血浆的生物标记。需要进一步的大规模研究来证实我们的发现。

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