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首页> 外文期刊>Cancer Medicine >Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma
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Long non‐coding RNA H19 promotes TDRG1 expression and cisplatin resistance by sequestering miRNA‐106b‐5p in seminoma

机译:长的非编码RNA H19通过在精原细胞瘤中隔离miRNA‐106b‐5p来促进TDRG1表达和顺铂耐药性

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The role of TDRG1 in tumorigenesis and the progression of seminoma, as well as its role in regulating chemosensitivity of seminoma to cisplatin through the PI3K/Akt/mTOR signaling pathway, has been previously defined. However, the detailed mechanism underlying TDRG1 expression and concomitant chemoresistance conditions are unknown. Furthermore, it has been reported that non‐protein‐coding RNAs play an important role in a variety of vital processes including cellular chemosensitivity. However, the role of non‐protein‐coding RNAs in regulating the chemosensitivity of seminoma remains unknown. In this study, using microarray analysis, we found that long non‐coding RNA H19 was upregulated while miRNA‐106b‐5p was downregulated in an established cisplatin‐resistant TCam‐2 cell line. Moreover, H19 acts as a miRNA‐106b‐5p sponge and thus impairs the function of miRNA‐106b‐5p on its target gene, TDRG1. Based on these findings, we propose that H19 promotes the expression of TDRG1 by sequestering miRNA‐106b‐5p and uses this mechanism to facilitate cell survival in cisplatin‐based chemotherapeutic conditions. These findings elucidate the mechanisms, at least partially, applied to deregulate TDRG1 and cisplatin sensitivity, and may provide new therapeutic possibilities for chemoresistant seminoma.
机译:先前已经定义了TDRG1在肿瘤发生和精原细胞瘤进展中的作用,以及通过PI3K / Akt / mTOR信号通路调节精原细胞对顺铂的化学敏感性的作用。但是,TDRG1表达和伴随的化学抗性条件的详细机制尚不清楚。此外,据报道,非蛋白质编码RNA在包括细胞化学敏感性在内的各种重要过程中也起着重要作用。然而,非蛋白编码的RNA在调节精原细胞瘤的化学敏感性中的作用仍是未知的。在这项研究中,我们使用微阵列分析发现,在已建立的顺铂耐药性TCam-2细胞系中,长的非编码RNA H19被上调,而miRNA-106b-5p被下调。此外,H19充当miRNA‐106b‐5p海绵,因此损害了miRNA‐106b‐5p在其靶基因TDRG1上的功能。基于这些发现,我们建议H19通过螯合miRNA-106b-5p来促进TDRG1的表达,并利用这种机制促进在基于顺铂的化学治疗条件下的细胞存活。这些发现至少部分阐明了解除TDRG1和顺铂敏感性的机制,并可能为化学耐药性精原细胞瘤提供新的治疗可能性。

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