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PDK1 稳定的长链非编码 RNA SPRY4-IT1 通过激活 NF-κB 信号通路促进乳腺癌进展。

PDK1-stabilized LncRNA SPRY4-IT1 promotes breast cancer progression via activating NF-κB signaling pathway.

机构信息

Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing, China.

Department of Orthopedics, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Mol Carcinog. 2023 Jul;62(7):1009-1024. doi: 10.1002/mc.23542. Epub 2023 Apr 12.

Abstract

Pyruvate dehydrogenase kinase 1 (PDK1) is a widely known glycolytic enzyme, and some evidence showed that PDK1 promoted breast cancer by multiple approaches. However, very few lncRNAs have been identified to be associated with PDK1 in breast cancer in previous research. In this study, we found that lncRNA sprouty4-intron transcript 1 (SPRY4-IT1) was regulated by PDK1 with correlation analysis, and PDK1 upregulated SPRY4-IT1 remarkably in breast cancer cells, as PDK1 interacted with SPRY4-IT1 in the nucleus and significantly enhanced the stability of SRPY4-IT1. Furthermore, SPRY4-IT1 was highly expressed in breast cancer, significantly promoted the proliferation and inhibited apoptosis of breast cancer cells. In terms of mechanism, SPRY4-IT1 inhibited the transcription of NFKBIA and the expression of IκBα, thus promoting the formation of p50/p65 complex and activating NF-κB signaling pathway, which facilitated survival of breast cancer cells. Therefore, our finding reveals that PDK1/SPRY4-IT1/NFKBIA axis plays a crucial role that promoting tumor progression, and SPRY4-IT1 knockdown incombined with PDK1 inhibitor is promising to be a new therapeutic strategy in breast cancer.

摘要

丙酮酸脱氢酶激酶 1(PDK1)是一种广泛存在的糖酵解酶,有证据表明 PDK1 通过多种途径促进乳腺癌的发生。然而,在之前的研究中,很少有长链非编码 RNA(lncRNA)被鉴定与乳腺癌中的 PDK1 相关。在这项研究中,我们发现 lncRNA 芽卷曲蛋白 4 内含子转录本 1(SPRY4-IT1)受 PDK1 调控,PDK1 在乳腺癌细胞中显著上调 SPRY4-IT1 的表达,因为 PDK1 在核内与 SPRY4-IT1 相互作用,并显著增强 SPRY4-IT1 的稳定性。此外,SPRY4-IT1 在乳腺癌中高表达,显著促进乳腺癌细胞的增殖并抑制细胞凋亡。在机制方面,SPRY4-IT1 抑制 NFKBIA 的转录和 IκBα 的表达,从而促进 p50/p65 复合物的形成并激活 NF-κB 信号通路,促进乳腺癌细胞的存活。因此,我们的发现揭示了 PDK1/SPRY4-IT1/NFKBIA 轴在促进肿瘤进展中起着关键作用,SPRY4-IT1 敲低与 PDK1 抑制剂联合使用有望成为乳腺癌的一种新的治疗策略。

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