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三七皂苷通过调节SNHG6/miR-137轴使结肠癌细胞对放疗增敏。

Panax notoginseng saponins radiosensitize colorectal cancer cells by regulating the SNHG6/miR-137 axis.

作者信息

Xu Caihui, Liu Teng, Liu Haiyan, Chen Gongbin, Guo Yinmou

机构信息

Department of Oncology, Shangqiu First People's Hospital No. 292, South Kaixuan Road, Suiyang District Shangqiu 476100 Henan China

Xinxiang Medical University Hongqi District Xinxiang Henan China.

出版信息

RSC Adv. 2019 Nov 26;9(66):38558-38567. doi: 10.1039/c9ra07622k. eCollection 2019 Nov 25.

Abstract

Panax notoginseng saponins (PNS) have recently attracted great attention for their anti-cancer activity in colorectal cancer (CRC). The aim of this study was to explore the functional role and underlying mechanisms of PNS on CRC radiosensitivity. Cell viability was assessed by a Cell Counting kit-8 assay. Cell survival and apoptosis were determined using colony formation assay and flow cytometry, respectively. Quantitative real-time PCR was used to quantify the levels of SNHG6 and miR-137. The targeted correlation between SNHG6 and miR-137 was validated by dual-luciferase reporter and RNA immunoprecipitation assays. Our data supported that PNS weakened the viability of CRC cells. Moreover, PNS promoted the radiosensitivity of CRC cells. Mechanistically, PNS enhanced CRC cell radiosensitivity by upregulating SNHG6. SNHG6 directly targeted miR-137 and inhibited miR-137 expression. MiR-137 was involved in the regulatory effect of SNHG6 on CRC cell radiosensitivity. Furthermore, PNS increased miR-137 expression through SNHG6 in CRC cells. Our study suggested that PNS promoted radiosensitivity in CRC cells at least partly through regulating the SNHG6/miR-137 axis, providing a novel understanding of the anti-cancer mechanism of PNS in CRC.

摘要

三七总皂苷(PNS)因其在结直肠癌(CRC)中的抗癌活性最近备受关注。本研究旨在探讨PNS对CRC放射敏感性的功能作用及潜在机制。通过细胞计数试剂盒-8法评估细胞活力。分别使用集落形成试验和流式细胞术测定细胞存活率和凋亡情况。采用定量实时PCR定量SNHG6和miR-137的水平。通过双荧光素酶报告基因和RNA免疫沉淀试验验证SNHG6与miR-137之间的靶向相关性。我们的数据支持PNS削弱了CRC细胞的活力。此外,PNS促进了CRC细胞的放射敏感性。机制上,PNS通过上调SNHG6增强CRC细胞的放射敏感性。SNHG6直接靶向miR-137并抑制miR-137表达。MiR-137参与了SNHG6对CRC细胞放射敏感性的调节作用。此外,PNS通过SNHG6增加CRC细胞中miR-137的表达。我们的研究表明,PNS至少部分通过调节SNHG6/miR-137轴促进CRC细胞的放射敏感性,为PNS在CRC中的抗癌机制提供了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c082/9075843/33d46a7fcc06/c9ra07622k-f1.jpg

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