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长非编码 RNA SCARNA2 通过调节 miR-342-3p 的表达诱导皮肤鳞状细胞癌的进展。

Long non-coding RNA SCARNA2 induces cutaneous squamous cell carcinoma progression via modulating miR-342-3p expression.

机构信息

Department of Dermatology, The First Affiliated Hospital of Guizhou University of Chinese Medicine, Guizhou, 550001, China.

出版信息

J Gene Med. 2020 Dec;22(12):e3242. doi: 10.1002/jgm.3242. Epub 2020 Nov 8.

Abstract

BACKGROUND

Long non-coding RNAs (lncRNAs) play important roles in the progression of tumors. However, the function and expression of SCARNA2 in cutaneous squamous cell carcinoma (cSCC) is still unreported.

METHODS

A quantitative polymerase chain reaction was applied to study the expression of SCARNA2 and miR-342-3p. Cell counting kit-8, flow cytometry and transwell assays were performed to study cell growth, cycle and cell invasion.

RESULTS

We found that SCARNA2 expression is up-regulated in cSCC cell lines and SCARNA2 expression is higher in cSCC tissues than in adjacent non-tumor specimens. Ectopic expression of SCARNA2 promoted cell growth, cell cycle and invasion in SCC13 cells. In addition, the data indicate that miR-342-3p expression is down-regulated in cSCC cell lines and miR-342-3p is down-regulated in cSCC tissues compared to adjacent non-tumor specimens. We showed that the SCARNA2 expression is negatively associated with miR-342-3p in cSCC. Moreover, we noted that SCARNA2 sponges miR-342-3p expression in cSCC cells. Overexpression of SCARNA2 suppressed the miR-342-3p expressed in SCC13 cells. We found that elevated expression of SCARNA2 promotes cell growth, cell cycle and invasion via regulating miR-342-3p expression in SCC13 cells.

CONCLUSIONS

These data suggest that SCARNA2 acts in an oncogenic role and may be a potential target for cSCC.

摘要

背景

长链非编码 RNA(lncRNA)在肿瘤的进展中发挥着重要作用。然而,SCARNA2 在皮肤鳞状细胞癌(cSCC)中的功能和表达仍未被报道。

方法

采用实时定量聚合酶链反应检测 SCARNA2 和 miR-342-3p 的表达。细胞计数试剂盒-8(CCK-8)、流式细胞术和 Transwell 实验分别用于研究细胞生长、周期和细胞侵袭。

结果

我们发现 SCARNA2 在 cSCC 细胞系中表达上调,并且 SCARNA2 在 cSCC 组织中的表达高于相邻非肿瘤标本。SCARNA2 过表达促进 SCC13 细胞的生长、细胞周期和侵袭。此外,数据表明 miR-342-3p 在 cSCC 细胞系中表达下调,并且 miR-342-3p 在 cSCC 组织中表达低于相邻非肿瘤标本。我们表明,在 cSCC 中,SCARNA2 的表达与 miR-342-3p 呈负相关。此外,我们注意到 SCARNA2 在 cSCC 细胞中海绵吸附 miR-342-3p。SCARNA2 的过表达抑制了 SCC13 细胞中 miR-342-3p 的表达。我们发现,在 SCC13 细胞中,上调 SCARNA2 的表达通过调节 miR-342-3p 的表达促进细胞生长、细胞周期和侵袭。

结论

这些数据表明,SCARNA2 发挥致癌作用,可能是 cSCC 的潜在治疗靶点。

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