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SLIT2表达的变化与人类卵巢透明细胞癌细胞的迁移相关。

Changes in SLIT2 expression are associated with the migration of human ovarian clear cell carcinoma cells.

作者信息

Lin Cuei-Jyuan, Huang Way-Ren, Wu Chia-Zhen, Tseng Ruo-Chia

机构信息

Department of Laboratory Medicine, Keelung Chang Gung Memorial Hospital, Keelung 20401, Taiwan, R.O.C.

GLORIA Operation Center, National Tsing Hua University, Hsinchu 30013, Taiwan, R.O.C.

出版信息

Oncol Lett. 2021 Jul;22(1):551. doi: 10.3892/ol.2021.12812. Epub 2021 May 24.

Abstract

Ovarian clear cell carcinoma (OCCC) is characterized by a poor survival of patients, which is mainly due to metastasis and treatment failure. Slit guidance ligand 2 (SLIT2), a secreted protein, has been reported to modulate the migration of neural cells and human cancer cells. However, the effect of changes in SLIT2 expression on the regulation of cell migration in OCCC remains unknown. The present study examined alterations in SLIT2 expression using OCCC cell models, including low- and high-mobility SKOV3 cells, as well as OCCC tissues. DNA methylation analysis suggested that promoter hypermethylation was responsible for the low expression levels of SLIT2 in OCCC cells. The demethylating agent 5-Aza-deoxycytosine was able to restore SLIT2 expression at both the mRNA and protein levels in high-mobility SKOV3 cells that harbored the relevant methylated promoter. Overexpression of SLIT2 inhibited the migration of high-mobility OCCC cells, as well as decreased the protein expression levels of β-catenin, phosphorylated (p)AKT and snail family transcriptional repressor 1 (SNAI1). On the other hand, knockdown of SLIT2 increased the migration of low-mobility OCCC cells, and enhanced the protein expression levels of β-catenin, pAKT and SNAI1. Overall, the results of the present study provided evidence that low expression levels of SLIT2 were associated with increased OCCC cell migration, and that SLIT2 may act as a suppressor gene of cancer cell migration.

摘要

卵巢透明细胞癌(OCCC)的特点是患者生存率低,这主要是由于转移和治疗失败。Slit引导配体2(SLIT2)是一种分泌蛋白,据报道可调节神经细胞和人类癌细胞的迁移。然而,SLIT2表达变化对OCCC细胞迁移调控的影响仍不清楚。本研究使用OCCC细胞模型,包括低迁移率和高迁移率的SKOV3细胞以及OCCC组织,检测了SLIT2表达的变化。DNA甲基化分析表明,启动子高甲基化是OCCC细胞中SLIT2低表达水平的原因。去甲基化剂5-氮杂-脱氧胞苷能够在具有相关甲基化启动子的高迁移率SKOV3细胞中,在mRNA和蛋白质水平上恢复SLIT2的表达。SLIT2的过表达抑制了高迁移率OCCC细胞的迁移,同时降低了β-连环蛋白、磷酸化(p)AKT和蜗牛家族转录抑制因子1(SNAI1)的蛋白质表达水平。另一方面,敲低SLIT2增加了低迁移率OCCC细胞的迁移,并提高了β-连环蛋白、pAKT和SNAI1的蛋白质表达水平。总体而言,本研究结果表明,SLIT2低表达水平与OCCC细胞迁移增加有关,并且SLIT2可能作为癌细胞迁移的抑制基因发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7de/8170186/75632232efc1/ol-22-01-12812-g00.jpg

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