企业档案
会员类型:旗舰版
已获得阿仪网信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
阿仪网旗舰版会员:9年
最后认证时间:
注册号: 【已认证】
法人代表: 【已认证】
参观次数:7948944
手机网站:http://wap.app17.com/c137908/
旗舰版网址:http://www.yajiml.com
技术文章
文献引用产品:人宫颈癌细胞CaSKi
点击次数:998 发布时间:2026/4/15 16:54:19
文章标题:Exogenous Na2SiO3 Mitigates the Adverse Effects of Drought Stress on Cucumber Seed Germination by Regulating the AsA-GSH Cycle
作者列表:Kexin Chen, Zitong Liu, Xin Meng, Shuyan Jiang, Li Jin, Shuya Wang, Shuchao Huang, Jian Lyu, Ning Jin, Jihua Yu
发表时间:2026-2-18
期刊:Horticulturae
影响因子:3
DOI:10.3390/horticulturae12020243
主要研究成果:Abstract
Cervical cancer (CC) remains a significant global health burden despite advances in prevention and screening. Emerging evidence highlights the critical role of long non-coding RNAs (lncRNAs) and RNA modifications in tumorigenesis. Here, we identified LINC01094 as a highly expressed lncRNA in CC through TCGA analysis and clinical specimens. Functional studies, including CCK-8 method, flow cytometry, Transwell and Western blot assays, demonstrated that LINC01094 knockdown suppressed cell proliferation, migration, and epithelial-mesenchymal transition while promoting apoptosis in CC cells (Caski and SiHa). Mechanistically, NSUN2-mediated 5-methylcytosine methylation stabilized LINC01094, enhancing its expression in CC. Furthermore, LINC01094 facilitated ZNF582-dependent transcriptional activation of SIRT1, promoted the deacetylation and degradation of p53. Rescue experiments confirmed that ectopic expression of either LINC01094 or SIRT1 reversed the tumor-suppressive effects of NSUN2 or LINC01094 knockdown, respectively. Collectively, NSUN2-mediated stabilization of LINC01094 upregulated SIRT1 expression, thereby suppressing the p53 pathway and accelerating CC progression. These findings uncover a novel NSUN2/LINC01094/SIRT1 axis as an epigenetic-transcriptional driver of CC, offering potential therapeutic targets.
原创作者:上海雅吉生物科技有限公司






