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MYB/LINC00092调节轴促进了乳头甲状腺癌的进展
Lian Cheng1,2, Xian Deng3,4, Yuan Le5
1Department of General Surgery (Thyroid Surgery), Affiliated Hospital of Southwest Medical University, Southwest Medical University, Luzhou, China.
Endokrynologia Polska
|March 18, 2024
概括
长非编码RNA LINC00092 作为状甲状腺癌 (PTC) 的瘤抑制剂. MYB通过直接或通过miR-4741.1抑制LINC00092来促进PTC进展.
科学领域:
- 内分泌学 在内分泌学.
- 分子生物学分子生物学
- 在瘤学瘤学.
背景情况:
- 甲状腺癌是一种普遍存在的内分泌恶性瘤.
- 乳头甲状腺癌 (PTC) 的进展涉及复杂的分子机制.
- 长非编码RNAs (lncRNAs) 在癌症发展中起着关键作用.
研究的目的:
- 为了阐明LINC00092在乳头甲状腺癌 (PTC) 进展中的分子机制.
- 在PTC中调查MYB,LINC00092和miR-4741之间的监管关系.
- 确定LINC00092在PTC中作为潜在的瘤抑制剂的作用.
主要方法:
- 在癌症基因组图集中的LINC00092表达的分析甲状腺癌 (TCGA-THCA) 患者队列和PTC细胞系.
- 功能测试包括MTT和伤口愈合测试,以评估细胞增殖和迁移.
- 染色体免疫沉 (Q-ChIP) 和光酶记者测定用于验证转录和miRNA-mRNA标.
主要成果:
- 发现LINC00092表达在甲状腺癌中被抑制,并且与高级TNM阶段负面相关.
- LINC00092抑制了皮质-介质细胞过渡 (EMT),迁移和PTC细胞的增殖.
- MYB被确定为一种直接抑制LINC00092的转录因子,并且还诱导miR-4741,这反过来抑制LINC00092,形成一个促进EMT的MYB-miR-4741-LINC00092轴.
结论:
- 在PTC中,LINC00092作为瘤抑制器IncRNA的功能.
- MYB-LINC00092轴,涉及MYB (部分通过miR-4741) 对LINC00092的直接和间接压制,有助于PTC的进展.
- 包括MYB,LINC00092和miR-4741在内的连贯的前循环调节了PTC的发展.
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