版权说明 操作指南
首页 > 成果 > 详情

HNRNPA2B1 and HNRNPR stabilize ASCL1 in an m6A-dependent manner to promote neuroblastoma progression

认领
导出
Link by DOI
反馈
分享
QQ微信 微博
成果类型:
期刊论文
作者:
Hu, Ting;Zeng, Chong;Song, Zhihao;Liu, Qing;Chen, Si;...
通讯作者:
Huang, Wei;Li, HY;Huang, W;Ma, QQ
作者机构:
[Hu, Ting; Song, Zhihao; Huang, Wei; Liu, Qing; Li, Haoyu] Cent South Univ, Xiangya Hosp, Dept Neurosurg, Changsha 410008, Peoples R China.
[Hu, Ting; Song, Zhihao; Liu, Qing; Li, Haoyu] Inst Skull Base Surg & Neurooncol Hunan Prov, Changsha 410008, Peoples R China.
[Hu, Ting; Song, Zhihao; Huang, Wei; Liu, Qing; Li, Haoyu] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Peoples R China.
[Zeng, Chong] Univ South China, Affiliated Hosp 7, Hengyang Med Sch, Dept Med, Changsha 410119, Peoples R China.
[Chen, Si; Li, Haoyu] Cent South Univ, Xiangya Hosp, Dept Ophthalmol, Changsha 410008, Peoples R China.
通讯机构:
[Huang, W ; Huang, W; Li, HY ] C
[Ma, QQ ] P
Cent South Univ, Xiangya Hosp, Dept Neurosurg, Changsha 410008, Peoples R China.
Inst Skull Base Surg & Neurooncol Hunan Prov, Changsha 410008, Peoples R China.
Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Peoples R China.
语种:
英文
关键词:
ASCL1;HNRNPA2B1;HNRNPR;N6-methyladenosine (m6A);Neuroblastoma
期刊:
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
ISSN:
0925-4439
年:
2024
卷:
1870
期:
3
页码:
167050
基金类别:
CRediT authorship contribution statement Ting Hu: Writing – original draft, Visualization, Validation, Methodology, Investigation. Chong Zeng: Writing – original draft, Visualization, Validation, Methodology, Investigation. Zhihao Song: Visualization, Validation. Qing Liu: Resources, Formal analysis. Si Chen: Software. Wei Huang: Writing – review & editing, Supervision, acquisition, Conceptualization. Qianquan Ma: Writing – review & editing, Supervision, Resources, Conceptualization. Haoyu Li: Writing – review & editing,
机构署名:
本校为其他机构
院系归属:
医学院
摘要:
HNRNPA2B1 and HNRNPR stabilize ASCL1 mRNA in neuroblastoma, but whether their regulatory effects depend on m6A modification and whether their function involves ASCL1 remain unknown. This study investigated the m6A-dependent binding of HNRNPA2B1 and HNRNPR to ASCL1 and subsequent regulation, as well as the expression, clinical significance, and function of HNRNPA2B1 and HNRNPR in neuroblastoma. We revealed that METTL14 mediated ASCL1 m6A modification to stabilize ASCL1. HNRNPA2B1 and HNRNPR significantly enriched ASCL1 mRNA by binding to the 5' and 3' untranslated regions, respectively, and MET...

反馈

验证码:
看不清楚,换一个
确定
取消

成果认领

标题:
用户 作者 通讯作者
请选择
请选择
确定
取消

提示

该栏目需要登录且有访问权限才可以访问

如果您有访问权限,请直接 登录访问

如果您没有访问权限,请联系管理员申请开通

管理员联系邮箱:yun@hnwdkj.com