N6-methyladenosine modified LINC00901 promotes pancreatic cancer progression through IGF2BP2/MYC axis
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N6-methyladenosine modified LINC00901 promotes pancreatic cancer progression through IGF2BP2/MYC axis
Genes & DiseasesVol. 10, Issue 2, (2023)
作者机构:
1. Department of Colorectal Surgery, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College,Zhejiang,Hangzhou,China,310014
2. Key Laboratory of Tumor Molecular Diagnosis and Individualized Medicine of Zhejiang Province, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College,Zhejiang,Hangzhou,China,310014
3. Department of Nephrology, The Children's Hospital, Zhejiang University School of Medicine, National Research Center for Child Health,Zhejiang,Hangzhou,China,310052
4. Department of Surgical Oncology, The Children's Hospital, Zhejiang University School of Medicine, National Research Center for Child Health,Zhejiang,Hangzhou,China,310052
5. Department of Medical Oncology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College,Zhejiang,Hangzhou,China,310014
6. Department of Pulmonary Medicine, Tongji Hospital, Tongji University,Shanghai,China,200065
7. Cancer Center and Research Institute, University of Mississippi Medical Center,MS,Jackson,USA,39216
8. Department of Pharmacology/Toxicology, University of Mississippi Medical Center,MS,Jackson,USA,39216
Wan-Xin Peng, Fei Liu, Jia-Hong Jiang, et al. N6-methyladenosine modified LINC00901 promotes pancreatic cancer progression through IGF2BP2/MYC axis. [J]. Genes & Diseases 10(2).(2023)
DOI:
Wan-Xin Peng, Fei Liu, Jia-Hong Jiang, et al. N6-methyladenosine modified LINC00901 promotes pancreatic cancer progression through IGF2BP2/MYC axis. [J]. Genes & Diseases 10(2).(2023) DOI: 10.1016/j.gendis.2022.02.014.
N6-methyladenosine modified LINC00901 promotes pancreatic cancer progression through IGF2BP2/MYC axis
摘要
Abstract
umulating evidence indicates that RNA methylation at N
6
-methyladenosine (m6A) plays an important regulatory role in gene expression and aberrant mRNA m6A modification is often associated with a variety of cancers. However
little is known whether and how m6A-modification impacts long non-coding RNA (lncRNA) and lncRNA-mediated tumorigenesis
particularly in pancreatic ductal adenocarcinoma (PDAC). In the present study
we report that a previously uncharacterized lncRNA
LINC00901
promotes pancreatic cancer cell growth and invasion and moreover
LINC00901 is subject to m6A modification which regulates its expression. In this regard
YTHDF1 serves as a reader for the m6A modified LINC00901 and downregulates the LINC00901 level. Notably
two conserved m6A sites in LINC00901 are critical to the recognition of LINC00901 by YTHDF1. Finally
RNA sequencing (RNA-seq) and gene function analysis revealed that LINC00901 positively regulates MYC through upregulation of IGF2BP2
a known RNA binding protein that can enhance MYC mRNA stability. Together
our results suggest that there is a LINC00901-IGF2BP2-MYC axis through which LINC00901 promotes PDAC progression in an m6A dependent manner.
The m6A regulator KIAA1429 stabilizes RAB27B mRNA and promotes the progression of chronic myeloid leukemia and resistance to targeted therapy
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Regulation mechanism and pathogenic role of lncRNA plasmacytoma variant translocation 1 (PVT1) in human diseases
PTPN18 promotes colorectal cancer progression by regulating the c-MYC-CDK4 axis
M6A modification of circNSUN2 promotes colorectal liver metastasis
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