N6-Methyladenosine-Mediated Overexpression of Long Noncoding Rna ADAMTS9-AS2 Triggers Neuroblastoma Differentiation via Regulating lin28B/Let-7/MYCN Signaling

Authors

Yun Liu
Jun Zhang
Fang Cao
Xiaobao Dong
Jie Li
Yanna Cao
Zhanglin Li
Yan Guo
Jie Yan
Yuanyuan Liu
Qiang Zhao

Publication Date

11-22-2023

Journal

JCI Insight

Abstract

Neuroblastomas have shed light on the differentiation disorder that is associated with spontaneous regression or differentiation in the same tumor at the same time. Long noncoding RNAs (lncRNAs) actively participate in a broad spectrum of biological processes. However, the detailed molecular mechanisms underlying lncRNA regulation of differentiation in neuroblastomas remain largely unknown. Here, we sequenced clinical samples of ganglioneuroma, ganglioneuroblastoma, and neuroblastoma. We compared transcription profiles of neuroblastoma cells, ganglion cells, and intermediate state cells; verified the profiles in a retinoic acid-induced cell differentiation model and clinical samples; and screened out the lncRNA ADAMTS9 antisense RNA 2 (ADAMTS9-AS2), which contributed to neuroblastoma differentiation. ADAMTS9-AS2 upregulation in neuroblastoma cell lines inhibited proliferation and metastatic potential. Additional mechanistic studies illustrated that the interactions between ADAMTS9-AS2 and LIN28B inhibited the association between LIN28B and primary let-7 (pri-let-7) miRNA, then released pri-let-7 into cytoplasm to form mature let-7, resulting in the inhibition of oncogene MYCN activity that subsequently affected cancer stemness and differentiation. Furthermore, we showed that the observed differential expression of ADAMTS9-AS2 in neuroblastoma cells was due to N6-methyladenosine methylation. Finally, ADAMTS9-AS2 upregulation inhibited proliferation and cancer stem-like capabilities in vivo. Taken together, these results show that ADAMTS9-AS2 loss leads to malignant neuroblastoma by increasing metastasis and causing dysfunctional differentiation.

Keywords

Humans, RNA, Long Noncoding, N-Myc Proto-Oncogene Protein, Cell Differentiation, Neuroblastoma, ADAMTS9 Protein, RNA-Binding Proteins, Oncology

Comments

Supplementary Materials

PMID: 37991019