Oncofetal IGF2BP3-mediated control of microRNA structural diversity in the malignancy of early- stage lung adenocarcinoma

• 成果类型: Article
• 署名作者: Fujiwara, Yuko; Takahashi, Ryou-u; Saito, Motonobu; Umakoshi, Michinobu; Shimada, Yoko; Koyama, Kei; Yatabe, Yasushi; Watanabe, Shun-ichi; Koyota, Souichi; Minamiya, Yoshihiro; Tahara, Hidetoshi; Kono, Koji; Shiraishi, Kouya; Kohno, Takashi; Goto, Akiteru; Tsuchiya, Naoto
• 署名单位: National Cancer Center - Japan; Hiroshima University; Fukushima Medical University; Akita University; National Cancer Center - Japan; National Cancer Center - Japan; National Cancer Center - Japan; Akita University; Akita University; National Cancer Center - Japan
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-9507
• DOI: 10.1073/pnas.2407016121
• 发表日期: 2024-09-03
• 关键词: rna-binding proteins; 3' adenylation; cancer; complex; expression; mir-21; gene; identification; metastasis; biogenesis

摘要

The nature of microRNA (miRNA) dysfunction in carcinogenesis remains controversial because of the complex connection between miRNA structural diversity and biological processes. Here, we found that oncofetal IGF2BP3 regulates the selective production of a subset of 3 '- isoforms (3 '- isomiRs), including miR-21-5p and Let- 7 family, which induces significant changes in their cellular seed occupancy and structural components, establishing a cancer- specific gene expression profile. The D- score, reflecting dominant production of a representative miR- 21-5p+C (a 3 '- isomiR), discriminated between clinical early- stage lung adenocarcinoma (LUAD) cases with low and high recurrence risks, and was associated with molecular features of cell cycle progression, epithelial-mesenchymal transition pressure, and immune evasion. We found that IGF2BP3 controls the production of miR- 21-5p+C by directing the nuclear Drosha complex to select the cleavage site. IGF2BP3 was also involved in the production of 3 '- isomiRs of miR- 425- 5p and miR- 454- 3p. IGF2BP3- regulated these three miRNAs are suggested to be associated with the regulation of p53, TGF- beta, and TNF pathways in LUAD. Knockdown of IGF2BP3 also induced a selective upregulation of Let- 7 3 '- isomiRs, leading to increased cellular Let- 7 seed occupancy and broad repression of its target genes encoding cell cycle regulators. The D- score is an index that reflects this cellular situation. Our results suggest that the aberrant regulation of miRNA structural diversity is a critical component for controlling cellular networks, thus supporting the establishment of a malignant gene expression profile in early stage LUAD.