N6-methyladenosine methyltransferase WTAP-stabilized FOXD2-AS1 promotes the osteosarcoma progression through m6A/FOXM1 axis

Long noncoding RNAs (lncRNAs) play critical roles in tumor progression regulation, including osteosarcoma. Evidence indicates that N-6-methyladenosine (m(6)A) modification modulates mRNA stability to regulate osteosarcoma tumorigenesis. Here, present research aims to detect the roles of m(6)A-modified lncRNA FOXD2-AS1 in the osteosarcoma pathophysiological process. Clinical data unveiled that osteosarcoma patients with higher FOXD2-AS1 expression had a poorer overall survival rate compared to those with lower FOXD2-AS1 expression. Functional research illuminated that FOXD2-AS1 accelerated the migration, proliferation and tumor growth in vitro and in vivo. Mechanistically, a remarkable m(6)A-modified site was found on the 3MODIFIER LETTER PRIME-UTR of FOXD2-AS1, and m(6)A methyltransferase WTAP (Wilms' tumor 1 associated protein) promoted the methylation modification, thus enhancing the stability of FOXD2-AS1 transcripts. Furthermore, FOXD2-AS1 interacted with downstream target FOXM1 mRNA through m(6)A sites, forming a FOXD2-AS1/m(6)A/FOXM1 complex to heighten FOXM1 mRNA stability. In conclusion, these findings propose a novel regulatory mechanism in which m(6)A-modified FOXD2-AS1 accelerates the osteosarcoma progression through m(6)A manner, which may provide new concepts for osteosarcoma tumorigenesis.

Automated summary

This study reveals the critical role of m(6)A-modified lncRNA FOXD2-AS1 in osteosarcoma progression, by enhancing the stability of FOXD2-AS1 transcripts and forming a complex with FOXM1 mRNA, thereby promoting migration, proliferation, and tumor growth.