AUTHOR=Wang Li , Zeng Yuefen , Zhang Ying , Zhu Yun , Xu Shuangyan , Liang Zuohui 

TITLE=Acetylcytidine modification of DDX41 and ZNF746 by N-acetyltransferase 10 contributes to chemoresistance of melanoma

JOURNAL=Frontiers in Oncology

VOLUME=14

YEAR=2024

URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2024.1448890

DOI=10.3389/fonc.2024.1448890

ISSN=2234-943X

ABSTRACT=<sec><title>Background</title><p>Rapidly developed chemoresistance to dacarbazine (DTIC) is a major obstacle in the clinical management of melanoma; however, the roles and mechanisms of epi-transcriptomic RNA modification in this process have not been investigated.</p></sec><sec><title>Method</title><p>DTIC-resistant (DR) melanoma cells were established for bulk RNA sequencing. The expressions of mRNAs were detected using qRT-PCR, and protein levels were determined using Western blotting and immunohistochemistry. Acetylated RNAs were detected by dot blotting and immunoprecipitation sequencing (acRIP-seq). A lung metastasis mouse model of melanoma was established to evaluate the anti-melanoma effects <italic>in vivo</italic>.</p></sec><sec><title>Results</title><p>We identified that the expression of <italic>N</italic>-acetyltransferase 10 (NAT10), a catalytic enzyme for the <italic>N</italic><sup>4</sup>-acetylcytidine (ac4C) modification of RNA, was significantly upregulated in the DR cells. Clinically, NAT10 expression was elevated in disease progression samples and predicted a poor outcome. Using ac4C RNA immunoprecipitation (ac4C-RIP), we found that the mRNAs of two C2H2 zinc finger transcriptional factors, <italic>DDX41</italic> and <italic>ZNF746</italic>, were targets of NAT10-mediated ac4C modification. Gain- and loss-of-function experiments in NAT10, or in DDX41 and ZNF746, altered the chemosensitivity of melanoma accordingly, and the two target genes also negatively correlated with clinical outcomes. Finally, pharmacological inhibition of NAT10 with Remodelin sensitized melanoma cells to DTIC treatment <italic>in vitro</italic> and in a mouse xenograft model.</p></sec><sec><title>Conclusion</title><p>Our study elucidates the previously unrecognized role of NAT10-mediated ac4C modification in the chemoresistance of melanoma and provides a rationale for developing new strategies to overcome chemoresistance in melanoma patients.</p></sec>