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ABSTRACT: Background
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.Method
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 in vivo.Results
We identified that the expression of N-acetyltransferase 10 (NAT10), a catalytic enzyme for
SUBMITTER: Wang L
PROVIDER: S-EPMC11377236 | biostudies-literature | 2024
REPOSITORIES: biostudies-literature