Combined SNPs sequencing and a... Note

Combined SNPs sequencing and allele specific proteomics capture reveal functional causality underpinning the 2p25 prostate cancer susceptibility locus

Here the authors reveal that the prostate cancer risk variant rs4519489 enhances binding of the oncogenic transcription factor USF1, upregulating NOL10. Elevated NOL10 promotes tumor progression, highlighting the rs4519489–USF1–NOL10 axis as a potential biomarker and therapeutic target.