Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Urology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Cancer Sci. 2021 Jan;112(1):323-330. doi: 10.1111/cas.14695. Epub 2020 Nov 24.
Although Y-box binding protein-1 (YB-1) is known to be overexpressed in prostate cancer, especially castration-resistant prostate cancer (CRPC), the mechanism of its overexpression remains unclear. We aimed to elucidate the mechanism of YB-1 overexpression in CRPC. Gene amplification in CRPC cells and tissues was examined by public database analysis, and digital PCR. The significance of YB-1 amplification for the YB-1/androgen receptor (AR) axis and prognosis was examined by public database analysis and immunohistochemistry. YB-1 amplification was mainly observed in CRPC tissues by public database analysis and confirmed in CRPC cells and tissues by digital PCR. Expression of YB-1 was increased in CRPC tissues compared with treatment-naïve tissues. Furthermore, YB-1 and phosphorylated YB-1 levels were associated with AR and AR V7 expression levels. Finally, YB-1 amplification was associated with poor outcomes in CRPC. Taken together, the present findings suggest that YB-1 amplification contributes to progression to CRPC through regulation of AR and AR V7 expressions, and that YB-1 is a promising therapeutic target in CRPC.
虽然 Y 盒结合蛋白-1(YB-1)已知在前列腺癌中过表达,尤其是在去势抵抗性前列腺癌(CRPC)中,但它过表达的机制仍不清楚。我们旨在阐明 CRPC 中 YB-1 过表达的机制。通过公共数据库分析和数字 PCR 检查 CRPC 细胞和组织中的基因扩增。通过公共数据库分析和免疫组织化学检查 YB-1 扩增对 YB-1/雄激素受体(AR)轴和预后的意义。通过公共数据库分析主要观察到 CRPC 组织中的 YB-1 扩增,并通过数字 PCR 在 CRPC 细胞和组织中得到证实。与未经治疗的组织相比,CRPC 组织中 YB-1 的表达增加。此外,YB-1 和磷酸化 YB-1 水平与 AR 和 AR V7 表达水平相关。最后,YB-1 扩增与 CRPC 的不良预后相关。总之,这些发现表明,YB-1 扩增通过调节 AR 和 AR V7 的表达促进 CRPC 的进展,YB-1 是 CRPC 有前途的治疗靶点。