Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.
School of Nursing, Suzhou Vocational Health College, Suzhou, China.
Cell Death Dis. 2021 Oct 25;12(11):998. doi: 10.1038/s41419-021-04278-3.
Prostate cancer is still one of the most common malignancies in men all around the world. The mechanism of how prostate cancer initiates and develops is still not clear. Here in this study, we show that tumor suppressor ZBTB38 could suppress the migration and proliferation of prostate cancer cells. We find lower ZBTB38 expression in prostate cancer tissues, which also strongly predicts a poorer prognosis of prostate cancer. ZBTB38 binds DKK1 (Dickkopf WNT signaling pathway inhibitor 1) locus and promotes DKK1 expression in prostate cancer cell lines. Consistently, reduction of DKK1 expression significantly restores ZBTB38-mediated suppression of migration and proliferation of prostate cancer cell lines. Mechanistically, we find that ZBTB38 primarily binds the promoters of target genes, and differentially regulates the expression of 1818 genes. We also identify PRKDC (protein kinase, DNA-activated, catalytic subunit) as a ZBTB38-interacting protein that could repress the function of ZBTB38 in suppressing migration and proliferation of prostate cancer cells. Taken together, our results indicate that ZBTB38 could repress cell migration and proliferation in prostate cancer via promoting DKK1 expression, and also provide evidence supporting ZBTB38 as a potential prognosis marker for prostate cancer.
前列腺癌仍然是全世界男性最常见的恶性肿瘤之一。前列腺癌发生和发展的机制尚不清楚。在本研究中,我们表明肿瘤抑制因子 ZBTB38 可以抑制前列腺癌细胞的迁移和增殖。我们发现前列腺癌组织中 ZBTB38 的表达较低,这也强烈预示着前列腺癌的预后较差。ZBTB38 结合 DKK1(Dickkopf WNT 信号通路抑制剂 1)基因座并促进前列腺癌细胞系中 DKK1 的表达。一致地,降低 DKK1 的表达显著恢复了 ZBTB38 介导的对前列腺癌细胞系迁移和增殖的抑制作用。在机制上,我们发现 ZBTB38 主要结合靶基因的启动子,并差异调节 1818 个基因的表达。我们还鉴定出 PRKDC(蛋白激酶,DNA 激活,催化亚基)作为 ZBTB38 相互作用蛋白,可抑制 ZBTB38 抑制前列腺癌细胞迁移和增殖的功能。总之,我们的结果表明 ZBTB38 可以通过促进 DKK1 的表达来抑制前列腺癌细胞的迁移和增殖,并为 ZBTB38 作为前列腺癌潜在预后标志物提供证据支持。