School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, 710061, China.
Department of Chemistry, Faculty of Science, Universiti Malaya, 50603, Kuala Lumpur, Malaysia.
Acta Pharmacol Sin. 2024 Jul;45(7):1520-1529. doi: 10.1038/s41401-024-01254-3. Epub 2024 Mar 22.
Parkin (PARK2) deficiency is frequently observed in various cancers and potentially promotes tumor progression. Here, we showed that Parkin expression is downregulated in liver cancer tissues, which correlates with poor patient survival. Parkin deficiency in liver cancer cells promotes migration and metastasis as well as changes in EMT and metastasis markers. A negative correlation exists between TMEFF1 and Parkin expression in liver cancer cells and tumor tissues. Parkin deficiency leads to upregulation of TMEFF1 which promotes migration and metastasis. TMEFF1 transcription is activated by Parkin-induced endogenous TGF-β production and subsequent phosphorylation of Smad2/3 and its binding to TMEFF1 promotor. TGF-β inhibitor and TMEFF1 knockdown can reverse shParkin-induced cell migration and changes of EMT markers. Parkin interacts with and promotes the ubiquitin-dependent degradation of HIF-1α/HIF-1β and p53, which accounts for the suppression of TGF-β production. Our data have revealed that Parkin deficiency in cancer leads to the activation of the TGF-β/Smad2/3 pathway, resulting in the expression of TMEFF1 which promotes cell migration, EMT, and metastasis in liver cancer cells.
Parkin(PARK2)缺失在各种癌症中经常观察到,并可能促进肿瘤进展。在这里,我们表明 Parkin 在肝癌组织中表达下调,与患者生存不良相关。肝癌细胞中的 Parkin 缺失促进迁移和转移以及 EMT 和转移标志物的变化。肝癌细胞和肿瘤组织中 TMEFF1 和 Parkin 的表达呈负相关。Parkin 缺失导致 TMEFF1 的上调,从而促进迁移和转移。TMEFF1 转录被 Parkin 诱导的内源性 TGF-β产生以及随后的 Smad2/3 磷酸化及其与 TMEFF1 启动子的结合所激活。TGF-β 抑制剂和 TMEFF1 敲低可逆转 shParkin 诱导的细胞迁移和 EMT 标志物的变化。Parkin 与 HIF-1α/HIF-1β 和 p53 相互作用,并促进其泛素依赖性降解,从而抑制 TGF-β 的产生。我们的数据表明,癌症中的 Parkin 缺失导致 TGF-β/Smad2/3 通路的激活,导致 TMEFF1 的表达,从而促进肝癌细胞的细胞迁移、EMT 和转移。