Zhou Xiaohua, Gao Fuping, Xu Guangqi, Puyang Yongqiang, Rui Hongqing, Li Junsheng
School of Medicine, Southeast University, China.
Department of General Surgery, Nanjing Gaochun People's Hospital, China.
Heliyon. 2024 Jun 7;10(11):e32676. doi: 10.1016/j.heliyon.2024.e32676. eCollection 2024 Jun 15.
Siah E3 ubiquitin protein ligase 1 (SIAH1) has been reported to participate in the development of several human cancers, including gastric cancer. However, the effect and mechanism of SIAH1 on the migration and invasion of gastric cancer cells need be further explored. Here, we first analyzed the clinical value of SIAH1 in gastric cancer, and found that SIAH1 was up-regulated in gastric cancer and associated with a poor prognosis. In addition, silencing of SIAH1 significantly inhibited the migration and invasion of gastric cancer cells through inhibiting the expression of matrix metalloproteinase-9 (MMP9), while overexpression of SIAH1 had the opposite effect. Molecularly, we provided the evidence that reversion-inducing cysteine-rich protein with Kazal motifs (RECK) was a potential substrate of SIAH1. We determined that SIAH1 could destabilize RECK through promoting its ubiquitination and degradation via proteasome pathway. We also found RECK was involved in SIAH1-regulated gastric cancer cell migration and invasion. In conclusion, SIAH1 is up-regulated in gastric cancer, which promotes the migration and invasion of gastric cancer cells through regulating RECK-MMP9 pathway.
据报道,Siah E3泛素蛋白连接酶1(SIAH1)参与包括胃癌在内的多种人类癌症的发展。然而,SIAH1对胃癌细胞迁移和侵袭的影响及机制仍需进一步探索。在此,我们首先分析了SIAH1在胃癌中的临床价值,发现SIAH1在胃癌中上调且与预后不良相关。此外,沉默SIAH1通过抑制基质金属蛋白酶-9(MMP9)的表达显著抑制了胃癌细胞的迁移和侵袭,而SIAH1的过表达则产生相反的效果。在分子层面,我们提供证据表明富含Kazal基序的逆转诱导型富含半胱氨酸蛋白(RECK)是SIAH1的潜在底物。我们确定SIAH1可通过促进RECK经蛋白酶体途径的泛素化和降解使其不稳定。我们还发现RECK参与了SIAH1调控的胃癌细胞迁移和侵袭。总之,SIAH1在胃癌中上调,通过调节RECK-MMP9途径促进胃癌细胞的迁移和侵袭。