Zhang Xiaoxia, Wei Yujie, Wu Fanqi, Li Mei, Han Cong, Huo Chengdong, Li Zhi, Tang Futian, He Wenting, Zhao Yang, Li Yumin
Department of the Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, 730030, China.
Key Laboratory of Digestive System Tumors of Gansu Province, Lanzhou, 730030, China.
J Cancer Res Clin Oncol. 2024 Apr 24;150(4):210. doi: 10.1007/s00432-024-05669-7.
Gastric cancer (GC) is prevalent as one of the most common malignant tumors globally, with a particularly high incidence in China. The role of UBE2L3 in the initiation and progression of various cancers has been well documented, but its specific significance in GC is not yet fully elucidated. The objective of this study is to examine the expression and importance of UBE2L3 in human gastric cancer tissues.
Immunohistochemical staining and survival analysis were conducted on 125 cases of GC. Western blot and quantitative real-time polymerase chain reaction (qRT-PCR) were employed to assess the expression of UBE2L3 in GC cell lines. Cell lines with UBE2L3 knockdown and overexpression were cultured through lentivirus transfection and subsequently assessed using Western blot analysis. The involvement of UBE2L3 in the proliferation, invasion, and apoptosis of GC cells was confirmed through in vitro experiments, and its capacity to facilitate tumor growth was also validated in in vivo studies.
The up-regulation of UBE2L3 expression was observed in GC, and its high expression was found to be significantly associated with the degree of differentiation (χ = 6.153, P = 0.0131), TNM stage (χ = 6.216, P = 0.0447), and poor overall survival. In vitro, UBE2L3 has been shown to enhance functions in GC cell lines, such as promoting proliferation and invasion, and inhibiting apoptosis. In vivo experiments have validated the role of UBE2L3 in promoting tumor growth.
The findings of our study demonstrate the significant involvement of UBE2L3 in the pathogenesis and advancement of gastric cancer, suggesting its potential as a therapeutic target.
胃癌(GC)是全球最常见的恶性肿瘤之一,在中国发病率尤其高。已有充分文献记载泛素结合酶E2L3(UBE2L3)在各种癌症的发生和发展中所起的作用,但其在胃癌中的具体意义尚未完全阐明。本研究的目的是检测UBE2L3在人胃癌组织中的表达及其重要性。
对125例胃癌患者进行免疫组织化学染色和生存分析。采用蛋白质免疫印迹法(Western blot)和定量实时聚合酶链反应(qRT-PCR)评估UBE2L3在胃癌细胞系中的表达。通过慢病毒转染培养UBE2L3基因敲低和过表达的细胞系,随后用蛋白质免疫印迹分析进行评估。通过体外实验证实UBE2L3参与胃癌细胞的增殖、侵袭和凋亡,其促进肿瘤生长的能力也在体内研究中得到验证。
在胃癌中观察到UBE2L3表达上调,发现其高表达与分化程度(χ = 6.153,P = 0.0131)、TNM分期(χ = 6.216,P = 0.0447)及总体生存率差显著相关。在体外,UBE2L3已被证明可增强胃癌细胞系的功能,如促进增殖和侵袭以及抑制凋亡。体内实验证实了UBE2L3在促进肿瘤生长中的作用。
我们的研究结果表明UBE2L3在胃癌的发病机制和进展中起重要作用,提示其作为治疗靶点的潜力。