解剖学报2024,Vol.55Issue(2) :203-209.DOI:10.16098/j.issn.0529-1356.2024.02.011

上皮细胞转化序列2通过调控p33生长抑制因子1表达影响食管鳞状细胞癌细胞的体外转移活性

Epithelial transformation sequence 2 affecting the in vitro metastatic activity of esophageal squamous carcinoma cells by regulating the expression of p33 inhibitor growth-1

汪洋 吴振华 吕红博 罗洞波
解剖学报2024,Vol.55Issue(2) :203-209.DOI:10.16098/j.issn.0529-1356.2024.02.011

上皮细胞转化序列2通过调控p33生长抑制因子1表达影响食管鳞状细胞癌细胞的体外转移活性

Epithelial transformation sequence 2 affecting the in vitro metastatic activity of esophageal squamous carcinoma cells by regulating the expression of p33 inhibitor growth-1

汪洋 1吴振华 2吕红博 1罗洞波1
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作者信息

  • 1. 新疆医科大学附属肿瘤医院胸外科二病区,乌鲁木齐 830011
  • 2. 新疆医科大学附属肿瘤医院胸外科一病区,乌鲁木齐 830011
  • 折叠

摘要

目的 探讨上皮细胞转化序列 2(ECT2)与p33 生长抑制因子 1(p33ING1)的表达水平对食管鳞状细胞癌(ESCC)细胞转移活性的影响.方法 采用免疫组织化学法和免疫印迹法检测食管鳞癌组织和癌旁组织中ECT2 和p33ING1 的表达情况.将人食管鳞癌细胞系 KYSE140 细胞分为 4 组:空白组、阴性对照组(pcDNA 3.1 NC)组、过表达组(pcDNA 3.1 ECT2)和抑制表达组(si ECT2).采用MTT法和细胞集落形成实验研究细胞的增殖和生长能力,Transwell实验和划痕实验研究细胞的侵袭和迁移能力,并用流式细胞术检测细胞凋亡率和细胞周期,Western blotting检测ECT2 对p33ING1 蛋白的影响.结果 在食管鳞癌组织中ECT2 表达增加,p33ING1 表达降低.过表达ECT2 能够显著增加KYSE140 细胞的生长、集落形成、迁移以及侵袭能力,并能降低KYSE140 细胞的凋亡率和p33ING1 的表达;此外,抑制 ECT2 表达后能够逆转上述变化.结论 ECT2 高表达能够促进食管鳞癌KYSE140 细胞的生长、转移,并抑制其凋亡,其机制可能与 ECT2 能够抑制 p33ING1 表达相关.

Abstract

Objective To investigate the effects of epithelial transformation sequence 2(ECT2)and p33ING1 on the metastatic activity of esophageal squamous cell carcinoma(ESCC)cells.Methods The expressions of ECT2 and p33ING1 in esophageal squamous cell carcinoma tissues and adjacent tissues were detected by immunohistochemistry and Western blotting.Human esophageal squamous carcinoma cell line KYSE140 cells were divided into 4 groups:blank group,negative control(pcDNA 3.1 NC)group,overexpression group(pcDNA 3.1 ECT2)and inhibited expression group(si ECT2).MTT assay and cell colony formation assay were used to study the proliferation and growth ability of cells,Transwell assay and scratch assay used to study the invasion and migration ability of cells,and flow cytometry used to detect apoptosis and cell cycle,Western blotting used to detect the effect of ECT2 on p33ING1 protein.Results ECT2 expression increased and p33ING1 expression decreased in esophageal squamous cell carcinoma tissues.Overexpression of ECT2 significantly increased the growth,colony formation,migration and invasion abilities of KYSE140 cells,and decreased the apoptosis rate and p33ING1 expression of KYSE140 cells.In addition,inhibition of ECT2 expression could reverse the above changes.Conclusion The high expression of ECT2 can promote the growth and metastasis of esophageal squamous cell carcinoma KYSE140 cells and inhibit their apoptosis.The mechanism may be related to the inhibition of p33ING1 expression by ECT2.

关键词

上皮细胞转化序列/2/p33/生长抑制因子/1/食管鳞状细胞癌/转移/免疫印迹法

Key words

Epithelial cell transformation sequence 2/p33 inhibitor of growth-1/Esophageal squamous carcinoma/Metastasis/Western blotting

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基金项目

新疆维吾尔自治区自然科学基金(2021D01C397)

出版年

2024
解剖学报
中国解剖学会

解剖学报

CSTPCD
影响因子:0.462
ISSN:0529-1356
参考文献量15
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