癌变·畸变·突变 ›› 2023, Vol. 35 ›› Issue (6): 412-419.doi: 10.3969/j.issn.1004-616x.2023.06.002

• 论著 • 上一篇    下一篇

TONSL在食管癌中的表达及其影响食管鳞癌细胞增殖的机制

郑雅琪1, 赵子婷2, 潘德渊2, 刘禄鑫1, 许秀娥1, 廖连娣1, 王少洪3, 李恩民2, 许丽艳1   

  1. 1. 汕头大学医学院病理教研室, 广东 汕头 515041;
    2. 汕头大学医学院生物化学与分子生物学教研室, 广东 汕头 515041;
    3. 汕头市中心医院病理科, 广东 汕头 515041
  • 收稿日期:2023-04-11 修回日期:2023-06-25 出版日期:2023-11-30 发布日期:2023-12-09
  • 通讯作者: 李恩民;许丽艳
  • 作者简介:郑雅琪,E-mail:1913828712@qq.com。
  • 基金资助:
    国家重点研发计划“精准医学研究”重点专项(2016YFC0901400);2021年广东省科技专项(210729156901797)

The expression of tonsoku-like DNA repair protein in esophageal carcinoma and its effect on the proliferation of esophageal squamous cell carcinoma

ZHENG Yaqi1, ZHAO Ziting2, PAN Deyuan2, LIU Luxin1, XU Xiue1, LIAO Liandi1, WANG Shaohong3, LI Enmin2, XU Liyan1   

  1. 1. Department of Pathology, Shantou University Medical College, Shantou 515041;
    2. Department of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041;
    3. Department of Pathology, Shantou Central Hospital, Shantou 515041, Guangdong, China
  • Received:2023-04-11 Revised:2023-06-25 Online:2023-11-30 Published:2023-12-09

摘要: 目的:探讨tonsoku样DNA修复蛋白(TONSL)在食管癌组织中的表达及其对食管鳞癌细胞增殖的影响及机制。方法:利用cBioPortal、GEPIA和PRIDE等数据库分析在食管癌组织中,TONSL基因组拷贝数及其转录和翻译水平的变化。通过免疫组织化学实验检测TONSL蛋白在食管鳞癌和正常食管组织中的表达。利用siRNA干扰构建TONSL瞬时敲降食管鳞癌细胞模型,并采用集落形成实验和EdU实验检测TONSL敲降对食管鳞癌细胞增殖能力的影响。Western blot检测TONSL敲降后食管鳞癌细胞中DNA损伤修复相关标志蛋白ATM丝氨酸/苏氨酸激酶(ATM)和检查点激酶2(CHK2)及其磷酸化激活水平的变化。结果:与正常食管组织比较,食管癌基因组、转录组和蛋白质组的数据库分析结果显示,TONSL在食管癌组织中拷贝数增加表达,其mRNA和蛋白质表达水平在食管癌组织中均上调(P<0.05),且TONSL高表达与食管癌患者不良预后相关(P<0.05);免疫组织化学验证结果也表明TONSL蛋白在食管鳞癌组织中表达上调(P<0.001)。集落形成实验和EdU实验结果显示,与对照组相比,TONSL敲降后食管鳞癌细胞增殖能力减弱(P<0.05),并且在敲降TONSL后,食管鳞癌细胞DNA损伤修复相关蛋白ATM和CHK2的磷酸化水平均上调(均为P<0.05)。结论:TONSL在食管鳞癌中表达上调,并通过参与食管鳞癌细胞DNA损伤修复促进食管鳞癌细胞增殖。

关键词: 食管鳞癌, tonsoku样DNA修复蛋白, 细胞增殖, DNA损伤修复

Abstract: OBJECTIVE:To investigate the expression of tonsoku-like DNA repair protein (TONSL) in esophageal carcinoma and its effect and mechanism on the proliferation of esophageal squamous cell carcinoma. METHODS:Databases such as cBioPortal,GEPIA and PRIDE were used to analyze changes in TONSL genome copy number and its transcription and translation levels in esophageal cancer. The expression of TONSL in esophageal squamous cell carcinoma and normal esophageal tissues was detected by immunohistochemistry. Small interfering RNA (siRNA) was used to construct a TONSL knockdown esophageal squamous cell model. The effect of TONSL knockdown on the proliferation of esophageal squamous cell carcinoma cells was studied by colony formation assay and EdU assay,while the changes of phosphorylated activation levels of ATM serine/threonine kinase (ATM) and checkpoint kinase 2 (CHK2),two DNA damage repair related marker proteins in esophageal squamous cell carcinoma cells was detected by Western blot. RESULTS:Compared with normal esophageal tissue,copy number amplification of TONSL was common in esophageal cancer,and its mRNA and protein levels in esophageal cancer were up-regulated compared with those in normal esophageal tissues (P<0.05),and high TONSL expression was associated with poor prognosis of patients with esophageal carcinoma (P<0.05). The results of immunohistochemistry also showed that TONSL was up-regulated in esophageal squamous cell carcinoma. The results of colony formation assay and EdU assay showed that knockdown of TONSL inhibited the proliferation of esophageal squamous cell carcinoma cells (P<0.05). Moreover,TONSL knockdown induced up-regulation of the phosphorylation of ATM serine/threonine kinase (ATM) and checkpoint kinase 2 (CHK2) in esophageal squamous cell carcinoma cells. CONCLUSION:TONSL was up-regulated in esophageal squamous cell carcinoma and promoted the proliferation of esophageal squamous cell carcinoma by participating in DNA damage repair.

Key words: esophageal squamous cell carcinomar, TONSL, cell proliferation, DNA damage repair

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