Journal of Shanghai Jiao Tong University (Medical Science) >

2025 , Vol. 45 >Issue 9: 1149 - 1160

DOI: https://doi.org/10.3969/j.issn.1674-8115.2025.09.007

Basic research

Construction of a truncated cylindromatosis tumor suppressor deubiquitinase plasmid and its regulation of the phenotypes of gastric cancer cells

  • PAERHATI Nadina ,
  • ZHANG Pengshan ,
  • XU Yitian ,
  • CHEN Yunqi ,
  • HUANG Chen
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  • Department of Gastrointestinal Surgery, General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200080, China
HUANG Chen, E-mail: richard-hc@hotmail.com.

Received date: 2024-12-13

  Accepted date: 2025-04-08

  Online published: 2025-09-30

Supported by

National Natural Science Foundation of China(82072662);“Two-hundred Talents” Program of Shanghai Jiao Tong University School of Medicine(20191425);Medical and Engineering Cross Research Fund from Shanghai Jiao Tong University “Jiao Tong University Star” Program;East Talents Program's Top-Notch Project (2023);Featured National Leading Talents of Shanghai General Hospital

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Abstract

Objective ·To construct truncations of CYLD, and to preliminarily analyze their effects on the proliferation of gastric cancer cells. Methods ·TCGA, GTEx, and Kaplan-Meier Plotter databases were used to analyze the differences in the expression levels of CYLD between gastric cancer tissues and normal tissues, and their relationship with the prognosis of gastric cancer patients. Immunohistochemistry and Western blotting were used to detect the expression of CYLD in cancer tissues and adjacent noncancerous tissues. Western blotting and qRT-PCR were used to analyze the protein and mRNA expression levels of CYLD in gastric mucosal epithelial cells and gastric cancer cells. According to the sequence and structural characteristics of CYLD gene, primers were designed to construct its truncations. Their expression was detected and identified by agarose gel electrophoresis and Western blotting, and localization was observed by immunofluorescence. In the human gastric adenocarcinoma cells (AGS) with CYLD knockdown, blank NC was added to the control group, and the full-length CYLD, enzyme-inactivated mutant, and three truncated plasmids were added to the experimental group. The proliferation changes of cells in each group were detected by CCK-8 and plate cloning assays. Co-immunoprecipitation, deubiquitination, and Western blotting assays were performed to examine the binding ability of full-length CYLD, the enzyme-inactivated mutant, and the truncated variants to CAMK2A, the level of CAMK2A deubiquitination, and the expression of STAT3 and p-STAT3 proteins. Results ·CYLD expression in normal gastric tissues and cells was significantly higher than in gastric cancer tissues and cells, and the prognosis of patients with high expression of CYLD was better. The truncations of human CYLD were successfully constructed, and full length CYLD, enzyme-inactivated mutant, and truncations were mainly localized in the cytoplasm. Knockdown of CYLD in gastric cancer cells significantly enhanced the proliferative ability of gastric cancer cells. Reconstitution of CYLD-knockdown cells with CYLD-WT, or truncated variants containing the CAP3 or USP domains significantly inhibited the proliferation of gastric cancer cells. In addition, CYLD bound to CAMK2A mediated K63 deubiquitination modification, and inhibited CAMK2A-induced phosphorylation of STAT3. Conclusion ·The human CYLD truncation plasmids are successfully constructed, and the full length CYLD and its CAP3 and USP segments significantly inhibit the proliferation of gastric cancer cells.

Key words： deubiquitinase; gastric cancer; cylindromatosis (CYLD); truncation; poliferation; CAMK2A; STAT3

Cite this article

PAERHATI Nadina , ZHANG Pengshan , XU Yitian , CHEN Yunqi , HUANG Chen . Construction of a truncated cylindromatosis tumor suppressor deubiquitinase plasmid and its regulation of the phenotypes of gastric cancer cells[J]. Journal of Shanghai Jiao Tong University (Medical Science), 2025 , 45(9) : 1149 -1160 . DOI: 10.3969/j.issn.1674-8115.2025.09.007

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