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已发表论文

含 MAM 结构域 2(MAMDC2)影响人类胃癌的侵袭和转移

 

Authors Shen J, Gao G , Liu S

Received 11 January 2025

Accepted for publication 22 May 2025

Published 26 May 2025 Volume 2025:18 Pages 679—693

DOI http://doi.org/10.2147/OTT.S516982

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Lukas Hawinkels

Jiaofeng Shen,1,* Guangyu Gao,1,* Songtao Liu1,2 

1Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, People’s Republic of China; 2Department of Ultrasound, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Songtao Liu, Department of Ultrasound, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, People’s Republic of China, Email 20185233105@stu.suda.edu.cn

Background: Gastric cancer (GC) is the fifth most prevalent cancer worldwide and the fourth leading cause of cancer-related mortality. MAM Domain Containing 2 (MAMDC2) has been involved in many cancers. However, the impact of MAMDC2 on gastric cancer was unclear. This study aimed to investigate the role and mechanism of MAMDC2 in gastric cancer.
Methods: Differential genes in gastric cancer are analyzed by GEO, TCGA, MSigDB database, R-packet limma, and Wilcoxon test. Survival analysis is performed through the R package survival. Construct a PPI network through the STRING database. Enrichment analysis is performed by Metascape. The infiltration level of gastric cancer immune cells is calculated by CIBERSORT. In addition, the expression of MAMDC2 was analyzed by immunohistochemistry and quantitative real-time polymerase chain reaction (RT-qPCR). siMAMDC2 was used to knock down the specific gene. Cell counting kit-8 (CCK-8) assay, colony formation assay, and cell migration were applied to evaluate the function of MAMDC2 in gastric cancer cells.
Results: In the present study, we revealed a significant upregulation of MAMDC2 in gastric cancer tissues and cells. Knocking down MAMDC2 inhibited the proliferation and migration of gastric cancer cells, while overexpression of MAMDC2 produced the opposite results. Furthermore, MAMDC2 may be an independent factor in poor prognosis in gastric cancer patients.
Conclusion: These results illustrated that MAMDC2 promoted the proliferation and migration of gastric cancer cells. The newly identified MAMDC2 provides novel insight into the pathogenesis of gastric cancer.

Keywords: MAMDC2, gastric cancer, GEO, CCK-8, invasion

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