SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition

Background: SQSTM1/p62 is an autophagy-related receptor protein that participates in regulating tumorigenesis and multiple signaling pathways. Gastric cancer (GC) is a common tumor in the digestive tract and continues to pose a significant threat to human health. Therefore, this study aims to invest...

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Main Authors: Yan Xu, Ciba Zhu, Chenglou Zhu, Lingzhi Peng, Dandan Ji, Qiong Wu, Pengwei Bai, Zhaozhao Bai, Mingxu Da
Format: Article
Language:English
Published: Elsevier 2024-02-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844024004407
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author Yan Xu
Ciba Zhu
Chenglou Zhu
Lingzhi Peng
Dandan Ji
Qiong Wu
Pengwei Bai
Zhaozhao Bai
Mingxu Da
author_facet Yan Xu
Ciba Zhu
Chenglou Zhu
Lingzhi Peng
Dandan Ji
Qiong Wu
Pengwei Bai
Zhaozhao Bai
Mingxu Da
author_sort Yan Xu
collection DOAJ
description Background: SQSTM1/p62 is an autophagy-related receptor protein that participates in regulating tumorigenesis and multiple signaling pathways. Gastric cancer (GC) is a common tumor in the digestive tract and continues to pose a significant threat to human health. Therefore, this study aims to investigate the impact of p62 on gastric cancer. Methods: Immunohistochemistry and Western blotting were employed to assess the expression level of the p62 protein in gastric cancer tissues and its correlation with prognosis. Subsequently, in vitro cell experiments were conducted to determine the role of p62 in gastric cancer cell proliferation, migration, and metastasis. Result: The expression of p62 in gastric cancer tissues was significantly higher than in normal tissues. The expression of p62 was positively correlated with poor prognosis in gastric cancer patients. In vitro cell experiments indicated that p62 promotes gastric cancer cell proliferation and migration. Mechanistically, elevated p62 expression induced epithelial-mesenchymal transition (EMT), leading to upregulation of E-cadherin and downregulation of N-cadherin and vimentin. Conclusion: This study provides novel and robust evidence for the mechanism by which elevated p62 expression promotes the progression of gastric cancer. It offers promising therapeutic targets for anti-tumor treatment strategies in gastric cancer patients.
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spelling doaj.art-15da4275df364bffaca5dc9a3bc7f81d2024-02-17T06:38:09ZengElsevierHeliyon2405-84402024-02-01103e24409SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transitionYan Xu0Ciba Zhu1Chenglou Zhu2Lingzhi Peng3Dandan Ji4Qiong Wu5Pengwei Bai6Zhaozhao Bai7Mingxu Da8The First School of Clinical Medicine, Gansu University of Chinese Medicine, Lanzhou,730000, ChinaThe First School of Clinical Medicine, Gansu University of Chinese Medicine, Lanzhou,730000, ChinaThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, ChinaThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China; Co-corresponding author.The First School of Clinical Medicine, Gansu University of Chinese Medicine, Lanzhou,730000, ChinaThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, ChinaClinical Medical College of Ningxia Medical University, 750000, Yinchuan, ChinaClinical Medical College of Ningxia Medical University, 750000, Yinchuan, ChinaThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China; Department of Surgical Oncology, Gansu Provincial Hospital, Lanzhou, 730000, China; Corresponding author.Background: SQSTM1/p62 is an autophagy-related receptor protein that participates in regulating tumorigenesis and multiple signaling pathways. Gastric cancer (GC) is a common tumor in the digestive tract and continues to pose a significant threat to human health. Therefore, this study aims to investigate the impact of p62 on gastric cancer. Methods: Immunohistochemistry and Western blotting were employed to assess the expression level of the p62 protein in gastric cancer tissues and its correlation with prognosis. Subsequently, in vitro cell experiments were conducted to determine the role of p62 in gastric cancer cell proliferation, migration, and metastasis. Result: The expression of p62 in gastric cancer tissues was significantly higher than in normal tissues. The expression of p62 was positively correlated with poor prognosis in gastric cancer patients. In vitro cell experiments indicated that p62 promotes gastric cancer cell proliferation and migration. Mechanistically, elevated p62 expression induced epithelial-mesenchymal transition (EMT), leading to upregulation of E-cadherin and downregulation of N-cadherin and vimentin. Conclusion: This study provides novel and robust evidence for the mechanism by which elevated p62 expression promotes the progression of gastric cancer. It offers promising therapeutic targets for anti-tumor treatment strategies in gastric cancer patients.http://www.sciencedirect.com/science/article/pii/S2405844024004407SQSTM1/p62Gastric cancerEMTPrognosis
spellingShingle Yan Xu
Ciba Zhu
Chenglou Zhu
Lingzhi Peng
Dandan Ji
Qiong Wu
Pengwei Bai
Zhaozhao Bai
Mingxu Da
SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition
Heliyon
SQSTM1/p62
Gastric cancer
EMT
Prognosis
title SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition
title_full SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition
title_fullStr SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition
title_full_unstemmed SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition
title_short SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition
title_sort sqstm1 p62 promotes the progression of gastric cancer through epithelial mesenchymal transition
topic SQSTM1/p62
Gastric cancer
EMT
Prognosis
url http://www.sciencedirect.com/science/article/pii/S2405844024004407
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