ZFP36L1 Promotes Gastric Cancer Progression via Regulating JNK and p38 MAPK Signaling Pathways

Author:

Zhou Fenghua1ORCID,Ding Kang1ORCID,Zhang Fengping1ORCID,Qi Gaoxiu2ORCID,Lin Meng1ORCID,Chen Min2ORCID,Chen Yanchun3ORCID,Zheng Jie1ORCID

Affiliation:

1. Department of Pathology, Weifang Medical University, Weifang, Shandong, P.R. China

2. Department of Pathology, Affiliated hospital, Weifang Medical University, Weifang, Shandong, PR China

3. Department of Histology and Embryology, Weifang Medical University, Weifang, Shandong, P.R. China

Abstract

Background: The RNA-binding protein Zinc Finger Protein 36 like 1(ZFP36L1) plays an important role in regulating the AU-rich elements (AREs) in the 3′ untranslated region (3′ UTR) of mRNAs, indicating a potential link between its expression and cancers. However, the role and mechanism of ZFP36L1 in gastric cancer (GC) are unclear. Objective: This study aimed to explore the role and mechanism of ZFP36L1 in gastric cancer. Material and Method: GC tissue samples and matched normal gastric tissues were collected, and the ZFP36L1 expression in these samples was evaluated by immunohistochemistry analysis. GC cells with different differentiation were selected for in vitro experiments. The ZFP36L1 expression in GC cells was examined by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot analysis. The viability and invasiveness of GC cells were assayed by 5-Ethynyl-2-deoxyuridine (EdU) and Transwell assays, respectively. Western blot assay was used to detect the expression of epithelial-to-mesenchymal transition (EMT) related proteins and proteins of the c-Jun N-terminal kinase (JNK) and p38 Mitogen-Activated Protein Kinase (MAPK) signaling pathways. Results: ZFP36L1 is overexpressed in GC tissues. Patients with high ZFP36L1 expression have a poor prognosis. Moreover, ZFP36L1 is overexpressed in the cell lines with a high degree of malig-nancy. ZFP36L1 increases cell proliferation, invasion, and migration in vitro. Furthermore, ZFP36L1 induces EMT. The JNK inhibitor and p38 inhibitor alone or in combination affect the biological function of GC cells. Furthermore, ZFP36L1 promotes GC progression by inhibiting JNK and p38 MAPK signaling pathways. Conclusion: RNA-binding protein ZFP36L1 exerts a role in the occurrence of gastric cancer by the regulation of the JNK and p38 MAPK signaling pathways. The combination of inhibitors of the JNK and p38 MAPK signaling pathways could be a novel treatment strategy for gastric cancer.

Funder

Shandong Province National Natural Science Foundation

Foundation Key Project of Shandong Province Higher Educational Science and Technology Program of China

Support Program for Youth Innovation technology in Colleges and Universities of Shandong Province of China

National Science Foundation of China

Shandong medical and health science and technology development plan project

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology (medical),Cancer Research,Drug Discovery,Oncology,General Medicine

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