The prognostic value of microRNA‐200 family expression in digestive system tumors: A meta‐analysis and validation

Author:

Wu Xiaoshuang1ORCID,Heng Jinghua2,Li Mengxiang3,Deng Danxia2,Wu Bingli2,Wang Muting4,Li Sanqiang5,Gao Shegan1,Qi Yijun1,Li Enmin2

Affiliation:

1. State Key Laboratory of Esophageal Cancer Prevention & Treatment, Henan Key Laboratory of Microbiome and Esophageal Cancer Prevention and Treatment; Henan Key Laboratory of Cancer Epigenetics; Cancer Hospital, The First Affiliated Hospital, College of Clinical Medicine Medical College of Henan University of Science and Technology Luoyang Henan China

2. The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Department of Biochemistry and Molecular Biology Shantou University Medical College Shantou Guangdong China

3. Department of Mathematics and Physics Luoyang Institute of Science and Technology Luoyang Henan China

4. The Department of Cardio‐Thoracic Surgery Shantou Central Hospital Shantou Guangdong China

5. School of Basic Medicine and Forensic Medicine Henan University of Science and Technology Luoyang Henan China

Abstract

AbstractThe relevance of miR‐200 family in the prognosis of digestive system tumors remains controversial. Through a systematic review of the pertinent literature using online databases including PubMed, EMBASE, The Cochrane Library, and Web of Science, our pooled‐analysis revealed that miR‐200 family downregulation was significantly correlated with poor overall survival (OS, hazard ratio [HR] > 1) and disease‐free survival (HR > 1) in digestive malignancies. Consistently, subgroup analyzes of various organ tissues, univariate analysis, gastric cancer, pancreatic cancer, and patients of American descent revealed the hazardous effects of miR‐200 family downregulation. In contrast, low miR‐200 family expression in blood samples predicted favorable OS (HR < 1). Moreover, lower expression levels of miR‐200c‐5p and miR‐429 were validated in esophageal squamous cell carcinoma (ESCC) tissues. Both the protein and messenger RNA expression levels of Paralemmin‐2 (PALM2) and Mitotic Arrest Deficient 2‐Like Protein (MAD2L1), regulated by miR‐200c‐5p, were notably higher in ESCC, and increased protein levels of PALM2 and MAD2L1 were correlated with adverse OS. PALM2 overexpression significantly enhanced ESCC cell migration. In conclusion, our study highlights the prognostic value of miR‐200 family in digestive system tumors, and the decrease of miR‐200c‐5p may promote ESCC invasion through upregulation of PALM2 and MAD2L1.

Publisher

Wiley

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