1. HIP1R acts as a tumor suppressor in gastric cancer by promoting cancer cell apoptosis and inhibiting migration and invasion through modulating Akt
- Author
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Fei Zhang, Qiong Xiao, Huiyuan Guan, Zhenning Wang, Peng Gao, Xin Wang, Yongxi Song, Zhonghua Wu, Jin-Liang Zhu, and Jinxin Shi
- Subjects
Male ,0301 basic medicine ,Microbiology (medical) ,Tumor suppressor gene ,huntingtin‐interacting protein 1‐related ,Clinical Biochemistry ,migration ,Flow cytometry ,03 medical and health sciences ,0302 clinical medicine ,Cell Movement ,Stomach Neoplasms ,Biomarkers, Tumor ,Tumor Cells, Cultured ,medicine ,Humans ,Immunology and Allergy ,Neoplasm Invasiveness ,Cytotoxicity ,Protein kinase B ,Research Articles ,Adaptor Proteins, Signal Transducing ,Cell Proliferation ,medicine.diagnostic_test ,Chemistry ,gastric cancer ,Microfilament Proteins ,Biochemistry (medical) ,apoptosis ,Public Health, Environmental and Occupational Health ,Cancer ,Hematology ,Middle Aged ,Prognosis ,invasion ,medicine.disease ,Gene Expression Regulation, Neoplastic ,Survival Rate ,Medical Laboratory Technology ,030104 developmental biology ,Apoptosis ,030220 oncology & carcinogenesis ,Cancer research ,Immunohistochemistry ,Female ,Proto-Oncogene Proteins c-akt ,Intracellular ,Research Article - Abstract
Background Huntingtin‐interacting protein 1‐related (HIP1R) is a multi‐domain gene that exerts many cellular functions including altering T cell–mediated cytotoxicity and controlling intracellular trafficking. However, its clinical significance and function in gastric cancer (GC) have not been described. Methods The expression levels of HIP1R were tested by the transcriptional and translational expression analysis and immunohistochemistry (IHC) in matched adjacent non‐tumorous vs tumor tissue specimens. The biological function of HIP1R on apoptosis, migration, and proliferation was evaluated by flow cytometry, Transwell, Cell Counting Kit‐8 (CCK‐8) assays, colony formation assays, and EdU labeling assays, respectively. Results We found downregulated HIP1R in GC compared with adjacent non‐tumorous tissue, and HIP1R expression associated with N classification. We further found that the expression of HIP1R could induce apoptosis and inhibit proliferation, migration, invasion of GC cells, possibly through modulating Akt. Conclusions Our data indicate that HIP1R may act as a potential diagnostic biomarker and a tumor suppressor gene in GC, potentially representing a novel therapeutic target for future GC treatment.
- Published
- 2020
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