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  1. Artikel ; Online: Huntingtin-associated protein 1 is a potential tumor suppressor for gastric cancer

    Qu, Ye-Min / Chen, Ai / Zhao, Xue / Wang, Zan / Guo, Dong / Shao, Shu-Li / Tao, Yuan-Yong / Li, Qiu-Jing / Wang, Ming-Yi / Ma, Wan-Shan

    Mol Biol Rep. 2023 Feb., v. 50, no. 2 p.1517-1531

    2023  

    Abstract: BACKGROUND: Gastric cancer is heterogeneous cancer and the causes of this disease are complex. New diagnostic and therapeutic targets are urgently needed to explore. Huntingtin-associated protein 1 (HAP1) is directly related to Huntington’s disease (HD). ...

    Abstract BACKGROUND: Gastric cancer is heterogeneous cancer and the causes of this disease are complex. New diagnostic and therapeutic targets are urgently needed to explore. Huntingtin-associated protein 1 (HAP1) is directly related to Huntington’s disease (HD). However, patients with Huntington’s disease have a lower incidence of cancer. Therefore, we are committed to studying the correlation between HAP1 and gastric carcinogenesis and development. METHODS AND RESULTS: Immunohistochemical staining, western blot analysis, and RT-qPCR were conducted to explore the localization and expression of HAP1 in gastric cancer. To study the biological significance of HAP1, we overexpressed HAP1 in both MKN28 and AGS cell lines by lentivirus infection. To explore the role of HAP1 in cell proliferation, the cells counting assay, EdU incorporation assay, and colony formation assay were carried out. We performed the wound healing assay and transwell assay to study the cell migration and invasion. To further investigate whether HAP1 could regulate gastric cancer cell death during glucose deprivation, Annexin V-FITC/PI staining was performed. In our study, we elucidated that HAP1 was downregulated in gastric cancer. What’s more, overexpressing HAP1 inhibited cell proliferation, cell migration and invasion, and triggered apoptosis during glucose deprivation. More importantly, the antitumor properties and mechanisms of HAP1 have been elucidated further in gastric cancer. CONCLUSIONS: Taken together, the available evidence implies that HAP1 may serve as a potential tumor suppressor, making it a significant target in preventing and treating gastric cancer. This research provides a theoretical basis for the early diagnosis, clinical targeted therapy, and prognosis evaluation of gastric cancer.
    Schlagwörter Western blotting ; apoptosis ; carcinogenesis ; cell movement ; cell proliferation ; early diagnosis ; glucose ; immunohistochemistry ; neoplasm cells ; prognosis ; stomach neoplasms ; therapeutics
    Sprache Englisch
    Erscheinungsverlauf 2023-02
    Umfang p. 1517-1531.
    Erscheinungsort Springer Netherlands
    Dokumenttyp Artikel ; Online
    ZDB-ID 186544-4
    ISSN 1573-4978 ; 0301-4851
    ISSN (online) 1573-4978
    ISSN 0301-4851
    DOI 10.1007/s11033-022-08090-w
    Datenquelle NAL Katalog (AGRICOLA)

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  2. Artikel ; Online: Huntingtin-associated protein 1 is a potential tumor suppressor for gastric cancer.

    Qu, Ye-Min / Chen, Ai / Zhao, Xue / Wang, Zan / Guo, Dong / Shao, Shu-Li / Tao, Yuan-Yong / Li, Qiu-Jing / Wang, Ming-Yi / Ma, Wan-Shan

    Molecular biology reports

    2022  Band 50, Heft 2, Seite(n) 1517–1531

    Abstract: Background: Gastric cancer is heterogeneous cancer and the causes of this disease are complex. New diagnostic and therapeutic targets are urgently needed to explore. Huntingtin-associated protein 1 (HAP1) is directly related to Huntington's disease (HD). ...

    Abstract Background: Gastric cancer is heterogeneous cancer and the causes of this disease are complex. New diagnostic and therapeutic targets are urgently needed to explore. Huntingtin-associated protein 1 (HAP1) is directly related to Huntington's disease (HD). However, patients with Huntington's disease have a lower incidence of cancer. Therefore, we are committed to studying the correlation between HAP1 and gastric carcinogenesis and development.
    Methods and results: Immunohistochemical staining, western blot analysis, and RT-qPCR were conducted to explore the localization and expression of HAP1 in gastric cancer. To study the biological significance of HAP1, we overexpressed HAP1 in both MKN28 and AGS cell lines by lentivirus infection. To explore the role of HAP1 in cell proliferation, the cells counting assay, EdU incorporation assay, and colony formation assay were carried out. We performed the wound healing assay and transwell assay to study the cell migration and invasion. To further investigate whether HAP1 could regulate gastric cancer cell death during glucose deprivation, Annexin V-FITC/PI staining was performed. In our study, we elucidated that HAP1 was downregulated in gastric cancer. What's more, overexpressing HAP1 inhibited cell proliferation, cell migration and invasion, and triggered apoptosis during glucose deprivation. More importantly, the antitumor properties and mechanisms of HAP1 have been elucidated further in gastric cancer.
    Conclusions: Taken together, the available evidence implies that HAP1 may serve as a potential tumor suppressor, making it a significant target in preventing and treating gastric cancer. This research provides a theoretical basis for the early diagnosis, clinical targeted therapy, and prognosis evaluation of gastric cancer.
    Mesh-Begriff(e) Humans ; Stomach Neoplasms/genetics ; Nerve Tissue Proteins/metabolism ; Huntington Disease/metabolism ; Apoptosis/genetics ; Cell Death ; Cell Proliferation/genetics ; Cell Line, Tumor
    Chemische Substanzen Nerve Tissue Proteins
    Sprache Englisch
    Erscheinungsdatum 2022-12-13
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 186544-4
    ISSN 1573-4978 ; 0301-4851
    ISSN (online) 1573-4978
    ISSN 0301-4851
    DOI 10.1007/s11033-022-08090-w
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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