SH3BP1 Regulates Melanoma Progression Through Race1/Wace2 Signaling Pathway.

Background: SH3-domain binding protein-1 (SH3BP1), which specifically inactivates Rac1 and its target protein Wave2, has been shown to be an important regulator of cancer metastasis. However, the effects of SH3BP1 in melanoma progression remain unclear. The current study aimed to explore the functio...

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Publicado en:Clinical Medicine Insights: Oncology pp. 1 - 12
Autores principales: Sun, Ting, Tong, Wenxian, Pu, Jie, Yu, Zhiguo, Kang, Zhengchun
Formato: pictorial research tables/charts Journal Article
Publicado: Sage Publications Inc. 4/21/2023
Acceso en línea:Ver este registro en EBSCOhost
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      jtl: Clinical Medicine Insights: Oncology
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      dt: 4/21/2023
      pid: 344
      pub: Sage Publications Inc.
      place: Thousand Oaks, California
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        10.1177/11795549231168075
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        atl: SH3BP1 Regulates Melanoma Progression Through Race1/Wace2 Signaling Pathway.
      aug:
        au:
          Sun, Ting
          Tong, Wenxian
          Pu, Jie
          Yu, Zhiguo
          Kang, Zhengchun
        affil: Department of Dermatology, Middle Military Command General Hospital of PLA, Wuhan, China
      sug:
        subj:
          Proteins Pharmacodynamics
          Melanoma Prognosis
          Disease Progression
          Signal Transduction
          Animal Studies
          Neoplasm Metastasis
          Reverse Transcriptase Polymerase Chain Reaction
          Gene Expression
          Bioinformatics
          In Vitro Studies
          In Vivo Studies
          Cell Proliferation
          Cell Movement
          Cell Line, Tumor
      ab: Background: SH3-domain binding protein-1 (SH3BP1), which specifically inactivates Rac1 and its target protein Wave2, has been shown to be an important regulator of cancer metastasis. However, the effects of SH3BP1 in melanoma progression remain unclear. The current study aimed to explore the function of SH3BP1 in melanoma and its possible molecular mechanism. Methods: TCGA database was used to analyze the expression of SH3BP1 in melanoma. Then, reverse transcription–quantitative polymerase chain reaction was performed to detect the expression of SH3BP1 in melanoma tissues and cells. Next, genes related to SH3BP1 were analyzed by LinkedOmics database, and protein interactions were analyzed by STRING database. These genes were further subjected to Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis. In addition, the signaling pathway of SH3BP1 action was screened by bioinformatics analysis. Finally, the function of SH3BP1 and its mediated signaling pathway in melanoma progression were investigated in vitro and in vivo. Results: SH3BP1 was significantly upregulated in melanoma tissues and cells. The pathways regulated by SH3BP1 are closely related to the occurrence and development of tumors. And we found that overexpression of SH3BP1 promoted the proliferation, migration, and invasion of melanoma cells by increasing Rac1 activity and Wave2 protein levels in vitro. Similarly, overexpression of SH3BP1 facilitated melanoma progression by upregulating Wave2 protein expression in vivo. Conclusion: In summary, this study revealed for the first time that SH3BP1 promoted melanoma progression through Rac1/Wave2 signaling pathway, providing a new therapeutic target for melanoma.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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