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Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) as an undetermined tool in tumor cells.
Azimnasab-Sorkhabi, Parviz; Soltani-Asl, Maryam; Kfoury Junior, Jose Roberto.
Afiliação
  • Azimnasab-Sorkhabi P; Department of Surgery, School of Veterinary Medicine and Animal Sciences, University of Sao Paulo, Sao Paulo, Brazil. Sorkhabi.parviz@gmail.com.
  • Soltani-Asl M; Department of Surgery, School of Veterinary Medicine and Animal Sciences, University of Sao Paulo, Sao Paulo, Brazil.
  • Kfoury Junior JR; Department of Surgery, School of Veterinary Medicine and Animal Sciences, University of Sao Paulo, Sao Paulo, Brazil.
Hum Cell ; 36(4): 1225-1232, 2023 Jul.
Article em En | MEDLINE | ID: mdl-36907978
In the tumor microenvironment, the function of T cells is a fate-changer for tumor progression. In the meantime, CD28 and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) are vital role players in the controlling activity of T cells as an activator and deactivator, respectively. In T cells in comparison to CD28, the molecular mechanism of CTLA-4 is unclear. In addition, despite the fact that most tumor cell types express CTLA-4, its role in tumor cells is not well understood and only few studies focused on the role of CTLA-4 signaling in tumor cells. It is illustrated that CTLA-4 signaling causes PD-L1 expression in tumor cells. However, numerous characteristics of CTLA-4 signaling in tumor cells are ambiguous and require to be described. In this article, we proposed that the CTLA-4 signaling during immunotherapy with anti-CTLA-4 antibodies may cause poor responses by patients. In addition, we attract attention to several fundamental questions regarding CTLA-4 signaling in tumor cells. Overall, the CTLA-4 signaling function and the related gaps about its role in tumor cells in the present review are challenged.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T Citotóxicos / Antígenos CD28 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Cell Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil País de publicação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T Citotóxicos / Antígenos CD28 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Cell Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil País de publicação: Japão