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Deregulation of interferon-gamma receptor 1 expression and its implications for lung adenocarcinoma progression.
Tecalco-Cruz, Angeles C; Medina-Abreu, Karen H; Oropeza-Martínez, Enrique; Zepeda-Cervantes, Jesus; Vázquez-Macías, Aleida; Macías-Silva, Marina.
Afiliação
  • Tecalco-Cruz AC; Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, CDMX 03100, Mexico. angeles.tecalco@uacm.edu.mx.
  • Medina-Abreu KH; Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, CDMX 03100, Mexico.
  • Oropeza-Martínez E; Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, CDMX 03100, Mexico.
  • Zepeda-Cervantes J; Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.
  • Vázquez-Macías A; Colegio de Ciencias y Humanidades, Universidad Autónoma de la Ciudad de México, CDMX 03100, Mexico.
  • Macías-Silva M; Instituo de Fisiología Celular, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.
World J Clin Oncol ; 15(2): 195-207, 2024 Feb 24.
Article em En | MEDLINE | ID: mdl-38455133
ABSTRACT
Interferon-gamma (IFN-γ) plays a dual role in cancer; it is both a pro- and an antitumorigenic cytokine, depending on the type of cancer. The deregulation of the IFN-γ canonic pathway is associated with several disorders, including vulnerability to viral infections, inflammation, and cancer progression. In particular, the interplay between lung adenocarcinoma (LUAD) and viral infections appears to exist in association with the deregulation of IFN-γ signaling. In this mini-review, we investigated the status of the IFN-γ signaling pathway and the expression level of its components in LUAD. Interestingly, a reduction in IFNGR1 expression seems to be associated with LUAD progression, affecting defenses against viruses such as severe acute respiratory syndrome coronavirus 2. In addition, alterations in the expression of IFNGR1 may inhibit the antiproliferative action of IFN-γ signaling in LUAD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: World J Clin Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: México

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: World J Clin Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: México