Your browser doesn't support javascript.
loading
GATA6 inhibits the biological function of non-small cell lung cancer by modulating glucose metabolism.
Ju, Weiwei; Lin, Lijuan; Zhang, Qifang; Lv, Xiumei; Teng, Shaohui; Hong, Yu; Shao, Zhixiang; Na, Hanyun; Yu, Shengjin.
Afiliación
  • Ju W; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China.
  • Lin L; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China.
  • Zhang Q; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China.
  • Lv X; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China.
  • Teng S; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China.
  • Hong Y; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China.
  • Shao Z; Pathology Department, Dandong First Hospital, Dandong, 118003, China.
  • Na H; Pathology Department, Dandong First Hospital, Dandong, 118003, China.
  • Yu S; Institute of Molecular Medicine, Medical College of Liaodong University, Dandong, 118003, China. yubing557@163.com.
J Cancer Res Clin Oncol ; 150(3): 126, 2024 Mar 14.
Article en En | MEDLINE | ID: mdl-38483616
ABSTRACT

PURPOSE:

This study aims to explore the role of GATA6 in lung cancer, with a focus on its impact on metabolic processes.

METHODS:

We assessed GATA6 expression in lung cancer tissues and its association with patient prognosis. In vitro cell function experiments were conducted to investigate the effects of altered GATA6 levels on lung cancer cell proliferation and migration. Mechanistic insights were gained by examining GATA6's influence on glucose metabolism-related genes, particularly its effect on c-Myc mRNA expression.

RESULTS:

Our study revealed significant down-regulation of GATA6 in lung cancer tissues, and this down-regulation was strongly correlated with unfavorable patient prognosis. Elevating GATA6 levels effectively inhibited the proliferation and migration of lung cancer cells in our cell function experiments. Mechanistically, we found that GATA6 suppressed the expression of c-Myc mRNA, impacting genes related to glucose metabolism. As a result, glucose uptake and metabolism in lung cancer cells were disrupted, ultimately impeding their malignant behaviors.

CONCLUSION:

Our study provides crucial insights into the metabolic regulation of GATA6 in lung cancer cells. These findings have the potential to offer a solid theoretical foundation for the development of novel clinical treatments for lung cancer.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: J Cancer Res Clin Oncol Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: J Cancer Res Clin Oncol Año: 2024 Tipo del documento: Article País de afiliación: China