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Exploration of the Correlation Between GRHL1 Expression and Tumor Microenvironment in Endometrial Cancer and Immunotherapy.
Guo, Suyang; Bai, Wenqi; Cui, Fengjie; Chen, Xin; Fang, Xiaojing; Shen, Honghong; Gu, Xianhua.
Afiliación
  • Guo S; Department of Gynecology Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
  • Bai W; Department of Gynecology Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
  • Cui F; Department of Gynecology Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
  • Chen X; Department of Gynecology Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
  • Fang X; Department of Gynecology Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
  • Shen H; Department of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
  • Gu X; Department of Gynecology Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu, People's Republic of China.
Pharmgenomics Pers Med ; 17: 91-103, 2024.
Article en En | MEDLINE | ID: mdl-38586176
ABSTRACT

Introduction:

GRHL1 belongs to the family of Grainyhead-like (GRHL). Previous studies have shown that dysregulation of growth and survival pathways is associated with the GRHL family of gene cancers. Immunotherapy with checkpoint inhibitors has changed the treatment paradigm for many tumors, including endometrial cancer (EC). However, the effect of GRHL1 on immunotherapy in EC and its relationship with immune cell infiltration are poorly understood.

Methods:

Differential expression of GRHL1 between EC and normal EC tissues was analyzed by searching the TCGA database, and the results were verified utilizing immunohistochemistry analyses. Next, the relationship between GRHL1, CD8+ T cells and tumor microenvironment (TME) was also investigated, and the effect of GRHL1 expression on immunotherapy in EC was evaluated.

Results:

According to the findings, EC tissues had elevated expression levels of GRHL1 relative to normal tissues. Patients with EC who expressed GRHL1 at high levels experienced worse overall survival (OS) and Progression-free survival (PFS) than those whose expression was lower. In addition, GRHL1 expression was negatively correlated with CD8+ T cells, and patients with high GRHL1 expression were less effective in receiving immunotherapy.

Conclusion:

The expression of GRHL1 was high in EC patients, and high expression of GRHL1 inhibits the proliferation of CD8+ T cells in the tumor microenvironment of EC and affect the efficacy of immunotherapy.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmgenomics Pers Med Año: 2024 Tipo del documento: Article Pais de publicación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmgenomics Pers Med Año: 2024 Tipo del documento: Article Pais de publicación: Nueva Zelanda