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Cuprotosis Patterns Are Associated with Tumor Mutation Burden and Immune Landscape in Lung Adenocarcinoma.
Liu, Tingting; Cai, Liangliang; Hua, Hujia; Jiang, Xingyu; Xu, Xintian; Zhang, Tianyi; Huang, Wenqing; Qian, Li; Bai, Hua; Duan, Jianchun.
Afiliación
  • Liu T; College of Veterinary Medicine, Yangzhou University, Yangzhou 225001, China.
  • Cai L; Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
  • Hua H; Jiangsu Key Laboratory of Experimental and Translational Non-coding RNA Research, Yangzhou, China.
  • Jiang X; CAMS Key Laboratory of Translational Research on Lung Cancer, State Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences Peking Union Medical College, Beijing 100
  • Xu X; Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
  • Zhang T; Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
  • Huang W; Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
  • Qian L; Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
  • Bai H; Department of Central Laboratory, Shanghai Children's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Duan J; Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
J Oncol ; 2022: 9772208, 2022.
Article en En | MEDLINE | ID: mdl-36467497
ABSTRACT

Background:

The association involving cuprotosis, molecular subtype, and specific immune cell groups in the tumor microenvironment has been focused on by more recent studies. In lung adenocarcinoma (LUAD), the potential functions of cuprotosis remain elusive.

Methods:

The cuprotosis regulations and tumor immune profile of 567 LUAD patients and the correlation between the cuprotosis patterns and the immune landscape were comprehensively evaluated. The cuprotosisScore was calculated using principal component analysis (PCA). The prognostic significance of the cuprotosisScore was evaluated by Cox regression statistics analysis.

Results:

Five cuprotosisClusters (named mc1, 2, 3, 4, 5)-characterized by differences in expression of immunomodulatory genes, mRNA, or lncRNA expression, and prognosis were identified. We established cuprotosisScore to quantify the cuprotosis pattern of individual LUAD patients. As is shown in further analyses, the cuprotosisScore was a relatively potential independent prognostic factor of LUAD involved in mc1. Finally, the prognostic value of the cuprotosisScore and its association with tumor immune microenvironment (iTME) of LUAD in five cuprotosisClusters were verified.

Conclusions:

We demonstrated the correlation between cuprotosis modification, the molecular subtype, and tumor immune landscape in LUAD. The cuprotosisCluster with high cuprotosisScore and high tumor mutation burden (TMB) was identified with a good prognosis and immune functions. The comprehensive evaluation of cuprotosis patterns in individual LUAD patients enhances the understanding of iTME and gives a new insight toward improved immune treatment strategies for LUAD patients.

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Año: 2022 Tipo del documento: Article