4.5 Article

Pan-Cancer analyses of Necroptosis-Related genes as a potential target to predict immunotherapeutic outcome

Journal

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
Volume 27, Issue 2, Pages 204-221

Publisher

WILEY
DOI: 10.1111/jcmm.17634

Keywords

cancer; immunotherapy; mutation; necroptosis; tumour microenvironment

Ask authors/readers for more resources

In this study, a systematic analysis of the necroptosis mechanism in cancer was conducted using The Cancer Genome Atlas and Genotype-Tissue Expression databases. The results revealed the correlation between necroptosis and cancer prognosis, DNA methylation status, tumour mutative burden, microsatellite instability, immune cell infiltration, and explored the relationship between necroptosis and immunotherapy prognosis for the first time. This study provides important evidence for a comprehensive understanding of the carcinogenicity of necroptosis in different types of cancer and suggests that necroptosis can be used as a potential target for tumor immunotherapy.
Necroptosis is a unique programmed death mechanism of necrotic cells. However, its role and specific mechanism in cancer remain unclear, and a systematic pan-cancer analysis of necroptosis is yet to be conducted. Thus, we performed a specific pan-cancer analysis using The Cancer Genome Atlas and Genotype-Tissue Expression databases to analyse necroptosis expression in terms of cancer prognosis, DNA methylation status, tumour mutative burden, microsatellite instability, immune cell infiltration in different types of cancer and molecular mechanisms. For the first time, we explored the correlation between necroptosis and immunotherapy prognosis. Thus, our study provides a relatively comprehensive understanding of the carcinogenicity of necroptosis in different types of cancer. It is suggested that necroptosis can be used to evaluate the sensitivity of different patients to immunotherapy and may become a potential target for tumour immunotherapy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available