Evidence map›Paper›PMID 36238158›Full record

ArticleFrontiers in genetics2022

Characterizing the prognostic and therapeutic value of necroptosis in sarcoma based on necroptosis subtypes.

Yibo Ma, Qihang Yuan, Shiping He, Xiulin Mao, Shuo Zheng, Changjian Chen

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yibo MaGraduate School of Dalian Medical University, Dalian Medical University, Dalian, China.
Qihang YuanDepartment of General Surgery, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Shiping HeDepartment of Orthopedics, Subei People's Hospital Affiliated to Yangzhou University, Yangzhou, China.
Xiulin MaoDepartment of Anesthesiology, Dalian Municipal Central Hospital, Dalian, China.
Shuo ZhengThe Second Ward of Department of Orthopedics, The Second Hospital of Dalian Medical University, Dalian, China.
Changjian ChenThe First Ward of Department of Orthopedics, The Second Hospital of Dalian Medical University, Dalian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Necroptosis, a type of necrotic cell death independent of caspase regulation, is mainly mediated by receptor interacting serine/threonine kinase 1 (RIPK1), receptor interacting serine/threonine kinase 3 (RIPK3) and mixed lineage kinase domain-like (MLKL). Necroptosis plays an essential role in many tumors. However, the potential roles of necroptosis in tumor microenvironment (TME) of sarcoma (SARC) remain unknown. This study analyzed the expression, prognosis, genetic alterations of necroptosis genes in SARC. We identified two subtypes (cluster A and B) by performing unsupervised consensus clustering. Cluster A and B greatly differed in prognosis and immune infiltration, with cluster A showing more favorable prognosis, higher immune infiltration and higher expression levels of necroptosis genes than cluster B. Based on the differentially expressed genes (DEGs) between two clusters, a necroptosis scoring system was developed for predicting overall survival of SARC patients. Patients with high necroptosis score had worse survival status, with a decreased infiltration level of most immune cells. Our findings demonstrated the potential role of necroptosis in regulating tumor microenvironment and the prognostic value of necroptosis-related genes for SARC patients.

Indexed as

bioinformatics analysisimmune infiltrationnecroptosisprognosissarcomasubtypes

Identifiers

PMID36238158
PMCPMC9552825

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.