Evidence map›Paper›PMID 39148138›Full record

ArticleBiology direct2024

Disulfidptosis signature predicts immune microenvironment and prognosis of gastric cancer.

Zitao Liu, Liang Sun, Wenjie Zhu, Jinfeng Zhu, Changlei Wu, Xingyu Peng, Huakai Tian, Chao Huang, Zhengming Zhu

Abstract read
In one paragraph

Article in Biology direct, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
–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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Zitao Liu *Department of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China.
Liang SunDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China. sunliang960724@163.com.
Wenjie Zhu *Department of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China.
Jinfeng ZhuHunan Provincial Key Laboratory of the Research and Development of Novel Pharmaceutical Preparations, Changsha Medical University, Changsha, Hunan, P. R. China.
Changlei Wu *Department of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China.
Xingyu PengDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China.
Huakai TianDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, P. R. China.
Chao HuangDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China.
Zhengming ZhuDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University, MinDe Road, Nanchang, Jiangxi, P. R. China. zhengmingzhu28@126.com.

Funding

Jiangxi Provincial Natural Science Foundation Key Project 20232ACB206032Jiangxi Provincial Natural Science Foundation Key Project 20232BAB216088
6 · The paper itself

Abstract

backgroundDisulfidptosis is a newly identified mechanism of cell death triggered by disulfide stress. Thus, gaining a comprehensive understanding of the disulfidptosis signature present in gastric cancer (GC) could greatly enhance the development of personalized treatment strategies for this disease.

methodsWe employed consensus clustering to identify various subtypes of disulfidptosis and examined the distinct tumor microenvironment (TME) associated with each subtype. The Disulfidptosis (Dis) score was used to quantify the subtype of disulfidptosis in each patient. Subsequently, we assessed the predictive value of Dis score in terms of GC prognosis and immune efficacy. Finally, we conducted in vitro experiments to explore the impact of Collagen X (COL10A1) on the progression of GC.

resultsTwo disulfidptosis-associated molecular subtypes (Discluster A and B) were identified, each with distinct prognosis, tumor microenvironment (TME), immune cell infiltration, and biological pathways. Discluster A, characterized by high expression of disulfidptosis genes, exhibited a high immune score but poor prognosis. Furthermore, the Dis score proved useful in predicting the prognosis and immune response in GC patients. Those in the low Dis score group showed better prognosis and increased sensitivity to immunotherapy. Finally, our experimental findings validated that downregulation of COL10A1 expression attenuates the proliferation and migration capabilities of GC cells while promoting apoptosis.

conclusionsThis study demonstrates that the disulfidptosis signature can assist in risk stratification and personalized treatment for patients with GC. The results offer valuable theoretical support for anti-tumor strategies.

Indexed as

Stomach NeoplasmsTumor MicroenvironmentApoptosisCell Line, TumorHumansPrognosisDisulfidptosisGastric cancerImmunotherapyPrognosisTumor microenvironment

Identifiers

PMID39148138
PMCPMC11325698

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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.