Evidence map›Paper›PMID 42159885›Full record

ArticleDiscover oncology2026

Constructing and investigating a disulfidptosis-associated LncRNA signature for prognostic prediction in gastric cancer.

Namei Li, Zhongyi Tong, Xiaoling She

Abstract read
In one paragraph

Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Namei LiDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, PR China.
Zhongyi TongDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, PR China.
Xiaoling SheDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, PR China. shexiaoling72@csu.edu.cn.

Funding

The Natural Science Foundation of Hunan Province 2021JJ30956The Natural Science Foundation of Hunan Province 2024JJ9229
6 · The paper itself

Abstract

backgroundGastric cancer (GC) prognosis remains poor, necessitating reliable biomarkers. Disulfidptosis represents a promising therapeutic frontier. This study aimed to construct a prognostic model based on disulfidptosis-related LncRNAs (DRLs) and investigate their function.

methodsDRLs were screened from TCGA-STAD using Pearson correlation and LASSO-COX regression to build a prognostic signature. Its accuracy was evaluated via Kaplan-Meier analysis, time-dependent ROC curves, and decision curve analysis. A key DRL was functionally validated in vitro and in vivo.

resultsWe established a six-DRL signature (AC090809.1, CYP4A22-AS1, AL356417.2, Z94721.2, FP325313.3, ERICH3-AS1) that effectively stratified patients into risk groups with distinct survival (P < 0.05). The risk score was an independent prognostic factor, with robust predictive AUCs for 1-, 2-, and 3-year survival. AL356417.2 was upregulated in GC and linked to poor outcome. Its knockdown inhibited cell viability, induced F-actin depolymerization, increased cystine uptake, and suppressed tumor growth in mice.

conclusionWe developed a novel DRL-based prognostic model and identified AL356417.2 as a functional regulator suppressing disulfidptosis, providing mechanistic insights and a potential therapeutic target for GC.

Indexed as

DisulfidptosisGastric cancerLncRNAPrognostic signature

Identifiers

PMID42159885
PMCPMC13365117

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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.