Evidence map›Paper›PMID 41234897›Full record

ArticleTranslational cancer research2025

A novel disulfidptosis-related lncRNAs index to predict prognosis and therapeutic target in hepatocellular carcinoma.

Xun-Feng Gao, Xiao-Lu Xu, Jin-Hui Zhang, Heng Zhang, Li-Quan Cai, Feng Gao, Jin-Long Zhang, Dan Yu, Qin-Wen Tai

Abstract read
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Article in Translational cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Disulfidptosis: molecular mechanisms and therapeutic targets.Signal transduction and targeted therapy · 2026
    Review
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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Xun-Feng Gao *General Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.ORCID https://orcid.org/0009-0004-0857-5850
Xiao-Lu Xu *Xingdong Community Health Service Center, Shenzhen Baoan People's Hospital, Shenzhen, China.
Jin-Hui ZhangGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Heng ZhangGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Li-Quan CaiGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Feng GaoGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jin-Long ZhangGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Dan YuGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Qin-Wen TaiGeneral Surgery Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Characterized by its significant occurrence and high fatality, hepatocellular carcinoma (HCC) presents a challenge with treatments frequently leading to less than ideal results. The mechanism of action behind disulfidptosis, a newly identified pathway of cell death, is not well comprehended when related to HCC. This research aims to investigate a model that employs long non-coding RNA (lncRNA) associated with disulfidptosis for predicting the prognosis of liver cancer and identifying potential therapeutic measures. Methods: The Cancer Genome Atlas (TCGA) and the International Cancer Genome Consortium (ICGC) provided tissue specimens from 374 and 243 cases of HCC, respectively, along with samples from 50 and 202 healthy liver tissues. By employing differential analysis and Pearson correlation, we identified lncRNAs associated with disulfidptosis. Cox and least absolute shrinkage and selection operator (LASSO) regression analyses were then utilized to assess risk and construct a prognostic model for these lncRNAs. The model's predictive performance underwent evaluation through survival analysis, receiver operating characteristic (ROC), and C-index. Furthermore, our study delved into potential therapeutic roles of disulfidptosis-related lncRNAs in HCC, scrutinizing pathways, exploring the tumor microenvironment, and investigating immune evasion mechanisms. Results: The prognostic model that we developed comprises five lncRNAs associated with disulfidptosis: Conclusions: A prognostic model concerning disulfidptosis-related lncRNAs was constructed to predict outcomes in HCC. This model provides insights into molecular mechanisms, characterizes the tumor microenvironment, and predicts patient responses to immunotherapy and targeted treatments.

Indexed as

disulfidptosisdrug sensitivityHepatocellular carcinoma (HCC)long non-coding RNA (lncRNA)prognosis

Identifiers

PMID41234897
PMCPMC12605202

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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.