Evidence map›Paper›PMID 39261898›Full record

ArticleWorld journal of surgical oncology2024

As a novel prognostic model for breast cancer, the identification and validation of telomere-related long noncoding RNA signatures.

Wei Zhao, Beibei Li, Mingxiang Zhang, Peiyao Zhou, Yongyun Zhu

Abstract readValidation Study
In one paragraph

Article in World journal of surgical oncology, 2024. 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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2 · The registry

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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

5 authors.

Wei Zhao *Department of Oncology, Gongli Hospital of Shanghai Pudong New Area, Shanghai, 200135, China.
Beibei Li *Department of Laboratory, Shanghai Pudong New Area Gongli Hospital, Shanghai, 200127, China.
Mingxiang Zhang *Thyroid and Breast Surgery Department, Shanghai Pudong New Area People's Hospital, 490 Chuanhuan South Road, Chuansha New Town, Pudong New Area, Shanghai, 200000, China.
Peiyao ZhouThyroid and Breast Surgery Department, Shanghai Pudong New Area People's Hospital, 490 Chuanhuan South Road, Chuansha New Town, Pudong New Area, Shanghai, 200000, China.
Yongyun ZhuDepartment of Oncology, Gongli Hospital of Shanghai Pudong New Area, Shanghai, 200135, China. zhuyongyun@shpdph.com.

Funding

Pudong New Area Health Research General Project PW2023A-18Pudong New District Health Committee Discipline Leader Program PWRd2023-10
6 · The paper itself

Abstract

backgroundTelomeres are a critical component of chromosome integrity and are essential to the development of cancer and cellular senescence. The regulation of breast cancer by telomere-associated lncRNAs is not fully known, though. The goals of this study were to describe predictive telomere-related LncRNAs (TRL) in breast cancer and look into any possible biological roles for these RNAs.

methodsWe obtained RNA-seq data, pertinent clinical data, and a list of telomere-associated genes from the cancer genome atlas and telomere gene database, respectively. We subjected differentially expressed TRLs to co-expression analysis and univariate Cox analysis to identify a prognostic TRL. Using LASSO regression analysis, we built a prognostic model with 14 TRLs. The accuracy of the model's prognostic predictions was evaluated through the utilization of Kaplan-Meier (K-M) analysis as well as receiver operating characteristic (ROC) curve analysis. Additionally, immunological infiltration and immune drug prediction were done using this model. Patients with breast cancer were divided into two subgroups using cluster analysis, with the latter analyzed further for variations in response to immunotherapy, immune infiltration, and overall survival, and finally, the expression of 14-LncRNAs was validated by RT-PCR.

resultsWe developed a risk model for the 14-TRL, and we used ROC curves to demonstrate how accurate the model is. The model may be a standalone prognostic predictor for patients with breast cancer, according to COX regression analysis. The immune infiltration and immunotherapy results indicated that the high-risk group had a low level of PD-1 sensitivity and a high number of macrophages infiltrating. In addition, we've discovered a number of small-molecule medicines with considerable for use in treating high-risk groups. The cluster 2 subtype showed the highest immune infiltration, the highest immune checkpoint expression, and the worst prognosis among the two subtypes defined by cluster analysis, which requires more attention and treatment.

conclusionAs a possible biomarker, the proposed 14-TRL signature could be utilized to evaluate clinical outcomes and treatment efficacy in breast cancer patients.

Indexed as

Biomarkers, TumorBreast NeoplasmsRNA, Long NoncodingTelomereFemaleFollow-Up StudiesGene Expression ProfilingGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMiddle AgedPrognosisROC CurveSurvival RateBiomarkers, TumorRNA, Long NoncodingBreast cancerImmunotherapylncRNAPrognosisTelomereTME

Identifiers

PMID39261898
PMCPMC11389561

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LicenceCC BY-NC-ND
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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.