Evidence map›Paper›PMID 39514138›Full record

ArticleDiscover oncology2024

Construction of a novel mitochondrial oxidative stress-related genes prognostic system and molecular subtype characterization for breast cancer.

Ying Liu, Yang Li, Yanzheng Zhu, Min Wang, Zheyao Luan

Abstract read
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Article in Discover 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ying Liu *Department of Breast Surgery, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Yang Li *Department of Breast Surgery, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Yanzheng ZhuDepartment of Internal Medicine, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Min WangDepartment of Digestive Endoscopy, Dezhou Hospital, Qilu Hospital, Shandong University, Jinan, China.
Zheyao LuanDepartment of Physical Examination, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China. luanzheyao@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBreast cancer (BRCA) is the most common malignant tumor among women, characterized by high incidence rates and mortality rates. Oxidative stress and immunity, particularly in relation to mitochondria, have emerged as pivotal factors in breast carcinogenesis. Nonetheless, limited research has explored the specific contribution of mitochondrial oxidative stress to the prognosis of BRCA.

methodIn this study, we conducted univariate and multivariate Cox regression analyses to pinpoint independent prognostic genes associated with mitochondrial oxidative stress (MOSRGs) and their correlation with BRCA clinical outcomes. Subsequently, we developed a robust and accurate MOS scoring system for BRCA patients based on these identified independent prognostic MOSRGs.

resultOur findings were further substantiated by immune infiltration and somatic mutation analyses, providing additional evidence that the MOS scoring system holds predictive value for clinical outcomes in patients and correlates directly with three subtypes of BRCA. In vitro experiments in the MCF7 cell and breast tissue further verified the mRNA and protein expression level of independent prognostic genes, validating the consistency of the MOS prognostic signatures in BRCA.

conclusionThis research has unveiled a novel prognostic scoring system, providing valuable insights for improving patient prognosis assessment and developing individualized treatment strategies in BRCA patients.

Indexed as

Breast cancerImmune infiltrationMitochondriaOxidative stressPrognostic model

Identifiers

PMID39514138
PMCPMC11549074

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