基于THRSP和ACACA蛋白组织表达预测乳腺癌患者预后的Nomogram模型构建

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Pharmacogenomics & Personalized Medicine Pub Date : 2025-07-31 eCollection Date: 2025-01-01 DOI:10.2147/PGPM.S516843
Benkai Wei, Fan Li, Huanhuan Yan, Jun Shen
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引用次数: 0

摘要

背景:本研究旨在分析甲状腺激素应答点14 (THRSP)和乙酰辅酶a羧化酶α (ACACA)蛋白在乳腺癌肿瘤组织中的表达及其与乳腺癌患者临床病理和预后的关系。此外,本研究还构建了预测乳腺癌患者预后的nomogram模型。方法:回顾性分析2019年10月至2021年3月在我院行手术治疗的202例乳腺癌患者,收集患者肿瘤组织及非肿瘤组织标本。免疫组化检测THRSP和ACACA蛋白表达。采用多因素COX回归分析影响乳腺癌患者预后的危险因素。利用R软件中的“rms”包建立生存nomogram模型,并对模型的有效性进行评价。结果:乳腺癌患者肿瘤组织中THRSP和ACACA蛋白的表达高于非肿瘤组织(p < 0.05)。有淋巴结转移的乳腺癌患者中THRSP和ACACA蛋白的表达高于无淋巴结转移的乳腺癌患者(p < 0.05)。Cox回归分析显示,TNM分期、淋巴结转移、Ki-67高表达、THRSP高表达、ACACA高表达均为乳腺癌患者预后的危险因素(p < 0.05)。模态图模型的c指数为0.704 (95% CI: 0.596~0.892)。该模型预测的1年、2年和3年生存auc分别为0.802、0.769和0.770。标定曲线表明,模型与理想曲线拟合良好。决策曲线分析显示该模型具有较高的临床实用性。结论:基于THRSP和ACACA蛋白构建的nomogram模型可为乳腺癌患者的预后评估提供参考价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Construction of a Nomogram Model for Predicting Prognosis in Breast Cancer Patients Based on the Expression of THRSP and ACACA Proteins Tissues.

Construction of a Nomogram Model for Predicting Prognosis in Breast Cancer Patients Based on the Expression of THRSP and ACACA Proteins Tissues.

Construction of a Nomogram Model for Predicting Prognosis in Breast Cancer Patients Based on the Expression of THRSP and ACACA Proteins Tissues.

Construction of a Nomogram Model for Predicting Prognosis in Breast Cancer Patients Based on the Expression of THRSP and ACACA Proteins Tissues.

Background: This study aimed to analyze the expression of thyroid hormone-responsive spot 14 (THRSP) and acetyl-CoA carboxylase alpha (ACACA) proteins in breast cancer tumor tissues and their relationship with clinicopathology and prognosis of breast cancer patients. In addition, a nomogram model to predict the prognosis of breast cancer patients was constructed in this study.

Methods: Retrospective analysis of 202 cases of breast cancer patients who underwent surgical treatment in our hospital from October 2019 to March 2021, and collection of patients' cancer tissues and non-Tumor tissue specimens. Immunohistochemistry was used to detect THRSP and ACACA protein expression. Multivariate COX regression was used to analyze the risk factors affecting the prognosis of breast cancer patients. The "rms" package in R software was used to build a survival nomogram model and evaluate the effectiveness of the model.

Results: The expression of THRSP and ACACA proteins in tumor tissues of breast cancer patients was higher than that in non-tumor tissues (p < 0.05). The expression of THRSP and ACACA proteins in breast cancer patients with lymph node metastasis was higher than that in patients without lymph node metastasis (p < 0.05). Cox regression analysis showed that TNM stage III, lymph node metastasis, high expression of Ki-67, high expression of THRSP, and high expression of ACACA were all risk factors for the prognosis of breast cancer patients (p < 0.05). The C-index of the nomogram model was 0.704 (95% CI: 0.596~0.892). The predicted 1-, 2- and 3-year survival AUCs of this nomogram model were 0.802, 0.769 and 0.770, respectively. The calibration curve showed that the model fit the ideal curve well. Decision curve analysis showed the high clinical utility of the model.

Conclusion: The nomogram model constructed based on THRSP and ACACA proteins may provide a reference value for the prognostic evaluation of breast cancer patients.

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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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