Predictive and Prognostic Value of TRIM58 Protein Expression in Patients with Breast Cancer Receiving Neoadjuvant Chemotherapy

被引:2
|
作者
Zheng, Yi-Zi [1 ]
Li, Jia-Ying [2 ,3 ]
Ning, Lv-Wen [3 ]
Xie, Ni [3 ,4 ]
机构
[1] Shenzhen Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp 2, Shenzhen Breast Tumor Res Ctr Diag & Treatment,Dep, Shenzhen, Guangdong, Peoples R China
[2] Univ South China, Hengyang Med Sch, Hengyang, Hunan, Peoples R China
[3] Shenzhen Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp 2, Biobank, Shenzhen, Guangdong, Peoples R China
[4] Shenzhen Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp 2, Biobank, 3002 Sungang West Rd, Shenzhen 518035, Guangdong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
chemosensitivity; pathological complete response; biomarker; patient stratification; predictive diagnostics; TUMOR SIZE; FAMILY PROTEINS; GENES; METASTASIS; RESISTANCE; MORTALITY; ROLES;
D O I
10.2147/BCTT.S387209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Tripartite motif-containing protein (TRIM) family members play crucial roles in carcinogenesis and chemotherapy resistance. In this study, we aimed to determine whether TRIM58 protein expression is related to patient responses to neoadjuvant therapy (NAT) and their survival outcome. Methods: Immunohistochemistry was performed on female breast cancer samples from biopsies before NAT in Shenzhen Second People's Hospital. Univariate and multivariate logistic regression tests were used to analyze the association between TRIM58 protein expression and pathological complete response (pCR). The Cox proportional hazards model was used to calculate the adjusted hazard ratio (HR) with a 95% confidence interval (95% CI). The Kaplan-Meier plotter database was used to analyze the prognostic value of Results: High TRIM58 expression was associated with small tumor size in all the patients (n = 58). Multivariate analysis suggested that low TRIM58 expression was an independent predictive factor for higher pCR (odds ratio = 0.06, 95% CI 0.005-0.741, P = 0.028). The Kaplan-Meier Plotter dataset suggested that the TRIM58 high-expression group showed a worse 5-year overall survival than the low-expression group (HR = 1.34, 95% CI 1.07-1.67, P = 0.01). Pathway analysis revealed the potential mechanisms of TRIM58 in chemoresistance. Discussion: Our study suggests that TRIM58 is a promising biomarker for both neoadjuvant chemosensitivity and long-term clinical outcomes in breast cancer. It may also help to identify candidate responders and determine treatment strategies.
引用
收藏
页码:475 / 487
页数:13
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