BIRC5 expression by race, age and clinical factors in breast cancer patients.

IF 7.4 1区 医学 Q1 Medicine
Alina M Hamilton, Andrea Walens, Sarah C Van Alsten, Linnea T Olsson, Joseph Nsonwu-Farley, Xiaohua Gao, Erin L Kirk, Charles M Perou, Lisa A Carey, Melissa A Troester, Yara Abdou
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引用次数: 0

Abstract

Purpose: Survivin/BIRC5 is a proliferation marker that is associated with poor prognosis in breast cancer and an attractive therapeutic target. However, BIRC5 has not been well studied among racially diverse populations where aggressive breast cancers are prevalent.

Experimental design: We studied BIRC5 expression in association with clinical and demographic variables and as a predictor of recurrence in 2174 participants in the Carolina Breast Cancer Study (CBCS), a population-based study that oversampled Black (n = 1113) and younger (< 50 years; n = 1137) participants with breast cancer. For comparison, similar analyses were conducted in The Cancer Genome Atlas [TCGA N = 1094, Black (n = 183), younger (n = 295)]. BIRC5 was evaluated as a continuous and categorical variable (highest quartile vs. lower three quartiles).

Results: Univariate, continuous BIRC5 expression was higher in breast tumors from Black women relative to non-Black women in both estrogen receptor (ER)-positive and ER-negative tumors and in analyses stratified by stage (i.e., within Stage I, Stage II, and Stage III/IV tumors). Within CBCS and TCGA, BIRC5-high was associated with young age (< 50 years) and Black race, as well as hormone receptor-negative tumors, non-Luminal A PAM50 subtypes, advanced stage, and larger tumors (> 2 cm). Relative to BIRC5-low, BIRC5-high tumors were associated with poor 5-year recurrence-free survival (RFS) among ER-positive tumors, both in unadjusted models [HR (95% CI): 2.7 (1.6, 4.6)] and after adjustment for age and stage [Adjusted HR (95% CI): 1.87 (1.07, 3.25)]. However, this relationship was not observed among ER-negative tumors [Crude HR (95% CI): 0.7 (0.39, 1.2); Adjusted HR (95% CI): 0.67 (0.37, 1.2)].

Conclusion: Black and younger women with breast cancer have a higher burden of BIRC5-high tumors than older and non-Black women. Emerging anti-survivin treatment strategies may be an important future direction for equitable breast cancer outcomes.

按种族、年龄和临床因素分列的乳腺癌患者中 BIRC5 的表达情况。
目的:Survivin/BIRC5 是一种与乳腺癌不良预后相关的增殖标志物,也是一个有吸引力的治疗靶点。然而,在侵袭性乳腺癌流行的不同种族人群中,对 BIRC5 的研究还不够深入:实验设计:我们研究了 BIRC5 表达与临床和人口统计学变量的关系,并将其作为卡罗莱纳乳腺癌研究(CBCS)2174 名参与者的复发预测因子:在雌激素受体(ER)阳性和ER阴性肿瘤中,以及在按分期进行的分层分析中(即在I期、II期和III/IV期肿瘤中),黑人妇女的乳腺肿瘤中BIRC5的单变量连续表达均高于非黑人妇女。在CBCS和TCGA中,BIRC5高与年轻(2厘米)有关。在未经调整的模型中[HR(95% CI):2.7(1.6,4.6)]以及调整年龄和分期后[调整后 HR(95% CI):1.87(1.07,3.25)],相对于 BIRC5 低,BIRC5 高的肿瘤与ER阳性肿瘤的 5 年无复发生存率(RFS)低有关。然而,在ER阴性肿瘤中没有观察到这种关系[粗略HR(95% CI):0.7(0.39,1.2);调整后HR(95% CI):0.67(0.37,1.2)]:结论:与年龄较大的非黑人女性相比,黑人和年轻女性乳腺癌患者患 BIRC5 高肿瘤的比例更高。新出现的抗生存素治疗策略可能是未来实现乳腺癌公平治疗的一个重要方向。
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来源期刊
CiteScore
12.00
自引率
0.00%
发文量
76
审稿时长
12 weeks
期刊介绍: Breast Cancer Research, an international, peer-reviewed online journal, publishes original research, reviews, editorials, and reports. It features open-access research articles of exceptional interest across all areas of biology and medicine relevant to breast cancer. This includes normal mammary gland biology, with a special emphasis on the genetic, biochemical, and cellular basis of breast cancer. In addition to basic research, the journal covers preclinical, translational, and clinical studies with a biological basis, including Phase I and Phase II trials.
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