Flanagan Meghan R, Doody David R, Voutsinas Jenna, Wu Qian, Banda Kalyan, Sharifi Nima, Li Christopher I, Gadi Vijayakrishna K
Breast Section, Department of Surgery, University of Washington, Seattle, WA, USA.
Division of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Ann Surg Oncol. 2022 Oct;29(11):7194-7201. doi: 10.1245/s10434-022-12088-w. Epub 2022 Jul 1.
Homozygous inheritance of a single-nucleotide polymorphism (1245A > C) in HSD3B1 results in an adrenal permissive phenotype of increased adrenal steroid precursor conversion to potent androgens. This is associated with poor outcomes in prostate cancer. We hypothesized that inheritance of the HSD3B1 adrenal permissive genotype would similarly negatively impact breast cancer outcomes.
Germline HSD3B1 was sequenced in 644 postmenopausal women diagnosed between 2004 and 2015 with stage I-III estrogen receptor-positive (ER), HER2/neu-negative (HER2) breast cancer enrolled in a population-based study in western Washington. Primary endpoint was distant metastatic recurrence according to genotype. Secondary endpoint was breast cancer-specific survival. Hazard ratios (HR) were calculated using cause-specific Cox regression accounting for competing risks.
Adrenal restrictive genotype (homozygous wild type) was most prevalent (47%), followed by heterozygous (44%) and adrenal permissive (9%). There were no significant differences comparing demographic, tumor, or treatment characteristics apart from higher frequency of adrenal permissive genotype among non-Hispanic white participants (p = 0.04). After accounting for competing risks, the cumulative incidence of distant metastatic recurrence (15 events) was significantly higher among participants with adrenal permissive compared with the adrenal restrictive genotype (HR 4.9, 95% CI 1.32-18.4, p = 0.02). The adrenal permissive genotype was also predictive of breast cancer-specific mortality (HR 3.5, 95% CI 1.27-9.59, p = 0.02).
Inheritance of the HSD3B1 adrenal permissive genotype is associated with increased incidence of distant metastasis and higher cause-specific mortality in postmenopausal ER/HER2 breast cancer. Further research is necessary to understand the effect of excess adrenal androgen metabolism in promoting breast cancer growth and progression.
HSD3B1基因中一个单核苷酸多态性(1245A > C)的纯合子遗传导致肾上腺许可表型,即肾上腺类固醇前体向强效雄激素的转化率增加。这与前列腺癌的不良预后相关。我们推测,HSD3B1肾上腺许可基因型的遗传同样会对乳腺癌的预后产生负面影响。
对2004年至2015年间在华盛顿州西部一项基于人群的研究中确诊为I - III期雌激素受体阳性(ER)、HER2/neu阴性(HER2)乳腺癌的644名绝经后女性进行种系HSD3B1测序。主要终点是根据基因型的远处转移复发情况。次要终点是乳腺癌特异性生存率。使用考虑竞争风险的病因特异性Cox回归计算风险比(HR)。
肾上腺限制性基因型(纯合野生型)最为常见(47%),其次是杂合子(44%)和肾上腺许可型(9%)。除了非西班牙裔白人参与者中肾上腺许可基因型的频率较高外(p = 0.04),在人口统计学、肿瘤或治疗特征方面没有显著差异。在考虑竞争风险后,肾上腺许可型参与者的远处转移复发累积发生率(15例事件)显著高于肾上腺限制性基因型参与者(HR 4.9,95% CI 1.32 - 18.4,p = 0.02)。肾上腺许可基因型也可预测乳腺癌特异性死亡率(HR 3.5,95% CI 1.27 - 9.59,p = 0.02)。
HSD3B1肾上腺许可基因型的遗传与绝经后ER/HER2乳腺癌远处转移发生率增加和更高的病因特异性死亡率相关。有必要进一步研究以了解过量肾上腺雄激素代谢在促进乳腺癌生长和进展中的作用。