University of North Carolina at Chapel Hill, Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, United States of America.
University of North Carolina at Chapel Hill, Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, United States of America.
Gynecol Oncol. 2022 May;165(2):248-256. doi: 10.1016/j.ygyno.2022.02.021. Epub 2022 Mar 8.
Black women suffer a higher mortality from endometrial cancer (EC) than White women. Potential biological causes for this disparity include a higher prevalence of obesity and more lethal histologic/molecular subtypes. We hypothesize that another biological factor driving this racial disparity could be the EC microbiome.
Banked tumor specimens of postmenopausal, Black and White women undergoing hysterectomy for early stage endometrioid EC were identified. The microbiota of the tumors were characterized by bacterial 16S rRNA sequencing. The microbial component of endometrioid ECs in The Cancer Genome Atlas (TCGA) database were assessed for comparison.
95 early stage ECs were evaluated: 23 Black (24%) and 72 White (76%). Microbial diversity was increased (p < 0.001), and Firmicutes, Cyanobacteria and OD1 phyla abundance was higher in tumors from Black versus White women (p < 0.001). Genus level abundance of Dietzia and Geobacillus were found to be lower in tumors of obese Black versus obese White women (p < 0.001). Analysis of early stage ECs in TCGA found that microbial diversity was higher in ECs from Black versus White women (p < 0.05). When comparing ECs from obese Black versus obese White women, 5 bacteria distributions were distinct, with higher abundance of Lactobacillus acidophilus in ECs from Black women being the most striking difference. Similarly in TCGA, Dietzia and Geobacillus were more common in ECs from White women compared to Black.
Increased microbial diversity and the distinct microbial profiles between ECs of obese Black versus obese White women suggests that intra-tumoral bacteria may contribute to EC disparities and pathogenesis.
黑人女性患子宫内膜癌(EC)的死亡率高于白人女性。这种差异的潜在生物学原因包括肥胖症的高发和更致命的组织学/分子亚型。我们假设,导致这种种族差异的另一个生物学因素可能是 EC 微生物组。
确定了因早期子宫内膜样 EC 而接受子宫切除术的绝经后黑人女性和白人女性的肿瘤标本。通过细菌 16S rRNA 测序来描述肿瘤的微生物群。评估了癌症基因组图谱(TCGA)数据库中子宫内膜样 EC 的微生物成分进行比较。
评估了 95 例早期 EC:23 例黑人(24%)和 72 例白人(76%)。与白人女性相比,黑人女性肿瘤中的微生物多样性增加(p < 0.001),厚壁菌门、蓝细菌门和 OD1 门的丰度更高(p < 0.001)。在肥胖的黑人女性与肥胖的白人女性的肿瘤中,发现 Dietzia 和 Geobacillus 属的丰度较低(p < 0.001)。TCGA 中早期 EC 的分析发现,黑人 EC 中的微生物多样性高于白人 EC(p < 0.05)。当比较肥胖的黑人 EC 与肥胖的白人 EC 时,有 5 种细菌分布存在差异,黑人女性 EC 中嗜酸乳杆菌的丰度更高是最显著的差异。同样在 TCGA 中,与黑人女性相比,Dietzia 和 Geobacillus 在白人女性的 EC 中更为常见。
肥胖的黑人 EC 与肥胖的白人 EC 之间微生物多样性增加和独特的微生物特征表明,肿瘤内细菌可能导致 EC 差异和发病机制。