Alves da Quinta Daniela, Rocha Darío, Yáñez Cristian, Binato Renata, Soares-Lima Sheila Coelho, Huang Xiaosong, Ganiewich Daiana, Zavala Valentina A, Sans Monica, Lopez-Vazquez Alejandra, Quintero Jael, Valenzuela Olivia, Quintero-Ramos Antonio, Del Toro-Arreola Alicia, Cerda Mauricio, Marcelain Katherine, Crocamo Susanne, Nagai Maria Aparecida, Carraro Dirce M, Marques Marcia Maria Chiquitelli, Gómez Jorge, Artagaveytia Nora, Daneri-Navarro Adrian, Müller Bettina G, Retamales Javier, Velazquez Carlos, Fernández Elmer A, Podhajcer Osvaldo L, Abdelhay Eliana, Verdugo Ricardo A, Llera Andrea S, Fejerman Laura
Laboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir-CONICET, Ciudad de Buenos Aires, Argentina.
Universidad Argentina de la Empresa (UADE), Instituto de Tecnología (INTEC), Buenos Aires, Argentina.
Cancer Res Commun. 2025 Jul 1;5(7):1070-1081. doi: 10.1158/2767-9764.CRC-25-0014.
This study investigates the relationship between genetic ancestry, breast cancer subtypes, and survival outcomes among 951 locally advanced breast cancer cases from Argentina, Brazil, Chile, Mexico, and Uruguay, participating in the Molecular Profile of Breast Cancer Study. Array-based genotyping and ADMIXTURE analysis were used for genetic ancestry evaluation. Breast cancer subtypes were defined by IHC and the gene expression-based PAM50 algorithm. The distribution of genetic ancestry, including European, Indigenous American (IA), African (AFR), and East Asian components, revealed a heterogeneous genetic admixture across countries, with the highest IA ancestry observed in Chile (30.9%) and Mexico (30.8%). Testing the relationship between genetic ancestry and breast cancer subtypes demonstrated that a 10% increase in European ancestry was significantly associated with a 14% decrease in the odds of developing HER2-enriched breast cancer, after adjustment by age, nodal status, and the AFR component (adj. P = 0.021, luminal A as reference). Accordingly, a 10% increase in IA ancestry was associated with a 21% increase in the probability of having HER2-enriched breast cancer (adj. P = 0.022). IA ancestry also significantly increased overall survival after adjustment by age, nodal status, and AFR ancestry, although this result is controversial and may be affected by the size and heterogeneity of the Molecular Profile Breast Cancer Study cohort. Our research confirms previous findings of a high prevalence of HER2-dependent breast tumors among Hispanic/Latina women and strengthens the hypotheses of the existence of either population-specific genetic variant(s) or of other ancestry-correlated factors that impact HER2 expression in breast cancer consistently across different Latin American regions.
The evidence in this work supports the idea that factors linked to genetic ancestry influence the prevalence of breast cancer subtypes in Latin America, potentially affecting treatment needs in the region.
本研究调查了来自阿根廷、巴西、智利、墨西哥和乌拉圭的951例局部晚期乳腺癌病例的遗传血统、乳腺癌亚型与生存结果之间的关系,这些病例参与了乳腺癌分子谱研究。基于阵列的基因分型和ADMIXTURE分析用于遗传血统评估。乳腺癌亚型通过免疫组化和基于基因表达的PAM50算法定义。遗传血统的分布,包括欧洲、美洲原住民(IA)、非洲(AFR)和东亚成分,显示出各国之间存在异质的遗传混合,其中智利(30.9%)和墨西哥(30.8%)的IA血统最高。测试遗传血统与乳腺癌亚型之间的关系表明,在调整年龄、淋巴结状态和AFR成分后,欧洲血统增加10%与HER2富集型乳腺癌发病几率显著降低14%相关(调整后P = 0.021,以腔面A型为参照)。相应地,IA血统增加10%与患HER2富集型乳腺癌的概率增加21%相关(调整后P = 0.022)。在调整年龄、淋巴结状态和AFR血统后,IA血统也显著提高了总生存率,尽管这一结果存在争议,可能受乳腺癌分子谱研究队列的规模和异质性影响。我们的研究证实了先前关于西班牙裔/拉丁裔女性中HER2依赖性乳腺肿瘤患病率较高的发现,并强化了以下假设:存在特定人群的基因变异或其他与血统相关的因素,这些因素在不同拉丁美洲地区一致地影响乳腺癌中HER2的表达。
这项工作中的证据支持了这样一种观点,即与遗传血统相关的因素影响拉丁美洲乳腺癌亚型的患病率,可能影响该地区的治疗需求。