Trembath Hannah E, Spanheimer Philip M
Department of Surgery, University of North Carolina, Chapel Hill, North Carolina.
Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Cancer Res. 2025 Feb 1;85(3):407-409. doi: 10.1158/0008-5472.CAN-24-3879.
Racial disparities in cancer outcomes are well documented across tumor types. For patients with breast cancer, Black women are more likely to present with more aggressive molecular features and more likely to die from disease, even after accounting for those features. Recent efforts have been aimed at developing translational model systems for precision medicine strategies, and a major focus has been on patient-derived organoids. Organoids allow for robust in vitro experimental platforms, including drug and CRISPR screens while maintaining more complex cancer and tumor microenvironment subpopulations than cell lines. For results that are broadly translationally relevant, it is important that cancer models are derived from the spectrum of human disease and humans with disease. In this issue of Cancer Research, Madorsky Rowdo and colleagues derive breast cancer organoids from patients with African ancestry and use CRISPR-Cas9 screens to identify novel therapeutic vulnerabilities. These findings demonstrate the promise of representative cancer model systems to facilitate discoveries that are most likely to translate to improved therapy for all patients. See related article by Madorsky Rowdo et al., p. 551.
癌症治疗结果中的种族差异在各种肿瘤类型中都有充分记录。对于乳腺癌患者,黑人女性更有可能表现出更具侵袭性的分子特征,并且即使考虑到这些特征,她们死于疾病的可能性也更高。最近的努力旨在开发用于精准医学策略的转化模型系统,其中一个主要重点是患者来源的类器官。类器官提供了强大的体外实验平台,包括药物和CRISPR筛选,同时比细胞系保留了更复杂的癌症和肿瘤微环境亚群。对于具有广泛转化相关性的结果而言,癌症模型源自人类疾病谱和患病个体非常重要。在本期《癌症研究》中,马多尔斯基·罗多及其同事从具有非洲血统的患者中获取乳腺癌类器官,并使用CRISPR-Cas9筛选来识别新的治疗弱点。这些发现证明了具有代表性的癌症模型系统有助于发现最有可能转化为改善所有患者治疗效果的疗法的前景。见马多尔斯基·罗多等人的相关文章,第551页。