Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Department of medical laboratory technology, Taibah University, Al-Madinah al-Munawwarah, Saudi Arabia.
Nat Commun. 2023 Sep 13;14(1):5665. doi: 10.1038/s41467-023-40841-6.
Triple-negative breast cancer (TNBC) patients have a poor prognosis and few treatment options. Mouse models of TNBC are important for development of new therapies, however, few mouse models represent the complexity of TNBC. Here, we develop a female TNBC murine model by mimicking two common TNBC mutations with high co-occurrence: amplification of the oncogene MYC and deletion of the tumor suppressor PTEN. This Myc;Ptenfl model develops heterogeneous triple-negative mammary tumors that display histological and molecular features commonly found in human TNBC. Our research involves deep molecular and spatial analyses on Myc;Ptenfl tumors including bulk and single-cell RNA-sequencing, and multiplex tissue-imaging. Through comparison with human TNBC, we demonstrate that this genetic mouse model develops mammary tumors with differential survival and therapeutic responses that closely resemble the inter- and intra-tumoral and microenvironmental heterogeneity of human TNBC, providing a pre-clinical tool for assessing the spectrum of patient TNBC biology and drug response.
三阴性乳腺癌(TNBC)患者的预后较差,治疗选择有限。TNBC 的小鼠模型对于新疗法的开发非常重要,但很少有小鼠模型能够代表 TNBC 的复杂性。在这里,我们通过模拟两种常见的高共发生 TNBC 突变:癌基因 MYC 的扩增和肿瘤抑制基因 PTEN 的缺失,开发了一种女性 TNBC 小鼠模型。Myc;Ptenfl 模型发展为具有异质性的三阴性乳腺肿瘤,显示出人类 TNBC 中常见的组织学和分子特征。我们的研究涉及对 Myc;Ptenfl 肿瘤的深入分子和空间分析,包括批量和单细胞 RNA 测序,以及多重组织成像。通过与人类 TNBC 进行比较,我们证明这种遗传小鼠模型发展出的乳腺肿瘤具有不同的生存和治疗反应,与人类 TNBC 的肿瘤内和肿瘤间以及微环境异质性非常相似,为评估患者 TNBC 生物学和药物反应的范围提供了一种临床前工具。