Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States of America; Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, United States of America; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, United States of America.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States of America; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, United States of America.
Biochim Biophys Acta Rev Cancer. 2024 Sep;1879(5):189163. doi: 10.1016/j.bbcan.2024.189163. Epub 2024 Jul 29.
Women that present to the clinic with established breast cancer metastases have limited treatment options. Yet, the majority of preclinical studies are actually not directed at developing treatment regimens for established metastatic disease. In this review we will discuss the current state of preclinical macro-metastatic breast cancer models, including, but not limited to syngeneic GEMM, PDX and xenografts. Challenges within these models which are often overlooked include fluorophore-immunogenic neoantigens, differences in experimental vs spontaneous metastasis and tumor heterogeneity. Furthermore, due to cell plasticity in the tumor immune microenvironment (TIME) of the metastatic landscape, the treatment efficacy of newly approved immune checkpoint blockade (ICB) may differ in metastatic sites as compared to primary localized tumors.
已经发生乳腺癌转移的女性到诊所就诊时,可选的治疗方法有限。然而,大多数临床前研究实际上并不是针对已确立的转移性疾病来制定治疗方案的。在这篇综述中,我们将讨论目前临床前大转移乳腺癌模型的现状,包括但不限于同源基因工程小鼠模型(GEMM)、PDX 模型和异种移植模型。这些模型中经常被忽视的挑战包括荧光免疫原性新抗原、实验性转移与自发性转移以及肿瘤异质性的差异。此外,由于转移部位肿瘤免疫微环境(TIME)中的细胞可塑性,新批准的免疫检查点阻断(ICB)的治疗效果可能与原发性局限性肿瘤不同。