Department of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, Ohio, USA.
Cancer Res. 2011 Feb 15;71(4):1203-7. doi: 10.1158/0008-5472.CAN-10-3263. Epub 2011 Feb 8.
Solid human tumors and their surrounding microenvironment are hypothesized to coevolve in a manner that promotes tumor growth, invasiveness, and spread. Mouse models of cancer have focused on genetic changes in the epithelial tumor cells and therefore have not robustly tested this hypothesis. We have recently developed a murine breast cancer model that ablates the PTEN tumor suppressor pathway in stromal fibroblasts. Remarkably, the model resembles human breast tumors both at morphologic and molecular levels. We propose that such models reflect subtypes of tumor-stromal coevolution relevant to human breast cancer, and will therefore be useful in defining the mechanisms that underpin tumor-stroma cross-talk. Additionally, these models should also aid in molecularly classifying human breast tumors on the basis of both the microenvironment subtypes they contain as well as on the tumor subtype.
实体瘤及其周围的微环境被认为是共同进化的,这种进化促进了肿瘤的生长、侵袭和扩散。癌症的小鼠模型主要关注上皮肿瘤细胞的遗传变化,因此并没有强有力地验证这一假设。我们最近开发了一种乳腺癌小鼠模型,该模型可使基质成纤维细胞中的抑癌基因 PTEN 失活。值得注意的是,该模型在形态和分子水平上均与人类乳腺癌相似。我们提出,此类模型反映了与人类乳腺癌相关的肿瘤-基质共同进化的亚型,因此将有助于确定肿瘤-基质相互作用的机制。此外,这些模型还应该有助于根据其包含的微环境亚型以及肿瘤亚型对人类乳腺癌进行分子分类。