Jamerson M Hunter, Johnson Michael D, Dickson Robert B
Department of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
J Mammary Gland Biol Neoplasia. 2004 Jan;9(1):27-37. doi: 10.1023/B:JOMG.0000023586.69263.0b.
The proto-oncogene c- myc is involved in regulating proliferation and apoptosis, and its deregulation via genomic and postgenomic mechanisms, contributes to the development and progression of multiple human cancers, including those of the breast. Deregulated expression of c-Myc also contributes to neoplastic transformation by altering cellular differentiation pathways and by facilitating mutagenesis through induction of genomic instability. Transgenic and gene-knockout mice are frequently utilized to resolve the mechanisms through which specific genes influence the development and progression of malignancies. In this review, we discuss how research findings obtained from various c- myc transgenic mammary tumor models help to improve our resolution of c-Myc's role both in tumorigenesis of the murine mammary gland and cancer of the human breast.
原癌基因c-myc参与调控细胞增殖和凋亡,其通过基因组和后基因组机制失调,会促使包括乳腺癌在内的多种人类癌症发生发展。c-Myc的表达失调还会通过改变细胞分化途径以及诱导基因组不稳定促进诱变,从而导致肿瘤转化。转基因和基因敲除小鼠常被用于解析特定基因影响恶性肿瘤发生发展的机制。在本综述中,我们将讨论从各种c-myc转基因乳腺肿瘤模型获得的研究结果如何有助于提高我们对c-Myc在小鼠乳腺肿瘤发生及人类乳腺癌中作用的认识。