Kern F G, McLeskey S W, Zhang L, Kurebayashi J, Liu Y, Ding I Y, Kharbanda S, Chen D, Miller D, Cullen K
Lombardi Cancer Research Center, Georgetown University Medical Center, Washington, DC 20007.
Breast Cancer Res Treat. 1994;31(2-3):153-65. doi: 10.1007/BF00666149.
The MCF-7 human breast carcinoma cell line has been used as a recipient for eukaryotic plasmid expression vectors to determine the effects of growth factor and growth factor receptor overexpression on the estrogen-dependent, antiestrogen sensitive and poorly metastatic phenotypes exhibited by this line. Overexpression of some members of the erbB family of ligands and receptors were found to have some effects on these phenotypes. However, only when two members of the fibroblast growth factor family, FGF-1 and FGF-4, were overexpressed was progressive in vivo growth observed is either ovariectomized nude mice without estrogen supplementation or in mice that received tamoxifen treatment. FGF transfected cells also exhibited an increased ability to form micrometastases. The implications of these results with regard to the possible role of the paracrine and autocrine effects of angiogenic growth factor production in breast cancer progression are discussed.
MCF-7人乳腺癌细胞系已被用作真核质粒表达载体的受体,以确定生长因子和生长因子受体过表达对该细胞系所表现出的雌激素依赖性、抗雌激素敏感性和低转移表型的影响。erbB配体和受体家族的一些成员过表达被发现对这些表型有一些影响。然而,只有当成纤维细胞生长因子家族的两个成员FGF-1和FGF-4过表达时,在未补充雌激素的去卵巢裸鼠或接受他莫昔芬治疗的小鼠中才观察到体内渐进性生长。FGF转染的细胞形成微转移的能力也有所增强。讨论了这些结果对于血管生成生长因子产生的旁分泌和自分泌效应在乳腺癌进展中可能作用的意义。