Li P, Barraclough R, Fernig D G, Smith J A, Rudland P S
Cancer and Polio Research Fund Laboratories, School of Biological Sciences, University of Liverpool, UK.
Int J Exp Pathol. 1998 Aug;79(4):193-206. doi: 10.1046/j.1365-2613.1998.00068.x.
The rodent and human nonpregnant mammary glands contain epithelial, intermediate and myoepithelial cells which have all been isolated as cell lines in vitro. Transforming growth factor-alpha (TGF alpha) and basic fibroblast growth factor (bFGF) are produced by myoepithelial cells and can stimulate the growth of intermediate stem cells in vitro. Epithelial and intermediate cells behave like stem cells in vitro, since they can differentiate into alveolar-like an myoepithelial cells. The myoepithelial differentiation pathway is associated with the early expression of a calcium-binding regulatory protein called p9Ka and the protease, Cathepsin D. Myoepithelial cells are also present in benign lesions but not in malignant mammary carcinomas of rats or humans, whose resultant cell lines fail to differentiate completely along the myoepithelial cell pathway. Loss of the myoepithelial cell in some invasive carcinomas may be compensated, at least in part, by changes in malignant cells. Over-expression of TGF alpha and/or erbB receptors may reduce the requirement for TGF alpha, whilst ectopic production of bFGF and its receptors and p9Ka/Cathespin D may assist in tumorigenesis and in metastasis, respectively. Thus compensation for, or retention of, molecules potentially involved in the differentiation of mammary cells may be a mechanism by which malignancy progresses in some human invasive carcinomas.
啮齿动物和人类的非妊娠乳腺包含上皮细胞、中间细胞和肌上皮细胞,这些细胞均已在体外分离为细胞系。转化生长因子-α(TGFα)和碱性成纤维细胞生长因子(bFGF)由肌上皮细胞产生,并且在体外能够刺激中间干细胞的生长。上皮细胞和中间细胞在体外表现得像干细胞,因为它们能够分化为肺泡样细胞和肌上皮细胞。肌上皮细胞的分化途径与一种名为p9Ka的钙结合调节蛋白和蛋白酶组织蛋白酶D的早期表达相关。肌上皮细胞也存在于良性病变中,但在大鼠或人类的恶性乳腺癌中不存在,其产生的细胞系无法完全沿着肌上皮细胞途径分化。在一些浸润性癌中,肌上皮细胞的缺失可能至少部分地由恶性细胞的变化来补偿。TGFα和/或erbB受体的过度表达可能会降低对TGFα的需求,而bFGF及其受体以及p9Ka/组织蛋白酶D的异位产生可能分别有助于肿瘤发生和转移。因此,对可能参与乳腺细胞分化的分子进行补偿或保留可能是某些人类浸润性癌中恶性肿瘤进展的一种机制。