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S100P钙结合蛋白的过表达与体外人乳腺上皮细胞的永生化及体内乳腺癌发生的早期阶段相关。

S100P calcium-binding protein overexpression is associated with immortalization of human breast epithelial cells in vitro and early stages of breast cancer development in vivo.

作者信息

Guerreiro Da Silva I D, Hu Y F, Russo I H, Ao X, Salicioni A M, Yang X, Russo J

机构信息

Breast Cancer Research Laboratory, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

出版信息

Int J Oncol. 2000 Feb;16(2):231-40.

Abstract

The mechanism of cell immortalization of human breast epithelial cells leading to neoplastic transformation is not clear. The isolation and characterization of a spontaneously immortalized human breast epithelial cell line, MCF-10F, have provided a valuable tool to identify genes involved in this process. Using the technique of differential display, we have identified seven cDNA bands differentially displayed in the MCF-10F cells when compared with the mortal S130 cells from which MCF-10F was originated. One of these bands was isolated and cloned. Sequence analysis revealed 99% homology to the EF-hand calcium-binding protein S100P (Placental). The clone was overexpressed in the immortal cell line MCF-10F when compared to the mortal counterpart S130 or other primary cultures of human breast epithelial cells. In addition, it was highly expressed in chemically transformed breast epithelial cell lines (BP1E and D3. 1), breast cancer cell line T47D, as well as in three invasive ductal carcinomas when compared to their normal adjacent tissue. The S100P protein was localized by immunohistochemistry, using a monoclonal antibody against the same amino acid sequence of the gene cloned, in ductal hyperplasias, in situ and invasive ductal carcinoma, but not in the normal tissues. We concluded that S100P overexpression is an early event that might play an important role in the immortalization of human breast epithelial cells in vitro and tumor progression in vivo.

摘要

人乳腺上皮细胞永生化并导致肿瘤转化的机制尚不清楚。一种自发永生化的人乳腺上皮细胞系MCF-10F的分离和鉴定,为识别参与这一过程的基因提供了一个有价值的工具。利用差异显示技术,我们鉴定出了7条在MCF-10F细胞中差异显示的cDNA条带,这些条带是与MCF-10F起源的有限传代S130细胞相比得到的。其中一条条带被分离并克隆。序列分析显示其与EF手型钙结合蛋白S100P(胎盘型)有99%的同源性。与有限传代的对应细胞S130或其他人乳腺上皮细胞原代培养物相比,该克隆在永生化细胞系MCF-10F中过表达。此外,与正常相邻组织相比,它在化学转化的乳腺上皮细胞系(BP1E和D3.1)、乳腺癌细胞系T47D以及3例浸润性导管癌中高表达。使用针对克隆基因相同氨基酸序列的单克隆抗体,通过免疫组织化学方法对S100P蛋白进行定位,结果显示其在导管增生、原位癌和浸润性导管癌中表达,但在正常组织中不表达。我们得出结论,S100P过表达是一个早期事件,可能在人乳腺上皮细胞体外永生化和体内肿瘤进展中起重要作用。

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