𝔖 Bobbio Scriptorium
✦   LIBER   ✦

New model of ErbB-2 over-expression in human mammary luminal epithelial cells

✍ Scribed by Robert A. Harris; Thomas J. Eichholtz; Ian D. Hiles; Martin J. Page; Michael J. O'Hare


Publisher
John Wiley and Sons
Year
1999
Tongue
French
Weight
324 KB
Volume
80
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.

✦ Synopsis


The ErbB-2 receptor has been strongly implicated in the development of breast cancer. To establish a new model system to investigate the role of erbB-2 in tumorigenesis of the breast, the conditionally immortalised human mammary luminal epithelial cell line HB4a was transfected with erbB-2 cDNA. Biological and biochemical characterisation of the resulting cell lines demonstrated that high levels of ErbB-2 expression were sufficient to cause transformation in vitro but did not cause tumours in vivo. Transformation by overexpression of ErbB-2 correlated with ligand-independent tyrosine phosphorylation of ErbB-2 and the adaptor protein Shc. Over-expression of ErbB-2 also resulted in the ligandindependent constitutive association between Shc and another adaptor protein, Grb2, indicating that receptor activation was sufficient to activate downstream signalling pathways. Using the model described, it was found that elevation of ErbB-2 expression levels caused marked quantitative and qualitative alterations in responses to the ligands epidermal growth factor and heregulin. Data indicate a central role for ErbB-2 in mediating the responses induced by these ligands and suggest that these altered ligand-dependent responses play an important role in tumorigenesis in vivo. Int.


πŸ“œ SIMILAR VOLUMES


MMP-2 mediates ethanol-induced invasion
✍ Zunji Ke; Hong Lin; Zhiqin Fan; Tian-Quan Cai; Rebecca A. Kaplan; Cuiling Ma; Ki πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 French βš– 515 KB

## Abstract Ethanol is a tumor promoter and may enhance the metastasis of breast cancer. We have previously demonstrated that over‐expression of ErbB2 promoted ethanol‐mediated invasion of mammary epithelial cells and breast cancer cells. However, the underlying cellular/molecular mechanisms remain

Over-expression of erbB-2/neu is paralle
✍ Hedvika Lazar; Anna Baltzer; Claude Gimmi; Andreas Marti; Rolf Jaggi πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 French βš– 411 KB πŸ‘ 2 views

The erbB-2/neu oncogene is frequently over-expressed in many different tumors in humans, including those of breast and ovary. The oncogene encodes a receptor tyrosine kinase closely related to the epidermal-growth-factor receptor. We studied effects on differentiation and cell death of erbB-2/neu du

Differential signal transduction of alte
✍ Allison B. Moffa; Stephen P. Ethier πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 373 KB

## Abstract Gene amplification and protein overexpression of fibroblast growth factor receptor 2 (FGFR2) characterize the SUM‐52 breast cancer cell line developed in our laboratory. SUM‐52 cells express nine distinct alternatively spliced isoforms of FGFR2. Among these isoforms are two otherwise id

Induction or suppression of expression o
✍ Yanbo Sun; Hong Lin; Yunfeng Zhu; Cuiling Ma; Jianping Ye; Jia Luo πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 287 KB πŸ‘ 1 views

## Abstract The ErbB family of receptor kinases is composed of four members: epidermal growth factor receptor (EGFR/ErbB1), ErbB2/neu, ErbB3, and ErbB4. Amplification of the ErbB2/neu is found in about 30% of breast cancer patients and is associated with a poor prognosis. Heregulin (HRG) activates

Enhanced expression of heregulin in c-er
✍ G. Mincione; C. Bianco; S. Kannan; G. Colletta; F. Ciardiello; M. Sliwkowski; Y. πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 978 KB

Heregulin P1 was found to stimulate the anchorage-dependent, serum-free growth of nontransformed human MCF-1 OA mammary epithelial cells. Unlike epidermal growth factor, transforming growth factor a, or amphiregulin, heregulin P I was also able to induce the anchorage-independent growth of MCF-1OA c