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Updated: Aug 28, 2026

In Vitro Evaluation of Oncogenic Transformation in Human Mammary Epithelial Cells
Published on: September 24, 2020
Increased expression of specific protein tyrosine phosphatases in human breast epithelial cells neoplastically
Y F Zhai1, H Beittenmiller, B Wang
1Department of Pharmacology, Michigan State University, East Lansing 48824.
Abstract:
Protein tyrosine phosphorylation/dephosphorylation is a fundamental mechanism in the regulation of cell proliferation and neoplastic transformation; this metabolic process is modulated by the opposing activities of protein tyrosine kinases and protein tyrosine phosphatases (PTPases). While the role of protein tyrosine kinases has been examined extensively in human breast tumorigenesis, the role of PTPases in this process is virtually unknown. To address this issue, an activated neu oncogene was introduced into an immortalized nontumorigenic human breast epithelial cell line (184B5). This resulted in a substantial increase in P185neu expression, which led to the formation of progressively growing carcinomas after such cells were inoculated into athymic nude mice. Importantly, a striking increase in the expression of specific PTPases, LAR and PTP1B, was observed in 3 independently neu transformed cell lines and their derived tumors. This elevation was verified at both the mRNA and protein levels. TC-PTP PTPase expression was only slightly increased in these neu transformed cells, and no expression of CD45 PTPase was observed. The level of neu expression, as well as the differential expression between P185neu and LAR/PTP1B, directly correlated with tumorigenicity. Furthermore, rat mammary carcinomas with elevated neu expression (neu-induced) also had sharply elevated LAR-PTPase expression when compared to rat mammary carcinomas with little or no neu expression (7,12-dimethylbenzanthracene induced); the level of expression of LAR PTPase was directly correlated with the level of neu expression. Thus, our results provide the first evidence that, in human breast carcinoma cells and in rat mammary carcinomas that have an induced increase in neu expression, a consistent and substantial increase in the expression of specific PTPases occurs. The relationship between P185neu-protein tyrosine kinase expression and specific PTPase expression may play a critical role in human breast tumorigenesis.
Insights
This study reveals that specific protein tyrosine phosphatases (PTPases), LAR and PTP1B, are significantly upregulated in human breast cancer cells and rat mammary tumors. This PTPase upregulation correlates with neu oncogene expression and tumorigenicity, suggesting a key role in breast cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Protein tyrosine phosphorylation/dephosphorylation regulates cell proliferation and is modulated by protein tyrosine kinases and phosphatases (PTPases).
- The role of PTPases in human breast tumorigenesis is largely unexplored, unlike the extensive research on protein tyrosine kinases.
Purpose of the Study:
- To investigate the role of specific PTPases in human breast tumorigenesis.
- To determine if PTPase expression is altered in response to neu oncogene activation and subsequent tumor formation.
Main Methods:
- Activated neu oncogene introduced into a human breast epithelial cell line (184B5).
- Tumorigenicity assessed by inoculation into athymic nude mice.
- Expression levels of specific PTPases (LAR, PTP1B, TC-PTP, CD45) analyzed at mRNA and protein levels in cell lines and tumors.
- Comparison with rat mammary carcinomas induced by neu or 7,12-dimethylbenzanthracene.
Main Results:
- Neu-transformed cells and derived tumors showed a striking increase in LAR and PTP1B PTPase expression at both mRNA and protein levels.
- TC-PTP expression showed only a slight increase, and CD45 expression was undetectable.
- Elevated neu expression and differential expression of P185neu with LAR/PTP1B correlated directly with tumorigenicity.
- Rat mammary carcinomas with elevated neu expression exhibited sharply increased LAR-PTPase expression compared to those with low neu expression.
Conclusions:
- This study provides the first evidence of consistent and substantial increases in specific PTPase expression (LAR, PTP1B) in human breast carcinoma cells and neu-induced rat mammary carcinomas.
- The observed relationship between P185neu-protein tyrosine kinase expression and specific PTPase expression may be critical in human breast tumorigenesis.
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