Proteomic and PROTEOMEX profiling of mammary cancer progression in a HER-2/neu oncogene-driven animal model system

PROTEOMICS ◽  
2010 ◽  
Vol 10 (21) ◽  
pp. 3835-3853 ◽  
Author(s):  
Stefania Croci ◽  
Christian V. Recktenwald ◽  
Rudolf Lichtenfels ◽  
Giordano Nicoletti ◽  
Sven P. Dressler ◽  
...  
2011 ◽  
Vol 5 (3-4) ◽  
pp. 200-200
Author(s):  
Stefania Croci ◽  
Christian V. Recktenwald ◽  
Rudolf Lichtenfels ◽  
Giordano Nicoletti ◽  
Sven P. Dressler ◽  
...  

2003 ◽  
Vol 49 (10) ◽  
pp. 1579-1598 ◽  
Author(s):  
Walter P Carney ◽  
Rainer Neumann ◽  
Allan Lipton ◽  
Kim Leitzel ◽  
Suhail Ali ◽  
...  

Abstract Background: The HER-2/neu oncogene and its p185 receptor protein are indicators of a more aggressive form of breast cancer. HER-2/neu status guides Herceptin therapy, specifically directed to the extracellular domain (ECD) of the HER-2/neu oncoprotein. The HER-2/neu ECD is shed from cancer cells into the circulation and is measurable by immunoassay. Methods: We performed a systematic review of the peer-reviewed literature on circulating ECD with respect to prevalence, prognosis, prediction of response to therapy, and monitoring of breast cancer. Results: The prevalence of increased ECD in patients with primary breast cancer varied between 0% and 38% (mean, 18.5%), whereas in metastatic disease the range was from 23% to 80% (mean, 43%). Some women with HER-2/neu-negative tumors by tissue testing develop increased ECD concentrations in metastatic disease. Increased ECD has been correlated with indicators of poor prognosis, e.g., overall survival and disease-free survival. Increased ECD predicts a poor response to hormone therapy and some chemotherapy regimens but can predict improved response to combinations of Herceptin and chemotherapy. Many studies support the value of monitoring ECD during breast cancer progression because serial increases precede the appearance of metastases and longitudinal ECD changes parallel the clinical course of disease. Conclusions: The monitoring of circulating HER-2/neu ECD provides a tool for assessing prognosis, for predicting response to therapy, and for earlier detection of disease progression and timely intervention with appropriate therapy.


Author(s):  
V.J. Montpetit ◽  
S. Dancea ◽  
L. Tryphonas ◽  
D.F. Clapin

Very large doses of pyridoxine (vitamin B6) are neurotoxic in humans, selectively affecting the peripheral sensory nerves. We have undertaken a study of the morphological and biochemical aspects of pyridoxine neurotoxicity in an animal model system. Early morphological changes in dorsal root ganglia (DRG) associated with pyridoxine megadoses include proliferation of neurofilaments, ribosomes, rough endoplasmic reticulum, and Golgi complexes. We present in this report evidence of the formation of unique aggregates of microtubules and membranes in the proximal processes of DRG which are induced by high levels of pyridoxine.


Cancers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2342 ◽  
Author(s):  
Lucie Brisson ◽  
Stéphanie Chadet ◽  
Osbaldo Lopez-Charcas ◽  
Bilel Jelassi ◽  
David Ternant ◽  
...  

The P2X7 receptor is an ATP-gated cation channel with a still ambiguous role in cancer progression, proposed to be either pro- or anti-cancerous, depending on the cancer or cell type in the tumour. Its role in mammary cancer progression is not yet defined. Here, we show that P2X7 receptor is functional in highly aggressive mammary cancer cells, and induces a change in cell morphology with fast F-actin reorganization and formation of filopodia, and promotes cancer cell invasiveness through both 2- and 3-dimensional extracellular matrices in vitro. Furthermore, P2X7 receptor sustains Cdc42 activity and the acquisition of a mesenchymal phenotype. In an immunocompetent mouse mammary cancer model, we reveal that the expression of P2X7 receptor in cancer cells, but not in the host mice, promotes tumour growth and metastasis development, which were reduced by treatment with specific P2X7 antagonists. Our results demonstrate that P2X7 receptor drives mammary tumour progression and represents a pertinent target for mammary cancer treatment.


Oncogene ◽  
1998 ◽  
Vol 17 (16) ◽  
pp. 2087-2093 ◽  
Author(s):  
Lin Chen ◽  
Weijie Zhang ◽  
Nevis Fregien ◽  
Michael Pierce
Keyword(s):  
Her 2 ◽  

1999 ◽  
Vol 1 (2) ◽  
pp. 47-47
Author(s):  
H F L Mark ◽  
D Feldman ◽  
S Das ◽  
H Kye ◽  
C-L Sun ◽  
...  

2018 ◽  
Vol 303 (1) ◽  
pp. 24-29 ◽  
Author(s):  
Joshua B. Gross ◽  
Amanda K. Powers

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