Literature DB >> 16491398

The role of insulin dependent NO synthesis in the impaired production of maspin in human breast cancer.

G V Girish1, G Bhattacharya, A Kumar Sinha.   

Abstract

PURPOSE: The synthesis of maspin, a protein with various anti-breast cancer properties has been reported to be produced in normal breast tissue but not in breast cancer cells. We investigated the role of insulin receptors and their upregulation by prostaglandin E(1) in vitro for the stimulation of NO synthesis by the hormone, and its consequence on maspin production in normal neutrophils and malignant cells in breast cancer.
METHODS: Maspin and NO were determined by ELISA and methemoglobin method, respectively.
RESULTS: The treatment of neutrophils and malignant breast cancer cells with prostaglandin E(1) resulted in partial restoration of the impaired receptor numbers, and resulted in partial normalization of NO and maspin production in these cells compared to normal counterparts. It was not feasible to stimulate NO synthesis to normal ranges by the upregulation of receptor number due to intrinsic decrease of insulin receptors in breast cancer cells. However, aspirin, which was found to stimulate NO synthesis to normal ranges, normalized maspin production in these cells in breast cancer.
CONCLUSION: The impaired maspin production was found to be the consequence of impaired insulin induced NO production in breast cancer due to the decrease of insulin receptor binding. Restoration of NO production by aspirin can be useful for the restoration of maspin production in breast cancer.

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Year:  2006        PMID: 16491398     DOI: 10.1007/s00432-006-0087-7

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  42 in total

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3.  Blocking tumor growth, invasion, and metastasis by maspin in a syngeneic breast cancer model.

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4.  Preparation of iodine-125-labeled insulin for radioimmunoassay: comparison of lactoperoxidase and chloramine-T iodination.

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5.  Maspin is an intracellular serpin that partitions into secretory vesicles and is present at the cell surface.

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Journal:  J Histochem Cytochem       Date:  1997-12       Impact factor: 2.479

6.  Targeted expression of maspin in tumor vasculatures induces endothelial cell apoptosis.

Authors:  Zhigang Li; Heidi Y Shi; Ming Zhang
Journal:  Oncogene       Date:  2005-03-17       Impact factor: 9.867

7.  Burn-activated neutrophils and tumor necrosis factor-alpha alter endothelial cell actin cytoskeleton and enhance monolayer permeability.

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8.  Maspin, a serpin with tumor-suppressing activity in human mammary epithelial cells.

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Journal:  Science       Date:  1994-01-28       Impact factor: 47.728

9.  Impairment of stimulation by estrogen of insulin-activated nitric oxide synthase in human breast cancer.

Authors:  Manti Guha; Jaydip Biswas; Jaya Tirkey; A Kumar Sinha
Journal:  Int J Cancer       Date:  2002-07-20       Impact factor: 7.396

10.  Impaired binding of insulin to erythrocyte membrane receptor and the activation of nitric oxide synthase by the hormone in human breast cancer.

Authors:  S Chakraborty; G V Girish; A K Sinha
Journal:  J Cancer Res Clin Oncol       Date:  2004-02-19       Impact factor: 4.553

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Authors:  Udayan Ray; Gausal A Khan; Kushal Chakraborty; Shyamali Basuroy; Sharmistha Chakraborty Patra; Gannareddy Girish; G Bhattacharya; Asru K Sinha
Journal:  J Thromb Thrombolysis       Date:  2012-04       Impact factor: 2.300

2.  The Role of Neutrophil Estrogen Receptor Status on Maspin Synthesis via Nitric Oxide Production in Human Breast Cancer.

Authors:  Karabi Ganguly Bhattacharjee; Mau Bhattacharyya; Umesh Chandra Halder; Pradipta Jana; Asru K Sinha
Journal:  J Breast Cancer       Date:  2012-06-28       Impact factor: 3.588

3.  The "Cross Talk" between the Receptors of Insulin, Estrogen and Progesterone in Neutrophils in the Synthesis of Maspin through Nitric Oxide in Breast Cancer.

Authors:  Karabi Ganguly Bhattacharjee; Mau Bhattacharyya; Umesh Chandra Halder; Pradipta Jana; Asru K Sinha
Journal:  Int J Biomed Sci       Date:  2012-06
  3 in total

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