Grape seed proanthocyanidins inhibit the growth of human non-small cell lung cancer xenografts by targeting insulin-like growth factor binding protein-3, tumor cell proliferation, and angiogenic factors
Autor: | Syed M. Meeran, Nandan Katiyar, Suhail Akhtar, Santosh K. Katiyar |
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Rok vydání: | 2009 |
Předmět: |
Cancer Research
Pathology medicine.medical_specialty Lung Neoplasms Angiogenesis medicine.medical_treatment Mice Nude Apoptosis Insulin-like growth factor-binding protein Mice In vivo Carcinoma Non-Small-Cell Lung Cell Line Tumor medicine Animals Humans Proanthocyanidins Lung cancer Cell Proliferation biology Grape Seed Extract Cell growth business.industry Plant Extracts Growth factor medicine.disease Xenograft Model Antitumor Assays In vitro respiratory tract diseases Diet Blot Insulin-Like Growth Factor Binding Protein 3 Oncology biology.protein Cancer research Angiogenesis Inducing Agents business |
Zdroj: | Clinical cancer research : an official journal of the American Association for Cancer Research. 15(3) |
ISSN: | 1078-0432 |
Popis: | Purpose: Lung cancer is a leading cause of cancer-related deaths worldwide. Here, we assessed the chemotherapeutic effect of grape seed proanthocyanidins (GSPs) on human non-small cell lung cancer (NSCLC) cells in vitro and in vivo using a tumor xenograft model. Experimental Design: The effects of GSPs on human NSCLC cell lines in terms of cellular proliferation were determined. The chemotherapeutic effects of a GSP- supplemented AIN76A control diet fed to nude mice bearing tumor xenografts (A549 and H1299) were evaluated in terms of biomarkers of cell proliferation and angiogenesis and on insulin-like growth factor binding protein-3 using immunohistochemical detection, ELISA, and Western blotting. Results: In vitro treatment of NSCLC cells with GSPs resulted in inhibition of cellular proliferation. Administration of GSPs (0.1%, 0.2%, and 0.5%, w/w) as a supplement of an AIN76A control diet resulted in a dose-dependent inhibition of the growth of NSCLC (A549 and H1299) tumor xenografts in athymic nude mice (25-76%; P < 0.05-0.001). The growth-inhibitory effect of GSPs on the NSCLC xenograft tumors was associated with the enhancement of the levels of insulin-like growth factor binding protein-3 in the tumor microenvironment and plasma and antiproliferative, antiangiogenic, and proapoptotic effects. Conclusions: This preclinical study reveals for the first time that dietary GSPs have the ability to inhibit the growth of human NSCLC tumor xenografts grown in vivo in athymic nude mice. More studies are needed to develop GSPs as a pharmacologically safe agent for the prevention of lung cancer in humans. |
Databáze: | OpenAIRE |
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