دورية أكاديمية

Cancer Malignancy Is Enhanced by Glyceraldehyde-Derived Advanced Glycation End-Products.

التفاصيل البيبلوغرافية
العنوان: Cancer Malignancy Is Enhanced by Glyceraldehyde-Derived Advanced Glycation End-Products.
المؤلفون: Takino, Jun-Ichi, Yamagishi, Sho-Ichi, Takeuchi, Masayoshi
المصدر: Journal of Oncology; 2010, p1-8, 8p, 1 Black and White Photograph, 4 Graphs
مصطلحات موضوعية: CANCER, CANCER cells, LUNG cancer, CELL proliferation, CANCER treatment
مستخلص: The receptor for advanced glycation end-products (RAGEs) is associated with the malignancy of cancer. A recent study has suggested that glyceraldehyde-derived AGEs (Glycer-AGEs) enhanced the malignancy of melanoma cells, but glucose-derived AGEs did not.However, the effects of Glycer-AGEs on other cancer cells remain poorly understood, and themolecularmechanisms behind the above-mentioned effect have not been clarified. The present paper aimed to examine the effect of Glycer-AGEs on cultured lung cancer A549 cells. RAGE was expressed in A549 cells. Glycer-AGEs significantly attenuated cell proliferation. Furthermore, Glycer-AGEs enhanced the migration capacity of the cells by activating Rac1 via ROS and also increased their invasion capacity. We demonstrated that Glycer-AGEs enhanced the migration and invasion of A549 cells rather than their proliferation. These results suggest that Glycer-AGEs play a critical role in the malignancy of cancer rather than its proliferation and are potential targets for therapeutic intervention. [ABSTRACT FROM AUTHOR]
Copyright of Journal of Oncology is the property of Hindawi Limited and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:16878450
DOI:10.1155/2010/739852