Cancer Malignancy Is Enhanced by Glyceraldehyde-Derived Advanced Glycation End-Products英文文献资料.docVIP
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Cancer Malignancy Is Enhanced by Glyceraldehyde-Derived Advanced Glycation End-Products英文文献资料
HindawiPublishingCorporation
JournalofOncology
Volume2010,ArticleID739852,8pages
doi:10.1155/2010/739852
ResearchArticle
CancerMalignancyIsEnhancedbyGlyceraldehyde-Derived
AdvancedGlycationEnd-Products
Jun-IchiTakino, Sho-IchiYamagishi, andMasayoshiTakeuchi
1 2 1
1
DepartmentofLifePharmacy,FacultyofPharmaceuticalSciences,HokurikuUniversity,Ho-3Kanagawa-machi,
Kanazawa920-1181,Japan
2
DepartmentofPathophysiologyandTherapeuticsofDiabeticVascularComplications,KurumeUniversitySchoolofMedicine,
67Asahimachi,Kurume830-0011,Japan
CorrespondenceshouldbeaddressedtoMasayoshiTakeuchi,m-takeuchi@hokuriku-u.ac.jp
Received2November2009;Revised24April2010;Accepted9May2010
AcademicEditor:JamesL.Mulshine
Copyright?2010Jun-IchiTakinoetal. This is an open access article distributed under the Creative Commons Attribution
License,whichpermitsunrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkisproperly
cited.
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
AGEsdidnot.However,thee?ectsofGlycer-AGEsonothercancercellsremainpoorlyunderstood,andthemolecularmechanisms
behind the above-mentioned e?ect have not been clari?ed. The present paper aimed to examine the e?ect of Glycer-AGEs
onculturedlungcancerA549cells.RAGEwasexpressedinA549cells.Glycer-AGEssigni?cantlyattenuatedcellproliferation.
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.TheseresultssuggestthatGlycer-AGEsplayacriticalroleinthemalignancyofcancerratherthanitsproliferation
andarepotentialtargetsfortherapeuticintervention.
1.Introduction
reportshavesuggestedth
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