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In situ identification and localization of IGHA2 in the breast tumor microenvironment by mass spectrometry

DC Field Value Language
dc.contributor.author김백길-
dc.contributor.author조남훈-
dc.contributor.author최영득-
dc.contributor.author최윤표-
dc.contributor.author강숙희-
dc.contributor.author고명청-
dc.date.accessioned2014-12-19T17:15:26Z-
dc.date.available2014-12-19T17:15:26Z-
dc.date.issued2012-
dc.identifier.issn1535-3893-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/91071-
dc.description.abstractModifications in the tumor microenvironment (TME) play a major role in the establishment, progression, and metastasis of cancer. Matrix-assisted laser desorption/ionization-mass spectrometry imaging (MALDI-MSI) is a powerful technique that enables the simultaneous identification and localization of biological compounds within tissues. To detect markers of early TME remodeling in invasive breast cancer, we used MALDI-MSI to compare the molecular profiles of tissues from the breast cancer interface zone, tumor zone, and normal-tissue zone. Using direct-tissue MALDI tandem mass spectrometry (MS/MS), we identified immunoglobulin heavy constant alpha 2 (IGHA2) as a new, zone-specific protein in the breast TME. The zone-specific expression of IGHA2 was verified by immunoblotting and immunohistochemical analysis. IGHA2 expression was consistently positive in tumor cells that were metastatic to regional nodes, with intense expression along the cytoplasmic borders. As a factor related to an increased percentage of nodes with tumor metastasis, IGHA2 expression was upregulated 3.745-fold in cases with an increased number of cancerous nodes (p = 0.0468). Our results provide the first evidence of IGHA2 as a marker of the early process of TME remodeling in invasive breast cancer. Furthermore, IGHA2 may be a novel marker for regional metastases in the lymph nodes of patients with breast cancer.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfJOURNAL OF PROTEOME RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHBiomarkers, Tumor-
dc.subject.MESHBreast/chemistry-
dc.subject.MESHBreast/pathology-
dc.subject.MESHBreast Neoplasms/chemistry*-
dc.subject.MESHBreast Neoplasms/metabolism-
dc.subject.MESHCarrier Proteins/analysis*-
dc.subject.MESHCarrier Proteins/chemistry-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHImmunoglobulin Heavy Chains/analysis*-
dc.subject.MESHImmunoglobulin Heavy Chains/chemistry-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHMolecular Imaging/methods-
dc.subject.MESHNeoplasm Metastasis-
dc.subject.MESHReproducibility of Results-
dc.subject.MESHSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods*-
dc.subject.MESHTandem Mass Spectrometry/methods-
dc.subject.MESHTumor Microenvironment/physiology*-
dc.titleIn situ identification and localization of IGHA2 in the breast tumor microenvironment by mass spectrometry-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorSuki Kang-
dc.contributor.googleauthorHeysun Maeng-
dc.contributor.googleauthorBaek Gil Kim-
dc.contributor.googleauthorGao Ming Qing-
dc.contributor.googleauthorYoon Pyo Choi-
dc.contributor.googleauthorHak Yong Kim-
dc.contributor.googleauthorPan Soo Kim-
dc.contributor.googleauthorYangsun Kim-
dc.contributor.googleauthorYoung Hwan Kim-
dc.contributor.googleauthorYoung Deuk Choi-
dc.contributor.googleauthorNam Hoon Cho-
dc.identifier.doi10.1021/pr3003672-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00484-
dc.contributor.localIdA03812-
dc.contributor.localIdA04111-
dc.contributor.localIdA04143-
dc.contributor.localIdA00044-
dc.contributor.localIdA00116-
dc.relation.journalcodeJ01720-
dc.identifier.eissn1535-3907-
dc.identifier.pmid22894699-
dc.identifier.urlhttp://pubs.acs.org/doi/abs/10.1021/pr3003672-
dc.subject.keywordbreast cancer-
dc.subject.keywordIGHA2-
dc.subject.keywordMALDI-MSI-
dc.subject.keywordtissue MALDI MS/MS-
dc.subject.keywordtumor microenvironment-
dc.contributor.alternativeNameKim, Baek Gil-
dc.contributor.alternativeNameCho, Nam Hoon-
dc.contributor.alternativeNameChoi, Young Deuk-
dc.contributor.alternativeNameChoi, Yoon Pyo-
dc.contributor.alternativeNameKang, Suki-
dc.contributor.alternativeNameGao, Ming Qing-
dc.contributor.affiliatedAuthorKim, Baek Gil-
dc.contributor.affiliatedAuthorCho, Nam Hoon-
dc.contributor.affiliatedAuthorChoi, Young Deuk-
dc.contributor.affiliatedAuthorChoi, Yoon Pyo-
dc.contributor.affiliatedAuthorKang, Suki-
dc.contributor.affiliatedAuthorGao, Ming Qing-
dc.citation.volume11-
dc.citation.number9-
dc.citation.startPage4567-
dc.citation.endPage4574-
dc.identifier.bibliographicCitationJOURNAL OF PROTEOME RESEARCH, Vol.11(9) : 4567-4574, 2012-
dc.identifier.rimsid33317-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Urology (비뇨의학교실) > 1. Journal Papers

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