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Sequential production and activation of matrix-metalloproteinase-9 (MMP-9) with breast cancer progression

DC Field Value Language
dc.contributor.author노재경-
dc.date.accessioned2021-09-28T08:07:59Z-
dc.date.available2021-09-28T08:07:59Z-
dc.date.issued1996-04-
dc.identifier.issn0167-6806-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/183437-
dc.description.abstractThe degradation of the basement membrane by matrix-metalloproteinase(MMP) and serine protease is a critical pointin tumor invasion and metastasis. We measured theactivity of MMP-9 from 28 normal, 12 benignand 126 breast cancer tissues using gelatin zymographywith an image analysis system. ProMMP-9 was expressedin 17.5% of the cancer patients compared to2.5% in 40 non-cancerous tissues (p=0.014).The mature form of MMP-9 (82 kD) wasexpressed only in T2–T4 stages. During the earlyphase of breast cancer (DCIS and T1 stage)progression, only production of proMMP-9 increased. However, asthe cancer grew or invaded skin (T2–T4), orwith lymphovascular permeation, both production and activation ofMMP-9 increased. In conclusion, proMMP-9 production was themain cause of increased MMP-9 activity during theearly phase, while both production and activation increasedin the late phase of breast cancer.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherKluwer Academic-
dc.relation.isPartOfBREAST CANCER RESEARCH AND TREATMENT-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHBreast Neoplasms / enzymology*-
dc.subject.MESHBreast Neoplasms / pathology*-
dc.subject.MESHCollagenases / biosynthesis*-
dc.subject.MESHCollagenases / metabolism*-
dc.subject.MESHDisease Progression-
dc.subject.MESHEnzyme Activation-
dc.subject.MESHHumans-
dc.subject.MESHMatrix Metalloproteinase 9-
dc.titleSequential production and activation of matrix-metalloproteinase-9 (MMP-9) with breast cancer progression-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSun Young Rha-
dc.contributor.googleauthorJoo Hang Kim-
dc.contributor.googleauthorJae Kyung Roh-
dc.contributor.googleauthorKyong Sik Lee-
dc.contributor.googleauthorJin Sik Min-
dc.contributor.googleauthorByung Soo Kim-
dc.contributor.googleauthorHyun Cheol Chung-
dc.identifier.doi10.1023/A:1005701231871-
dc.contributor.localIdA01290-
dc.relation.journalcodeJ00403-
dc.identifier.eissn1573-7217-
dc.identifier.pmid9131273-
dc.identifier.urlhttp://link.springer.com/article/10.1023/A:1005701231871-
dc.contributor.alternativeNameRoh, Jae Kyung-
dc.contributor.affiliatedAuthor노재경-
dc.citation.volume42-
dc.citation.number2-
dc.citation.startPage175-
dc.citation.endPage181-
dc.identifier.bibliographicCitationBREAST CANCER RESEARCH AND TREATMENT, Vol.42(2) : 175-181, 1996-04-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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