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Ectopic expression of neutrophil gelatinase-associated lipocalin suppresses the invasion and liver metastasis of colon cancer cells

DC Field Value Language
dc.contributor.author홍순원-
dc.date.accessioned2015-06-10T12:27:28Z-
dc.date.available2015-06-10T12:27:28Z-
dc.date.issued2006-
dc.identifier.issn0020-7136-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/109837-
dc.description.abstractNeutrophil gelatinase-associated lipocalin (NGAL), also known as lipocalin 2, is a 25-kDa lipocalin initially purified from neutrophil granules. It is thought to play a role in regulating cellular growth since its expression is highly upregulated in a variety of proliferative cells such as cancer cells. However, experimental evidence showing a clear causal relationship between NGAL expression and the proliferation of tumor cells is lacking. Here, we found NGAL expression in highly and poorly metastatic colon cancer cell lines of the same genetic origin correlated inversely with the metastatic potential of these cells, which suggests NGAL participates in the metastatic process. To explore the role NGAL plays in tumor growth and metastasis, the KM12SM human colon cancer cell line, which is highly metastatic while showing decreased NGAL expression, was genetically manipulated to overexpress NGAL. The effects of this on tumor growth and liver metastasis were then analyzed using experimental animal models established by injecting BALB/c nude mice with tumor cells subcutaneously or intrasplenically. Ectopic expression of NGAL in the colon cancer cells had little effect on the growth and viability of the tumor cells both in vitro and in vivo. However, NGAL expression not only suppressed the ability of the colon carcinoma cells to invade Matrigel in vitro, it also substantially inhibited liver metastasis in an experimental animal model. Collectively, these results indicate that NGAL may be a candidate metastasis suppressor in colon cancer cells.-
dc.description.statementOfResponsibilityopen-
dc.format.extent2490~2497-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAcute-Phase Proteins/biosynthesis*-
dc.subject.MESHAcute-Phase Proteins/physiology*-
dc.subject.MESHBlotting, Western-
dc.subject.MESHCell Proliferation-
dc.subject.MESHCollagen-
dc.subject.MESHColonic Neoplasms/pathology*-
dc.subject.MESHDrug Combinations-
dc.subject.MESHFlow Cytometry-
dc.subject.MESHGene Expression Profiling-
dc.subject.MESHHumans-
dc.subject.MESHLaminin-
dc.subject.MESHLipocalin-2-
dc.subject.MESHLipocalins-
dc.subject.MESHLiver Neoplasms/physiopathology-
dc.subject.MESHLiver Neoplasms/prevention & control-
dc.subject.MESHLiver Neoplasms/secondary*-
dc.subject.MESHNeoplasm Invasiveness-
dc.subject.MESHProteoglycans-
dc.subject.MESHProto-Oncogene Proteins/biosynthesis*-
dc.subject.MESHProto-Oncogene Proteins/physiology*-
dc.subject.MESHTumor Cells, Cultured-
dc.titleEctopic expression of neutrophil gelatinase-associated lipocalin suppresses the invasion and liver metastasis of colon cancer cells-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorHo-Jeong Lee-
dc.contributor.googleauthorEun-Kyoung Lee-
dc.contributor.googleauthorKong-Ju Lee-
dc.contributor.googleauthorSoon-Won Hong-
dc.contributor.googleauthorYeup Yoon-
dc.contributor.googleauthorJang-Seong Kim-
dc.identifier.doi10.1002/ijc.21657-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA04411-
dc.relation.journalcodeJ01092-
dc.identifier.eissn1097-0215-
dc.identifier.pmid16381001-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1002/ijc.21657/abstract-
dc.subject.keywordneutrophil-
dc.subject.keywordgelatinase‐associated lipocalin-
dc.subject.keywordmetastasis suppressor gene-
dc.subject.keywordcolonic neoplasms-
dc.subject.keywordexperimental liver neoplasm-
dc.contributor.alternativeNameHong, Soon Won-
dc.contributor.affiliatedAuthorHong, Soon Won-
dc.rights.accessRightsnot free-
dc.citation.volume118-
dc.citation.number10-
dc.citation.startPage2490-
dc.citation.endPage2497-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF CANCER, Vol.118(10) : 2490-2497, 2006-
dc.identifier.rimsid50307-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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