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dc.creatorLiu, Jian-Miao
dc.creatorKusinski, Michal
dc.creatorIlić, Vesna
dc.creatorBignon, Jerome
dc.creatorHajem, Neila
dc.creatorKomorowski, Jan
dc.creatorKuzdak, Krzysztof
dc.creatorStepien, Henryk
dc.creatorWdzieczak-Bakala, Joanna
dc.date.accessioned2021-04-20T12:15:05Z
dc.date.available2021-04-20T12:15:05Z
dc.date.issued2008
dc.identifier.issn0250-7005
dc.identifier.urihttp://rimi.imi.bg.ac.rs/handle/123456789/204
dc.description.abstractBackground: The natural tetrapeptide acetyl-SerAsp-Lys-Pro (AcSDKP), generated from thymosin beta 4 following its cleavage by prolyl oligopeptidase (POP), is a physiological stimulator of angiogenesis. Because of the critical role of neovascularisation in tumor development, the expression of AcSDKP and the activity of POP were examined in different human solid malignancies. Materials and Methods: The expression of AcSDKP and the activity of POP were evaluated in human blood samples and tissue specimens of thyroid goiter and thyroid papillary carcinoma as well as in commercial cancer tissue microarray. Results: A significantly increased concentration of AcSDKP in intratumoral blood and enhanced tissular activity of POP were detected in cancer patients. The expression of AcSDKP in human breast, colon, head and neck, kidney, lung, skin, ovary and prostate cancer tissues was shown to be greater than that in normal tissues. Conclusion: AcSDKP and POP contribute to the malignant phenotype and these molecules are potentiel markers of cancer.en
dc.publisherInt Inst Anticancer Research, Athens
dc.relationCentre of Excellence MolMed [QJK3-CD-2002-30326]
dc.relationInstitut de Chimie des Substances Naturelles, CNRSCentre National de la Recherche Scientifique (CNRS)
dc.rightsrestrictedAccess
dc.sourceAnticancer Research
dc.subjectAcSDKPen
dc.subjectPOPen
dc.subjectmarkeren
dc.subjectangiogenesisen
dc.subjectthyroid tumoren
dc.subjectcanceren
dc.titleOverexpression of the Angiogenic Tetrapeptide AcSDKP in Human Malignant Tumorsen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage2817
dc.citation.issue5A
dc.citation.other28(5A): 2813-2817
dc.citation.rankM23
dc.citation.spage2813
dc.citation.volume28
dc.identifier.pmid19035315
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_rimi_204
dc.identifier.wos000260554900042
dc.type.versionpublishedVersion


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