Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:12220625rdf:typepubmed:Citationlld:pubmed
pubmed-article:12220625lifeskim:mentionsumls-concept:C0086418lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C0007634lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C0205065lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C0087071lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C1155299lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C0021467lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C0021469lld:lifeskim
pubmed-article:12220625lifeskim:mentionsumls-concept:C0205197lld:lifeskim
pubmed-article:12220625pubmed:issue1-3lld:pubmed
pubmed-article:12220625pubmed:dateCreated2002-9-10lld:pubmed
pubmed-article:12220625pubmed:abstractTextThe two known mechanisms for telomere maintenance in eukaryocytes are telomerase in telomerase-positive cells and alternative lengthening of telomeres (ALT) in telomerase-negative cells. We report here that telomere maintenance in the telomerase-positive human ovarian SKOV-3 cells was not affected by inhibition of telomerase. For comparison, the effect of telomerase inhibitors on telomere maintenance in another telomerase-positive cell line (i.e. human pharynx FaDu cells) and the telomerase-negative human osteosarcoma Saos-2 cells was examined. Telomerase activity was measured using a modified telomeric repeat amplification protocol and telomere length was measured using a solution hybridization-based method and fluorescence in situ hybridization. A reverse transcriptase inhibitor (3'-azido-deoxythymidine or AZT) and an antisense against a component of human telomerase RNA (antisense hTR) were used to inhibit telomerase. FaDu and SKOV-3 cells showed comparable baseline telomerase activity. Telomerase activity in both cells was inhibited about equally by AZT (maximal inhibition of approximately 80%) and by expression of antisense hTR (complete inhibition in SKOV-3 cells and maximal inhibition of approximately 80% in FaDu cells). However, treatment with telomerase inhibitors resulted in approximately 50% telomere shortening in FaDu cells but had no effect on SKOV-3 nor Saos-2 cells. SKOV-3 cells did not show the characteristic features of ALT (i.e. heterogeneous telomere length and promyelocytic leukemia bodies), whereas these ALT features were observed in Saos-2 cells. Collectively, these results suggest the existence of a telomerase-independent mechanism of telomere maintenance in the telomerase-positive SKOV-3 cells.lld:pubmed
pubmed-article:12220625pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12220625pubmed:languageenglld:pubmed
pubmed-article:12220625pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12220625pubmed:citationSubsetIMlld:pubmed
pubmed-article:12220625pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12220625pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12220625pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12220625pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12220625pubmed:statusMEDLINElld:pubmed
pubmed-article:12220625pubmed:monthSeplld:pubmed
pubmed-article:12220625pubmed:issn0014-5793lld:pubmed
pubmed-article:12220625pubmed:authorpubmed-author:AuJessie...lld:pubmed
pubmed-article:12220625pubmed:authorpubmed-author:LuJieJlld:pubmed
pubmed-article:12220625pubmed:authorpubmed-author:GanYueboYlld:pubmed
pubmed-article:12220625pubmed:authorpubmed-author:MoYiqunYlld:pubmed
pubmed-article:12220625pubmed:authorpubmed-author:JohnstonJeffr...lld:pubmed
pubmed-article:12220625pubmed:authorpubmed-author:WientjesM...lld:pubmed
pubmed-article:12220625pubmed:issnTypePrintlld:pubmed
pubmed-article:12220625pubmed:day11lld:pubmed
pubmed-article:12220625pubmed:volume527lld:pubmed
pubmed-article:12220625pubmed:ownerNLMlld:pubmed
pubmed-article:12220625pubmed:authorsCompleteYlld:pubmed
pubmed-article:12220625pubmed:pagination10-4lld:pubmed
pubmed-article:12220625pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:meshHeadingpubmed-meshheading:12220625...lld:pubmed
pubmed-article:12220625pubmed:year2002lld:pubmed
pubmed-article:12220625pubmed:articleTitleTelomere maintenance in telomerase-positive human ovarian SKOV-3 cells cannot be retarded by complete inhibition of telomerase.lld:pubmed
pubmed-article:12220625pubmed:affiliationCollege of Pharmacy, The Ohio State University, 500 West 12th Avenue, Columbus, OH 43210, USA.lld:pubmed
pubmed-article:12220625pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12220625pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:12220625lld:pubmed