About: Autophagy is preferred pathway of camptothecin-induced programmed cell death of v-myb-transformed monoblasts     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
Description
  • A damage of programmed cell death pathways is a frequent event during malignant transformation. In this study, we analyzed programmed cell daeth (PCD) in v-myb-transformed BM2 and human U937 promonocytes induced by arsenic trioxide,cycloheximide and camtothecin. The presence of functional v-Myb protein pre-determined the BM2 cells to autophagic pathway of PCD in response to the DNA-damaging agents. The absence of transactivating v-Myb protein allowed activation of PCD pathway marked by mitochondrial membrane depolarization and resulting in necrosis. the fact that the antiapoptotic function of the Myb protein can be overcome by alternative PCD pathway suggests that understanding of molecular mechanisms of autophagy could improve therapy of cancer cells suffering from defective apoptosis.
  • A damage of programmed cell death pathways is a frequent event during malignant transformation. In this study, we analyzed programmed cell daeth (PCD) in v-myb-transformed BM2 and human U937 promonocytes induced by arsenic trioxide,cycloheximide and camtothecin. The presence of functional v-Myb protein pre-determined the BM2 cells to autophagic pathway of PCD in response to the DNA-damaging agents. The absence of transactivating v-Myb protein allowed activation of PCD pathway marked by mitochondrial membrane depolarization and resulting in necrosis. the fact that the antiapoptotic function of the Myb protein can be overcome by alternative PCD pathway suggests that understanding of molecular mechanisms of autophagy could improve therapy of cancer cells suffering from defective apoptosis. (en)
  • Malignitransfrmaci často doprovází poškození drah programované buněčné smri (PCD). V této práci jsme analyzovali PCD monoblastů transformovaných v-myb a promonocytů U937, která byla indukována oxidem adrzenitým, cykloheximidem a kamptotecinem. Přítomnost funkčního proteinu v-Myb predeterminovala buňky BM2 vystavená činidlům poškozujícím DNA k PCD autofagií. Nepřítomnost funkčního proteinu v-Myb umožnila aktivaci dráhy PCD doprovázené depolarizací mitochondriální membrány a vedoucí k nekróze. Fakt, že antiapoptotická funkce onkoproteinu v-Myb může být překonána indukcí alternativní dráhy PCD naznačuje, že pochopení molekulárníchmechanismů autofagie by mohlo přispět ke zlepšení terapie nádorových buněk se sníženou schopností apoptózy. (cs)
Title
  • Autophagy is preferred pathway of camptothecin-induced programmed cell death of v-myb-transformed monoblasts
  • Monoblasty transformované onkogenem v-myb a ovlivněné kamptotecinem odumírají autofagií (cs)
  • Autophagy is preferred pathway of camptothecin-induced programmed cell death of v-myb-transformed monoblasts (en)
skos:prefLabel
  • Autophagy is preferred pathway of camptothecin-induced programmed cell death of v-myb-transformed monoblasts
  • Monoblasty transformované onkogenem v-myb a ovlivněné kamptotecinem odumírají autofagií (cs)
  • Autophagy is preferred pathway of camptothecin-induced programmed cell death of v-myb-transformed monoblasts (en)
skos:notation
  • RIV/00216224:14310/05:00012715!RIV06-MSM-14310___
http://linked.open.../vavai/riv/strany
  • S49-S50
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA301/03/1055), Z(MSM0021622415)
http://linked.open...iv/cisloPeriodika
  • Suppl. 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 513424
http://linked.open...ai/riv/idVysledku
  • RIV/00216224:14310/05:00012715
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • v-Myb; apoptosis; autophagy; camptohecin (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • CZ - Česká republika
http://linked.open...ontrolniKodProRIV
  • [DA37B8B59D9F]
http://linked.open...i/riv/nazevZdroje
  • Journal of Applied Biomedicine
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 3/2005
http://linked.open...iv/tvurceVysledku
  • Horváth, Viktor
  • Souček, Karel
  • Šmarda, Jan
  • Ondroušková, Eva
http://linked.open...n/vavai/riv/zamer
issn
  • 1214-0287
number of pages
http://localhost/t...ganizacniJednotka
  • 14310
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 75 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software