About: Transport and cytotoxicity of paclitaxel, docetaxel, and novel taxanes in human breast cancer cells     Goto   Sponge   NotDistinct   Permalink

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Description
  • Tato studie srovnávává cytotoxicitu a transport paclitaxel a docetaxelu s novými taxany u lidských buněk nádorů prsu. Tyto zkoumané buněčné linie se liší v expresi membránových ABC transportérů. Na základě reverzní transkripční polymerázy bylo odhaleno, že buňky NCI/ADR-RES exprimují vyšší hladinu P glycoproteinu na úrovni mRNA, který chybí u buněk MDA-MB-435, u nich byla zvýšená hladina MRP2. Buňky NCI/ADR/RES jsou hodně rezistentnější vúči paclitaxelu a docetaxelu než buňky MDA-MB-435, ale obě linie podobně senzitivní vúči novým taxanům. Buňky NCI/ADR-RES absorbují přibližně 20krát méně [14C]paclitaxelu, 7 krát méně docetaxelu a přibližně stejně nových taxanů jako buňky MDA-MB-435. SB-T-1103 a SB-T-1216 neovlivňují transport paclitaxelu, ale SB-T-1214 snižuje uptake u obou buňěčných linií. To vede k závěru, že nové taxany nejsou inhibitory P glykoproteinu. (cs)
  • This study compared cytotoxicity and transport of paclitaxel and docetaxel with novel taxanes in human breast cancer cells. The cell lines examined differ expression of ABC membrane transporters. Reverse transcription-polymerase chain reaction revealed that NCI/ADR-RES cells expressed high levels of P-glycoprotein mRNA, which was absent in MDA-MB-435 cells, while the opposite was true for MRP2 mRNA. NCI/ADR-RES cells were more resistant to paclitaxel and to docetaxel than MDA-MB-435 cells, but almost equally sensitive to novel taxanes. This complied with the fact that NCI/ADR-RES cells absorbed almost 20-fold less [14C]paclitaxel, about 7-fold less docetaxel, and almost equal amounts of SB-T-1103, SB-T-1214, and SB-T-1216 as the MDA-MB-435 cells. SB-T-1103 and SB-T-1216 did not influence transport of paclitaxel, but SB-T-1214 decreased [14C]paclitaxel uptake in both cell lines indicating inhibition of uptake. This suggests that the novel taxanes are not inhibitors of P-glycoprotein.
  • This study compared cytotoxicity and transport of paclitaxel and docetaxel with novel taxanes in human breast cancer cells. The cell lines examined differ expression of ABC membrane transporters. Reverse transcription-polymerase chain reaction revealed that NCI/ADR-RES cells expressed high levels of P-glycoprotein mRNA, which was absent in MDA-MB-435 cells, while the opposite was true for MRP2 mRNA. NCI/ADR-RES cells were more resistant to paclitaxel and to docetaxel than MDA-MB-435 cells, but almost equally sensitive to novel taxanes. This complied with the fact that NCI/ADR-RES cells absorbed almost 20-fold less [14C]paclitaxel, about 7-fold less docetaxel, and almost equal amounts of SB-T-1103, SB-T-1214, and SB-T-1216 as the MDA-MB-435 cells. SB-T-1103 and SB-T-1216 did not influence transport of paclitaxel, but SB-T-1214 decreased [14C]paclitaxel uptake in both cell lines indicating inhibition of uptake. This suggests that the novel taxanes are not inhibitors of P-glycoprotein. (en)
Title
  • Transport and cytotoxicity of paclitaxel, docetaxel, and novel taxanes in human breast cancer cells
  • Transport and cytotoxicity of paclitaxel, docetaxel, and novel taxanes in human breast cancer cells (en)
  • Transport a cytotoxicita paclitaxelu, docetaxelu a nových taxanů u lidských buněk nádorů prsu (cs)
skos:prefLabel
  • Transport and cytotoxicity of paclitaxel, docetaxel, and novel taxanes in human breast cancer cells
  • Transport and cytotoxicity of paclitaxel, docetaxel, and novel taxanes in human breast cancer cells (en)
  • Transport a cytotoxicita paclitaxelu, docetaxelu a nových taxanů u lidských buněk nádorů prsu (cs)
skos:notation
  • RIV/68378050:_____/05:00027660!RIV06-AV0-68378050
http://linked.open.../vavai/riv/strany
  • 95;105
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA305/04/0403), P(NL7567), Z(AV0Z50520514)
http://linked.open...iv/cisloPeriodika
  • 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
  • 547137
http://linked.open...ai/riv/idVysledku
  • RIV/68378050:_____/05:00027660
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • taxanes; uptake; ABC transporters (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [737D262FC7FD]
http://linked.open...i/riv/nazevZdroje
  • Naunyn-Schmiedeberg's Archiv of Pharmacology
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
  • 372
http://linked.open...iv/tvurceVysledku
  • Kovář, Jan
  • Truksa, Jaroslav
  • Chen, J.
  • Ehrlichová, Marie
  • Ojima, I.
  • Gut, I.
  • Václavíková, R.
  • Kuznetsova, L. V.
  • Pepe, A.
http://linked.open...n/vavai/riv/zamer
issn
  • 0028-1298
number of pages
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