-
Je něco špatně v tomto záznamu ?
Coupled expression of dipeptidyl peptidase-IV and fibroblast activation protein-α in transformed astrocytic cells
E. Balaziova, P. Busek, J. Stremenova, L. Sromova, E. Krepela, L. Lizcova, A. Sedo
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2011-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
- MeSH
- buněčná diferenciace MeSH
- buněčné extrakty chemie MeSH
- buněčné kultury MeSH
- dipeptidylpeptidasa 4 genetika metabolismus MeSH
- enzymatické testy MeSH
- genetická transkripce MeSH
- lidé MeSH
- membránové proteiny genetika metabolismus MeSH
- messenger RNA genetika metabolismus MeSH
- neuroglie enzymologie metabolismus MeSH
- rekombinantní proteiny genetika metabolismus MeSH
- serinové endopeptidasy genetika metabolismus MeSH
- transformované buněčné linie MeSH
- želatinasy genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Dipeptidyl peptidase-IV (DPP-IV) and fibroblast activation protein-α (FAP) are speculated to participate in the regulation of multiple biological processes, because of their unique enzymatic activity, as well as by non-hydrolytic molecular interactions. At present, the role of DPP-IV and FAP in the development and progression of various types of tumors, including glioblastoma, is intensively studied, and their functional crosstalk is hypothesized. In this article, we describe the correlative expression of DPP-IV and FAP mRNA in primary cell cultures derived from human glioblastoma and associated expression dynamics of both molecules in astrocytoma cell lines depending on culture conditions. Although the molecular mechanisms of DPP-IV and FAP co-regulations remain unclear, uncoupled expression of transgenic DPP-IV and the endogenous FAP suggests that it occurs rather at the transcriptional than at the posttranscriptional level. Understanding of the expressional and functional coordinations of DPP-IV and FAP may help clarify the mechanisms of biological roles of both molecules in transformed astrocytic cells.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12028348
- 003
- CZ-PrNML
- 005
- 20121107063219.0
- 007
- ta
- 008
- 120817e20110428ne f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1007/s11010-011-0828-z $2 doi
- 035 __
- $a (PubMed)21526345
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Balážiová, Eva $7 xx0126036 $u Institute of Biochemistry and Experimental Oncology of the 1st Faculty of Medicine, Charles University in Prague, U Nemocnice 5, Prague 2, 12853, Czech Republic.
- 245 10
- $a Coupled expression of dipeptidyl peptidase-IV and fibroblast activation protein-α in transformed astrocytic cells / $c E. Balaziova, P. Busek, J. Stremenova, L. Sromova, E. Krepela, L. Lizcova, A. Sedo
- 520 9_
- $a Dipeptidyl peptidase-IV (DPP-IV) and fibroblast activation protein-α (FAP) are speculated to participate in the regulation of multiple biological processes, because of their unique enzymatic activity, as well as by non-hydrolytic molecular interactions. At present, the role of DPP-IV and FAP in the development and progression of various types of tumors, including glioblastoma, is intensively studied, and their functional crosstalk is hypothesized. In this article, we describe the correlative expression of DPP-IV and FAP mRNA in primary cell cultures derived from human glioblastoma and associated expression dynamics of both molecules in astrocytoma cell lines depending on culture conditions. Although the molecular mechanisms of DPP-IV and FAP co-regulations remain unclear, uncoupled expression of transgenic DPP-IV and the endogenous FAP suggests that it occurs rather at the transcriptional than at the posttranscriptional level. Understanding of the expressional and functional coordinations of DPP-IV and FAP may help clarify the mechanisms of biological roles of both molecules in transformed astrocytic cells.
- 650 _2
- $a buněčné kultury $7 D018929
- 650 _2
- $a buněčná diferenciace $7 D002454
- 650 _2
- $a buněčné extrakty $x chemie $7 D002457
- 650 _2
- $a transformované buněčné linie $7 D002461
- 650 _2
- $a dipeptidylpeptidasa 4 $x genetika $x metabolismus $7 D018819
- 650 _2
- $a enzymatické testy $7 D057075
- 650 _2
- $a želatinasy $x genetika $x metabolismus $7 D018093
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a membránové proteiny $x genetika $x metabolismus $7 D008565
- 650 _2
- $a neuroglie $x enzymologie $x metabolismus $7 D009457
- 650 _2
- $a messenger RNA $x genetika $x metabolismus $7 D012333
- 650 _2
- $a rekombinantní proteiny $x genetika $x metabolismus $7 D011994
- 650 _2
- $a serinové endopeptidasy $x genetika $x metabolismus $7 D012697
- 650 _2
- $a genetická transkripce $7 D014158
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Busek, Petr
- 700 1_
- $a Stremeňová, Jarmila $7 xx0143383
- 700 1_
- $a Sromova, Lucie $u
- 700 1_
- $a Křepela, Evžen $7 xx0083612
- 700 1_
- $a Lizcova, Libuse
- 700 1_
- $a Šedo, Aleksi, $d 1967- $7 jn20000605245
- 773 0_
- $w MED00003385 $t Molecular and cellular biochemistry $x 1573-4919 $g Roč. 354, č. 1-2 (20110428), s. 283-9
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21526345 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m
- 990 __
- $a 20120817 $b ABA008
- 991 __
- $a 20121107063232 $b ABA008
- 999 __
- $a ok $b bmc $g 950390 $s 785694
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 354 $c 1-2 $d 283-9 $e 20110428 $i 1573-4919 $m Molecular and cellular biochemistry $n Mol Cell Biochem $x MED00003385
- LZP __
- $a Pubmed-20120817/11/04