-
Je něco špatně v tomto záznamu ?
Effect of cancer-associated fibroblasts on the migration of glioma cells in vitro
J. Trylcova, P. Busek, K. Smetana, E. Balaziova, B. Dvorankova, A. Mifkova, A. Sedo,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT12237
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
ProQuest Central
od 1997-12-01 do 2015-12-31
Medline Complete (EBSCOhost)
od 2005-01-01 do 2016-12-31
Health & Medicine (ProQuest)
od 1997-12-01 do 2015-12-31
Public Health Database (ProQuest)
od 1997-12-01 do 2015-12-31
ROAD: Directory of Open Access Scholarly Resources
od 1987
- MeSH
- aktiny biosyntéza MeSH
- fibroblasty patologie MeSH
- glioblastom genetika patologie MeSH
- kultivační média speciální * MeSH
- lidé MeSH
- nádorové buněčné linie MeSH
- nádorové mikroprostředí genetika MeSH
- pohyb buněk * MeSH
- proliferace buněk genetika MeSH
- regulace genové exprese u nádorů MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Cancer-associated fibroblasts (CAFs) significantly influence biological properties of many tumors. The role of these mesenchymal cells is also anticipated in human gliomas. To evaluate the putative role of CAFs in glioblastoma, we tested the effect of CAF conditioned media on the proliferation and chemotaxis of glioma cells. The proliferation of glioma cells was stimulated to similar extent by both the normal fibroblasts (NFs) and CAF-conditioned media. Nevertheless, CAF-conditioned media enhanced the chemotactic migration of glioma cells significantly more potently than the media from normal fibroblasts. In order to determine whether CAF-like cells are present in human glioblastomas, immunofluorescence staining was performed on tissue samples from 20 patients using markers typical for CAFs. This analysis revealed regular presence of mesenchymal cells expressing characteristic CAF markers α-smooth muscle actin and TE-7 in human glioblastomas. These observations indicate the potential role of CAF-like cells in glioblastoma biology.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16000254
- 003
- CZ-PrNML
- 005
- 20191015080501.0
- 007
- ta
- 008
- 160108s2015 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s13277-015-3259-8 $2 doi
- 035 __
- $a (PubMed)25712375
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Trylčová, Jana $u Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague, U Nemocnice 5, 128 53, Prague 2, Czech Republic. $7 _AN068677
- 245 10
- $a Effect of cancer-associated fibroblasts on the migration of glioma cells in vitro / $c J. Trylcova, P. Busek, K. Smetana, E. Balaziova, B. Dvorankova, A. Mifkova, A. Sedo,
- 520 9_
- $a Cancer-associated fibroblasts (CAFs) significantly influence biological properties of many tumors. The role of these mesenchymal cells is also anticipated in human gliomas. To evaluate the putative role of CAFs in glioblastoma, we tested the effect of CAF conditioned media on the proliferation and chemotaxis of glioma cells. The proliferation of glioma cells was stimulated to similar extent by both the normal fibroblasts (NFs) and CAF-conditioned media. Nevertheless, CAF-conditioned media enhanced the chemotactic migration of glioma cells significantly more potently than the media from normal fibroblasts. In order to determine whether CAF-like cells are present in human glioblastomas, immunofluorescence staining was performed on tissue samples from 20 patients using markers typical for CAFs. This analysis revealed regular presence of mesenchymal cells expressing characteristic CAF markers α-smooth muscle actin and TE-7 in human glioblastomas. These observations indicate the potential role of CAF-like cells in glioblastoma biology.
- 650 _2
- $a aktiny $x biosyntéza $7 D000199
- 650 _2
- $a nádorové buněčné linie $7 D045744
- 650 12
- $a pohyb buněk $7 D002465
- 650 _2
- $a proliferace buněk $x genetika $7 D049109
- 650 12
- $a kultivační média speciální $7 D017077
- 650 _2
- $a fibroblasty $x patologie $7 D005347
- 650 _2
- $a regulace genové exprese u nádorů $7 D015972
- 650 _2
- $a glioblastom $x genetika $x patologie $7 D005909
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a nádorové mikroprostředí $x genetika $7 D059016
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Bušek, Petr $7 xx0094315
- 700 1_
- $a Smetana, Karel, $d 1958- $7 jn20000710554
- 700 1_
- $a Balážiová, Eva $7 xx0126036
- 700 1_
- $a Dvořánková, Barbora, $d 1955- $7 xx0076196
- 700 1_
- $a Mifková, Alžběta $7 xx0228870
- 700 1_
- $a Šedo, Aleksi, $d 1967- $7 jn20000605245
- 773 0_
- $w MED00008757 $t Tumour biology the journal of the International Society for Oncodevelopmental Biology and Medicine $x 1423-0380 $g Roč. 36, č. 8 (2015), s. 5873-5879
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25712375 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20160108 $b ABA008
- 991 __
- $a 20191015080926 $b ABA008
- 999 __
- $a ok $b bmc $g 1102535 $s 924460
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 36 $c 8 $d 5873-5879 $e 20150225 $i 1423-0380 $m Tumor biology $n Tumor Biol $x MED00008757
- GRA __
- $a NT12237 $p MZ0
- LZP __
- $a Pubmed-20160108