Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Exosomes produced by melanoma cells significantly influence the biological properties of normal and cancer-associated fibroblasts

K. Strnadová, L. Pfeiferová, P. Přikryl, B. Dvořánková, E. Vlčák, J. Frýdlová, M. Vokurka, J. Novotný, J. Šáchová, M. Hradilová, J. Brábek, J. Šmigová, D. Rösel, K. Smetana, M. Kolář, L. Lacina

. 2022 ; 157 (2) : 153-172. [pub] 20211127

Jazyk angličtina Země Německo

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc22011151

Grantová podpora
No. 19-05048S Czech Science Foundation project
project CZ.02.1.01/0.0/0.0/16_019/0000785 "Centre for Tumour Ecology-Research of the Cancer Microenvironment Supporting Cancer Growth Spread" Operational Programme "Research, Development and Education"
PROGRESS Q28 Univerzita Karlova v Praze
CZ.02.1.01/0.0/0.0/16_013/0001775 ERDF
CZ.02.1.01/0.0/0.0/18_046/0016045 ERDF
LM2018129 MEYS

E-zdroje Online Plný text

NLK ProQuest Central od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2000-01-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest) od 1997-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1997-01-01 do Před 1 rokem
Public Health Database (ProQuest) od 1997-01-01 do Před 1 rokem

The incidence of cutaneous malignant melanoma is increasing worldwide. While the treatment of initial stages of the disease is simple, the advanced disease frequently remains fatal despite novel therapeutic options . This requires identification of novel therapeutic targets in melanoma. Similarly to other types of tumours, the cancer microenvironment plays a prominent role and determines the biological properties of melanoma. Importantly, melanoma cell-produced exosomes represent an important tool of intercellular communication within this cancer ecosystem. We have focused on potential differences in the activity of exosomes produced by melanoma cells towards melanoma-associated fibroblasts and normal dermal fibroblasts. Cancer-associated fibroblasts were activated by the melanoma cell-produced exosomes significantly more than their normal counterparts, as assessed by increased transcription of genes for inflammation-supporting cytokines and chemokines, namely IL-6 or IL-8. We have observed that the response is dependent on the duration of the stimulus via exosomes and also on the quantity of exosomes. Our study demonstrates that melanoma-produced exosomes significantly stimulate the tumour-promoting proinflammatory activity of cancer-associated fibroblasts. This may represent a potential new target of oncologic therapy .

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc22011151
003      
CZ-PrNML
005      
20240305135130.0
007      
ta
008      
220425s2022 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00418-021-02052-2 $2 doi
035    __
$a (PubMed)34837514
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Strnadová, Karolína $u Institute of Anatomy, 1st Faculty of Medicine, Charles University, 128 00, Prague 2, Czech Republic $u BIOCEV, 1st Faculty of Medicine, Charles University, 25250, Vestec, Czech Republic
245    10
$a Exosomes produced by melanoma cells significantly influence the biological properties of normal and cancer-associated fibroblasts / $c K. Strnadová, L. Pfeiferová, P. Přikryl, B. Dvořánková, E. Vlčák, J. Frýdlová, M. Vokurka, J. Novotný, J. Šáchová, M. Hradilová, J. Brábek, J. Šmigová, D. Rösel, K. Smetana, M. Kolář, L. Lacina
520    9_
$a The incidence of cutaneous malignant melanoma is increasing worldwide. While the treatment of initial stages of the disease is simple, the advanced disease frequently remains fatal despite novel therapeutic options . This requires identification of novel therapeutic targets in melanoma. Similarly to other types of tumours, the cancer microenvironment plays a prominent role and determines the biological properties of melanoma. Importantly, melanoma cell-produced exosomes represent an important tool of intercellular communication within this cancer ecosystem. We have focused on potential differences in the activity of exosomes produced by melanoma cells towards melanoma-associated fibroblasts and normal dermal fibroblasts. Cancer-associated fibroblasts were activated by the melanoma cell-produced exosomes significantly more than their normal counterparts, as assessed by increased transcription of genes for inflammation-supporting cytokines and chemokines, namely IL-6 or IL-8. We have observed that the response is dependent on the duration of the stimulus via exosomes and also on the quantity of exosomes. Our study demonstrates that melanoma-produced exosomes significantly stimulate the tumour-promoting proinflammatory activity of cancer-associated fibroblasts. This may represent a potential new target of oncologic therapy .
650    _2
$a exozómy $x metabolismus $7 D055354
650    _2
$a fibroblasty $x metabolismus $x patologie $7 D005347
650    _2
$a lidé $7 D006801
650    _2
$a melanom experimentální $x metabolismus $x patologie $7 D008546
650    _2
$a nádorové buňky kultivované $7 D014407
655    _2
$a časopisecké články $7 D016428
700    1_
$a Pfeiferová, Lucie $u Laboratory of Genomics and Bioinformatics, Institute of Molecular Genetics of the Czech Academy of Sciences, 142 20, Prague 4, Czech Republic $u Department of Informatics and Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Prague, Czech Republic $7 xx0314741
700    1_
$a Přikryl, Petr $u Institute of Pathological Physiology, 1st Faculty of Medicine, Charles University, 128 00, Praha, Czech Republic
700    1_
$a Dvořánková, Barbora $u Institute of Anatomy, 1st Faculty of Medicine, Charles University, 128 00, Prague 2, Czech Republic $u BIOCEV, 1st Faculty of Medicine, Charles University, 25250, Vestec, Czech Republic
700    1_
$a Vlčák, Erik $u Electron Microscopy Core Facility, Institute of Molecular Genetics of the Czech Academy of Sciences, 142 20, Prague 4, Czech Republic
700    1_
$a Frýdlová, Jana $u Institute of Pathological Physiology, 1st Faculty of Medicine, Charles University, 128 00, Praha, Czech Republic
700    1_
$a Vokurka, Martin $u Institute of Pathological Physiology, 1st Faculty of Medicine, Charles University, 128 00, Praha, Czech Republic
700    1_
$a Novotný, Jiří $u Laboratory of Genomics and Bioinformatics, Institute of Molecular Genetics of the Czech Academy of Sciences, 142 20, Prague 4, Czech Republic $u Department of Informatics and Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Prague, Czech Republic
700    1_
$a Šáchová, Jana $u Laboratory of Genomics and Bioinformatics, Institute of Molecular Genetics of the Czech Academy of Sciences, 142 20, Prague 4, Czech Republic
700    1_
$a Hradilová, Miluše $u Laboratory of Genomics and Bioinformatics, Institute of Molecular Genetics of the Czech Academy of Sciences, 142 20, Prague 4, Czech Republic
700    1_
$a Brábek, Jan $u BIOCEV, Faculty of Sciences, Charles University, 25250, Vestec, Czech Republic
700    1_
$a Šmigová, Jana $u BIOCEV, Faculty of Sciences, Charles University, 25250, Vestec, Czech Republic
700    1_
$a Rösel, Daniel $u BIOCEV, Faculty of Sciences, Charles University, 25250, Vestec, Czech Republic
700    1_
$a Smetana, Karel $u Institute of Anatomy, 1st Faculty of Medicine, Charles University, 128 00, Prague 2, Czech Republic $u BIOCEV, 1st Faculty of Medicine, Charles University, 25250, Vestec, Czech Republic
700    1_
$a Kolář, Michal $u Laboratory of Genomics and Bioinformatics, Institute of Molecular Genetics of the Czech Academy of Sciences, 142 20, Prague 4, Czech Republic. michal.kolar@img.cas.cz $u Department of Informatics and Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Prague, Czech Republic. michal.kolar@img.cas.cz
700    1_
$a Lacina, Lukáš $u Institute of Anatomy, 1st Faculty of Medicine, Charles University, 128 00, Prague 2, Czech Republic. lukas.lacina@lf1.cuni.cz $u BIOCEV, 1st Faculty of Medicine, Charles University, 25250, Vestec, Czech Republic. lukas.lacina@lf1.cuni.cz $u Department of Dermatovenereology, 1st Faculty of Medicine, Charles University and General University Hospital, 120 00, Prague 2, Czech Republic. lukas.lacina@lf1.cuni.cz $1 https://orcid.org/0000000217509933 $7 xx0106429
773    0_
$w MED00002042 $t Histochemistry and cell biology $x 1432-119X $g Roč. 157, č. 2 (2022), s. 153-172
856    41
$u https://pubmed.ncbi.nlm.nih.gov/34837514 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20220425 $b ABA008
991    __
$a 20240305135126 $b ABA008
999    __
$a ok $b bmc $g 1788973 $s 1162349
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2022 $b 157 $c 2 $d 153-172 $e 20211127 $i 1432-119X $m Histochemistry and cell biology $n Histochem Cell Biol $x MED00002042
GRA    __
$a No. 19-05048S $p Czech Science Foundation project
GRA    __
$a project CZ.02.1.01/0.0/0.0/16_019/0000785 "Centre for Tumour Ecology-Research of the Cancer Microenvironment Supporting Cancer Growth Spread" $p Operational Programme "Research, Development and Education"
GRA    __
$a PROGRESS Q28 $p Univerzita Karlova v Praze
GRA    __
$a CZ.02.1.01/0.0/0.0/16_013/0001775 $p ERDF
GRA    __
$a CZ.02.1.01/0.0/0.0/18_046/0016045 $p ERDF
GRA    __
$a LM2018129 $p MEYS
LZP    __
$a Pubmed-20220425

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...