• Je něco špatně v tomto záznamu ?

Melanoma cells influence the differentiation pattern of human epidermal keratinocytes

O. Kodet, L. Lacina, E. Krejčí, B. Dvořánková, M. Grim, J. Štork, D. Kodetová, Č. Vlček, J. Šáchová, M. Kolář, H. Strnad, K. Smetana,

. 2015 ; 14 (-) : 1. [pub] 20150105

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc15031531

Grantová podpora
NT13488 MZ0 CEP - Centrální evidence projektů

BACKGROUND: Nodular melanoma is one of the most life threatening tumors with still poor therapeutic outcome. Similarly to other tumors, permissive microenvironment is essential for melanoma progression. Features of this microenvironment are arising from molecular crosstalk between the melanoma cells (MC) and the surrounding cell populations in the context of skin tissue. Here, we study the effect of melanoma cells on human primary keratinocytes (HPK). Presence of MC is as an important modulator of the tumor microenvironment and we compare it to the effect of nonmalignant lowly differentiated cells also originating from neural crest (NCSC). METHODS: Comparative morphometrical and immunohistochemical analysis of epidermis surrounding nodular melanoma (n = 100) was performed. Data were compared to results of transcriptome profiling of in vitro models, in which HPK were co-cultured with MC, normal human melanocytes, and NCSC, respectively. Differentially expressed candidate genes were verified by RT-qPCR. Biological activity of candidate proteins was assessed on cultured HPK. RESULTS: Epidermis surrounding nodular melanoma exhibits hyperplastic features in 90% of cases. This hyperplastic region exhibits aberrant suprabasal expression of keratin 14 accompanied by loss of keratin 10. We observe that MC and NCSC are able to increase expression of keratins 8, 14, 19, and vimentin in the co-cultured HPK. This in vitro finding partially correlates with pseudoepitheliomatous hyperplasia observed in melanoma biopsies. We provide evidence of FGF-2, CXCL-1, IL-8, and VEGF-A participation in the activity of melanoma cells on keratinocytes. CONCLUSION: We conclude that the MC are able to influence locally the differentiation pattern of keratinocytes in vivo as well as in vitro. This interaction further highlights the role of intercellular interactions in melanoma. The reciprocal role of activated keratinocytes on biology of melanoma cells shall be verified in the future.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc15031531
003      
CZ-PrNML
005      
20191014105719.0
007      
ta
008      
151005s2015 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1186/1476-4598-14-1 $2 doi
035    __
$a (PubMed)25560632
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Kodet, Ondřej, $d 1983- $7 xx0170115
245    10
$a Melanoma cells influence the differentiation pattern of human epidermal keratinocytes / $c O. Kodet, L. Lacina, E. Krejčí, B. Dvořánková, M. Grim, J. Štork, D. Kodetová, Č. Vlček, J. Šáchová, M. Kolář, H. Strnad, K. Smetana,
520    9_
$a BACKGROUND: Nodular melanoma is one of the most life threatening tumors with still poor therapeutic outcome. Similarly to other tumors, permissive microenvironment is essential for melanoma progression. Features of this microenvironment are arising from molecular crosstalk between the melanoma cells (MC) and the surrounding cell populations in the context of skin tissue. Here, we study the effect of melanoma cells on human primary keratinocytes (HPK). Presence of MC is as an important modulator of the tumor microenvironment and we compare it to the effect of nonmalignant lowly differentiated cells also originating from neural crest (NCSC). METHODS: Comparative morphometrical and immunohistochemical analysis of epidermis surrounding nodular melanoma (n = 100) was performed. Data were compared to results of transcriptome profiling of in vitro models, in which HPK were co-cultured with MC, normal human melanocytes, and NCSC, respectively. Differentially expressed candidate genes were verified by RT-qPCR. Biological activity of candidate proteins was assessed on cultured HPK. RESULTS: Epidermis surrounding nodular melanoma exhibits hyperplastic features in 90% of cases. This hyperplastic region exhibits aberrant suprabasal expression of keratin 14 accompanied by loss of keratin 10. We observe that MC and NCSC are able to increase expression of keratins 8, 14, 19, and vimentin in the co-cultured HPK. This in vitro finding partially correlates with pseudoepitheliomatous hyperplasia observed in melanoma biopsies. We provide evidence of FGF-2, CXCL-1, IL-8, and VEGF-A participation in the activity of melanoma cells on keratinocytes. CONCLUSION: We conclude that the MC are able to influence locally the differentiation pattern of keratinocytes in vivo as well as in vitro. This interaction further highlights the role of intercellular interactions in melanoma. The reciprocal role of activated keratinocytes on biology of melanoma cells shall be verified in the future.
650    _2
$a dospělí $7 D000328
650    _2
$a senioři $7 D000368
650    12
$a mezibuněčná komunikace $7 D002450
650    12
$a buněčná diferenciace $x genetika $7 D002454
650    _2
$a nádorové buněčné linie $7 D045744
650    _2
$a chemokin CXCL1 $x farmakologie $7 D054360
650    _2
$a epidermis $x patologie $7 D004817
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a fibroblastový růstový faktor 2 $x farmakologie $7 D016222
650    _2
$a stanovení celkové genové exprese $7 D020869
650    _2
$a lidé $7 D006801
650    _2
$a interleukin-8 $x farmakologie $7 D016209
650    _2
$a keratin-10 $x metabolismus $7 D053550
650    _2
$a keratin-14 $x metabolismus $7 D053547
650    _2
$a keratinocyty $x cytologie $x účinky léků $x metabolismus $7 D015603
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a melanocyty $x metabolismus $7 D008544
650    _2
$a melanom $x metabolismus $x patologie $7 D008545
650    _2
$a lidé středního věku $7 D008875
650    _2
$a metastázy nádorů $7 D009362
650    _2
$a proteiny S100 $x metabolismus $7 D009418
650    _2
$a vaskulární endoteliální růstový faktor A $x farmakologie $7 D042461
650    _2
$a epidermální buňky $7 D000078404
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Lacina, Lukáš, $d 1979- $7 xx0106429
700    1_
$a Krejčí, Eliška $7 _AN057197
700    1_
$a Dvořánková, Barbora, $d 1955- $7 xx0076196
700    1_
$a Grim, Miloš, $d 1941- $7 jn20000602504
700    1_
$a Štork, Jiří, $d 1954- $7 jn20000402892
700    1_
$a Nováková Kodetová, Daniela, $d 1953- $7 jo2002104665
700    1_
$a Vlček, Čestmír $7 xx0122524
700    1_
$a Šáchová, Jana $7 xx0114863
700    1_
$a Kolář, Michal $d 1977- $7 xx0253415
700    1_
$a Strnad, Hynek $u 1st Faculty of Medicine, Institute of Anatomy, Charles University in Prague, U Nemocnice 3, CZ-12800 Prague, Czech Republic. strnad@img.cas.cz. $7 xx0125779
700    1_
$a Smetana, Karel, $d 1958- $7 jn20000710554
773    0_
$w MED00008245 $t Molecular cancer $x 1476-4598 $g Roč. 14, č. - (2015), s. 1
856    41
$u https://pubmed.ncbi.nlm.nih.gov/25560632 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20151005 $b ABA008
991    __
$a 20191014110143 $b ABA008
999    __
$a ok $b bmc $g 1092407 $s 914657
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 14 $c - $d 1 $e 20150105 $i 1476-4598 $m Molecular cancer $n Mol Cancer $x MED00008245
GRA    __
$a NT13488 $p MZ0
LZP    __
$a Pubmed-20151005

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...