-
Je něco špatně v tomto záznamu ?
Tail spontaneous metastatic mouse model: comparison of metastatic potential of orthotopic and heterotopic models imaged by GFP and RFP protein
V. Bobek, K. Kolostova, D. Pinterova, M. Boubelik, R. Gurlich, RM. Hoffman
Jazyk angličtina Země Řecko
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
Grantová podpora
NS9976
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Free Medical Journals
od 2004 do Před 2 roky
Open Access Digital Library
od 2004-01-01
PubMed
22021676
Knihovny.cz E-zdroje
- MeSH
- karcinom plic Lewisové metabolismus patologie MeSH
- luminescentní proteiny metabolismus MeSH
- melanom experimentální metabolismus patologie MeSH
- metastázy nádorů MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- zelené fluorescenční proteiny metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
Studies over the past decade have clearly shown that s.c. implant of primary and cultured tumor cells rarely leads to the occurrence of metastatic disease. Orthotopic transplantation of cell suspensions, surgical orthotopic implantation (SOI) of cancer tissue fragments resulted in metastases in many cancer types reaching 100% successful rate. We compared two metastatic models - heterotopic model of Lewis lung cancer and orthotopic B16 mouse melanoma. Both models were syngeneic with high metastatic ratio in C57BL/6 mice after transplantation of cancer cells, by injection into subcutaneous region of mice tail and without surgical intervention. The conclusion is that the localisation of cancer cell injection is a crucial condition for metastatic potential. The site with 100% haematogenous and lymph metastasis rate, after simple injection of cancer cells only, has been defined in mice, without dependence on the genetically predisposition and tumor cell line.
AntiCancer Inc San Diego CA USA
Department of Surgery University of California San Diego CA USA
Department of Tumor Biology 3rd Faculty of Medicine Charles University Prague Ruska 87 100 34 Prague
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12022307
- 003
- CZ-PrNML
- 005
- 20160405144950.0
- 007
- ta
- 008
- 120806s2011 gr f 000 0#eng||
- 009
- AR
- 035 __
- $a (PubMed)22021676
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gr
- 100 1_
- $a Bobek, Vladimír $7 xx0162734 $u Department of Tumor Biology, Third Faculty of Medicine Charles University Prague, Ruska 87, 100 34 Prague; Department of Surgery, Third Faculty of Medicine, Charles University and Faculy Hospital Kralovske Vinohrady, Prague, Czech Republic
- 245 10
- $a Tail spontaneous metastatic mouse model: comparison of metastatic potential of orthotopic and heterotopic models imaged by GFP and RFP protein / $c V. Bobek, K. Kolostova, D. Pinterova, M. Boubelik, R. Gurlich, RM. Hoffman
- 520 9_
- $a Studies over the past decade have clearly shown that s.c. implant of primary and cultured tumor cells rarely leads to the occurrence of metastatic disease. Orthotopic transplantation of cell suspensions, surgical orthotopic implantation (SOI) of cancer tissue fragments resulted in metastases in many cancer types reaching 100% successful rate. We compared two metastatic models - heterotopic model of Lewis lung cancer and orthotopic B16 mouse melanoma. Both models were syngeneic with high metastatic ratio in C57BL/6 mice after transplantation of cancer cells, by injection into subcutaneous region of mice tail and without surgical intervention. The conclusion is that the localisation of cancer cell injection is a crucial condition for metastatic potential. The site with 100% haematogenous and lymph metastasis rate, after simple injection of cancer cells only, has been defined in mice, without dependence on the genetically predisposition and tumor cell line.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a karcinom plic Lewisové $x metabolismus $x patologie $7 D018827
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a zelené fluorescenční proteiny $x metabolismus $7 D049452
- 650 _2
- $a luminescentní proteiny $x metabolismus $7 D008164
- 650 _2
- $a melanom experimentální $x metabolismus $x patologie $7 D008546
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a metastázy nádorů $7 D009362
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kološtová, Katarína $7 xx0207726 $u Department of Tumor Biology, Third Faculty of Medicine Charles University Prague, Ruska 87, Prague, Czech Republic
- 700 1_
- $a Pintérová, Daniela $7 xx0102048 $u Department of Tumor Biology, Third Faculty of Medicine Charles University Prague, Ruska 87, Prague, Czech Republic
- 700 1_
- $a Boubelík, Michael, $d -2009 $7 xx0153154 $u Department of Tumor Biology, Third Faculty of Medicine Charles University Prague, Ruska 87, Prague, Czech Republic
- 700 1_
- $a Gürlich, Robert, $d 1964- $7 xx0000272 $u Department of Surgery, Third Faculty of Medicine, Charles University and Faculy Hospital Kralovske Vinohrady, Prague, Czech Republic
- 700 1_
- $a Hoffman, Robert M. $u AntiCancer, Inc, San Diego, CA, USA.; Department of Surgery, University of California, San Diego, CA, USA
- 773 0_
- $w MED00175831 $t In vivo (Athens, Greece) $x 1791-7549 $g Roč. 25, č. 6 (2011), s. 849-852
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22021676 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m $z 0
- 990 __
- $a 20120806 $b ABA008
- 991 __
- $a 20160405145026 $b ABA008
- 999 __
- $a ok $b bmc $g 944220 $s 779604
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 25 $c 6 $d 849-852 $i 1791-7549 $m In Vivo $n In Vivo $x MED00175831
- GRA __
- $a NS9976 $p MZ0
- LZP __
- $b NLK111 $a Pubmed-20120806/12/01