About: Origin of cells cultured in vitro from human breast carcinomas traced by cyclin D1 and HER2/neu FISH signal numbers     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
Description
  • We investigated if malignant cells in situ additionally characterized by increased numbers of proto-oncogenes can be traced by the FISH method in the ex vivo-derived cultures. In 6 tumors (5 primary tumors, 1 cutaneous metastasis), increased numbers of FISH signals were found in 55-99% of cells. In cell populations maintained for up to 2-6 passages in vitro the incidence of cells with increased FISH signals was found to be low (2-16%). Moreover, the cells with multiplied signals that survived more than one passage in vitro were evidently unable to divide further. However, in all 6 tumors at least a small fraction of cells displaying only two signals of CCND1 or HER2/neu genes was identified directly in invasive tumor structures in the vicinity of cells with multiple signals. Our findings suggest that these invasive tumor cells displaying only two proto-oncogene signals were most probably involved in the initiation and propagation of ex vivo tumor-derived primary cell cultures.
  • We investigated if malignant cells in situ additionally characterized by increased numbers of proto-oncogenes can be traced by the FISH method in the ex vivo-derived cultures. In 6 tumors (5 primary tumors, 1 cutaneous metastasis), increased numbers of FISH signals were found in 55-99% of cells. In cell populations maintained for up to 2-6 passages in vitro the incidence of cells with increased FISH signals was found to be low (2-16%). Moreover, the cells with multiplied signals that survived more than one passage in vitro were evidently unable to divide further. However, in all 6 tumors at least a small fraction of cells displaying only two signals of CCND1 or HER2/neu genes was identified directly in invasive tumor structures in the vicinity of cells with multiple signals. Our findings suggest that these invasive tumor cells displaying only two proto-oncogene signals were most probably involved in the initiation and propagation of ex vivo tumor-derived primary cell cultures. (en)
  • Snažili jsme se zjistit, zda maligní buňky in situ charakterizované ještě zvýšeným počtem protoonkogenů mohou být v ex vivo odvozených kulturách zachyceny metodou FISH. V 6 nádorech (5 primárních nádorů, 1 kožní metastáza) byly zvýšené signály FISH nalezeny v 55-99% buněk. V buněčných populacích udržených až 2-6 pasáží in vitro byl výskyt nalezených zvýšených signálů FISH nízký (2-16%). Navíc buňky se znásobenými signály, které přežily více než jednu pasáž in vitro, se už evidentně nemohly množit. Ve všech 6 nádorech však byla přímo v invazivních strukturách poblíž buněk se znásobenými signály identifikována alespoň malá frakce buněk vykazujících pouze dva signály genů CCND1 či HER2/neu. Naše výsledky naznačují, že invazivní nádorové buňky vykazující pouze dva protoonkogenní signály se pravděpodobně podílely na iniciaci a propagaci primárních buněčných kultur odvozených ex vivo. (cs)
Title
  • Origin of cells cultured in vitro from human breast carcinomas traced by cyclin D1 and HER2/neu FISH signal numbers
  • Origin of cells cultured in vitro from human breast carcinomas traced by cyclin D1 and HER2/neu FISH signal numbers (en)
  • Původ buněk kultivovaných in vitro z buněk lidského karcinomu prsu zjišťovaný počtem signálů FISH pro cyklin D1 a HER2/neu (cs)
skos:prefLabel
  • Origin of cells cultured in vitro from human breast carcinomas traced by cyclin D1 and HER2/neu FISH signal numbers
  • Origin of cells cultured in vitro from human breast carcinomas traced by cyclin D1 and HER2/neu FISH signal numbers (en)
  • Původ buněk kultivovaných in vitro z buněk lidského karcinomu prsu zjišťovaný počtem signálů FISH pro cyklin D1 a HER2/neu (cs)
skos:notation
  • RIV/68378050:_____/05:00001378!RIV06-AV0-68378050
http://linked.open.../vavai/riv/strany
  • 1051;1058
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(NR8145), Z(AV0Z50520514)
http://linked.open...iv/cisloPeriodika
  • 2A
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 535020
http://linked.open...ai/riv/idVysledku
  • RIV/68378050:_____/05:00001378
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • breast carcinomas; primary cultures of carcinoma cells; cyclin D1 and HER2/neu by FISH (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GR - Řecká republika
http://linked.open...ontrolniKodProRIV
  • [82849FD1DE61]
http://linked.open...i/riv/nazevZdroje
  • Anticancer Research
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 25
http://linked.open...iv/tvurceVysledku
  • Veselý, Pavel
  • Matoušková, Eva
  • Brožová, Markéta
  • Chaloupková, Alena
  • Kudláčková, Iva
  • Netíková, I.
http://linked.open...n/vavai/riv/zamer
issn
  • 0250-7005
number of pages
is http://linked.open...avai/riv/vysledek of
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 58 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software