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High-throughput live cell imaging reveals differential inhibition of tumor cell proliferation by human fibroblasts

Flaberg, E. (author)
Karolinska Institutet
Markasz, L. (author)
Department of Microbiology, Tumor and Cell Biology (MTC), Center for Integrative Recognition in the Immune System (IRIS), Karolinska Institutet, Stockholm, Sweden
Petranyi, Gabor (author)
Department of Microbiology, Tumor and Cell Biology (MTC), Center for Integrative Recognition in the Immune System (IRIS), Karolinska Institutet, Stockholm, Sweden
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Stuber, G. (author)
Department of Microbiology, Tumor and Cell Biology (MTC), Center for Integrative Recognition in the Immune System (IRIS), Karolinska Institutet, Stockholm, Sweden
Dicsö, F. (author)
Division of Pediatrics, Jósa András County Hospital, Nyíregyháza, Hungary
Alchihabi, N. (author)
Division of Pediatrics, Jósa András County Hospital, Nyíregyháza, Hungary
Oláh, E. (author)
Department of Pediatrics, Medical and Health Science Center, Debrecen University, Debrecen, Hungary
Csízy, I. (author)
Department of Pediatrics, Medical and Health Science Center, Debrecen University, Debrecen, Hungary
Józsa, T. (author)
Department of Pediatrics, Medical and Health Science Center, Debrecen University, Debrecen, Hungary
Andrén, Ove, 1963- (author)
Örebro universitet,Hälsoakademin,Clinic of Urology, Örebro County Council, Örebro, Sweden
Johansson, J-E, 1956- (author)
Örebro universitet,Hälsoakademin,Clinic of Urology, Örebro County Council, Örebro, Sweden
Andersson, Swen-Olof, 1949- (author)
Örebro universitet,Hälsoakademin,Clinic of Urology, Örebro County Council, Örebro, Sweden
Klein, G. (author)
Karolinska Institutet
Szekely, L. (author)
Karolinska Institutet
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 (creator_code:org_t)
2010-12-29
2011
English.
In: International Journal of Cancer. - : Wiley-Blackwell. - 0020-7136 .- 1097-0215. ; 128:12, s. 2793-2802
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Increasing evidence indicates that cancer development requires changes both in the precancerous cells and in their microenvironment. To study one aspect of the microenvironmental control, we departed from Michael Stoker's observation (Stroker et al, J Cell Sci 1966;1:297-310) that normal fibroblasts can inhibit the growth of admixed cancer cells (neighbour suppression). We have developed a high-throughput microscopy and image analysis system permitting the examination of live mixed cell cultures growing on 384-well plates, at the single cell level and over time. We have tested the effect of 107 samples of low passage number (<5) primary human fibroblasts from pediatric and adult donors, on the growth of six human tumor cell lines. Three of the lines were derived from prostate carcinomas, two from lung carcinomas and one was an EBV transformed lymphoblastoid line. Labeled tumor cells were grown in the presence of unlabeled fibroblasts. The majority of the tested fibroblasts inhibited the proliferation of the tumor cells, compared to the control cultures where labeled tumor cells were co-cultured with unlabeled tumor cells. The proliferation inhibiting effect of the fibroblasts differed depending on their site of origin and the age of the donor. Inhibition required direct cell contact. Mouse 3T3 fibroblasts inhibited the growth of SV40-transformed 3T3 cells and human tumor cells, showing that the inhibitory effect could prevail across the species barrier. Our high-throughput system allows the quantitative analysis of the inhibitory effect of fibroblasts on the population level and the exploration of differences depending on the source of the normal cells.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

neighbour suppression; fibroblasts; tumor inhibition; high throughput microscopy

Publication and Content Type

ref (subject category)
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