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Sökning: WFRF:(Berger Klaus) > (2020-2023) > Primary and hTERT-T...

Primary and hTERT-Transduced Mesothelioma-Associated Fibroblasts but Not Primary or hTERT-Transduced Mesothelial Cells Stimulate Growth of Human Mesothelioma Cells

Ries, Alexander (författare)
Medical University of Vienna
Slany, Astrid (författare)
University of Vienna
Pirker, Christine (författare)
Medical University of Vienna
visa fler...
Mader, Johanna C. (författare)
University of Vienna
Mejri, Doris (författare)
Medical University of Vienna
Mohr, Thomas (författare)
Medical University of Vienna,University of Vienna
Schelch, Karin (författare)
Medical University of Vienna
Flehberger, Daniela (författare)
Medical University of Vienna
Maach, Nadine (författare)
Medical University of Vienna
Hashim, Muhammad (författare)
Medical University of Vienna
Hoda, Mir Alireza (författare)
Medical University of Vienna
Dome, Balazs (författare)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,Clinical Chemistry, Malmö,Lund University Research Groups,Semmelweis University,National Korányi Institute for Tuberculosis and Pulmonology, Hungary,Medical University of Vienna
Krupitza, Georg (författare)
Medical University of Vienna
Berger, Walter (författare)
Medical University of Vienna
Gerner, Christopher (författare)
University of Vienna
Holzmann, Klaus (författare)
Medical University of Vienna
Grusch, Michael (författare)
Medical University of Vienna
visa färre...
 (creator_code:org_t)
2023
2023
Engelska.
Ingår i: Cells. - 2073-4409. ; 12:15
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Pleural mesothelioma (PM) is an aggressive malignancy that develops in a unique tumor microenvironment (TME). However, cell models for studying the TME in PM are still limited. Here, we have generated and characterized novel human telomerase reverse transcriptase (hTERT)-transduced mesothelial cell and mesothelioma-associated fibroblast (Meso-CAF) models and investigated their impact on PM cell growth. Pleural mesothelial cells and Meso-CAFs were isolated from tissue of pneumothorax and PM patients, respectively. Stable expression of hTERT was induced by retroviral transduction. Primary and hTERT-transduced cells were compared with respect to doubling times, hTERT expression and activity levels, telomere lengths, proteomes, and the impact of conditioned media (CM) on PM cell growth. All transduced derivatives exhibited elevated hTERT expression and activity, and increased mean telomere lengths. Cell morphology remained unchanged, and the proteomes were similar to the corresponding primary cells. Of note, the CM of primary and hTERT-transduced Meso-CAFs stimulated PM cell growth to the same extent, while CM derived from mesothelial cells had no stimulating effect, irrespective of hTERT expression. In conclusion, all new hTERT-transduced cell models closely resemble their primary counterparts and, hence, represent valuable tools to investigate cellular interactions within the TME of PM.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

conditioned medium
hTERT
human telomerase reverse transcriptase
mesothelioma-associated fibroblasts
pleural mesothelial cells
pleural mesothelioma
tumor microenvironment

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