Transforming growth factor beta expression and transformation of rat lung epithelial cells by crystalline silica (quartz)
Autor: | Ekwere T. Ifon, Umberto Saffiotti, Alan D. Knapton, A. Olufemi Williams |
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Rok vydání: | 1996 |
Předmět: |
Cancer Research
Pathology medicine.medical_specialty biology Transforming growth factor beta biology.organism_classification Molecular biology Epithelium In vitro Malignant transformation Desmoplasia medicine.anatomical_structure Nude mouse Oncology Gene expression medicine biology.protein medicine.symptom Transforming growth factor |
Zdroj: | International Journal of Cancer. 65:639-649 |
ISSN: | 1097-0215 0020-7136 |
DOI: | 10.1002/(sici)1097-0215(19960301)65:5<639::aid-ijc14>3.0.co;2-2 |
Popis: | Crystalline silica (quartz) induces silicosis and associated peripheral lung carcinomas in rats. The role and pattern of expression of transforming growth factor (TGF)-beta1/beta2 mRNA transcripts were investigated in the fetal rat lung epithelial cell line FRLE, its neoplastic transformants and derived tumors in athymic nude mice. FRLE cells, treated with 100 microgram/cm2 of quartz in serum-free medium, gave rise to phenotypically altered, tumorigenic cells. Quartz-treated, transformed and tumorigenic cells, subcultured directly (QTT-C1) or after growth in soft agar (QTT-C2), formed tumors in athymic nude mice (QTT-T1). Cells subcultured from the tumors (QTT-T1C) were also tumorigenic in nude mice (QTT-T2). QTT-T1 and QTT-T2 tumors were poorly differentiated carcinomas with variable amounts of extracellular matrix-associated TGF-beta1 and desmoplasia. For comparison, a tumorigenic cell line derived from FRLE cells transformed with a mutated K-ras plasmid (RT-C1) and cells subcultured from a corresponding nude mouse tumor (RT-T1) and designated RT-T1C were used. Whereas TGF-beta1 and TGF-beta2 inhibited the growth of QTT-T1C and FRLE cells in a dose-dependent fashion, RT-T1C cells, containing an activated ras gene, were relatively unaffected. TGF-beta1 and TGF-beta2 mRNAs were expressed at higher levels in QTT-T1C cells than in FRLE and TR-T1C cells, and there was an increase in TGF-beta type II receptor (TGR-betaR) mRNA expression in QTT-T1C and RT-T1C cells compared to FRLE cells. Carcinomas in nude mice derived from QTT and RT cells and silicosis-associated lung carcinomas induced in rats by intra-tracheal quartz did not express either active or latent forms of TGF-beta1 protein on immunohistochemistry. The disparity between TGF-beta1 mRNA and TGF-beta1 protein expression in QTT tumors may be due to post-transcriptional regulation of TGF-beta1. |
Databáze: | OpenAIRE |
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