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1.
Braz. j. med. biol. res ; 43(1): 17-24, Jan. 2010. tab, ilus
Article Dans Anglais | LILACS | ID: lil-535634

Résumé

We have demonstrated that a synthetic DNA enzyme targeting early growth response factor-1 (Egr-1) can inhibit neointimal hyperplasia following vascular injury. However, the detailed mechanism of this inhibition is not known. Thus, the objective of the present study was to further investigate potential inhibitory mechanisms. Catalytic DNA (ED5) and scrambled control DNA enzyme (ED5SCR) were synthesized and transfected into primary cultures of rat vascular smooth muscle cells (VSMCs). VSMC proliferation and DNA synthesis were analyzed by the MTT method and BrdU staining, respectively. Egr-1, TGF-â1, p53, p21, Bax, and cyclin D1 expression was detected by RT-PCR and Western blot. Apoptosis and cell cycle assays were performed by FACS. Green fluorescence could be seen localized in the cytoplasm of 70.6 ± 1.52 and 72 ± 2.73 percent VSMCs 24 h after transfection of FITC-labeled ED5 and ED5SCR, respectively. We found that transfection with ED5 significantly inhibited cultured VSMC proliferation in vitro after 24, 48, and 72 h of serum stimulation, and also effectively decreased the uptake of BrdU by VSMC. ED5 specifically reduced serum-induced Egr-1 expression in VSMCs, further down-regulated the expression of cyclin D1 and TGF-â1, and arrested the cells at G0/G1, inhibiting entry into the S phase. FACS analysis indicated that there was no significant difference in the rate of apoptosis between ED5- and ED5SCR-transfected cells. Thus, ED5 can specifically inhibit Egr-1 expression, and probably inhibits VSMC proliferation by down-regulating the expressions of cyclin D1 and TGF-â1. However, ED5 has no effect on VSMC apoptosis.


Sujets)
Animaux , Rats , Prolifération cellulaire , Cycline D1/métabolisme , Facteur de transcription EGR-1/antagonistes et inhibiteurs , Protéines et peptides de signalisation intercellulaire/physiologie , Muscles lisses vasculaires/cytologie , Facteur de croissance transformant bêta-1/métabolisme , Apoptose/physiologie , Technique de Western , Domaine catalytique/physiologie , Cycline D1/physiologie , ADN , Régulation négative/physiologie , Hyperplasie/prévention et contrôle , Protéines et peptides de signalisation intercellulaire/métabolisme , Rat Wistar , RT-PCR , Tunique intime/anatomopathologie
2.
J Postgrad Med ; 2003 Jul-Sep; 49(3): 246-8
Article Dans Anglais | IMSEAR | ID: sea-116332

Résumé

Malignant fibrous histiocytomas (MFH) as primary renal tumours are rare, with less than 50 cases described in the literature. We report a case of primary renal MFH of giant cell type in a 56-year-old man, who presented with bilateral dull flank pain, intermittent gross haematuria and body weight loss (6 kg in 3 months). Intravenous urography, computerized tomography (CT) and magnetic resonance image (MRI) showed right ureteral stones with mild hydronephrosis, and a solid mass at the lower pole of the left kidney associated with staghorn calculi, as well as tumour thrombi in the left renal vein and inferior vena cava. Left radical nephrectomy and evacuation of tumour thrombi from the left renal vein and inferior vena cava were performed. Histopathologic examination revealed malignant fibrous histiocytoma (MFH) of giant cell type. To the best of our knowledge, this is the first report of primary renal MFH associated with staghorn calculi.


Sujets)
Tumeurs à cellules géantes/complications , Histiocytome fibreux bénin/complications , Humains , Calculs rénaux/complications , Tumeurs du rein/complications , Mâle , Adulte d'âge moyen
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