Holko Przemyslaw, Ligeza Janusz, Kisielewska Joanna, Kordowiak Anna M, Klein Andrzej
Department of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków.
Pol J Pathol. 2008;59(1):3-8.
Numerous studies have focused on the growth regulation effect of vanadium compounds. In our preliminary investigation we have observed growth inhibition of rat hepatoma cell line H35-19 by inorganic vanadium salts. The aim of the present study was to determine the effect of vanadyl sulphate (VOSO4) on autocrine growth and survival of tumorogenic lung (A549) and prostate (DU145) human cell lines. Additionally, non-carcinogenic human cell lines BEAS-2B (as a lung control) and PNT-2 (as a prostate control) were investigated. MTT, modified crystal violet staining, differential staining (HOECHST33258 and PI) methods and assay for anchorage-independent colony formation were used to investigate the effect of vanadyl sulphate. The results showed that VOSO4 significantly inhibited autocrine growth, decreased carcinoma cells viability and increased the ratio of apoptotic and necrotic cells compared to the controls. However, it should be noted that the examined "drug" significantly decreased viability of non-carcinogenic human cell lines (BEAS-2B, PNT-2).
众多研究聚焦于钒化合物的生长调节作用。在我们的初步研究中,我们观察到无机钒盐对大鼠肝癌细胞系H35 - 19的生长具有抑制作用。本研究的目的是确定硫酸氧钒(VOSO4)对致瘤性人肺(A549)和前列腺(DU145)细胞系自分泌生长和存活的影响。此外,还研究了非致癌性人细胞系BEAS - 2B(作为肺对照)和PNT - 2(作为前列腺对照)。采用MTT法、改良结晶紫染色法、鉴别染色法(HOECHST33258和PI)以及非贴壁依赖性集落形成试验来研究硫酸氧钒的作用效果。结果表明,与对照组相比,VOSO4显著抑制自分泌生长,降低癌细胞活力,并增加凋亡和坏死细胞的比例。然而,应当注意的是,所检测的“药物”显著降低了非致癌性人细胞系(BEAS - 2B、PNT - 2)的活力。