米托坦
微阵列
微阵列分析技术
肾上腺皮质癌
激素
内科学
生物
内分泌学
类固醇激素
细胞培养
基因表达
基因
癌症研究
化学
医学
生物化学
遗传学
作者
Adrienn Zsippai,Diána Rita Szabó,Zsófia Tömböl,Péter M. Szabó,Katalin Éder,Éva Pállinger,Rolf C. Gaillard,Attila Patócs,Sára Tóth,András Falus,Kàroly Rácz,Péter Igaz
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2012-09-01
卷期号:13 (12): 1351-1361
被引量:30
摘要
AIM: The adrenolytic agent mitotane is widely used in the treatment of adrenocortical cancer; however, its mechanism of action is poorly elucidated. We have studied mitotane-induced mRNA expression changes in the NCI-H295R adrenocortical cancer cell line. MATERIALS & METHODS: Cell viability and hormone assays were used to select the optimal mitotane concentration effectively inhibiting hormone secretion without affecting cell viability. RNA isolated from cultures treated for 48 and 72 h was subjected to Agilent 4×44K microarray platforms. Microarray results were validated by quantitative reverse-transcription PCR. RESULTS: Altogether, 117 significantly differentially expressed genes were detected at 48 h and 72 h (p < 0.05) in mitotane-treated samples relative to controls. Three significantly underexpressed genes involved in steroid hormone biosynthesis (HSD3B1, HSD3B2 and CYP21A2) and four significantly overexpressed genes (GDF15, ALDH1L2, TRIB3 and SERPINE2) have been validated. CONCLUSION: Gene-expression changes might be involved in the adrenal action of mitotane and in the inhibition of hormone secretion.
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