首页> 外文期刊>Endocrine Research >Expression of insulin-like growth factor I (IGF-I) gene and of genes for IGF-binding proteins 1, 2, 3, 4 (IGFBP-1-IGFBP-4) in non-neoplastic human thyroid cells and in certain human thyroid cancers. Effect of exogenous IGF-I on this expression.
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Expression of insulin-like growth factor I (IGF-I) gene and of genes for IGF-binding proteins 1, 2, 3, 4 (IGFBP-1-IGFBP-4) in non-neoplastic human thyroid cells and in certain human thyroid cancers. Effect of exogenous IGF-I on this expression.

机译:胰岛素样生长因子I(IGF-1)基因和IGF结合蛋白1、2、3、4(IGFBP-1-IGFBP-4)的基因在非肿瘤性人类甲状腺细胞和某些人类甲状腺中的表达癌症。外源IGF-1对此表达的影响。

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AIM: The aim of this study was to examine the expression of the IGF-I gene and of genes for IGFBP-1, -2, -3, and -4 in cells from nodular goiters (NG), and from different human thyroid carcinomas (papillary--PTC, anaplastic--ATC, and medullary--MTC), cultured in monolayers. The influence, exerted by exogenous IGF-I on the expression of these genes, was also investigated. METHODS: Thyroid tissue specimens were obtained from 65 patients during subtotal or total thyroidectomies. After approximately 2-3 weeks of culture, thyroid cells were incubated for 24 hours with IGF-I in concentrations of: 0, 1, 10 and 100 ng/ml. The total mRNA was isolated according to the method described by Chomczynski and Sacchi with our own modifications. Afterwards, mRNA encoding IGF-I, IGFBP-1-IGFBP-4 and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), were amplified, using the reverse transcription-polymerase chain reaction (RT-PCR); GAPDH gene served as a control gene. PCR products were electrophoresed and then submitted todensitometric analysis. RESULTS AND CONCLUSIONS: Our study has shown that in carcinoma cells (ATC, PTC, MTC), IGF-I reveals a stimulatory influence on the expression of its own gene, that effect being most distinctive in ATC cells. These facts indicate an important role of IGF-I in the pathogenesis and invasiveness of the analyzed malignant neoplasms.
机译:目的:本研究的目的是检查结节性甲状腺肿(NG)和人类甲状腺癌细胞中IGF-I基因和IGFBP-1,-2,-3和-4基因的表达(乳头-PTC,间变性-ATC和髓样-MTC),以单层培养。还研究了外源性IGF-1对这些基因表达的影响。方法:从65例甲状腺小结或全甲状腺切除术患者中获取甲状腺组织标本。培养约2-3周后,将甲状腺细胞与浓度为0、1、10和100 ng / ml的IGF-I孵育24小时。根据Chomczynski和Sacchi描述的方法,用我们自己的修饰分离总mRNA。然后,使用逆转录-聚合酶链反应(RT-PCR)扩增编码IGF-I,IGFBP-1-IGFBP-4和甘油醛-3-磷酸脱氢酶(GAPDH)的mRNA; GAPDH基因用作对照基因。对PCR产物进行电泳,然后进行光密度分析。结果与结论:我们的研究表明,在癌细胞(ATC,PTC,MTC)中,IGF-I揭示了对其自身基因表达的刺激作用,这种作用在ATC细胞中最为明显。这些事实表明IGF-I在所分析的恶性肿瘤的发病机理和侵袭性中具有重要作用。

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