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利用cDNA微阵列鉴定横纹肌肉瘤分化过程中表达的新基因。

Identification of novel genes expressed during rhabdomyosarcoma differentiation using cDNA microarrays.

作者信息

Carey Kate A, Segal David, Klein Reuben, Sanigorski Andrew, Walder Ken, Collier Gregory R, Cameron-Smith David

机构信息

Center for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Deakin University, Melbourne, Australia.

出版信息

Pathol Int. 2006 May;56(5):246-55. doi: 10.1111/j.1440-1827.2006.01958.x.

Abstract

Rhabdomyosarcomas (RMS) are highly aggressive tumors that are thought to arise as a consequence of the regulatory disruption of the growth and differentiation of skeletal muscle progenitor cells. Normal myogenesis is characterized by the expression of the myogenic regulatory factor gene family but, despite their expression in RMS, these tumor cells fail to complete the latter stages of myogenesis. The RMS cell line RD-A was treated with 12-O-tetradecanoylphorbol-13-acetate to induce differentiation and cultured for 10 days. RNA was extracted on days 1, 3, 6, 8 and 10. A human skeletal muscle cDNA microarray was developed and used to analyze the global gene expression of RMS tumors over the time-course of differentiation. As a comparison, the genes identified were subsequently examined during the differentiated primary human skeletal muscle cultures. Prothymosin alpha (PTMA), and translocase of inner mitochondrial membrane 10 (Tim10), two genes not previously implicated in RMS, showed reduced expression during differentiation. Marked differences in the expression of PTMA and Tim10 were observed during the differentiation of human primary skeletal muscle cells. These results identify several new genes with potential roles in the myogenic arrest present in rhabdomyosarcoma. PTMA expression in RMS biopsy samples might prove to be an effective diagnostic marker for this disease.

摘要

横纹肌肉瘤(RMS)是极具侵袭性的肿瘤,被认为是骨骼肌祖细胞生长和分化的调节紊乱所致。正常的肌生成以肌源性调节因子基因家族的表达为特征,然而,尽管这些肿瘤细胞在RMS中表达了这些基因,但它们未能完成肌生成的后期阶段。用12-O-十四酰佛波醇-13-乙酸酯处理RMS细胞系RD-A以诱导分化,并培养10天。在第1、3、6、8和10天提取RNA。开发了一种人类骨骼肌cDNA微阵列,并用于分析RMS肿瘤在分化时间过程中的整体基因表达。作为比较,随后在分化的原代人类骨骼肌培养物中检查鉴定出的基因。原胸腺素α(PTMA)和线粒体内膜转位酶10(Tim10)这两个以前未与RMS相关的基因,在分化过程中表达降低。在人类原代骨骼肌细胞分化过程中观察到PTMA和Tim10表达的显著差异。这些结果确定了几个在横纹肌肉瘤中存在的肌生成停滞中具有潜在作用的新基因。RMS活检样本中的PTMA表达可能被证明是该疾病的有效诊断标志物。

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