首页> 外文期刊>Teratogenesis, carcinogenesis, and mutagenesis >Evaluation of relationship between chromosome 22 and p53 gene alterations and the subtype of meningiomas by the interphase-FISH technique.
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Evaluation of relationship between chromosome 22 and p53 gene alterations and the subtype of meningiomas by the interphase-FISH technique.

机译:通过相间FISH技术评估22号染色体和p53基因改变与脑膜瘤亚型之间的关系。

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摘要

In this study, we investigated the relationship between genetic alterations such as chromosome 22 aneuploidy and p53 gene deletion, and the pathological types of meningioma of typical and aggressive forms. Thirty-four meningiomas (23 typical and 11 aggressive) were examined by application of fluorescence in situ hybridization (FISH) with chromosome 22 specific alpha satellite probe and a combination of p53 locus specific and chromosome 17 centromere specific alpha satellite probes, to evaluate the chromosome 22 aneuploidy and gain or loss of p53 gene along with chromosome 17. The results showed that, although chromosome 22 aneuploidy was seen in 7 out of 23 typical (30.4%) and 4 out of 11 aggressive meningiomas (36.3%), no p53 deletion was detected in typical meningiomas, and p53 deletion was detected in 3 out of 11 aggressive meningiomas (1 atypical and 2 malignant), which had recurrence. There were no simultaneous occurrences of p53 gene deletions between typical and aggressive meningiomas. The present findings indicate that the loss of chromosome 22 may be involved with tumorogenesis of typical and aggressive meningiomas, while p53 gene deletions may be involved with malignant progression and recurrence in the aggressive meningiomas. Copyright 2002 Wiley-Liss, Inc.
机译:在这项研究中,我们调查了遗传变异(如22号染色体非整倍性和p53基因缺失)与典型和侵袭性脑膜瘤的病理类型之间的关系。通过应用荧光原位杂交(FISH)与22号染色体特异性α卫星探针以及p53基因座特异性和17号染色​​体着丝粒特异性α卫星探针的组合,检查了34种脑膜瘤(典型23例,侵袭性11例),以评估该染色体22个非整倍性以及p53基因的获得或丢失以及17号染色​​体。结果显示,尽管在23个典型(30.4%)中有7个(30.4%)和11个侵袭性脑膜瘤中有4个(36.3%)可见22号染色体非整倍性,但没有p53缺失在典型的脑膜瘤中检测到p53缺失,在11例复发性侵袭性脑膜瘤中有3例(非典型性和2例恶性)中发现了p53缺失。在典型和侵袭性脑膜瘤之间没有同时发生p53基因缺失。目前的发现表明,第22号染色体的丢失可能与典型的和侵袭性脑膜瘤的肿瘤发生有关,而p53基因的缺失可能与侵袭性脑膜瘤的恶性进展和复发有关。版权所有2002 Wiley-Liss,Inc.

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