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作为鉴定结直肠癌中DNA杂合性缺失技术的Southern印迹法与聚合酶链反应的比较。

A comparison of Southern blot and polymerase chain reaction as techniques to identify loss of DNA heterozygosity in colorectal cancer.

作者信息

Hewett P J, Firgaira F, Morley A

机构信息

Department of Surgery, Flinders Medical Centre, Bedford Park, South Australia.

出版信息

Aust N Z J Surg. 1994 Aug;64(8):556-7. doi: 10.1111/j.1445-2197.1994.tb02285.x.

Abstract

Alterations in the tumour suppressor gene p53 have been found in a wide variety of tumours. The variable number tandem repeat present at the YNZ22 locus is a highly polymorphic marker closely linked to the p53 gene. Examination for loss of heterozygosity at the YNZ22 locus has been carried out by Southern blot or polymerase chain reaction (PCR). A comparison of these techniques shows a 100% concordance rate in normal tissue but a 90.9% rate in tumour tissue. Both false positive and false negative results were obtained. This must be considered in the interpretation of studies using PCR for this purpose.

摘要

在多种肿瘤中都发现了肿瘤抑制基因p53的改变。位于YNZ22位点的可变数目串联重复序列是一种与p53基因紧密连锁的高度多态性标记。通过Southern印迹法或聚合酶链反应(PCR)对YNZ22位点的杂合性缺失进行检测。对这些技术的比较显示,在正常组织中一致性率为100%,而在肿瘤组织中为90.9%。同时获得了假阳性和假阴性结果。在解释为此目的使用PCR的研究时必须考虑到这一点。

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