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使用一种新方法检测胰液中低丰度的p16和p53突变:有限稀释PCR的异源双链分析

Detecting low-abundance p16 and p53 mutations in pancreatic juice using a novel assay: heteroduplex analysis of limiting dilution PCRs.

作者信息

Bian Yansong, Matsubayashi Hiroyuki, Li Chung-Pin, Abe Tadayoshi, Canto Marcia, Murphy Kathleen M, Goggins Michael

机构信息

Department of Pathology, The Sol Goldman Center for Pancreatic Cancer Research, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21231, USA.

出版信息

Cancer Biol Ther. 2006 Oct;5(10):1392-9. doi: 10.4161/cbt.5.10.3453. Epub 2006 Oct 30.

Abstract

We have developed a simple, robust, highly-sensitive assay for identifying gene mutations in clinical samples. We applied this assay to detect p53 and p16 mutations in pancreatic juice obtained from patients undergoing evaluation and treatment of pancreatic disease. The assay strategy involves PCR amplifying DNA at limiting dilution (LD-PCR) followed by screening PCR products for mutations using temperature gradient capillary electrophoresis (TGCE). Compared to conventional TGCE, TGCE after LD-PCR significantly increased the number of detectable mutations in pancreatic duct juice. Using LD-PCR, mutations in p53 and/or p16 were found in the pancreatic juice of 12 of 20 individuals with pancreatic cancer compared to only 1 of 8 patients with chronic pancreatitis, 0 of 8 individuals without evidence of pancreatic disease (p<0.02). We conclude that limiting dilution PCR is an effective strategy for improving the detection of mutations in clinical samples and when applied to pancreatic juice to detect mutations of p53 and/or p16, it can help distinguish patients with pancreatic cancer from those without evidence of pancreatic neoplasia.

摘要

我们已经开发出一种简单、可靠、高灵敏度的检测方法,用于鉴定临床样本中的基因突变。我们将此检测方法应用于检测从接受胰腺疾病评估和治疗的患者获取的胰液中的p53和p16基因突变。该检测策略包括在有限稀释条件下进行PCR扩增DNA(LD-PCR),随后使用温度梯度毛细管电泳(TGCE)筛选PCR产物中的突变。与传统TGCE相比,LD-PCR后的TGCE显著增加了胰管液中可检测到的突变数量。使用LD-PCR,在20例胰腺癌患者中,有12例在胰液中发现了p53和/或p16基因突变,而在8例慢性胰腺炎患者中只有1例发现突变,8例无胰腺疾病证据的个体中未发现突变(p<0.02)。我们得出结论,有限稀释PCR是提高临床样本中突变检测的有效策略,当应用于胰液检测p53和/或p16突变时,它有助于区分胰腺癌患者和无胰腺肿瘤证据的患者。

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