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可切除性结直肠癌患者粪便中p53基因的突变

Mutations of the p53 gene in the stool of patients with resectable colorectal cancer.

作者信息

Eguchi S, Kohara N, Komuta K, Kanematsu T

机构信息

Department of Surgery II, Nagasaki University, School of Medicine, Japan.

出版信息

Cancer. 1996 Apr 15;77(8 Suppl):1707-10. doi: 10.1002/(SICI)1097-0142(19960415)77:8<1707::AID-CNCR43>3.0.CO;2-0.

Abstract

BACKGROUND

This study was undertaken to evaluate whether genetic analysis in the stool can be useful for detecting malignant tumors in the colon and rectum. We searched for the possible presence of mutations in the p53 gene in the stool of patients with resectable colorectal cancer. Alterations in the p53 gene are the most frequent among mutant genes related to colorectal cancer.

METHODS

Surgically resected tumor specimens and stool samples from 25 patients with colorectal cancer were examined for mutations of exons 5-8 of the p53 gene by polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP). Results were compared with those achieved by fecal occult blood testing.

RESULTS

Mutations of the p53 gene were found in the tumor tissues in 11 of 25 patients (44%). Of these 11 patients, 7 (64%) had evidence of alterations in the p53 gene within the stool. Of five patients who were negative for fecal occult blood testing, p53 mutations in the stool were evident in three patients.

CONCLUSIONS

This method of stool DNA analysis for tumor-specific mutations is expected to have a wide application in clinical screening for colorectal cancer.

摘要

背景

本研究旨在评估粪便中的基因分析对于检测结肠和直肠癌恶性肿瘤是否有用。我们在可切除的结直肠癌患者的粪便中寻找p53基因可能存在的突变。p53基因的改变是与结直肠癌相关的突变基因中最常见的。

方法

对25例结直肠癌患者手术切除的肿瘤标本和粪便样本,采用聚合酶链反应单链构象多态性(PCR-SSCP)检测p53基因第5-8外显子的突变。将结果与粪便潜血试验的结果进行比较。

结果

25例患者中有11例(44%)肿瘤组织中发现p53基因突变。在这11例患者中,7例(64%)粪便中有p53基因改变的证据。在5例粪便潜血试验阴性的患者中,有3例粪便中有明显的p53基因突变。

结论

这种用于肿瘤特异性突变的粪便DNA分析方法有望在结直肠癌的临床筛查中得到广泛应用。

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