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p53蛋白积累是巴雷特化生恶性潜能的特异性标志物。

p53 Protein accumulation is a specific marker of malignant potential in Barrett's metaplasia.

作者信息

Younes M, Ertan A, Lechago L V, Somoano J R, Lechago J

机构信息

Department of Pathology, Baylor College of Medicine and the Methodist Hospital, Houston, Texas 77030, USA.

出版信息

Dig Dis Sci. 1997 Apr;42(4):697-701. doi: 10.1023/a:1018828207371.

Abstract

Our aim was to determine the sensitivity and specificity of p53 accumulation as a marker of malignant potential in Barrett's metaplasia (BM). One hundred eighty biopsies from 61 patients with BM were evaluated for p53 accumulation by immunohistochemistry. Of 25 patients with LGD, 9 had p53-positive biopsies, and of these 5 (56%) developed HGD/CA, whereas 16 had p53-negative biopsies and none (0%) developed HGD/CA after similar follow-up times (P = 0.0108). As a marker of malignant potential in BM, p53 accumulation has a sensitivity of 100%, specificity of 93%, and a predictive value of a positive test of 0.56, compared to sensitivity of 100%, specificity of 64%, and predictive value of a positive test of 0.2 for a histologic diagnosis of LGD. We conclude that: (1) p53 accumulation is more specific and has better predictive value for subsequent development of HGD/CA than histologic diagnosis of LGD. (2) Patients with LGD and p53-positive biopsies are more likely to develop HGD/CA; therefore, they should be followed up more closely than those with LGD and p53-negative biopsies.

摘要

我们的目的是确定p53蛋白积累作为巴雷特化生(BM)恶性潜能标志物的敏感性和特异性。通过免疫组织化学对61例BM患者的180份活检样本进行p53蛋白积累评估。在25例低级别异型增生(LGD)患者中,9例活检样本p53呈阳性,其中5例(56%)进展为高级别异型增生(HGD)/癌,而16例活检样本p53呈阴性,在相似随访时间后无一例(0%)进展为HGD/癌(P = 0.0108)。作为BM恶性潜能的标志物,与组织学诊断LGD相比,p53蛋白积累的敏感性为100%,特异性为93%,阳性试验预测值为0.56,而组织学诊断LGD的敏感性为100%,特异性为64%,阳性试验预测值为0.2。我们得出结论:(1)与LGD的组织学诊断相比,p53蛋白积累对HGD/癌的后续发生更具特异性且具有更好的预测价值。(2)活检样本p53呈阳性的LGD患者更有可能进展为HGD/癌;因此,与活检样本p53呈阴性的LGD患者相比,对他们应进行更密切的随访。

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