Mutations of p53 in morphologically non-neoplastic mucosa of long-standing ulcerative colitis

被引:15
作者
Takaku, H
Ajioka, Y
Watanabe, H
Hashidate, H
Yamada, S
Yokoyama, J
Kazama, S
Suda, T
Hatakeyama, K
机构
[1] Niigata Univ, Sch Med, Dept Pathol 1, Niigata 9518510, Japan
[2] Niigata Univ, Sch Med, Dept Surg 1, Niigata 9518510, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2001年 / 92卷 / 02期
关键词
ulcerative colitis; colorectal cancer; dysplasia; p53; K-ras;
D O I
10.1111/j.1349-7006.2001.tb01073.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Two cases of ulcerative colitis (UC)-associated carcinoma or dysplasia and morphologically non-neoplastic mucosa with p53 protein overexpression ((MNNM-p53OE) were selected. DNA was extracted from the paraffin blocks of these lesions and exons 5-8 of the p53 gene were analyzed by PCR and direct sequencing, In addition, mutations in K-ras codon 12 were analyzed by PCR-RFLP methods, MNNM-p53OE was located surrounding and adjoining a coexisting carcinoma and/or dysplasia. A p53 mutation was detected in 12/22 (54.5%) MNNM-p53OE samples, 4/8 (50%) dysplasia samples and 8/8 (100%) carcinoma samples. The p53 mutations detected in MNNM-p53OE were identical to those demonstrated in the adjoining carcinoma and/or dysplasia. No K-ras codon 12 mutation was detected in ang of the samples. These results indicate that MNNM-p53OE mag share an identical clonal linkage with a coexisting carcinoma and/or dysplasia, and may be an initial and submorphological form of UC-associated neoplasia, Recognition of MNNM-p53OE in biopsy specimens may help to identify patients with UC at risk of developing colorectal carcinoma.
引用
收藏
页码:119 / 126
页数:8
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