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Mutations of p53 in Morphologically Non‐neoplastic Mucosa of Long‐standing Ulcerative Colitis

机译:长期溃疡性结肠炎的形态学非肿瘤性黏膜中p53突变

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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/j53 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 any of the samples. These results indicate that MNNM‐p53OE may 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.
机译:选择了2例溃疡性结肠炎(UC)相关癌或不典型增生以及形态学上非肿瘤性黏膜伴p53蛋白过度表达(MNNM-p53OE)的病例。从这些病变的石蜡块中提取DNA,并通过PCR和直接测序分析p53基因的5-8号外显子。另外,通过PCR-RFLP方法分析了K-ras密码子12中的突变。 MNNM-p53OE位于并存的癌和/或不典型增生周围。在12/22(54.5%)的MNNM-p53OE样本,4/8(50%)的不典型增生样本和8/8(100%)的癌症样本中检测到p53突变。在MNNM-p53OE中检测到的/ j53突变与在相邻的癌和/或不典型增生中证实的突变相同。在任何样品中均未检测到K-ras密码子12突变。这些结果表明,MNNM-p53OE可能与并存的癌和/或不典型增生共享相同的克隆连接,并且可能是UC相关性瘤形成的初始和亚形态学形式。在活检标本中识别MNNM-p53OE可能有助于鉴定患有大肠癌风险的UC患者。

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