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Variation in K‐ras Codon 12 Point Mutation Rate with Histological Atypia within Individual Colorectal Tumors

机译:大肠肿瘤内组织异型性的K-ras密码子12点突变率变化

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摘要

To elucidate genetic alteration in relation to morphology and also to confirm more directly the proposed adenoma‐carcinoma sequence, we analyzed thirty‐eight colorectal “cancer in adenoma” lesions exhibiting areas of different atypia, in terms of K‐ras codon 12 point mutation. The mutation incidence was 26.3% (10/38) for all cancerous areas. Well‐differentiated and very well‐differentiated carcinoma exhibited values of 17.6% (3/17) and 30.4% (7/23), respectively (statistically not significant). Positive cases of adenoma with severe atypia and adenoma with moderate or slight atypia were 26.7% (8/30) and 8.3% (3/36) respectively (statistically significant). Thus, K‐ras point mutation, as indicated previously, may play an important role in the early stages of colorectal tumorigenesis. As for the nature of the mutation, GGT(Gly) to GAT(Asp) was the most frequent (80%). Eight cases had mutations concurrently in different areas of the same tumor and in all of these the mutation was homogeneous (6 cases to GAT, 1 case to TGT and 1 case to GTT). This provides genetic support for the “adenoma‐carcinoma sequence” theory proposed on the basis of morphological considerations. All lesions with a mutation were of polypoid type, and no mutation was found in the flat type.
机译:为了阐明与形态相关的遗传改变,并更直接地确认拟议的腺瘤-癌序列,我们根据K-ras密码子12点突变分析了38个显示不同异型区域的结直肠“腺瘤癌”病变。所有癌变区域的突变发生率为26.3%(10/38)。高分化和高分化癌分别显示出17.6%(3/17)和30.4%(7/23)的值(统计学上不显着)。重度异型腺瘤和中度或轻度异型腺瘤的阳性病例分别为26.7%(8/30)和8.3%(3/36)(统计学意义)。因此,如前所述,K-ras点突变可能在结直肠肿瘤发生的早期阶段起重要作用。至于突变的性质,GGT(Gly)至GAT(Asp)是最常见的(80%)。 8例在同一肿瘤的不同区域同时发生突变,并且所有突变均是同质的(GAT为6例,TGT为1例,GTT为1例)。这为基于形态学考虑而提出的“腺瘤-癌序列”理论提供了遗传支持。所有具有突变的病变均为息肉状,扁平型未发现突变。

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