Brown S R, Finan P J, Cawkwell L, Quirke P, Bishop D T
Centre for Digestive Diseases, Leeds General Infirmary, Leeds, UK.
Gut. 1998 Oct;43(4):553-7. doi: 10.1136/gut.43.4.553.
Replication errors (RERs) characterise tumours of hereditary non-polyposis colorectal cancer (HNPCC). RER status may therefore improve identification of such families previously diagnosed by family history alone.
To assess RER and HNPCC frequency within a population of colorectal cancer patients and a regional population of family history defined (Amsterdam criteria) HNPCC families.
Family history was assessed by personal interview in a population of 479 patients with colorectal cancer attending one follow up clinic. Seven fluorescently labelled microsatellites were used to investigate RER frequency in colorectal cancers from 89 patients of this population with varying degrees of family history and 20 Amsterdam criteria positive families (four with a known germline mutation, 16 with unknown mutation status) from the regional population.
Only four of the follow up population (0.8%) came from families meeting the Amsterdam criteria with only one showing RERs. The frequency of RERs was similar in the early onset cancer group (less than 50 years of age), those with a family history, and those with no family history of colorectal cancer. From the regional population, RERs were identified in 4/4 families with a mutation but only 8/16 families with unknown mutation status.
No correlation was seen between RER status and strength of family history except in HNPCC families. Results also indicate that half of the Amsterdam criteria defined families do not exhibit RERs, perhaps suggesting a different mechanism of tumorigenesis.
复制错误(RERs)是遗传性非息肉病性结直肠癌(HNPCC)肿瘤的特征。因此,RER状态可能有助于更好地识别那些之前仅通过家族史诊断的此类家族。
评估结直肠癌患者群体以及符合家族史定义(阿姆斯特丹标准)的HNPCC家族的区域群体中的RER和HNPCC频率。
通过个人访谈对一家随访诊所的479例结直肠癌患者进行家族史评估。使用七个荧光标记的微卫星来研究该群体中89例具有不同家族史程度的患者的结直肠癌中的RER频率,以及来自区域群体的20个符合阿姆斯特丹标准的阳性家族(4个有已知种系突变,16个突变状态未知)中的RER频率。
随访人群中只有4例(0.8%)来自符合阿姆斯特丹标准的家族,其中只有1例显示RERs。RERs频率在早发性癌症组(年龄小于50岁)、有家族史的患者以及无结直肠癌家族史的患者中相似。在区域群体中,在4个有突变的家族中发现了RERs,但在16个突变状态未知的家族中只有8个发现了RERs。
除了在HNPCC家族中,未发现RER状态与家族史强度之间存在相关性。结果还表明,符合阿姆斯特丹标准的家族中有一半没有表现出RERs,这可能暗示了一种不同的肿瘤发生机制。