Brychtová V, Šefr R, Hrstka R, Vídeňská P, Bencsiková B, Hanáková B, Zdražilová Dubská L, Nenutil R, Budinská E
Klin Onkol. 2017 Spring;30(Supplementum1):153-155.
Colorectal carcinoma (CRC) is third most common cancer worldwide with very heterogenous character. In most cases, it is caused by sporadic events leading to disruption of epithelial cells of the colon. The minority evolves from germline mutations associated with hereditary cancer syndromes. Mechanisms leading to mutations of oncogenes, tumour suppressors and genes of DNA repair mechanisms include: 1. chromosomal instability, 2. microsatellite instability and 3. CpG island methylator phenotype. Microsatellite instability (MSI) usually arises from a germline mutation of the component of mismatch repair machinery (MMR) or somatic hypermethylation of the MLH1 promoter. The diagnostic approaches include PCR methods and immunohistochemistry for the detection of the loss of MMR part. The aim of our study was to characterise the cohort of ongoing study of gut microbiome in CRC patients considering MSI.
The consecutive study group consisted of 103 patients diagnosed with CRC. The cohort consisted of 45 women (43.7%) and 58 men (56.3%). Patient age at the time of diagnosis was within the range of 31-83 years (median 66 years). The expression of MLH1, MSH2, MSH6 and PMS2 proteins was detected by immunohistochemical method and the positivity was correlated with the stage and the localization of the primary tumour.
The MMR status was determined by immunohistochemical method in 43 (41.7%) from the existing total of 103 patients. MSI was detected in 11 (25.6%) cases while 32 (74.4%) were microsatellite stabile. With the respect to cancer clasification the most cases of MSI was detected in stage II (8 cases; 22.2%). In regard to localization of primary tumour, MSI rather correlates to right site CRC, while microsatellite stable tumours do not show any site preferences.
Considering low number of MMR status determination in study group, statistic evaluation is inaccurate so far. However there is a trend in our cohort in relation to determination of the portion of MSI in CRC population and also in localization of primary tumour according to literature.Key words: colorectal carcinoma - microsatellite instability - Lynch syndrome The work was supported by the project MEYS - NPS I - LO1413 and AZV 16-31966A. The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.Submitted: 13. 3. 2017Accepted: 26. 3. 2017.
结直肠癌(CRC)是全球第三大常见癌症,具有高度异质性。在大多数情况下,它是由导致结肠上皮细胞破坏的散发性事件引起的。少数病例由与遗传性癌症综合征相关的种系突变演变而来。导致癌基因、肿瘤抑制基因和DNA修复机制基因突变的机制包括:1. 染色体不稳定;2. 微卫星不稳定;3. CpG岛甲基化表型。微卫星不稳定(MSI)通常源于错配修复机制(MMR)成分的种系突变或MLH1启动子的体细胞高甲基化。诊断方法包括用于检测MMR部分缺失的PCR方法和免疫组织化学。我们研究的目的是在考虑MSI的情况下,对正在进行的CRC患者肠道微生物组研究队列进行特征描述。
连续研究组由103例诊断为CRC的患者组成。该队列包括45名女性(43.7%)和58名男性(56.3%)。诊断时患者年龄在31 - 83岁之间(中位数66岁)。通过免疫组织化学方法检测MLH1、MSH2、MSH6和PMS2蛋白的表达,并将阳性结果与原发肿瘤的分期和定位相关联。
在现有的103例患者中,通过免疫组织化学方法确定了43例(41.7%)的MMR状态。检测到11例(25.6%)为MSI,32例(74.4%)为微卫星稳定。就癌症分期而言,MSI在II期检测到的病例最多(8例;22.2%)。关于原发肿瘤的定位,MSI与右半结肠癌的相关性更高,而微卫星稳定的肿瘤没有显示出任何部位偏好。
考虑到研究组中MMR状态确定的病例数较少,目前统计评估不准确。然而,在我们的队列中,存在一种趋势,即根据文献确定CRC人群中MSI的比例以及原发肿瘤的定位。关键词:结直肠癌 - 微卫星不稳定 - 林奇综合征 本研究得到了项目MEYS - NPS I - LO1413和AZV 16 - 31966A的支持。作者声明他们在研究中使用的药物、产品或服务方面没有潜在的利益冲突。编辑委员会声明该手稿符合ICMJE对生物医学论文的建议。提交日期:2017年3月13日 接受日期:2017年3月26日