• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

老年结直肠癌患者中错配修复缺陷表型和V600E BRAF突变的高患病率。

High prevalence of deficient mismatch repair phenotype and the V600E BRAF mutation in elderly patients with colorectal cancer.

作者信息

Aparicio Thomas, Schischmanoff Olivier, Poupardin Cecile, Mary Florence, Soufir Nadem, Barrat Christophe, Bellaiche Guy, Boubaya Marouane, Choudat Laurence, Cucherousset Joel, DesGuetz Gaetan, Wind Philippe, Benamouzig Robert

机构信息

Gastroenterology, Avicenne Hospital, APHP, HUPSSD, Sorbonne-Paris Cité, University Paris 13, Bobigny, France.

Biochemistry, Avicenne Hospital, APHP, HUPSSD, Sorbonne-Paris Cité, University Paris 13, Bobigny, France.

出版信息

J Geriatr Oncol. 2014 Oct 1;5(4):384-8. doi: 10.1016/j.jgo.2014.08.002. Epub 2014 Aug 28.

DOI:10.1016/j.jgo.2014.08.002
PMID:25176643
Abstract

AIMS

Colorectal cancer (CRC) occurs mostly in the elderly. However, the biology of CRC in elderly has been poorly studied. This study examined the prevalence of deficient mismatch repair phenotype (dMMR) and BRAF mutations according to age.

PATIENTS AND METHODS

MMR phenotype was prospectively determined by molecular analysis in patients of all ages undergoing surgery for CRC. BRAF V600E mutation status was analysed in a subset of dMMR tumours.

RESULTS

A total of 754 patients who underwent surgery between 2005 and 2008 were included in the study. Amongst them, 272 (36%) were ≥75years old. The proportion of women <75 was 38% and that ≥75 was 53% (p<0.0001). The prevalence of dMMR was 19.4% in patients ≥75 and 10.7% in patients <75 (p=0.0017). For patients ≥75, the prevalence of dMMR was significantly higher in women than in men (27% vs 10.2%, respectively; p=0.003) but was similar in women and men <75 (12.5% vs 9.7%, respectively; p=0.4). We examined BRAF mutation status in 80 patients with dMMR tumours. The V600E BRAF mutation was significantly more frequent in patients ≥75 than in patients <75 (72.2% vs 11.4%, respectively; p<0.001). In patients ≥75, there was no difference in the prevalence of the BRAF V600E mutation according to sex (78% in women and 70% in men, p=0.9).

CONCLUSIONS

The prevalence of dMMR in CRC is high in patients over 75. In elderly patients, dMMR tumours are significantly more frequent in women than in men. The BRAF mutation is frequent in elderly patients with CRC.

摘要

目的

结直肠癌(CRC)大多发生于老年人。然而,老年CRC的生物学特性研究较少。本研究根据年龄检测错配修复缺陷表型(dMMR)和BRAF突变的发生率。

患者与方法

对所有接受CRC手术的各年龄段患者,通过分子分析前瞻性确定MMR表型。在一部分dMMR肿瘤患者中分析BRAF V600E突变状态。

结果

共有754例在2005年至2008年间接受手术的患者纳入本研究。其中,272例(36%)年龄≥75岁。年龄<75岁的女性比例为38%,年龄≥75岁的女性比例为53%(p<0.0001)。年龄≥75岁患者中dMMR的发生率为19.4%,年龄<75岁患者中为10.7%(p=0.0017)。对于年龄≥75岁的患者,女性dMMR的发生率显著高于男性(分别为27%和10.2%;p=0.003),但年龄<75岁的女性和男性相似(分别为12.5%和9.7%;p=0.4)。我们检测了80例dMMR肿瘤患者的BRAF突变状态。年龄≥75岁患者中V600E BRAF突变显著高于年龄<75岁患者(分别为72.2%和11.4%;p<0.001)。在年龄≥75岁的患者中,BRAF V600E突变的发生率根据性别无差异(女性为78%,男性为70%,p=0.9)。

结论

75岁以上CRC患者中dMMR的发生率较高。在老年患者中,dMMR肿瘤在女性中显著多于男性。BRAF突变在老年CRC患者中很常见。

相似文献

1
High prevalence of deficient mismatch repair phenotype and the V600E BRAF mutation in elderly patients with colorectal cancer.老年结直肠癌患者中错配修复缺陷表型和V600E BRAF突变的高患病率。
J Geriatr Oncol. 2014 Oct 1;5(4):384-8. doi: 10.1016/j.jgo.2014.08.002. Epub 2014 Aug 28.
2
Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancer.DNA错配修复缺陷与泰国散发性结直肠癌患者的良好预后相关。
World J Gastroenterol. 2015 Jan 21;21(3):926-34. doi: 10.3748/wjg.v21.i3.926.
3
Molecular subtypes in early colorectal cancer associated with clinical features and patient prognosis.早期结直肠癌的分子亚型与临床特征和患者预后相关。
Clin Transl Oncol. 2018 Nov;20(11):1422-1429. doi: 10.1007/s12094-018-1874-8. Epub 2018 May 25.
4
Clinicopathological features of mismatch repair protein expression patterns in colorectal cancer.结直肠癌错配修复蛋白表达模式的临床病理特征。
Pathol Res Pract. 2021 Jan;217:153288. doi: 10.1016/j.prp.2020.153288. Epub 2020 Nov 16.
5
Distinct Clinicopathological Patterns of Mismatch Repair Status in Colorectal Cancer Stratified by KRAS Mutations.KRAS 突变分层的结直肠癌错配修复状态的不同临床病理模式
PLoS One. 2015 Jun 4;10(6):e0128202. doi: 10.1371/journal.pone.0128202. eCollection 2015.
6
[Difference analysis of somatic mutations between deficient mismatch repair and proficient mismatch repair gene related with colorectal cancer].[与结直肠癌相关的错配修复缺陷和错配修复正常基因间体细胞突变的差异分析]
Zhonghua Zhong Liu Za Zhi. 2021 Oct 23;43(10):1088-1093. doi: 10.3760/cma.j.cn112152-20190719-00448.
7
Prognostic value of Lynch syndrome, BRAF , and RAS mutational status in dMMR/MSI-H metastatic colorectal cancer in a pooled analysis of Dutch and French cohorts.Lynch 综合征、BRAF 和 RAS 突变状态对荷兰和法国队列汇总分析中错配修复缺陷/微卫星高度不稳定转移性结直肠癌的预后价值。
Cancer Med. 2023 Aug;12(15):15841-15853. doi: 10.1002/cam4.6223. Epub 2023 Jun 16.
8
Clinicopathologic features and prognostic value of KRAS, NRAS and BRAF mutations and DNA mismatch repair status: A single-center retrospective study of 1,834 Chinese patients with Stage I-IV colorectal cancer.KRAS、NRAS 和 BRAF 基因突变及 DNA 错配修复状态的临床病理特征和预后价值:一项中国 1834 例Ⅰ-Ⅳ期结直肠癌患者的单中心回顾性研究。
Int J Cancer. 2019 Sep 15;145(6):1625-1634. doi: 10.1002/ijc.32489. Epub 2019 Jun 22.
9
Increased cancer predisposition in family members of colorectal cancer patients harboring the p.V600E BRAF mutation: a population-based study.结直肠癌患者携带 p.V600E BRAF 突变的家族成员中癌症易感性增加:一项基于人群的研究。
Cancer Epidemiol Biomarkers Prev. 2010 Jul;19(7):1831-9. doi: 10.1158/1055-9965.EPI-10-0055. Epub 2010 Jun 22.
10
New Therapeutic Opportunities Based on DNA Mismatch Repair and BRAF Status in Metastatic Colorectal Cancer.基于DNA错配修复和BRAF状态的转移性结直肠癌新治疗机会
Curr Oncol Rep. 2016 Mar;18(3):18. doi: 10.1007/s11912-016-0504-2.

引用本文的文献

1
Clinical, pathological, and adjuvant chemotherapy use differences among microsatellite unstable and microsatellite stable colon cancers.微卫星不稳定型和微卫星稳定型结肠癌在临床、病理及辅助化疗应用方面的差异。
J Natl Cancer Cent. 2024 Apr 25;4(2):169-175. doi: 10.1016/j.jncc.2024.04.003. eCollection 2024 Jun.
2
FOxTROT2: innovative trial design to evaluate the role of neoadjuvant chemotherapy for treating locally advanced colon cancer in older adults or those with frailty.FOxTROT2:一项创新性试验设计,旨在评估新辅助化疗治疗老年或虚弱局部晚期结肠癌的作用。
ESMO Open. 2023 Feb;8(1):100642. doi: 10.1016/j.esmoop.2022.100642. Epub 2022 Dec 20.
3
Comparison of universal screening in major lynch-associated tumors: a systematic review of literature.
大 Lynch 相关肿瘤的普遍筛查比较:文献系统评价。
Fam Cancer. 2022 Jan;21(1):57-67. doi: 10.1007/s10689-020-00226-w. Epub 2021 Jan 11.
4
Worldwide variation in lynch syndrome screening: case for universal screening in low colorectal cancer prevalence areas.林奇综合征筛查的全球差异:低结直肠癌患病率地区进行普遍筛查的理由。
Fam Cancer. 2021 Apr;20(2):145-156. doi: 10.1007/s10689-020-00206-0. Epub 2020 Sep 11.
5
Effect of Aspirin on Cancer Incidence and Mortality in Older Adults.阿司匹林对老年人癌症发病和死亡的影响。
J Natl Cancer Inst. 2021 Mar 1;113(3):258-265. doi: 10.1093/jnci/djaa114.
6
Clinicopathologic features and prognostic value of KRAS, NRAS and BRAF mutations and DNA mismatch repair status: A single-center retrospective study of 1,834 Chinese patients with Stage I-IV colorectal cancer.KRAS、NRAS 和 BRAF 基因突变及 DNA 错配修复状态的临床病理特征和预后价值:一项中国 1834 例Ⅰ-Ⅳ期结直肠癌患者的单中心回顾性研究。
Int J Cancer. 2019 Sep 15;145(6):1625-1634. doi: 10.1002/ijc.32489. Epub 2019 Jun 22.
7
Genetic and immunological biomarkers predict metastatic disease recurrence in stage III colon cancer.遗传和免疫生物标志物可预测 III 期结肠癌的转移疾病复发。
BMC Cancer. 2018 Oct 19;18(1):998. doi: 10.1186/s12885-018-4940-2.