• 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

KRAS、BRAF、PIK3CA 和 PTEN 在结直肠癌中的预后作用。

The prognostic role of KRAS, BRAF, PIK3CA and PTEN in colorectal cancer.

机构信息

Department of Medical Biosciences/Pathology, Umeå University, SE-901 85 Umeå, Sweden.

出版信息

Br J Cancer. 2013 May 28;108(10):2153-63. doi: 10.1038/bjc.2013.212. Epub 2013 May 9.

DOI:10.1038/bjc.2013.212
PMID:23660947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3670497/
Abstract

BACKGROUND

Mutations in KRAS, BRAF, PIK3CA and PTEN expression have been in focus to predict the effect of epidermal growth factor receptor-blocking therapy in colorectal cancer (CRC). Here, information on these four aberrations was collected and combined to a Quadruple index and used to evaluate the prognostic role of these factors in CRC.

PATIENTS

We analysed the mutation status in KRAS, BRAF and PIK3CA and PTEN expression in two separate CRC cohorts, Northern Sweden Health Disease Study (NSHDS; n=197) and Colorectal Cancer in Umeå Study (CRUMS; n=414). A Quadruple index was created, where Quadruple index positivity specifies cases with any aberration in KRAS, BRAF, PIK3CA or PTEN expression.

RESULTS

Quadruple index positive tumours had a worse prognosis, significant in the NSHDS but not in the CRUMS cohort (NSHDS; P=0.003 and CRUMS; P=0.230) in univariate analyses but significance was lost in multivariate analyses. When analysing each gene separately, only BRAF was of prognostic significance in the NSHDS cohort (multivariate HR 2.00, 95% CI: 1.16-3.43) and KRAS was of prognostic significance in the CRUMS cohort (multivariate HR 1.48, 95% CI: 1.02-2.16). Aberrations in PIK3CA and PTEN did not add significant prognostic information.

CONCLUSIONS

Our results suggest that establishment of molecular subgroups based on KRAS and BRAF mutation status is important and should be considered in future prognostic studies in CRC.

摘要

背景

KRAS、BRAF、PIK3CA 和 PTEN 表达的突变已成为预测结直肠癌(CRC)中表皮生长因子受体阻断治疗效果的焦点。在这里,收集了这四种异常的信息,并组合成一个四重指数,用于评估这些因素在 CRC 中的预后作用。

患者

我们在两个独立的 CRC 队列(瑞典北部健康疾病研究(NSHDS);n=197 和乌默奥 CRC 研究(CRUMS);n=414)中分析了 KRAS、BRAF 和 PIK3CA 的突变状态和 PTEN 表达。创建了一个四重指数,其中四重指数阳性指定 KRAS、BRAF、PIK3CA 或 PTEN 表达有任何异常的病例。

结果

四重指数阳性肿瘤的预后较差,在 NSHDS 队列中具有统计学意义,但在 CRUMS 队列中无统计学意义(NSHDS;P=0.003 和 CRUMS;P=0.230)在单因素分析中,但在多因素分析中失去了意义。当单独分析每个基因时,只有 BRAF 在 NSHDS 队列中具有预后意义(多因素 HR 2.00,95%CI:1.16-3.43),而 KRAS 在 CRUMS 队列中具有预后意义(多因素 HR 1.48,95%CI:1.02-2.16)。PIK3CA 和 PTEN 的异常并未提供显著的预后信息。

结论

我们的结果表明,基于 KRAS 和 BRAF 突变状态建立分子亚组很重要,在未来的 CRC 预后研究中应考虑这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/e8181a396ee7/bjc2013212f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/be00d6f6be2c/bjc2013212f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/f696ad00d3ff/bjc2013212f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/e8181a396ee7/bjc2013212f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/be00d6f6be2c/bjc2013212f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/f696ad00d3ff/bjc2013212f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/423f/3670497/e8181a396ee7/bjc2013212f3.jpg

相似文献

1
The prognostic role of KRAS, BRAF, PIK3CA and PTEN in colorectal cancer.KRAS、BRAF、PIK3CA 和 PTEN 在结直肠癌中的预后作用。
Br J Cancer. 2013 May 28;108(10):2153-63. doi: 10.1038/bjc.2013.212. Epub 2013 May 9.
2
The predictive value of KRAS, NRAS, BRAF, PIK3CA and PTEN for anti-EGFR treatment in metastatic colorectal cancer: A systematic review and meta-analysis.KRAS、NRAS、BRAF、PIK3CA和PTEN对转移性结直肠癌抗表皮生长因子受体治疗的预测价值:一项系统评价和荟萃分析。
Acta Oncol. 2014 Jul;53(7):852-64. doi: 10.3109/0284186X.2014.895036. Epub 2014 Mar 25.
3
Molecular alterations of Ras-Raf-mitogen-activated protein kinase and phosphatidylinositol 3-kinase-Akt signaling pathways in colorectal cancers from a tertiary hospital at Kuala Lumpur, Malaysia.马来西亚吉隆坡一所三级医院的结直肠癌中 Ras-Raf-丝裂原活化蛋白激酶和磷脂酰肌醇 3-激酶-Akt 信号通路的分子改变。
APMIS. 2013 Oct;121(10):954-66. doi: 10.1111/apm.12152. Epub 2013 Aug 29.
4
Impact of KRAS, BRAF, PIK3CA mutations, PTEN, AREG, EREG expression and skin rash in ≥ 2 line cetuximab-based therapy of colorectal cancer patients.KRAS、BRAF、PIK3CA 突变、PTEN、AREG、EREG 表达及皮疹对≥2 线基于西妥昔单抗治疗的结直肠癌患者的影响。
PLoS One. 2011 Jan 20;6(1):e15980. doi: 10.1371/journal.pone.0015980.
5
BRAF, KRAS and PIK3CA mutations in colorectal serrated polyps and cancer: primary or secondary genetic events in colorectal carcinogenesis?结直肠锯齿状息肉和癌症中的BRAF、KRAS及PIK3CA突变:结直肠癌发生过程中的原发性或继发性遗传事件?
BMC Cancer. 2008 Sep 9;8:255. doi: 10.1186/1471-2407-8-255.
6
Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis.KRAS、BRAF、NRAS 和 PIK3CA 基因突变对西妥昔单抗联合化疗治疗化疗耐药转移性结直肠癌疗效的影响:一项回顾性联盟分析。
Lancet Oncol. 2010 Aug;11(8):753-62. doi: 10.1016/S1470-2045(10)70130-3. Epub 2010 Jul 8.
7
DNA sequence profiles of the colorectal cancer critical gene set KRAS-BRAF-PIK3CA-PTEN-TP53 related to age at disease onset.与疾病发病年龄相关的结直肠癌关键基因 KRAS-BRAF-PIK3CA-PTEN-TP53 的 DNA 序列谱。
PLoS One. 2010 Nov 12;5(11):e13978. doi: 10.1371/journal.pone.0013978.
8
KRAS, BRAF and PIK3CA mutations and the loss of PTEN expression in Chinese patients with colorectal cancer.中国结直肠癌患者 KRAS、BRAF 和 PIK3CA 基因突变及 PTEN 表达缺失。
PLoS One. 2012;7(5):e36653. doi: 10.1371/journal.pone.0036653. Epub 2012 May 7.
9
Promising biomarkers for predicting the outcomes of patients with KRAS wild-type metastatic colorectal cancer treated with anti-epidermal growth factor receptor monoclonal antibodies: a systematic review with meta-analysis.抗表皮生长因子受体单克隆抗体治疗 KRAS 野生型转移性结直肠癌患者结局的有前途的生物标志物:系统评价与荟萃分析。
Int J Cancer. 2013 Oct 15;133(8):1914-25. doi: 10.1002/ijc.28153. Epub 2013 Jul 13.
10
Biomarkers of benefit from cetuximab-based therapy in metastatic colorectal cancer: interaction of EGFR ligand expression with RAS/RAF, PIK3CA genotypes.表皮生长因子受体(EGFR)配体表达与 RAS/RAF、PIK3CA 基因型与西妥昔单抗为基础的治疗转移性结直肠癌获益的相关性:生物标志物。
BMC Cancer. 2013 Feb 2;13:49. doi: 10.1186/1471-2407-13-49.

引用本文的文献

1
Targeting the MAP kinase pathway in colorectal cancer: A journey in personalized medicine.靶向结直肠癌中的丝裂原活化蛋白激酶通路:个性化医疗之旅。
Clin Cancer Res. 2025 May 1. doi: 10.1158/1078-0432.CCR-25-0107.
2
The role of PIK3CA gene mutations in colorectal cancer and the selection of treatment strategies.PIK3CA基因突变在结直肠癌中的作用及治疗策略的选择。
Front Pharmacol. 2024 Oct 30;15:1494802. doi: 10.3389/fphar.2024.1494802. eCollection 2024.
3
Identifying Genetic Mutation Status in Patients with Colorectal Cancer Liver Metastases Using Radiomics-Based Machine-Learning Models.

本文引用的文献

1
KRAS mutation status and clinical outcome of preoperative chemoradiation with cetuximab in locally advanced rectal cancer: a pooled analysis of 2 phase II trials.KRAS 突变状态和西妥昔单抗术前放化疗治疗局部晚期直肠癌的临床结局:2 项 II 期试验的汇总分析。
Int J Radiat Oncol Biol Phys. 2013 Jan 1;85(1):201-7. doi: 10.1016/j.ijrobp.2012.03.048. Epub 2012 Jun 5.
2
Clinical usefulness of KRAS, BRAF, and PIK3CA mutations as predictive markers of cetuximab efficacy in irinotecan- and oxaliplatin-refractory Japanese patients with metastatic colorectal cancer.KRAS、BRAF 和 PIK3CA 突变作为西妥昔单抗疗效预测标志物在伊立替康和奥沙利铂耐药的日本转移性结直肠癌患者中的临床意义。
Int J Clin Oncol. 2013 Aug;18(4):670-7. doi: 10.1007/s10147-012-0422-8. Epub 2012 May 26.
3
使用基于影像组学的机器学习模型识别结直肠癌肝转移患者的基因突变状态
Cancers (Basel). 2023 Nov 29;15(23):5648. doi: 10.3390/cancers15235648.
4
Unraveling the Role of Molecular Profiling in Predicting Treatment Response in Stage III Colorectal Cancer Patients: Insights from the IDEA International Study.解析分子谱分析在预测Ⅲ期结直肠癌患者治疗反应中的作用:来自IDEA国际研究的见解
Cancers (Basel). 2023 Sep 30;15(19):4819. doi: 10.3390/cancers15194819.
5
Glutamine Starvation Affects Cell Cycle, Oxidative Homeostasis and Metabolism in Colorectal Cancer Cells.谷氨酰胺饥饿影响结肠癌细胞的细胞周期、氧化稳态和代谢。
Antioxidants (Basel). 2023 Mar 10;12(3):683. doi: 10.3390/antiox12030683.
6
Comprehensive genomic profiling of colorectal cancer patients reveals differences in mutational landscapes among clinical and pathological subgroups.结直肠癌患者的综合基因组分析揭示了临床和病理亚组之间突变图谱的差异。
Front Oncol. 2022 Nov 10;12:1000146. doi: 10.3389/fonc.2022.1000146. eCollection 2022.
7
Identification of Lynch Syndrome in Patients with Endometrial Cancer Based on a Germline Next Generation Sequencing Multigene Panel Test.基于种系二代测序多基因检测panel对子宫内膜癌患者林奇综合征的鉴定
Cancers (Basel). 2022 Jul 13;14(14):3406. doi: 10.3390/cancers14143406.
8
Prognostic Value of Mutations in Colorectal Cancer Patients.结直肠癌患者基因突变的预后价值
Cancers (Basel). 2022 Jul 7;14(14):3320. doi: 10.3390/cancers14143320.
9
A RAS-Independent Biomarker Panel to Reliably Predict Response to MEK Inhibition in Colorectal Cancer.一种不依赖RAS的生物标志物组合,用于可靠预测结直肠癌对MEK抑制的反应。
Cancers (Basel). 2022 Jul 1;14(13):3252. doi: 10.3390/cancers14133252.
10
The role of the PTEN/mTOR axis in clinical response of rectal cancer patients.PTEN/mTOR 轴在直肠癌患者临床反应中的作用。
Mol Biol Rep. 2022 Sep;49(9):8461-8472. doi: 10.1007/s11033-022-07665-x. Epub 2022 Jun 21.
Mutation pattern of KRAS and BRAF oncogenes in colorectal cancer patients.结直肠癌患者 KRAS 和 BRAF 癌基因的突变模式。
Neoplasma. 2012;59(4):376-83. doi: 10.4149/neo_2012_049.
4
Concordance in KRAS and BRAF mutations in endoscopic biopsy samples and resection specimens of colorectal adenocarcinoma.结直肠腺癌内镜活检样本和切除标本中 KRAS 和 BRAF 突变的一致性。
Eur J Cancer. 2012 May;48(7):1108-15. doi: 10.1016/j.ejca.2012.02.054. Epub 2012 Mar 23.
5
Prognostic role of PIK3CA mutation in colorectal cancer: cohort study and literature review.PIK3CA 突变在结直肠癌中的预后作用:队列研究和文献回顾。
Clin Cancer Res. 2012 Apr 15;18(8):2257-68. doi: 10.1158/1078-0432.CCR-11-2410. Epub 2012 Feb 22.
6
BRAF mutations in colorectal cancer are associated with distinct clinical characteristics and worse prognosis.结直肠癌中的 BRAF 突变与独特的临床特征和较差的预后相关。
Dis Colon Rectum. 2012 Feb;55(2):128-33. doi: 10.1097/DCR.0b013e31823c08b3.
7
Predictive and prognostic roles of BRAF mutation in stage III colon cancer: results from intergroup trial CALGB 89803.BRAF 突变在 III 期结肠癌中的预测和预后作用:CALGB 89803 组间试验的结果。
Clin Cancer Res. 2012 Feb 1;18(3):890-900. doi: 10.1158/1078-0432.CCR-11-2246. Epub 2011 Dec 6.
8
PIK3CA kinase domain mutation identifies a subgroup of stage III colon cancer patients with poor prognosis.PIK3CA 激酶结构域突变鉴定出具有不良预后的 III 期结肠癌患者亚组。
Cell Oncol (Dordr). 2011 Dec;34(6):523-31. doi: 10.1007/s13402-011-0054-4. Epub 2011 Aug 10.
9
KRAS, BRAF and PIK3CA mutations in human colorectal cancer: relationship with metastatic colorectal cancer.KRAS、BRAF 和 PIK3CA 基因突变与人类结直肠癌:与转移性结直肠癌的关系。
Oncol Rep. 2011 Jun;25(6):1691-7. doi: 10.3892/or.2011.1217. Epub 2011 Mar 17.
10
Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis.KRAS、BRAF、NRAS 和 PIK3CA 基因突变对西妥昔单抗联合化疗治疗化疗耐药转移性结直肠癌疗效的影响:一项回顾性联盟分析。
Lancet Oncol. 2010 Aug;11(8):753-62. doi: 10.1016/S1470-2045(10)70130-3. Epub 2010 Jul 8.