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Molecular biomarkers of colorectal cancer: prognostic and predictive tools for clinical practice.结直肠癌的分子生物标志物:临床实践的预后和预测工具。
J Zhejiang Univ Sci B. 2012 Sep;13(9):663-75. doi: 10.1631/jzus.B1100340.
2
Pharmacogenetic influences on treatment response and toxicity in colorectal cancer.药物遗传学对结直肠癌治疗反应和毒性的影响。
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[Molecular biology in clinical cancer research: the example of digestive cancers].[临床癌症研究中的分子生物学:以消化系统癌症为例]
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Role of pharmacogenetics as predictive biomarkers of response and/or toxicity in the treatment of colorectal cancer.药物遗传学在结直肠癌治疗中作为反应和/或毒性预测生物标志物的作用。
Clin Colorectal Cancer. 2009 Jan;8(1):15-21. doi: 10.3816/CCC.2009.n.003.
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KRAS and BRAF mutations in advanced colorectal cancer are associated with poor prognosis but do not preclude benefit from oxaliplatin or irinotecan: results from the MRC FOCUS trial.晚期结直肠癌中的KRAS和BRAF突变与预后不良相关,但不排除从奥沙利铂或伊立替康治疗中获益:MRC FOCUS试验结果
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[New perspectives in predicting response to chemotherapy in colorectal cancer].
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CUDC-101 as a dual-target inhibitor of EGFR and HDAC enhances the anti-myeloma effects of bortezomib by regulating G2/M cell cycle arrest.CUDC-101 作为 EGFR 和 HDAC 的双重抑制剂,通过调节 G2/M 细胞周期阻滞增强硼替佐米的抗骨髓瘤作用。
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本文引用的文献

1
Validation study of a quantitative multigene reverse transcriptase-polymerase chain reaction assay for assessment of recurrence risk in patients with stage II colon cancer.用于评估 II 期结肠癌患者复发风险的定量多重逆转录-聚合酶链反应检测的验证研究。
J Clin Oncol. 2011 Dec 10;29(35):4611-9. doi: 10.1200/JCO.2010.32.8732. Epub 2011 Nov 7.
2
Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths.癌症统计数据,2011 年:消除社会经济和种族差异对癌症过早死亡的影响。
CA Cancer J Clin. 2011 Jul-Aug;61(4):212-36. doi: 10.3322/caac.20121. Epub 2011 Jun 17.
3
DNA mismatch repair status and colon cancer recurrence and survival in clinical trials of 5-fluorouracil-based adjuvant therapy.基于氟尿嘧啶的辅助治疗临床试验中 DNA 错配修复状态与结肠癌复发和生存的关系。
J Natl Cancer Inst. 2011 Jun 8;103(11):863-75. doi: 10.1093/jnci/djr153. Epub 2011 May 19.
4
Thymidine Phosphorylase/β-tubulin III expressions predict the response in Chinese advanced gastric cancer patients receiving first-line capecitabine plus paclitaxel.胸苷磷酸化酶/β-微管蛋白 III 表达预测中国晚期胃癌患者一线接受卡培他滨联合紫杉醇治疗的反应。
BMC Cancer. 2011 May 18;11:177. doi: 10.1186/1471-2407-11-177.
5
Use of a comprehensive panel of biomarkers to predict response to a fluorouracil-oxaliplatin regimen in patients with metastatic colorectal cancer.使用综合生物标志物面板预测转移性结直肠癌患者对氟尿嘧啶-奥沙利铂方案的反应。
Pharmacogenomics. 2011 Mar;12(3):433-42. doi: 10.2217/pgs.10.196.
6
Pharmacogenomic contribution to drug response.药物反应的药物基因组学贡献。
Cancer J. 2011 Mar-Apr;17(2):80-8. doi: 10.1097/PPO.0b013e3182147432.
7
ERCC1 and ERCC2 polymorphisms predict clinical outcomes of oxaliplatin-based chemotherapies in gastric and colorectal cancer: a systemic review and meta-analysis.ERCC1 和 ERCC2 多态性可预测胃癌和结直肠癌奥沙利铂为基础的化疗的临床结局:系统评价和荟萃分析。
Clin Cancer Res. 2011 Mar 15;17(6):1632-40. doi: 10.1158/1078-0432.CCR-10-2169. Epub 2011 Jan 28.
8
Targeted therapies as adjuvant treatment for early-stage colorectal cancer: first impressions and clinical questions.靶向治疗作为早期结直肠癌的辅助治疗:初步印象和临床问题。
Clin Colorectal Cancer. 2010 Dec;9(5):269-73. doi: 10.3816/CCC.2010.n.039.
9
Predictive value of VEGF gene polymorphisms for metastatic colorectal cancer patients receiving first-line treatment including fluorouracil, irinotecan, and bevacizumab.血管内皮生长因子基因多态性对接受氟尿嘧啶、伊立替康和贝伐单抗一线治疗的转移性结直肠癌患者的预测价值。
Int J Colorectal Dis. 2011 Feb;26(2):143-51. doi: 10.1007/s00384-010-1108-1. Epub 2010 Dec 29.
10
Multiple genetic polymorphisms in the prediction of clinical outcome of metastatic colorectal cancer patients treated with first-line FOLFOX-4 chemotherapy.多基因遗传多态性预测一线 FOLFOX-4 化疗治疗转移性结直肠癌患者的临床结局。
Pharmacogenet Genomics. 2011 Jan;21(1):18-25. doi: 10.1097/FPC.0b013e3283415124.

结直肠癌的分子生物标志物:临床实践的预后和预测工具。

Molecular biomarkers of colorectal cancer: prognostic and predictive tools for clinical practice.

机构信息

Cancer Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China.

出版信息

J Zhejiang Univ Sci B. 2012 Sep;13(9):663-75. doi: 10.1631/jzus.B1100340.

DOI:10.1631/jzus.B1100340
PMID:22949358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3437365/
Abstract

Colorectal cancer remains one of the most common types of cancer and leading causes of cancer death worldwide. Although we have made steady progress in chemotherapy and targeted therapy, evidence suggests that the majority of patients undergoing drug therapy experience severe, debilitating, and even lethal adverse drug events which considerably outweigh the benefits. The identification of suitable biomarkers will allow clinicians to deliver the most appropriate drugs to specific patients and spare them ineffective and expensive treatments. Prognostic and predictive biomarkers have been the subjects of many published papers, but few have been widely incorporated into clinical practice. Here, we want to review recent biomarker data related to colorectal cancer, which may have been ready for clinical use.

摘要

结直肠癌仍然是世界上最常见的癌症类型之一,也是癌症死亡的主要原因。尽管我们在化疗和靶向治疗方面取得了稳步进展,但有证据表明,大多数接受药物治疗的患者都经历了严重、衰弱甚至致命的药物不良事件,这些事件的影响远远超过了治疗的益处。合适的生物标志物的识别将使临床医生能够为特定患者提供最合适的药物,并使他们免受无效和昂贵的治疗。预后和预测生物标志物一直是许多已发表论文的主题,但很少有被广泛纳入临床实践。在这里,我们想回顾一下与结直肠癌相关的最近的生物标志物数据,这些数据可能已经准备好用于临床应用。