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J Gastrointest Oncol. 2018 Aug;9(4):E23-E27. doi: 10.21037/jgo.2018.05.10.
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FAM129B-dependent activation of NRF2 promotes an invasive phenotype in BRAF mutant melanoma cells.FAM129B 依赖性激活 NRF2 促进 BRAF 突变黑色素瘤细胞的侵袭表型。
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Mutation analysis of POLE gene in patients with early-onset colorectal cancer revealed a rare silent variant within the endonuclease domain with potential effect on splicing.对早发性结直肠癌患者 POLE 基因的突变分析显示,在内切酶结构域内存在一种罕见的沉默变异体,可能对剪接有影响。
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本文引用的文献

1
Inactivation of DNA repair triggers neoantigen generation and impairs tumour growth.DNA 修复失活会引发新抗原生成,并损害肿瘤生长。
Nature. 2017 Dec 7;552(7683):116-120. doi: 10.1038/nature24673. Epub 2017 Nov 29.
2
Durable complete remission following anti-EGFR antibodies in recurrent metastatic colorectal cancer.抗表皮生长因子受体(EGFR)抗体治疗复发性转移性结直肠癌后实现持久完全缓解。
J Oncol Pharm Pract. 2019 Jan;25(1):239-243. doi: 10.1177/1078155217730130. Epub 2017 Sep 26.
3
Mutational signature analysis identifies MUTYH deficiency in colorectal cancers and adrenocortical carcinomas.突变特征分析可鉴定出结直肠癌和肾上腺皮质癌中的MUTYH缺陷。
J Pathol. 2017 May;242(1):10-15. doi: 10.1002/path.4880. Epub 2017 Mar 29.
4
ESMO consensus guidelines for the management of patients with metastatic colorectal cancer.ESMO 共识指南:转移性结直肠癌患者的管理。
Ann Oncol. 2016 Aug;27(8):1386-422. doi: 10.1093/annonc/mdw235. Epub 2016 Jul 5.
5
Somatic c.34G>T KRAS mutation: a new prescreening test for MUTYH-associated polyposis?体细胞c.34G>T KRAS突变:一种用于MUTYH相关息肉病的新预筛查检测方法?
Cancer Genet. 2015 Jul-Aug;208(7-8):390-5. doi: 10.1016/j.cancergen.2015.04.005. Epub 2015 Apr 23.
6
Beyond KRAS status and response to anti-EGFR therapy in metastatic colorectal cancer.转移性结直肠癌中除KRAS状态及抗表皮生长因子受体治疗反应之外的因素
Pharmacogenomics. 2014 May;15(7):1043-52. doi: 10.2217/pgs.14.66.
7
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis.通过全外显子组下一代测序和生物信息学分析鉴定的 MSI 和 MSS 结直肠癌的体细胞突变谱。
PLoS One. 2010 Dec 22;5(12):e15661. doi: 10.1371/journal.pone.0015661.
8
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions.MYH 双等位基因突变可以通过 APC 或 MLH1 颠换使两条结直肠癌的遗传途径失活。
Fam Cancer. 2010 Dec;9(4):589-94. doi: 10.1007/s10689-010-9367-0.
9
Activating KRAS mutations and overexpression of epidermal growth factor receptor as independent predictors in metastatic colorectal cancer patients treated with cetuximab.KRAS 基因突变激活和表皮生长因子受体过表达是西妥昔单抗治疗转移性结直肠癌患者的独立预测指标。
Ann Surg. 2010 Feb;251(2):254-60. doi: 10.1097/SLA.0b013e3181bc9d96.
10
KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer.KRAS 突变状态可预测结直肠癌患者对西妥昔单抗治疗的反应。
Cancer Res. 2006 Apr 15;66(8):3992-5. doi: 10.1158/0008-5472.CAN-06-0191.

接受基于西妥昔单抗化疗治愈的不可切除转移性结直肠癌患者:一份具有新分子见解的病例报告

Unresectable metastatic colorectal cancer patient cured with cetuximab-based chemotherapy: a case report with new molecular insights.

作者信息

Cohen Romain, Sroussi Marine, Pilati Camilla, Houry Sidney, Laurent-Puig Pierre, André Thierry

机构信息

Sorbonne Université, Department of Oncology, AP-HP, Hôpital Saint-Antoine, Paris, France.

Laboratoire de médecine personnalisée, pharmacogénomique et optimisation thérapeutique (UMR-S1147) Université Paris Descartes, Sorbonne Paris Cité, INSERM, Paris, France.

出版信息

J Gastrointest Oncol. 2018 Aug;9(4):E23-E27. doi: 10.21037/jgo.2018.05.10.

DOI:10.21037/jgo.2018.05.10
PMID:30151276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6087863/
Abstract

Here we report the case of a 20-year-old patient who was diagnosed in 2002 with a metastatic colorectal cancer (CRC). He achieved a complete response under cetuximab-based therapy and remains without disease recurrence until now while chemotherapy was discontinued in 2009. The tumor exhibited high level of epidermal growth factor receptor () amplification, no mutation in , or genes and a microsatellite-stable (MSS) phenotype. Intriguingly this young patient was carrying a monoallelic germline mutation of that was associated with an inactivation of the second allele by loss of heterozygosity on tumor DNA. Moreover, this mutation was associated with a specific mutational signature on tumor level characterized by C > A single base substitutions and a higher mutational load than usually observed in MSS neoplasms. This case report paves the way for further researches on -associated cancers' sensitivity to anticancer therapies.

摘要

在此,我们报告一例20岁患者,其于2002年被诊断为转移性结直肠癌(CRC)。他在基于西妥昔单抗的治疗下实现了完全缓解,并且至今仍无疾病复发,而化疗于2009年停止。肿瘤表现出高水平的表皮生长因子受体()扩增,、或基因无突变,且为微卫星稳定(MSS)表型。有趣的是,这位年轻患者携带单等位基因种系突变,该突变与肿瘤DNA上杂合性缺失导致的第二个等位基因失活有关。此外,这种突变与肿瘤水平上的特定突变特征相关,其特征为C>A单碱基替换,且突变负荷高于MSS肿瘤通常观察到的水平。本病例报告为进一步研究相关癌症对抗癌治疗的敏感性铺平了道路。