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大多数早期胰腺上皮内瘤变中存在体细胞突变。

Presence of somatic mutations in most early-stage pancreatic intraepithelial neoplasia.

机构信息

Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Gastroenterology. 2012 Apr;142(4):730-733.e9. doi: 10.1053/j.gastro.2011.12.042. Epub 2012 Jan 5.

DOI:10.1053/j.gastro.2011.12.042
PMID:22226782
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3321090/
Abstract

More information is needed about genetic factors that initiate development of pancreatic intraepithelial neoplasms-the most common precursors of pancreatic ductal adenocarcinoma. We show that more than 99% of the earliest-stage, lowest-grade, pancreatic intraepithelial neoplasm-1 lesions contain mutations in KRAS, p16/CDKN2A, GNAS, or BRAF. These findings could improve our understanding of the development and progression of these premalignant lesions.

摘要

需要更多关于启动胰腺上皮内瘤变(胰腺导管腺癌最常见的前体)发展的遗传因素的信息。我们表明,超过 99%的最早阶段、最低级别、胰腺上皮内瘤变 1 病变含有 KRAS、p16/CDKN2A、GNAS 或 BRAF 的突变。这些发现可以提高我们对这些癌前病变发展和进展的理解。

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Presence of somatic mutations in most early-stage pancreatic intraepithelial neoplasia.大多数早期胰腺上皮内瘤变中存在体细胞突变。
Gastroenterology. 2012 Apr;142(4):730-733.e9. doi: 10.1053/j.gastro.2011.12.042. Epub 2012 Jan 5.
2
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本文引用的文献

1
Recurrent GNAS mutations define an unexpected pathway for pancreatic cyst development.GNAS 基因突变的反复出现为胰腺囊肿的发生发展开辟了一条意料之外的途径。
Sci Transl Med. 2011 Jul 20;3(92):92ra66. doi: 10.1126/scitranslmed.3002543.
2
Pancreatic cancer.胰腺癌。
Lancet. 2011 Aug 13;378(9791):607-20. doi: 10.1016/S0140-6736(10)62307-0. Epub 2011 May 26.
3
Genome-wide analysis of promoter methylation associated with gene expression profile in pancreatic adenocarcinoma.胰腺癌中与基因表达谱相关的启动子甲基化的全基因组分析。
Clin Cancer Res. 2011 Jul 1;17(13):4341-54. doi: 10.1158/1078-0432.CCR-10-3431. Epub 2011 May 24.
4
Oncogenic KRas suppresses inflammation-associated senescence of pancreatic ductal cells.致癌性 KRas 抑制胰腺导管细胞炎症相关的衰老。
Cancer Cell. 2010 Nov 16;18(5):448-58. doi: 10.1016/j.ccr.2010.10.020.
5
Pancreatic duct glands are distinct ductal compartments that react to chronic injury and mediate Shh-induced metaplasia.胰腺导管腺是独特的导管隔室,对慢性损伤有反应,并介导 Shh 诱导的化生。
Gastroenterology. 2010 Mar;138(3):1166-77. doi: 10.1053/j.gastro.2009.12.005. Epub 2009 Dec 21.
6
Increased Prevalence of Precursor Lesions in Familial Pancreatic Cancer Patients.家族性胰腺癌患者前驱病变的患病率增加。
Clin Cancer Res. 2009 Dec 15;15(24):7737-7743. doi: 10.1158/1078-0432.CCR-09-0004.
7
Senescence-messaging secretome: SMS-ing cellular stress.衰老信息分泌组:传递细胞应激信号
Nat Rev Cancer. 2009 Feb;9(2):81-94. doi: 10.1038/nrc2560. Epub 2009 Jan 9.
8
Core signaling pathways in human pancreatic cancers revealed by global genomic analyses.通过全基因组分析揭示的人类胰腺癌核心信号通路。
Science. 2008 Sep 26;321(5897):1801-6. doi: 10.1126/science.1164368. Epub 2008 Sep 4.
9
Gene expression profiles in pancreatic intraepithelial neoplasia reflect the effects of Hedgehog signaling on pancreatic ductal epithelial cells.胰腺上皮内瘤变中的基因表达谱反映了刺猬信号通路对胰腺导管上皮细胞的影响。
Cancer Res. 2005 Mar 1;65(5):1619-26. doi: 10.1158/0008-5472.CAN-04-1413.
10
Frequency of K-ras mutations in pancreatic intraductal neoplasias associated with pancreatic ductal adenocarcinoma and chronic pancreatitis: a meta-analysis.与胰腺导管腺癌和慢性胰腺炎相关的胰腺导管内瘤变中K-ras突变的频率:一项荟萃分析。
Neoplasia. 2005 Jan;7(1):17-23. doi: 10.1593/neo.04445.