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本文引用的文献

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Roles for KRAS in pancreatic tumor development and progression.KRAS 在胰腺肿瘤发生和发展中的作用。
Gastroenterology. 2013 Jun;144(6):1220-9. doi: 10.1053/j.gastro.2013.01.071.
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PI3K and MEK inhibitor combinations: examining the evidence in selected tumor types.PI3K 和 MEK 抑制剂联合治疗:在选定肿瘤类型中评估证据。
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Cancer statistics, 2013.癌症统计数据,2013 年。
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International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer.国际胰腺癌筛查(CAPS)联盟关于家族性胰腺癌高危患者管理的峰会。
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EGF receptor is required for KRAS-induced pancreatic tumorigenesis.表皮生长因子受体对于 KRAS 诱导的胰腺肿瘤发生是必需的。
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A randomized, placebo-controlled phase 2 study of ganitumab (AMG 479) or conatumumab (AMG 655) in combination with gemcitabine in patients with metastatic pancreatic cancer.一项吉妥珠单抗(AMG 479)或康奈妥单抗(AMG 655)联合吉西他滨治疗转移性胰腺癌患者的随机、安慰剂对照 2 期研究。
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Familial pancreatic cancer--current knowledge.家族性胰腺癌——现有知识。
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Enhanced cytotoxicity of PARP inhibition in mantle cell lymphoma harbouring mutations in both ATM and p53.同时存在 ATM 和 p53 突变的套细胞淋巴瘤中,聚腺苷二磷酸核糖聚合酶抑制剂的细胞毒性增强。
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Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations.BRCA1 和 BRCA2 基因突变个体的乳腺癌和卵巢癌以外的癌症风险。
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Genetic susceptibility to pancreatic cancer.胰腺癌的遗传易感性。
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胰腺腺癌的遗传决定因素及潜在治疗靶点

Genetic determinants and potential therapeutic targets for pancreatic adenocarcinoma.

作者信息

Reznik Robert, Hendifar Andrew E, Tuli Richard

机构信息

Department of Radiation Oncology, Cedars-Sinai Medical Center Los Angeles, CA, USA.

出版信息

Front Physiol. 2014 Mar 3;5:87. doi: 10.3389/fphys.2014.00087. eCollection 2014.

DOI:10.3389/fphys.2014.00087
PMID:24624093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3939680/
Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer deaths in both men and women in the United States, carrying a 5-year survival rate of approximately 5%, which is the poorest prognosis of any solid tumor type. Given the dismal prognosis associated with PDAC, a more thorough understanding of risk factors and genetic predisposition has important implications not only for cancer prevention, but also for screening techniques and the development of personalized therapies. While screening of the general population is not recommended or practicable with current diagnostic methods, studies are ongoing to evaluate its usefulness in people with at least 5- to 10-fold increased risk of PDAC. In order to help identify high-risk populations who would be most likely to benefit from early detection screening tests for pancreatic cancer, discovery of additional pancreatic cancer susceptibility genes is crucial. Thus, specific gene-based, gene-product, and marker-based testing for the early detection of pancreatic cancer are currently being developed, with the potential for these to be useful as potential therapeutic targets as well. The goal of this review is to provide an overview of the genetic basis for PDAC with a focus on germline and familial determinants. A discussion of potential therapeutic targets and future directions in screening and treatment is also provided.

摘要

胰腺导管腺癌(PDAC)是美国男性和女性癌症死亡的第四大主要原因,其5年生存率约为5%,是所有实体瘤类型中预后最差的。鉴于与PDAC相关的预后不佳,更全面地了解风险因素和遗传易感性不仅对癌症预防具有重要意义,而且对筛查技术和个性化治疗的发展也具有重要意义。虽然目前的诊断方法不建议或不适用于对普通人群进行筛查,但正在进行研究以评估其对胰腺癌风险至少增加5至10倍的人群的有效性。为了帮助识别最有可能从胰腺癌早期检测筛查试验中受益的高危人群,发现更多的胰腺癌易感基因至关重要。因此,目前正在开发基于特定基因、基因产物和标志物的胰腺癌早期检测测试,这些测试也有可能作为潜在的治疗靶点。本综述的目的是概述PDAC的遗传基础,重点是种系和家族决定因素。还讨论了潜在的治疗靶点以及筛查和治疗的未来方向。