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胰腺腺癌:流行病学与遗传学

Pancreatic adenocarcinoma: epidemiology and genetics.

作者信息

Flanders T Y, Foulkes W D

机构信息

Department of Medicine, McGill University, Montreal General Hospital, Quebec, Canada.

出版信息

J Med Genet. 1996 Nov;33(11):889-98. doi: 10.1136/jmg.33.11.889.

Abstract

Pancreatic adenocarcinoma is an important cause of death from cancer throughout the developed world. There are few established environmental risk factors, but a previous history of pancreatitis and exposure to tobacco and salted food appear to be the most important. A family history of pancreatic adenocarcinoma is not common in patients with this disease, but recent research has shown that pancreatic adenocarcinoma can be a feature of cancer susceptibility syndromes associated with germline mutations in p16, BRCA1, BRCA2, and APC. This highlights the need for a full family history in apparently sporadic cases. Somatic mutations in p16, BRCA2, and APC have also been reported in pancreatic cancer; however, K-RAS mutations appear to be the commonest oncogenic alteration. Recent advances in our understanding of the basis of hereditary cancer syndromes may be applicable to the diagnosis, treatment, and possibly prevention of pancreatic adenocarcinoma in the future.

摘要

在整个发达国家,胰腺腺癌是癌症致死的一个重要原因。已明确的环境风险因素较少,但胰腺炎病史以及接触烟草和腌制食品似乎是最重要的因素。胰腺腺癌患者中家族病史并不常见,但最近的研究表明,胰腺腺癌可能是与p16、BRCA1、BRCA2和APC种系突变相关的癌症易感性综合征的一个特征。这凸显了在看似散发的病例中获取完整家族病史的必要性。胰腺癌中也报道了p16、BRCA2和APC的体细胞突变;然而,K-RAS突变似乎是最常见的致癌改变。我们对遗传性癌症综合征基础的最新认识进展可能适用于未来胰腺腺癌的诊断、治疗以及预防。

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