New Strategies in Pancreatic Cancer: Emerging Epidemiologic and Therapeutic Concepts

被引:49
|
作者
Li, Donghui [1 ]
Abbruzzese, James L. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 426, Houston, TX 77030 USA
关键词
GENOME-WIDE ASSOCIATION; BODY-MASS INDEX; ABO BLOOD-GROUP; LIVER RECEPTOR HOMOLOG-1; VON-WILLEBRAND-FACTOR; DIABETES-MELLITUS; INSULIN-RECEPTOR; ENDOTHELIAL FUNCTION; METFORMIN; RISK;
D O I
10.1158/1078-0432.CCR-09-1942
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancer (PC) is a highly lethal disease with complex etiology involving both environmental and genetic factors. Although cigarette smoking is known to explain 25% of cases, data from recent studies suggest that obesity and long-term type II diabetes are two major modifiable risk factors for PC. Furthermore, obesity and diabetes seem to affect the clinical outcome of patients with PC. Understanding the mechanistic effects of obesity and diabetes on the pancreasmay identify new strategies for prevention or therapy. Experimental and epidemiologic evidence suggests that the antidiabetic drug metformin has protective antitumor activity in PC. In addition to insulin resistance and inflammation as mechanisms of carcinogenesis, obesity and diabetes are linked to impairments in endothelial function and coagulation status, which increase the risks of thrombosis and angiogenesis and, in turn, the risk of PC development and progression. The associations of the ABO blood group gene and NR5A2 gene variants with PC discovered by recent genome-wide association studies may link insulin resistance, inflammation, and thrombosis to pancreatic carcinogenesis. These exciting findings open new avenues for understanding the etiology of PC and provide opportunities for developing novel strategies for prevention and treatment of this disease. Clin Cancer Res; 16(17); 4313-8. (C) 2010 AACR.
引用
收藏
页码:4313 / 4318
页数:6
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