期刊文献+

Molecular targets for the treatment of pancreatic cancer:Clinical and experimental studies 被引量:5

Molecular targets for the treatment of pancreatic cancer:Clinical and experimental studies
下载PDF
导出
摘要 Pancreatic cancer is the fourth most common cause of cancer deaths worldwide. Although recent therapeutic developments for patients with pancreatic cancer have provided survival benefits, the outcomes for patients with pancreatic cancer remain unsatisfactory. Molecularly targeted cancer therapy has advanced in the past decade with the use of a number of pathways as candidates of therapeutic targets. This review summarizes the molecular features of this refractory disease while focusing on the recent clinical and experimental findings on pancreatic cancer. It also discusses the data supporting current standard clinical outcomes, and offers conclusions that may improve the management of pancreatic cancer in the future. Pancreatic cancer is the fourth most common cause of cancer deaths worldwide. Although recent therapeutic developments for patients with pancreatic cancer have provided survival benefits, the outcomes for patients with pancreatic cancer remain unsatisfactory. Molecularly targeted cancer therapy has advanced in the past decade with the use of a number of pathways as candidates of therapeutic targets. This review summarizes the molecular features of this refractory disease while focusing on the recent clinical and experimental findings on pancreatic cancer. It also discusses the data supporting current standard clinical outcomes, and offers conclusions that may improve the management of pancreatic cancer in the future.
出处 《World Journal of Gastroenterology》 SCIE CAS 2016年第2期776-789,共14页 世界胃肠病学杂志(英文版)
基金 Supported by(in part)Grant-in-Aid for Scientific Research No.23390329
关键词 PANCREATIC CANCER TARGETED therapy Tyrosinekinase INHIBITORS MICROENVIRONMENT CANCER stem cell Pancreatic cancer Targeted therapy Tyrosine kinase inhibitors Microenvironment Cancer stem cell
  • 相关文献

参考文献102

  • 1Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CACancer J Clin 2012; 62: 10-29 [PMID: 22237781 DOI: 10.3322/caac.20138].
  • 2Oettle H, Post S, Neuhaus P, Gellert K, Langrehr J, RidwelskiK, Schramm H, Fahlke J, Zuelke C, Burkart C, Gutberlet K,Kettner E, Schmalenberg H, Weigang-Koehler K, Bechstein WO,Niedergethmann M, Schmidt-Wolf I, Roll L, Doerken B, RiessH. Adjuvant chemotherapy with gemcitabine vs observation inpatients undergoing curative-intent resection of pancreatic cancer:a randomized controlled trial. JAMA 2007; 297: 267-277 [PMID:17227978 DOI: 10.1001/jama.297.3.267].
  • 3Borazanci E, Von Hoff DD. Nab-paclitaxel and gemcitabine for thetreatment of patients with metastatic pancreatic cancer. Expert RevGastroenterol Hepatol 2014; 8: 739-747 [PMID: 24882381 DOI:10.1586/17474124.2014.925799].
  • 4Thota R, Pauff JM, Berlin JD. Treatment of metastatic pancreaticadenocarcinoma: a review. Oncology (Williston Park) 2014; 28:70-74 [PMID: 24683721].
  • 5Jones S, Zhang X, Parsons DW, Lin JC, Leary RJ, Angenendt P,Mankoo P, Carter H, Kamiyama H, Jimeno A, Hong SM, Fu B, LinMT, Calhoun ES, Kamiyama M, Walter K, Nikolskaya T, NikolskyY, Hartigan J, Smith DR, Hidalgo M, Leach SD, Klein AP, JaffeeEM, Goggins M, Maitra A, Iacobuzio-Donahue C, Eshleman JR,Kern SE, Hruban RH, Karchin R, Papadopoulos N, Parmigiani G,Vogelstein B, Velculescu VE, Kinzler KW. Core signaling pathwaysin human pancreatic cancers revealed by global genomic analyses.Science 2008; 321: 1801-1806 [PMID: 18772397].
  • 6Rozenblum E, Schutte M, Goggins M, Hahn SA, Panzer S, ZahurakM, Goodman SN, Sohn TA, Hruban RH, Yeo CJ, Kern SE. Tumorsuppressivepathways in pancreatic carcinoma. Cancer Res 1997;57: 1731-1734 [PMID: 9135016].
  • 7Yashiro M, Carethers JM, Laghi L, Saito K, Slezak P, Jaramillo E,Rubio C, Koizumi K, Hirakawa K, Boland CR. Genetic pathwaysin the evolution of morphologically distinct colorectal neoplasms.Cancer Res 2001; 61: 2676-2683 [PMID: 11289147].
  • 8Moskaluk CA, Hruban RH, Kern SE. p16 and K-ras gene mutationsin the intraductal precursors of human pancreatic adenocarcinoma.Cancer Res 1997; 57: 2140-2143 [PMID: 9187111].
  • 9Hruban RH, van Mansfeld AD, Offerhaus GJ, van Weering DH,Allison DC, Goodman SN, Kensler TW, Bose KK, Cameron JL,Bos JL. K-ras oncogene activation in adenocarcinoma of the humanpancreas. A study of 82 carcinomas using a combination of mutant-enriched polymerase chain reaction analysis and allele-specificoligonucleotide hybridization. Am J Pathol 1993; 143: 545-554[PMID: 8342602].
  • 10Schutte M, Hruban RH, Geradts J, Maynard R, Hilgers W,Rabindran SK, Moskaluk CA, Hahn SA, Schwarte-Waldhoff I,Schmiegel W, Baylin SB, Kern SE, Herman JG. Abrogation ofthe Rb/p16 tumor-suppressive pathway in virtually all pancreaticcarcinomas. Cancer Res 1997; 57: 3126-3130 [PMID: 9242437].

同被引文献23

引证文献5

二级引证文献29

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部