期刊文献+

Promising molecular mechanisms responsible for gemcitabine resistance in cancer 被引量:3

原文传递
导出
摘要 Gemcitabine is the first-line treatment for pancreatic ductual adenocarcinoma(PDAC)as well as acts against a wide range of other solid tumors.Patients usually have a good initial response to gemcitabine-based chemotherapy but would eventually develop resistance.To improve survival and prognosis of cancer patients,better understanding of the mechanisms responsible for gemcitabine resistance and discovery of new therapeutic strategies are in great need.Amounting evidence indicate that the developmental pathways,such as Hedgehog(Hh),Wnt and Notch,become reactivated in gemcitabine-resistant cancer cells.Thus,the strategies for targeting these pathways may sensitize cancer cells to gemcitabine treatment.In this review,we will summarize recent development in this area of research and discuss strategies to overcome gemcitabine resistance.Given the cross-talk between these three developmental signaling pathways,designing clinical trials using a cocktail of inhibitory agents targeting all these pathways may be more effective.Ultimately,our hope is that targeting these developmental pathways may be an effective way to improve the gemcitabine treatment outcome in cancer patients.
出处 《Genes & Diseases》 SCIE 2015年第4期299-306,共8页 基因与疾病(英文)
基金 Current research in my laboratory is supported by grants from the National Cancer Institute CA155086 Riley Children’s Foundation,Wells Center for Pediatric Research and Shandong Provincial Natural Science Foundation of China ZR2015HM018。
  • 相关文献

参考文献1

二级参考文献19

  • 1SIEGEL R, NAISHADHAM D, JEMAL A. Cancerstatistics, 2013 [J]. CA Cancer J Clin, 2013, 63 (1) :11-30. 被引量:1
  • 2BURRIS H A 3RD, MOORE M J, ANDERSEN J, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial [ J ]. J Clin Oncol, 1997,15(6) :2403-2413. 被引量:1
  • 3SADE H,KRISHNA S, SARIN A. The anti-apoptotic effect of Notch-1 requires p561ck-dependent, Akt/ PKB-mediated signaling in T cells [ J ]. J Biol Chem, 2004,279 ( 4 ) : 2937-2944. 被引量:1
  • 4STYLIANOU S, CLARKE R B, BRENNAN K. Aberrant activation of notch signaling in human breast cancer [J]. Cancer Res, 2006,66(3) :1517-1525. 被引量:1
  • 5MUNGAMURI S K, YANG X, THOR A D, et al. Survival signaling by Notch1: mammalian target of rapamycin (mTOR) -dependent inhibition of p53 [ J]. Cancer Res, 2006,66(9) :4715-4724. 被引量:1
  • 6ULASOV I V, NANDI S, DEY M, et al. Inhibition of Sonic hedgehog and Notch pathways enhances sensitivity of CD133 ( + ) glioma stem cells to temozolomide therapy [J]. Mol Meal, 2011,17(1-2) :103-112. 被引量:1
  • 7PARK J T, CHEN X, TROPE C G, et al. Notch3 overexpression is related to the recurrence of ovarian cancer and confers resistance to carboplatin [ J ]. Am J Pathol, 2010,177(3) :1087-1094. 被引量:1
  • 8MENG R D,SHELTON C C, LI Y M, et al. gamma- Secretase inhibitors abrogate oxaliplatin-induced activation of the Notch-1 signaling pathway in colon cancer cells resulting in enhanced chemosensitivity [J]. Cancer Res, 2009,69(2) :573-582. 被引量:1
  • 9TASAKA T, AKIYOSHI T, YAMAGUCHI K, ct al. Gamma-secretase complexes regulate the responses of human pancreatic ductal adenocarcinoma cells to taxanes [J]. Anticancer Res, 2010,30(12) :4999- 5010. 被引量:1
  • 10GU F, MA Y, ZHANG Z, et al. Expression of Stat3 and Notchl is associated with cisplatin resistance in head and neck squamous cell carcinoma [ J ]. Oncol Rep, 2010,23(3) :671-676. 被引量:1

共引文献3

同被引文献8

引证文献3

二级引证文献8

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