Literature DB >> 24727386

Opportunities for translation: targeting DNA repair pathways in pancreatic cancer.

Elaina N Maginn1, Camila H de Sousa2, Harpreet S Wasan2, Euan A Stronach2.   

Abstract

Pancreatic ductal adenocarcinoma (PDAC) remains one of the poorest prognosis neoplasms. It is typified by high levels of genomic aberrations and copy-number variation, intra-tumoural heterogeneity and resistance to conventional chemotherapy. Improved therapeutic options, ideally targeted against cancer-specific biological mechanisms, are urgently needed. Although induction of DNA damage and/or modulation of DNA damage response pathways are associated with the activity of a number of conventional PDAC chemotherapies, the effectiveness of this approach in the treatment of PDAC has not been comprehensively reviewed. Here, we review chemotherapeutic agents that have shown anti-cancer activity in PDAC and whose mechanisms of action involve modulation of DNA repair pathways. In addition, we highlight novel potential targets within these pathways based on the emerging understanding of PDAC biology and their exploitation as targets in other cancers.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chemoresistance; DNA damage response and repair; DNA damaging agents; Pancreatic ductal adenocarcinoma

Mesh:

Substances:

Year:  2014        PMID: 24727386     DOI: 10.1016/j.bbcan.2014.04.002

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  8 in total

Review 1.  The evolution into personalized therapies in pancreatic ductal adenocarcinoma: challenges and opportunities.

Authors:  Anteneh A Tesfaye; Mandana Kamgar; Asfar Azmi; Philip A Philip
Journal:  Expert Rev Anticancer Ther       Date:  2017-12-19       Impact factor: 4.512

2.  Effect of DAPK1 gene on proliferation, migration, and invasion of carcinoma of pancreas BxPC-3 cell line.

Authors:  Yong Qin; Guan-Xiong Ye; Cheng-Jun Wu; Shi Wang; De-Biao Pan; Jin-Yan Jiang; Jing Fu; Sheng-Qian Xu
Journal:  Int J Clin Exp Pathol       Date:  2014-10-15

Review 3.  Preventing Damage Limitation: Targeting DNA-PKcs and DNA Double-Strand Break Repair Pathways for Ovarian Cancer Therapy.

Authors:  Daniela A Dungl; Elaina N Maginn; Euan A Stronach
Journal:  Front Oncol       Date:  2015-10-26       Impact factor: 6.244

4.  An ABCG2 non-substrate anticancer agent FL118 targets drug-resistant cancer stem-like cells and overcomes treatment resistance of human pancreatic cancer.

Authors:  Xiang Ling; Wenjie Wu; Chuandong Fan; Chao Xu; Jianqun Liao; Laurie J Rich; Ruea-Yea Huang; Elizabeth A Repasky; Xinjiang Wang; Fengzhi Li
Journal:  J Exp Clin Cancer Res       Date:  2018-10-03

5.  DNA damage induced by KP372-1 hyperactivates PARP1 and enhances lethality of pancreatic cancer cells with PARP inhibition.

Authors:  Talysa Viera; Praveen L Patidar
Journal:  Sci Rep       Date:  2020-11-19       Impact factor: 4.379

Review 6.  The Chromatin Response to Double-Strand DNA Breaks and Their Repair.

Authors:  Radoslav Aleksandrov; Rossitsa Hristova; Stoyno Stoynov; Anastas Gospodinov
Journal:  Cells       Date:  2020-08-07       Impact factor: 6.600

Review 7.  Take a Break to Repair: A Dip in the World of Double-Strand Break Repair Mechanisms Pointing the Gaze on Archaea.

Authors:  Mariarosaria De Falco; Mariarita De Felice
Journal:  Int J Mol Sci       Date:  2021-12-10       Impact factor: 5.923

8.  Tumor-selective use of DNA base excision repair inhibition in pancreatic cancer using the NQO1 bioactivatable drug, β-lapachone.

Authors:  Gaurab Chakrabarti; Molly A Silvers; Mariya Ilcheva; Yuliang Liu; Zachary R Moore; Xiuquan Luo; Jinming Gao; Glenda Anderson; Lili Liu; Venetia Sarode; David E Gerber; Sandeep Burma; Ralph J DeBerardinis; Stanton L Gerson; David A Boothman
Journal:  Sci Rep       Date:  2015-11-25       Impact factor: 4.996

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.