Literature DB >> 17504016

Therapeutic potential of drugs to modulate DNA repair in cancer.

Nicola Curtin1.   

Abstract

Most established cancer therapy regimes involve DNA-damaging chemotherapy or radiotherapy. The DNA repair capacity of the tumour, therefore, represents a mechanism of therapeutic resistance. Drugs to inhibit DNA repair pathways have been developed and they demonstrate good chemosensitisation and radiosensitisation activity in preclinical models. Two classes of DNA repair inhibitors have entered clinical trial and show promising activity. Genetic instability in tumours may be at least partially due to defects in DNA repair pathways; such defects may underlie the inherent sensitivity of some tumours to certain classes of anticancer agent. DNA repair defects may also make the tumour dependent on complimentary or back-up pathways; laboratory evidence shows that targeting these complimentary pathways results in tumour-selective therapy.

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Year:  2007        PMID: 17504016     DOI: 10.1517/14728222.11.6.783

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  7 in total

1.  Single-cell microarray enables high-throughput evaluation of DNA double-strand breaks and DNA repair inhibitors.

Authors:  David M Weingeist; Jing Ge; David K Wood; James T Mutamba; Qiuying Huang; Elizabeth A Rowland; Michael B Yaffe; Scott Floyd; Bevin P Engelward
Journal:  Cell Cycle       Date:  2013-02-19       Impact factor: 4.534

2.  Expression of PARP-1 and its active polymer PAR in prostate cancer and benign prostatic hyperplasia in Chinese patients.

Authors:  Wenqi Wu; Hanliang Zhu; Yeping Liang; Zhenzhen Kong; Xiaolu Duan; Shujue Li; Zhijian Zhao; Dong Yang; Guohua Zeng
Journal:  Int Urol Nephrol       Date:  2014-01-17       Impact factor: 2.370

3.  The DNA-damage response: new molecular insights and new approaches to cancer therapy.

Authors:  Stephen P Jackson
Journal:  Biochem Soc Trans       Date:  2009-06       Impact factor: 5.407

4.  Central nervous system penetration and enhancement of temozolomide activity in childhood medulloblastoma models by poly(ADP-ribose) polymerase inhibitor AG-014699.

Authors:  R A Daniel; A L Rozanska; E A Mulligan; Y Drew; H D Thomas; D J Castelbuono; Z Hostomsky; E R Plummer; D A Tweddle; A V Boddy; S C Clifford; N J Curtin
Journal:  Br J Cancer       Date:  2010-10-26       Impact factor: 7.640

5.  Liquid Chromatographic Determination of NSC 737664 (ABT-888: an Inhibitor of Poly(ADP-ribose) Polymerase (PARP)) in Plasma and Urine in a Phase 0 Clinical Trial.

Authors:  Lawrence R Phillips; Kimberly D Hill; Eva Majerova
Journal:  J Liq Chromatogr Relat Technol       Date:  2009-01       Impact factor: 1.312

6.  Downregulation of breast cancer resistance protein by long-term fractionated radiotherapy sensitizes lung adenocarcinoma to SN-38.

Authors:  Yuqing Wang; Jie Huang; Qiong Wu; Jingjing Zhang; Zhiyuan Ma; Shenglin Ma; Shirong Zhang
Journal:  Invest New Drugs       Date:  2021-01-21       Impact factor: 3.850

7.  BRCA1 promoter hypermethylation, 53BP1 protein expression and PARP-1 activity as biomarkers of DNA repair deficit in breast cancer.

Authors:  William Jacot; Simon Thezenas; Romain Senal; Cathy Viglianti; Anne-Claire Laberenne; Evelyne Lopez-Crapez; Frédéric Bibeau; Jean-Pierre Bleuse; Gilles Romieu; Pierre-Jean Lamy
Journal:  BMC Cancer       Date:  2013-11-05       Impact factor: 4.430

  7 in total

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