Anticancer effect of AZD2461 PARP inhibitor against colon cancer cells carrying wt or dysfunctional p53
Creators
- 1. Department of Experimental Medicine, "Sapienza" University of Rome, Italy. Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti (Italy)
- 2. Department of Radiological, Oncological and Pathological Sciences, "Sapienza" University of Rome, Rome (Italy)
- 3. Department of Radiotherapy, Policlinico Umberto I, "Sapienza" University of Rome, Rome (Italy)
- 4. Department of Research and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome (Italy)
- 5. Department of Neurosciences, Imaging and Clinical Sciences, University "G. D'Annunzio" Chieti (Italy)
Description
Colon cancer is one of the most common cancers, currently treated with traditional chemotherapies or alternative therapies. However, these treatments are still not enough effective and induce several side effects, so that the search of new therapeutic strategies is needed. The use of Poly-(ADP-ribose)-polymerase (PARP) inhibitors, although originally approved against BRCA-1 or BRCA-2 mutated cancers, has been extended, particularly in combination with other treatments, to cure cancers that do not display defects in DNA repair signaling pathways. The role of p53 oncosuppressor in the regulating the outcome of PARP inhibitor treatment remains an open issue. In this study, we addressed this topic by using a well-tolerated PARP 1/2/3 inhibitor, namely AZD2461, against colon cancer cell lines with different p53 status. We found that AZD2461 reduced cell proliferation in wtp53 and p53−/− cancer cells by increasing ROS and DNA damage, while R273H mutant (mut) p53 counteracted these effects. Moreover, AZD2461 improved the reduction of cell proliferation by low dose radiation (IR) in wtp53 cancer cells, in which a down-regulation of BRCA-1 occurred. AZD2461 did not affect cell proliferation of mutp53 colon cancer cells also in combination with low dose radiation, suggesting that only wt p53 or p53 null colon cancer cells could benefit AZD2461 treatment.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.yexcr.2021.112879Additional details
Identifiers
- DOI
- 10.1016/j.yexcr.2021.112879;
- PII
- S001448272100433X;
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 408
- Journal Issue
- 2
- Journal Page Range
- vp.
- ISSN
- 0014-4827
- CODEN
- ECREAL
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53119067
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ADP; CELL PROLIFERATION; CHEMOTHERAPY; DNA DAMAGES; DNA REPAIR; LARGE INTESTINE; MUTANTS; NEOPLASMS; POLYMERASES; RADIATION DOSES; RIBOSE; SIDE EFFECTS
- Descriptors DEC
- ALDEHYDES; BIOLOGICAL RECOVERY; BIOLOGICAL REPAIR; BODY; CARBOHYDRATES; DIGESTIVE SYSTEM; DISEASES; DOSES; ENZYMES; GASTROINTESTINAL TRACT; INTESTINES; MEDICINE; MONOSACCHARIDES; NUCLEOTIDES; NUCLEOTIDYLTRANSFERASES; ORGANIC COMPOUNDS; ORGANS; PENTOSES; PHOSPHORUS-GROUP TRANSFERASES; PROTEINS; REPAIR; SACCHARIDES; THERAPY; TRANSFERASES
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier Inc. All rights reserved.