DNA damage and repair capacity in patients with non-small cell lung cancer treated with polychemotherapy

<p style="margin-bottom: .0001pt; text-align: justify; line-height: 150%;"><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Introduction:</strong> In advanced stages of non-small cell lung cancer (NSCLC), treatment is based pri...

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Bibliographic Details
Main Authors: Anamarys Pandolfi Blanco, Sergio Fernández García, Gretel Riverón-Forment, Reinaldo Gutiérrez Gutiérrez, Judith Pupo Balboa, Aimara de Armas Santiesteban, Gisselle Lemus Molina, Yanet López IzadaI
Format: Article
Language:English
Published: Universidad de Ciencias Médicas de La Habana 2018-05-01
Series:Revista Habanera de Ciencias Médicas
Online Access:http://www.revhabanera.sld.cu/index.php/rhab/article/view/2208
Description
Summary:<p style="margin-bottom: .0001pt; text-align: justify; line-height: 150%;"><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Introduction:</strong> In advanced stages of non-small cell lung cancer (NSCLC), treatment is based primarily on polychemotherapy. The sensitivity and the phenomena of chemoresistance to the treatments used depend, among other factors, on the functionality of the various DNA repair mechanisms.<br /> </span><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Objective:</strong> To evaluate the effect of polychemotherapy with cisplatin and vinblastine on basal endogenous DNA damage, and the repair capacity of H<sub>2</sub>O<sub>2</sub>-induced damage in patients with advanced NSCLC.<br /> </span><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Material and Methods:</strong> A descriptive study with a prospective longitudinal design was carried out. We included 15 patients with NSCLC, aged between 44 and 77 years, (stages IIIb-IV), treated with cisplatin and vinblastine in the <em>Hospital Neumologico "Benefico Juridico"</em>, and 10 apparently healthy individuals (ages: 52-69 years) as control group. The alkaline variant of the comet assay was used to determine the endogenous basal DNA damage and its capacity to repair the damage induced with H<sub>2</sub>O<sub>2</sub> in lymphocytes isolated from patients before and after treatment and controls<strong>.<br /> </strong></span><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Results:</strong> The patients had no alterations in the endogenous basal damage before treatment, but there was a reduced repair capacity of the damage induced in the DNA by the peroxide in comparison with the control subjects. After treatment, a significant increase in DNA damage was observed, as well as an increase in DNA repair efficiency.<br /> </span><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Conclusions:</strong> The combined treatment of cisplatin and vinblastine in patients with NSCLC in advanced stages produced DNA damage and the efficiency of DNA repair increased. These genotoxicity markers could be used as predictors of response to this polychemotherapy regimen.</span></p><p style="margin-bottom: .0001pt; text-align: justify; line-height: 150%;"><span style="color: #000000; font-family: verdana; font-size: small;"><strong>Keywords:</strong>DNA damage, DNA repair capacity, non-small cell lung cancer, cisplatin, vinblastine, Comet Assay.</span></p>
ISSN:1729-519X