Evidence map›Paper›PMID 36327269›Full record

ArticlePloS one2022

DNA damage and antioxidant capacity in COPD patients with and without lung cancer.

Camila Freitas Dos Santos, Mariana Gobbo Braz, Nayara Micarelli de Arruda, Laura Caram, Duelene Ludimila Nogueira, Suzana Erico Tanni, Irma de Godoy, Renata Ferrari

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Implications of DNA damage in chronic lung disease.Frontiers in cell and developmental biology · 2024
    Review
  8. Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Camila Freitas Dos SantosUNINOVE, Bauru Campus, Bauru, Brazil.ORCID 0000-0002-3520-8974
Mariana Gobbo BrazBotucatu Medical School, GENOTOX Laboratory, São Paulo State University-UNESP, São Paulo, Brazil.
Nayara Micarelli de ArrudaBotucatu Medical School, GENOTOX Laboratory, São Paulo State University-UNESP, São Paulo, Brazil.ORCID 0000-0002-1937-1691
Laura CaramDepartment of Internal Medicine, Botucatu Medical School, São Paulo State University-UNESP, São Paulo, Brazil.
Duelene Ludimila NogueiraDepartment of Internal Medicine, Botucatu Medical School, São Paulo State University-UNESP, São Paulo, Brazil.
Suzana Erico TanniDepartment of Internal Medicine, Botucatu Medical School, São Paulo State University-UNESP, São Paulo, Brazil.
Irma de GodoyDepartment of Internal Medicine, Botucatu Medical School, São Paulo State University-UNESP, São Paulo, Brazil.
Renata FerrariDepartment of Internal Medicine, Botucatu Medical School, São Paulo State University-UNESP, São Paulo, Brazil.
Universidade Estadual Paulista (Unesp) · BRUniversidade Nove de Julho · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveChronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the lower airways, and COPD patients show two to five times higher risk of lung cancer than smokers with normal lung function. COPD is associated with increased oxidative stress, which may cause DNA damage and lung carcinogenesis. Our aim was to evaluate DNA damage and oxidative stress (lipid peroxidation and antioxidant status) and their relationship in patients with COPD with and without lung cancer.

methodsWe evaluated 18 patients with COPD, 18 with COPD with lung cancer, and 18 controls (former or current smokers). DNA damage was evaluated in peripheral blood lymphocytes using a comet assay; the concentration of malondialdehyde (MDA) and hydrophilic antioxidant performance (HAP) were measured in the plasma.

resultsDNA damage was higher in patients with COPD with cancer than in the controls (p = 0.003). HAP was significantly lower in patients with COPD with cancer than in those without cancer and controls. The presence of lung cancer and COPD showed a positive association with DNA strand breaks and the concentration of MDA.

conclusionCOPD with lung cancer was associated with elevated DNA damage in peripheral lymphocytes, and cancer and COPD showed a positive correlation with DNA damage. The antioxidant capacity showed a negative association with the interaction COPD and cancer and presence of COPD. The mechanisms underlying the increased incidence of lung cancer in COPD are unknown; DNA damage may be involved. Further research may provide insights into their development and treatment.

Indexed as

Lung NeoplasmsPulmonary Disease, Chronic ObstructiveAntioxidantsDNA DamageHumansOxidative StressSmokingAntioxidants

Identifiers

PMID36327269
PMCPMC9632772
OpenAlexW4308098919

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.