Evidence map›Paper›PMID 19267883›Full record

ArticleJournal of cellular and molecular medicine2009

Proteomics analysis of protein expression and specific protein oxidation in human papillomavirus transformed keratinocytes upon UVB irradiation.

Marzia Perluigi, Alessandra Giorgi, Carla Blarzino, Federico De Marco, Cesira Foppoli, Fabio Di Domenico, D Allan Butterfield, M Eugenia Schininà, Chiara Cini, Raffaella Coccia

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

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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

13 citing papers in PubMed.

  1. Article
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  7. Article
  8. Article
  9. Article
  10. Smoking and cervical cancer.ISRN obstetrics and gynecology · 2011
    Article
  11. Article
  12. Article
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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

10 authors.

Marzia PerluigiDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.
Alessandra GiorgiDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.
Carla BlarzinoDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.
Federico De MarcoLaboratory of Virology, "Regina Elena Institute for Cancer Research", Rome, Italy.
Cesira FoppoliCNR Institute of Molecular Biology and Pathology, Rome, Italy.
Fabio Di DomenicoDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.
D Allan ButterfieldDepartment of Chemistry, Center of Membrane Science, and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA.
M Eugenia SchininàDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.
Chiara CiniDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.
Raffaella CocciaDepartment of Biochemical Sciences, "Sapienza" University of Rome, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence supports the role of oxidative stress in cancer development. Ultraviolet (UV) irradiation is one of the major sources of oxidative stress through the generation of reactive oxygen species (ROS). Besides the physiological function of ROS in cellular homeostasis, accumulating reports suggest that ROS are involved in all stages of multistep cancer development. In order to investigate the involvement of oxidative damage into the mechanisms of tumour progression, we used a parallel proteomic approach to analyse the protein expression profile and to identify oxidatively modified proteins in human papillomavirus (HPV)-transformed keratinocytes (HK-168 cells) upon ultraviolet B (UVB) exposure. The HK-168 cells were obtained from normal human epidermal keratinocytes transfected with the whole genome of the high-risk HPV type 16, unanimously recognized as an etiological agent of cervical carcinoma. Because of its year-long latency, this tumour offers a convenient model to study the role of environmental concurring agents in the multistep malignant progression. By the protein expression profile, we identified 21 proteins that showed different expression levels in HK-168 cells treated with UVB in comparison with untreated cells. Focusing on the oxidative modifications occurring at the protein level, we identified five proteins that showed elevated protein carbonyls levels: alpha-enolase, heat shock protein 75, annexin 2, elongation factor Tu and elongation factor gamma. Our results indicate that UVB-induced oxidative stress perturbs the normal redox balance and shifts HPV-transformed keratinocytes into a state in which the carbonylation of specific proteins is systematically induced. We suggest that UVB-induced modulation of protein expression combined with oxidative modification lead to protein dysfunction that might contribute to the malignant progression of transformed cells.

Indexed as

ProteomicsUltraviolet RaysBlotting, WesternCell Line, TransformedElectrophoresis, Gel, Two-DimensionalHumansKeratinocytesOxidation-ReductionPapillomaviridaeProteinsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationProteins

Identifiers

PMID19267883
PMCPMC6512374

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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.