Cutaneous DNA Damage Caused by UV-A Irradiation

NCT ID: NCT00864955

Last Updated: 2009-09-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-03-31

Study Completion Date

2009-07-31

Brief Summary

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The DIMUVA study aims to evaluate the correlation between cutaneous phototype and the nature and quantity of damage caused to cutaneous DNA after exposure to UV-A radiation.

Detailed Description

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Due to their capacity to damage Deoxyribonucleic acid (DNA), Ultra-Violet (UV) radiation is one of the causes of skin cancers.

Until recently, the genotoxic effects of UV-A radiation, were poorly identified, in particular their capacity to lead to the dimerization of pyrimidine bases .

It is well known that the response to UV-A and UV-B radiations is different depending on the cutaneous phototype.

Thus, the aim of this study is to determine the correlation between cutaneous phototype and the quantity and nature (CPD or oxidative lesions) of damage caused to cutaneous DNA after an ex-vivo exposure to UV-A and UV-B radiations.

Conditions

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Healthy Volunteers

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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phototype 2

Volunteers with cutaneous phototype 2

Group Type EXPERIMENTAL

UVA and UVB irradiation

Intervention Type RADIATION

* 4 cutaneous biopsies for Ex-vivo irradiation
* Determination of the minimal erythemic dose of UVA and UVB for each volunteer

phototype 4

Volunteers with cutaneous phototype 4

Group Type EXPERIMENTAL

UVA and UVB irradiation

Intervention Type RADIATION

* 4 cutaneous biopsies for Ex-vivo irradiation
* Determination of the minimal erythemic dose of UVA and UVB for each volunteer

Interventions

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UVA and UVB irradiation

* 4 cutaneous biopsies for Ex-vivo irradiation
* Determination of the minimal erythemic dose of UVA and UVB for each volunteer

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* Male,
* Between 18 and 35 years old,
* Healthy volunteers,
* Cutaneous phototype 2 or 4 according to the Fitzpatrick classification,
* Affiliation to the French Social Security.

Exclusion Criteria

* History of photosensibility,
* Active smoking or stopped since less than one year,
* Dermatological pathology or treatment contra-indicating cutaneous irradiation and skin biopsies,
* Any chronic pathology susceptible to interfere with the evaluations related to the protocol,
* Allergy to local anaesthetics,
* Volunteers who take drugs and/or food complements acting on oxidative stress in the 8 weeks preceding inclusion,
* Volunteers who have take paracetamol or aspirin within 7 days prior to the inclusion visit,
* Subject in exclusion period for another biomedical research study,
* Subject having exceeded the threshold of annual compensation for biomedical research.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Commissariat A L'energie Atomique

OTHER_GOV

Sponsor Role collaborator

University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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University Hospital Grenoble

Principal Investigators

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Jean-Claude BEANI, Pr

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Grenoble

Locations

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Centre d'investigation Clinique ,University Hospital Grenoble

Grenoble, , France

Site Status

Department of Dermatology, University Hospital Grenoble

Grenoble, , France

Site Status

Countries

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France

References

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Brash DE. Sunlight and the onset of skin cancer. Trends Genet. 1997 Oct;13(10):410-4. doi: 10.1016/s0168-9525(97)01246-8.

Reference Type BACKGROUND
PMID: 9351343 (View on PubMed)

Melnikova VO, Ananthaswamy HN. Cellular and molecular events leading to the development of skin cancer. Mutat Res. 2005 Apr 1;571(1-2):91-106. doi: 10.1016/j.mrfmmm.2004.11.015.

Reference Type BACKGROUND
PMID: 15748641 (View on PubMed)

Cadet J, Sage E, Douki T. Ultraviolet radiation-mediated damage to cellular DNA. Mutat Res. 2005 Apr 1;571(1-2):3-17. doi: 10.1016/j.mrfmmm.2004.09.012. Epub 2005 Jan 26.

Reference Type BACKGROUND
PMID: 15748634 (View on PubMed)

Douki T, Reynaud-Angelin A, Cadet J, Sage E. Bipyrimidine photoproducts rather than oxidative lesions are the main type of DNA damage involved in the genotoxic effect of solar UVA radiation. Biochemistry. 2003 Aug 5;42(30):9221-6. doi: 10.1021/bi034593c.

Reference Type BACKGROUND
PMID: 12885257 (View on PubMed)

Dumaz N, Drougard C, Sarasin A, Daya-Grosjean L. Specific UV-induced mutation spectrum in the p53 gene of skin tumors from DNA-repair-deficient xeroderma pigmentosum patients. Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10529-33. doi: 10.1073/pnas.90.22.10529.

Reference Type BACKGROUND
PMID: 8248141 (View on PubMed)

Other Identifiers

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DCIC 08 13

Identifier Type: -

Identifier Source: org_study_id

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