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PMID: 16751059 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Genetic predictors of adverse radiotherapy effects: the Gene-PARE project.

International journal of radiation oncology, biology, physics ·Vol. 65 ·No. 3 ·2006-07-01 ·Pages 646-55

Ho AY, Atencio DP, Peters S, Stock RG, Formenti SC, Cesaretti JA, Green S, Haffty B, Drumea K, Leitzin L, Kuten A, Azria D, Ozsahin M, Overgaard J, Andreassen CN, Trop CS, Park J, Rosenstein BS

Abstract

The development of adverse effects resulting from the radiotherapy of cancer limits the use of this treatment modality. The validation of a test capable of predicting which patients would be most likely to develop adverse responses to radiation treatment, based on the possession of specific genetic variants, would therefore be of value. The purpose of the Genetic Predictors of Adverse Radiotherapy Effects (Gene-PARE) project is to help achieve this goal. A continuously expanding biorepository has been created consisting of frozen lymphocytes and DNA isolated from patients treated with radiotherapy. In conjunction with this biorepository, a database is maintained with detailed clinical information pertaining to diagnosis, treatment, and outcome. The DNA samples are screened using denaturing high performance liquid chromatography (DHPLC) and the Surveyor nuclease assay for variants in ATM, TGFB1, XRCC1, XRCC3, SOD2, and hHR21. It is anticipated that additional genes that control the biologic response to radiation will be screened in future work. Evidence has been obtained that possession of variants in genes, the products of which play a role in radiation response, is predictive for the development of adverse effects after radiotherapy. It is anticipated that the Gene-PARE project will yield information that will allow radiation oncologists to use genetic data to optimize treatment on an individual basis.

MeSH Terms
Ataxia Telangiectasia Mutated Proteins Cell Cycle Proteins/genetics Chromatography, High Pressure Liquid/methods DNA-Binding Proteins/genetics Deoxyribonuclease I/analysis Humans Mutation/genetics Neoplasms/radiotherapy Nuclear Proteins/genetics Phosphoproteins/genetics Polymorphism, Single Nucleotide/genetics Predictive Value of Tests Protein Serine-Threonine Kinases/genetics Radiation Injuries/genetics Radiation Tolerance/genetics Radiotherapy/adverse effects Superoxide Dismutase/genetics Transforming Growth Factor beta/genetics Transforming Growth Factor beta1 Tumor Suppressor Proteins/genetics X-ray Repair Cross Complementing Protein 1
Chemicals
Cell Cycle Proteins DNA-Binding Proteins Nuclear Proteins Phosphoproteins RAD21 protein, human TGFB1 protein, human Transforming Growth Factor beta Transforming Growth Factor beta1 Tumor Suppressor Proteins X-ray Repair Cross Complementing Protein 1 XRCC1 protein, human Superoxide Dismutase superoxide dismutase 2 ATM protein, human Ataxia Telangiectasia Mutated Proteins Protein Serine-Threonine Kinases Deoxyribonuclease I
Authors & Affiliations
18 authors, click to expand affiliations / ORCID
Ho Alice Y
Department of Radiation Oncology, Mount Sinai School of Medicine, New York, NY, USA.
Atencio David P
Peters Sheila
Stock Richard G
Formenti Silvia C
Cesaretti Jamie A
Green Sheryl
Haffty Bruce
Drumea Karen
Leitzin Larisa
Kuten Abraham
Azria David
Ozsahin Mahmut
Overgaard Jens
Andreassen Christian N
Trop Cynthia S
Park Janelle
Rosenstein Barry S
Article Info
Journal
International journal of radiation oncology, biology, physics
Abbr.
Int J Radiat Oncol Biol Phys
ISSN
0360-3016
Published
2006-07-01
Pages
646-55
Language
English
Region
United States
NLM ID
7603616
Subset
IM
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