HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

c-MYC is a radiosensitive locus in human breast cells.

Abstract
Ionising radiation is a potent human carcinogen. Epidemiological studies have shown that adolescent and young women are at increased risk of developing breast cancer following exposure to ionising radiation compared with older women, and that risk is dose-dependent. Although it is well understood which individuals are at risk of radiation-induced breast carcinogenesis, the molecular genetic mechanisms that underlie cell transformation are less clear. To identify genetic alterations potentially responsible for driving radiogenic breast transformation, we exposed the human breast epithelial cell line MCF-10A to fractionated doses of X-rays and examined the copy number and cytogenetic alterations. We identified numerous alterations of c-MYC that included high-level focal amplification associated with increased protein expression. c-MYC amplification was also observed in primary human mammary epithelial cells following exposure to radiation. We also demonstrate that the frequency and magnitude of c-MYC amplification and c-MYC protein expression is significantly higher in breast cancer with antecedent radiation exposure compared with breast cancer without a radiation aetiology. Our data also demonstrate extensive intratumor heterogeneity with respect to c-MYC copy number in radiogenic breast cancer, suggesting continuous evolution at this locus during disease development and progression. Taken together, these data identify c-MYC as a radiosensitive locus, implicating this oncogenic transcription factor in the aetiology of radiogenic breast cancer.
AuthorsM A Wade, N J Sunter, S E Fordham, A Long, D Masic, L J Russell, C J Harrison, V Rand, C Elstob, N Bown, D Rowe, C Lowe, G Cuthbert, S Bennett, S Crosier, C M Bacon, K Onel, K Scott, D Scott, L B Travis, F E B May, J M Allan
JournalOncogene (Oncogene) Vol. 34 Issue 38 Pg. 4985-94 (Sep 17 2015) ISSN: 1476-5594 [Electronic] England
PMID25531321 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Breast (cytology, radiation effects)
  • Breast Neoplasms (etiology, genetics)
  • Cell Line
  • DNA Copy Number Variations
  • Female
  • Genes, myc
  • Hodgkin Disease (radiotherapy)
  • Humans
  • Neoplasms, Radiation-Induced (genetics)
  • Polymorphism, Single Nucleotide
  • Radiation Dosage
  • Radiation Tolerance (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: