Influence of ionizing radiation on proliferation, c-myc expression and the induction of apoptotic cell death in two breast tumour cell lines differing in p53 status

• Published in: International journal of radiation biology Vol. 72; no. 5; pp. 547 - 559
• Main Authors: WATSON, N. C, DI, Y.-M, ORR, M. S, FORNARI, F. A, RANDOLPH, J. K, MAGNET, K. J, JAIN, P. T, GEVIRTZ, D. A
• Format: Journal Article
• Language: English
• Published: London Informa UK Ltd 01-11-1997; Taylor & Francis
• Subjects: Apoptosis - radiation effects; Biological and medical sciences; Biological effects of radiation; Breast Neoplasms - genetics; Breast Neoplasms - pathology; Cell Division - radiation effects; DNA Damage; Female; Fundamental and applied biological sciences. Psychology; G1 Phase; Genes, myc - radiation effects; Humans; Radiocontamination; Space life sciences; Tissues, organs and organisms biophysics; Tumor Cells, Cultured; Tumor Suppressor Protein p53 - analysis; Ionizing radiation; DNA; Established cell line; Radiation injury; Tumor; Gene expression; Apoptosis
• DOI: 10.1080/095530097143059
• EISSN: 1362-3095
• ISSN: 0955-3002

Purpose : To determine the capacity of ionizing radiation to inhibit proliferation, to suppress c- myc expression and to induce apoptotic cell death in the p53 wild-type MCF-7 cell line and the p53 mutated MDA-MB231 cell line. Materials and methods : Growth inhibition and cell killing were determined by cell number and trypan blue exclusion. Apoptosis was assessed through cell morphology and fluorescent endlabelling. c- myc expression was monitored by Northern blotting. Results : Inhibition of cell proliferation by ionizing radiation was similar in both cell lines. MDA-MB231 cells accumulated in G2 while MCF-7 cells accumulated in both the G1 and G2 phases of the cell cycle after irradiation. There was no evidence of apoptosis in either cell line. In MCF-7 cells, growth inhibition correlated closely with an early dose-dependent suppression of c- myc expression; in MDA-MB231 cells, there was no correspondence between growth inhibition and a transient, dose- independent reduction in c- myc message. Conclusions : These findings suggest that in the absence of classical apoptotic cell death, radiosensitivity is not predictably related to the p53 status of the cell. While both p53 and c- myc may be linked to the DNA damage response pathway, neither p53 nor c- myc are essential for growth arrest in response to ionizing radiation.