ATM protein expression correlates with radioresistance in primary glioblastoma cells in culture

Purpose: Glioblastoma multiforme (GBM) is one of the malignancies most resistant to radiation therapy. In contrast, cells derived from individuals with ataxia telangiectasia (AT) possessing mutations in the ATM gene, demonstrate increased sensitivity to ionizing radiation, Using a collection of glioma specimens adapted to tissue culture and several established GEM cell lines, we investigated the relationship between ATM protein expression and radiosensitivity. The three aims of our study were to: (1) quantify ATM protein levels in cultured glioma cells; (2) measure the correlation between ATM protein levels and radiation sensitivity; and (3) examine the dependence of ATM on p53 status. Methods and Materials: Glioma specimens were collected, catalogued, and adapted to grow in culture. Levels of ATM, p53, and p21 proteins were determined by Western blot. Radiation sensitivities were determined by clonogenic assays. p53 mutation status was determined by DNA sequencing. Correlations were identified by linear regression analysis. Results: ATM protein levels were variable in the primary gliomas, Glioma cell lines demonstrated significantly lower levels of ATM protein, Clonogenic assays of cell strains and cell lines yielded survival fractions (SF(2)s) consistent with the radioresistant behavior of GEM tumors in vivo. Regression analysis revealed a high correlation between ATM protein levels and SF, for primary glioma cell strains, but not for established GEM cell lines. p53 status failed to predict radiosensitivity. Conclusion: We have demonstrated that while our collection of low passage cell cultures depends on ATM for their resistance to IR, established cell lines may acquire adaptive characteristics which downplay the role of the ATM gene product in vitro. Therefore, attenuating ATM gene expression may be a successful strategy in the treatment of GEM tumors. (C) 2001 Elsevier Science Inc.