RT Journal Article SR Electronic T1 Spontaneous In Vitro Senescence of Glioma Cells Confirmed by an Antibody Against IDH1R132H JF Anticancer Research JO Anticancer Res FD International Institute of Anticancer Research SP 2859 OP 2867 VO 34 IS 6 A1 STOCZYNSKA-FIDELUS, EWELINA A1 OCH, WALDEMAR A1 RIESKE, PIOTR A1 BIENKOWSKI, MICHAL A1 BANASZCZYK, MATEUSZ A1 WINIECKA-KLIMEK, MARTA A1 ZIEBA, JOLANTA A1 JANIK, KAROLINA A1 ROSIAK, KAMILA A1 TREDA, CEZARY A1 STAWSKI, ROBERT A1 RADOMIAK-ZALUSKA, ANNA A1 PIASKOWSKI, SYLWESTER YR 2014 UL http://ar.iiarjournals.org/content/34/6/2859.abstract AB Background: We have recently suggested that glioblastoma cells become spontaneously senescent in cell culture conditions. The antibody specific against IDH1R132H offers the perfect opportunity to verify this hypothesis. Materials and Methods: We analyzed the features of senescence in 8 glioma cell cultures showing the IDH1R132H mutation based on combination of immunocytochemistry, enzymo-cytochemistry, BrdU incorporation assay and real-time microscopic observation. Results: We report that glioma cells showing the IDH1R132H mutation become rapidly and spontaneously senescent in vitro. Senescence was observed in both classical and novel serum-free cell culture conditions. Importantly, the senescent IDH1R132H-positive cells showed the expression of stemness marker (SOX2). Conclusion: In vitro senescence appeared to be the main reason of the difficulties in any kind culturing of glioma cells. 3D cell cultures prolonged the survival and in vitro proliferation of neoplastic IDH1R132H-positive cells, however, did not enhance the stabilization efficiency. Senescence of glioma cells is spontaneously triggered in vitro, which offers the opportunity of potential new therapeutic strategies based on this phenomenon.