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. Author manuscript; available in PMC: 2012 May 1.
Published in final edited form as: J Neurooncol. 2010 Sep 4;103(1):87–102. doi: 10.1007/s11060-010-0374-7

Fig. 1.

Fig. 1

The effect of expression of −17a.a./+KTS and +17a.a./+KTS WT1 isoforms on glioma chemosensitivity to BCNU. ATP assays, performed 5 days after treatment, were used as a surrogate of cell survival. Percent survival was normalized to untreated controls. a WT1 (−17a.a./+KTS) LNZ308 cells were consistently more chemoresistant compared to the other cells, particularly in the 100–200 μM range. b LN229 and c U87MG cells show little or no benefit from WT1 expression. d Expression of −17a.a./+KTS WT1 in LNZ308 cells was investigated further. Additional experiments performed with more replicates confirm a survival benefit at 100 or 150 μM of BCNU