Inhibition of NEDD8-activating enzyme (NAE) has emerged as a highly promising approach to treat cancer through the adenosine sulfamate analog MLN4924. Here, we show that selective pressure results in HCT116 colorectal carcinoma cells with decreased MLN4924 sensitivity and identify a single-nucleotide transition that changes alanine 171 to threonine (A171T) of the NAE subunit UBA3. This reduces the enzyme's affinity for MLN4924 and ATP while increasing NEDD8 activation at physiological ATP concentrations. Expression of UBA3 A171T is sufficient to decrease MLN4924 sensitivity of naive HCT116 cells, indicating that it is a dominant suppressor of MLN4924-mediated cell death. Our data suggest that the on-target potency of MLN4924 selects for a point mutation in NAE that overcomes the molecule's inhibitory effects, allowing cancer cell survival.
A gatekeeper residue for NEDD8-activating enzyme inhibition by MLN4924.
MLN4924 抑制 NEDD8 激活酶的门控残基
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作者:Toth Julia I, Yang Li, Dahl Russell, Petroski Matthew D
| 期刊: | Cell Reports | 影响因子: | 6.900 |
| 时间: | 2012 | 起止号: | 2012 Apr 19; 1(4):309-16 |
| doi: | 10.1016/j.celrep.2012.02.006 | 研究方向: | 信号转导 |
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