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ABSTRACT: Context
Mutations in the gene encoding Mediator complex subunit MED12 are dominant drivers of uterine fibroids (UFs) in women of diverse racial and ethnic origins. Previously, we showed that UF-linked mutations in MED12 disrupt its ability to activate cyclin C-CDK8/19 in Mediator. However, validation of Mediator kinase disruption in the clinically relevant setting of MED12-mutant UFs is currently lacking.Objective
The objective of this study was twofold. First, to extend the ethnic distribution profile of MED12 mutations by establishing their frequency in UFs from Hispanic women of South Texas. Second, to examine the impact of MED12 mutations on Mediator kinase activity in patient-derived UFs.Methods
We screened 219 UFs from 76 women, including 170 tumors from 57 Hi
SUBMITTER: Park MJ
PROVIDER: S-EPMC6194812 | biostudies-literature | 2018 Nov
REPOSITORIES: biostudies-literature