Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:1.1.1.41 (
isocitrate dehydrogenase
)
3,101
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The Hedgehog (Hh) pathway regulates the growth of a subset of adult gliomas and better definition of Hh-responsive subtypes could enhance the clinical utility of monitoring and targeting this pathway in patients. Somatic mutations of the
isocitrate dehydrogenase
(
IDH
) genes occur frequently in WHO grades II and III gliomas and WHO grade IV secondary glioblastomas. Hh pathway activation in WHO grades II and III gliomas suggests that it might also be operational in glioblastomas that developed from lower-grade lesions. To evaluate this possibility and to better define the molecular and histopathological glioma subtypes that are Hh-responsive,
IDH
genes were sequenced in adult glioma specimens assayed for an operant Hh pathway. The proportions of grades II-IV specimens with
IDH
mutations correlated with the proportions that expressed elevated levels of the Hh gene target
PTCH1
. Indices of an operational Hh pathway were measured in all primary cultures and xenografts derived from
IDH
-mutant glioma specimens, including
IDH
-mutant glioblastomas. In contrast, the Hh pathway was not operational in glioblastomas that lacked
IDH
mutation or history of antecedent lower-grade disease.
IDH
mutation is not required for an operant pathway however, as significant Hh pathway modulation was also measured in grade III gliomas with wild-type
IDH
sequences. These results indicate that the Hh pathway is operational in grades II and III gliomas and glioblastomas with molecular or histopathological evidence for evolvement from lower-grade gliomas. Lastly, these findings suggest that gliomas sharing this molecularly defined route of progression arise in Hh-responsive cell types.
...
PMID:Identification of Hedgehog pathway responsive glioblastomas by isocitrate dehydrogenase mutation. 2306 52