Glioma (KEGG map)
This KEGG map shows the two genetic roads to glioblastoma: primary tumours amplify EGFR and lose PTEN and p16, secondary tumours from lower-grade astrocytomas over-express PDGF and CDK4 and lose TP53 and RB. It explains why growth-factor and cell-cycle drugs are the main targeted options in brain tumours, and why paediatric low-grade gliomas with BRAF changes respond to MAPK inhibitors.
Overview
Gliomas are the most common primary brain tumours, more than 40 percent of central nervous system neoplasms, and include astrocytomas, oligodendrogliomas, mixed gliomas and ependymomas. KEGG map hsa05214 draws the routes to glioblastoma, the most malignant infiltrating astrocytoma. Primary glioblastoma arises de novo in older patients and typically shows EGFR amplification or mutation, p16 (CDKN2A) and p14ARF deletion and PTEN mutation or deletion. Secondary glioblastoma progresses from low-grade or anaplastic astrocytoma in younger patients and frequently shows PDGF and PDGFR over-expression, CDK4 or MDM2 amplification, TP53 mutation and RB1 loss. Both routes converge on the same effectors: RAS-ERK, PI3K-AKT (unleashed by PTEN loss), PLC-gamma/calcium signalling from EGFR and PDGFR, and loss of the p16-CDK4/6-RB and p14ARF-MDM2-p53 checkpoints.
Weller and colleagues, Nature Reviews Disease Primers, 2015 (doi:10.1038/nrdp.2015.17) review the field: IDH mutation separates lower-grade and secondary tumours from IDH wild-type primary glioblastoma, MGMT promoter methylation predicts benefit from temozolomide, and BRAF V600E and KIAA1549-BRAF fusions characterise many paediatric low-grade gliomas.
What drugs do about it: temozolomide with radiotherapy remains the standard for glioblastoma, with bevacizumab used for symptomatic control; vorasidenib treats IDH-mutant grade 2 glioma; in paediatric low-grade glioma the BRAF-MAPK arm is drugged with tovorafenib (listed by KEGG) and with dabrafenib plus trametinib for BRAF V600E tumours, and the MEK inhibitors selumetinib and mirdametinib treat NF1-related tumours. EGFR and PDGFR inhibitors have so far failed in glioblastoma, partly because of the blood-brain barrier and tumour heterogeneity.
In one picture
Two roads to the same wreck. On the fast road (primary glioblastoma) the accelerator is welded down (EGFR) and the main brake line is cut (PTEN). On the slow road (secondary glioblastoma) a different accelerator is pressed (PDGF) and the brakes wear out one by one (TP53, RB). In children's low-grade gliomas a single stuck relay (BRAF) is the fault, which is why one drug can help.
Diagram
top- Paediatric low-grade glioma: BRAF-MAPK inhibitors tovorafenib (listed by KEGG), dabrafenib plus trametinib for BRAF V600E, selumetinib or mirdametinib for NF1-related tumours
- IDH-mutant grade 2 glioma: vorasidenib
- Glioblastoma: temozolomide with radiotherapy (MGMT methylated tumours benefit most), bevacizumab for symptom control
- EGFR and PDGFR inhibitors and CDK4/6 inhibitors have not yet shown benefit in glioblastoma trials
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