- Open Access
Identification of targets for rational pharmacological therapy in childhood craniopharyngioma
- Jacob M. Gump1Email author,
- Andrew M. Donson2,
- Diane K. Birks3,
- Vladimir M. Amani2,
- Karun K. Rao2,
- Andrea M. Griesinger2,
- B. K. Kleinschmidt-DeMasters3, 4,
- James M. Johnston5,
- Richard C. E. Anderson6,
- Amy Rosenfeld7,
- Michael Handler3, 8,
- Lia Gore2, 9,
- Nicholas Foreman2, 9 and
- Todd C. Hankinson3, 8, 10Email author
© Gump et al.; licensee BioMed Central. 2015
- Received: 4 May 2015
- Accepted: 5 May 2015
- Published: 21 May 2015
Pediatric adamantinomatous craniopharyngioma (ACP) is a histologically benign but clinically aggressive brain tumor that arises from the sellar/suprasellar region. Despite a high survival rate with current surgical and radiation therapy (75–95 % at 10 years), ACP is associated with debilitating visual, endocrine, neurocognitive and psychological morbidity, resulting in excheptionally poor quality of life for survivors. Identification of an effective pharmacological therapy could drastically decrease morbidity and improve long term outcomes for children with ACP.
Using mRNA microarray gene expression analysis of 15 ACP patient samples, we have found several pharmaceutical targets that are significantly and consistently overexpressed in our panel of ACP relative to other pediatric brain tumors, pituitary tumors, normal pituitary and normal brain tissue. Among the most highly expressed are several targets of the kinase inhibitor dasatinib – LCK, EPHA2 and SRC; EGFR pathway targets – AREG, EGFR and ERBB3; and other potentially actionable cancer targets – SHH, MMP9 and MMP12. We confirm by western blot that a subset of these targets is highly expressed in ACP primary tumor samples.
We report here the first published transcriptome for ACP and the identification of targets for rational therapy. Experimental drugs targeting each of these gene products are currently being tested clinically and pre-clinically for the treatment of other tumor types. This study provides a rationale for further pre-clinical and clinical studies of novel pharmacological treatments for ACP. Development of mouse and cell culture models for ACP will further enable the translation of these targets from the lab to the clinic, potentially ushering in a new era in the treatment of ACP.
- Pilocytic Astrocytoma
- Malignant Peripheral Nerve Sheath Tumor
- Oncology Drug
Adamantinomatous craniopharyngioma (ACP) is the most common non-neural brain tumor with an incidence of approximately 1.9 cases/million patient-years in children [1–3]. Due to its sensitive sellar/suprasellar location and propensity to form large cysts, ACP often compresses and damages vital structures of the pituitary, hypothalamus and visual apparatus. Although seemingly well-demarcated on neuroimaging studies, histology reveals finger-like protrusions extending into neighboring visual and hypothalamic structures, eliciting tissue damage and gliosis . This propensity to invade adjacent structures, in addition to the difficult surgical location, often precludes total resection in order to avoid the significantly increased risk of visual and hypothalamic damage associated with attempts to completely remove the tumor [5–8]. The current standard of subtotal resection followed by radiation reduces some of the morbidity, however, it makes recurrence relatively common, even after apparently successful primary therapy. Outcomes after recurrence are poorer, with significantly higher mortality and morbidity than after primary treatment [9–11].
While conservative surgery and radiation confer low mortality, the morbidity for survivors is still unacceptably high. Variable morbidities are associated with ACP but include endocrine, neurological, vascular, psychological and visual deficits . As a result, ACP has been associated with the lowest quality of life (QoL) scores of any pediatric brain tumor . Lifelong care is necessary for most childhood craniopharyngioma patients and ACP and is considered by many to be a chronic disease . The introduction of rational therapy to treat craniopharyngioma could drastically reduce the morbidity associated with both the primary disease and current treatments by reducing the extent of resection and/or reducing or eliminating the need for subsequent radiation. Such a paradigm change in ACP treatment is critical to improving long term QoL for patients with this debilitating disease.
Progress regarding our understanding of the biological drivers of ACP growth has been slowed by the relative rarity of the tumor and the recalcitrance of ACP cells to laboratory growth. Lack of knowledge of the underlying biology, combined with the clinical complexity of ACP have led to an absence of standard systemic antitumor therapies. Few attempts to remedy this deficit have been made, in part because current therapy has acceptable survival outcomes. Nevertheless, substantial progress has been made recently through tissue banking collaborations and “omics” approaches.
Virtually all craniopharyngiomas in childhood are of the adamantinomatous type (ACP), contrasting with adults in whom up to 10 % of craniopharyngiomas are papillary, and are now known to be driven by BRAF V600E mutations . The only known genetic alterations in adamatinomatous craniopharyngioma (ACP) are point mutations in exon 3 of CTNNB1 that lead to β-catenin accumulation and upregulation of downstream target gene expression. While the reported frequency of CTNNB1 sequence alterations ranges from 16–100 % [16–19], Brastianos and colleagues  recently used whole exome sequencing and mass spectrometric genotyping to identify CTNNB1 mutations in 92–96 % of ACP. It is likely, however, that genetic, epigenetic or other biological factors in addition to CTNNB1 mutation contribute to the pathogenesis of ACP. For instance, Larkin and colleagues  described 2 tumors that harbored alterations in both CTNNB1 and BRAF. Furthermore, ACP tumors with CTNNB1 mutation contain cells that do not demonstrate intranuclear β-catenin accumulation  and it has been suggested that some of the cells that comprise the tumor may not actually be CTNNB1 mutant “tumor” cells at all . EGFR pathway activation has also recently been identified as a driver of migration and growth using in-vitro and xenotransplant models of ACP, supporting the testing of EGFR targeted therapies [23, 24]. In addition, through an embryonic mouse model of human ACP, the role of pituitary stem cells in ACP tumorigenesis is being explored [22, 25, 26].
The recent identification of BRAF mutations in papillary craniopharyngioma changes the paradigm in treating this (primarily adult) tumor because of the availability of BRAF V600E-specific inhibitors. By contrast, the identification of β-catenin/Wnt signaling as a driver of adamantinomatous craniopharyngioma (ACP) is of little use in guiding therapy because inhibitors of Wnt signaling downstream of β-catenin/TCF/LEF are not yet clinically viable . Global gene expression analysis is therefore critical for determining the epigenetic effect of aberrant β-catenin driven transcription in ACP in order to find targets for rational therapy [22, 28].
β-catenin and BRAF mutational status of tumor and age of 15 ACP patient cohort used in transcriptome study
Age at Dx
Nucleic acid extraction, amplification and microarray preparation
RNA from all surgical specimens was extracted, amplified, labeled and hybridized to Affymetrix HG-U113 plus 2 microarray chips (Affymetrix, Santa Clara, CA, USA) according to manufacturer’s instructions and as described previously . SNaPshot analysis for CTNNB1 and BRAF mutations was performed at the University of Colorado Pathology Core per manufacturer’s instructions and as described previously [22, 30]. Patient characteristics, including presence or absence of CTNNB1 mutations by SNaPshot analysis, are shown in Table 1. SNaPshot analysis was also used to examine BRAF mutational status (Table 1), specifically BRAF V600E, which was recently identified in papillary craniopharyngioma . This mutation was not found in any ACP sample tested.
Microarray data analysis
Data analysis was performed in R (http://www.r-project.org), using packages publicly available through Bioconductor (http://www.bioconductor.org). As a first step, the scanned microarray data were background corrected and normalized using the gcRMA algorithm  resulting in log 2 gene expression values. Publically available microarray CEL file data were obtained for 9 normal pituitary and 14 pituitary adenoma samples from GEO (GSE26966); these samples were chosen because they were processed in the same manner as ours and through the same microarray core lab . These were combined with the ACP, other tumor, and normal brain cohort as detailed above. Multiple probesets for a gene were then collapsed to 1 entry per gene, based on the mean best-expressed probeset for that gene. Hierarchical clustering was performed using the normalized gene expression data. Distances based on Spearman correlations were calculated for input to an agglomerative algorithm with use of complete linkage, as implemented in the Bioconductor hclust function. These microarray data have been deposited in the National Center for Biotechnology Information Gene Expression Omnibus (GEO) database  and are publicly accessible through GEO Series accession number GSE68015 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68015).
Differential gene expression between ACP and multiple other tumor and normal tissue types was calculated using the Bioconductor limma function . Data were filtered before input to eliminate genes not expressed in any samples or that showed only limited variance across samples. The limma function performs pair-wise comparisons between a target group and each of the other user-defined groups in the dataset. It uses an Empirical Bayes approach to calculate a moderated t-statistic and calculates a false discovery rate (FDR) that accounts for multiple testing both within and across groups. The unique molecular signature of ACP was defined as genes that showed significant differential expression in all of the pair-wise comparisons (FDR ≤0.1 and mean fold difference ≥1.5) and for which the mean difference was in the same direction when compared with all of the other clusters (i.e., either all upregulated or all downregulated in all of the comparisons with respect to ACP).
In further analyses, individual tumor gene expression of select genes involved in putative ACP development/biology were extracted from the normalized dataset. For these comparisons, normalized hybridization intensity values for a selected gene for individual ACP samples were presented as fold-difference relative to the average of all other tumor and normal samples.
Data analysis using hierarchical clustering, NIH Database for Annotation, Visualization, and Integrated Discovery (DAVID) bioinformatics tools has been previously described . Functional analysis of genes was performed with DAVID using the Gene Ontology, Protein Analysis Through Evolutionary Relationships (PANTHER) Biological Process and KEGG databases [35–37]. ACP upregulated genes were compared to known targets of FDA approved and other oncology drugs that had reached clinical trial stage, as published in the literature and compiled in Ingenuity’s KnowledgeBase (Ingenuity Systems, www.ingenuity.com). Oncology drug target gene expression in individual ACP samples (n = 15) was compared to all other tumor and normal tissue combined and assigned percentile scores. Drug target genes that were consistently highly expressed (>66th percentile) in all ACP samples were identified, and then ranked according to the highest average percentile expression.
Western blot validation of functional isoforms of putative drug targets
Protein levels of a selection of putative drug target genes in ACP were examined by Western blot analysis to validate the results of microarray analysis. Snap frozen tumor samples were homogenized in RIPA buffer (Sigma) supplemented with protease and phosphatase inhibitors (Roche). This study utilized 6 ACP samples and 3 each of AT/RT, EPN, GBM, MED, PA and normal brain (obtained from autopsy material). Proteins samples (30 μg) were resolved on a 26 well Criterion Gel (BioRad) and transferred to Immobilon PVDF membrane (Millipore). Membranes were probed with antibodies to SHH (Millipore #06-1106; 1:1000), MMP9 (Cell Signaling #3852; 1:1000), MMP12 (R&D Systems #AF917; 1:1000) and Actin (Cell Signaling #12262; 1:10,000).
Identification of potential drug targets and ACP signature genes
Top 20 therapeutic target genes overexpressed in ACP compared to normal brain tissues and a variety of CNS and peripheral malignancies
# of ACP >66th %-ile
matrix metallopeptidase 12
sonic hedgehog homolog
interleukin 2 receptor, beta
lymphocyte-specific protein tyrosine kinase
EPH receptor A2
phosphoinositide-3-kinase, catalytic, delta
interleukin 6 receptor
matrix metallopeptidase 9
epithelial cell adhesion molecule
v-src sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog
v-erb-b2 erythroblastic leukemia viral oncogene homolog 3
tumor necrosis factor (ligand) superfamily, member 11
mitogen-activated protein kinase 14
prostaglandin-endoperoxide synthase 2
related RAS viral (r-ras) oncogene homolog
proteasome (prosome, macropain) subunit, beta type, 1
epidermal growth factor receptor
Cetuximab, Erlotinib, Gefitinib, Lapatinib, etc.
Transcriptome microarray clustering analyses
Gene expression signature recapitulates ACP histopathological characteristics
Enriched ontology terms associated with ACP-exclusive genes. Limma identified 384 genes that were exclusively expressed in ACP compared to a normal brain tissues and a variety of CNS and peripheral malignancies. DAVID was used to identify 23 enriched ontologies (FDR < 0.005) that are shown ranked according to fold enrichment. Abbreviation: Ontology ID prefix GO, Gene ontology biological process; BP, panther biological process; HSA, KEGG pathway; FDR, Benjamini false discovery rate adjusted p-value
Odontogenesis of dentine-containing tooth
Epidermal cell differentiation
Epithelial cell differentiation
Cell adhesion-mediated signaling
Cytokine-cytokine receptor interaction
Skeletal system development
Cell structure and motility
Regulation of cell proliferation
Wnt pathway genes are expressed homogeneously and not at abnormally high levels in ACP (Fig. 4b), with the exception of the transcription factor (TCF)/lymphoid enhancer-binding factor (LEF) targets LEF1 and WNT5A. However, consistent with the hypothesis that aberrant Wnt signaling (via mutant β-catenin) is responsible for the pathogenesis of ACP, β-catenin/TCF/LEF target genes are overexpressed an average of 32 fold over the other samples (Fig. 4c).
Identification of potential therapeutic targets in our transcriptomic analysis confirmed findings of previous studies that had identified SHH and EGFR pathway activity in ACP and provide further evidence that therapies targeting these pathways could be used successfully in treating ACP. Transcriptomic analysis of ACP generated in a mouse model demonstrated high levels of SHH gene expression, suggesting a mitogenic autocrine/paracrine loop . A subsequent study identified upregulation of members of the SHH signaling pathway in human specimens . In vitro and xenotransplant model studies have demonstrated that EGFR activation is responsible for driving growth and migration in ACP [23, 24]. The proven clinical utility of EGFR inhibition in the treatment of cancer makes EGFR targeted drugs an attractive approach to ACP treatment. Our identification of high levels of EGFR ligand AREG provide a potential mechanism for EGFR activation in ACP that warrants further exploration. Furthermore, AREG has been implicated as a paracrine/juxtacrine regulator of cell survival in other cancers and epidermal cell types . It has also recently been suggested that ACP may be paracrine in nature (i.e. the CTNNB1 mutant cells may promote the proliferation of another cell type that actually populates the tumor) . This hypothesis could explain the extensive intratumoral heterogeneity in ACP and perhaps the difficulty we and others have found in obtaining “pure” tumor samples to accurately identify CTNNB1 mutations .
We also identified a number of additional novel potential drug targets. One group, including LCK, EPHA2 and SRC, is targeted by the kinase inhibitor dasatinib. Hundreds of trials are now underway using dasatinib to treat a wide variety of cancers beyond the few for which it currently has FDA approval. A second group of targets we identified are extracellular proteases, of which many were strongly represented in our analysis; two in particular, MMPs 9 and 12, are targeted by the drug AZD1236. MMP12, which we found expressed at very high levels, is a proteolytic factor that may contribute to the significant invasive phenotype that is a hallmark of ACP . Previous studies have attempted to correlate proteinase activity with biological course in ACP  including a study that confirmed the presence of MMP9 by immunohistochemistry .
The results of this transcriptomic study of human pediatric ACP shed further light on the biology of this tumor, reflect the odontogenic and epithelial characteristics in the pathology of ACP and recapitulate the origins of ACP from oral ectoderm. The origins of ACP have long been the subject of speculation due to the oddity of their morphology and location. Many consider ACP to be a congenital midline developmental malformation, but the (albeit infrequent) occurrence of ACP in late adulthood and variable presentation are difficult to reconcile with this hypothesis. The recognition that β-catenin dysregulation is responsible for ACP have led to two conflicting mouse models for the formation of ACP – in mice an ACP-like tumor can develop from targeted CTNNB1 mutations in either pituitary oral ectoderm precursors in developing mice embryos or in pituitary stem cells in post-natal mice . The data presented here are consistent with the theory that ACP is a congenital malformation that develops from the improper closure of the craniophyrangeal duct from the oral ectoderm-derived remnants of Rathke’s pouch [46–48] (Table 3). However, these data are not completely inconsistent with the hypothesis that ACP arises from an anterior pituitary stem cell that transdifferentiates toward an oral epithelial phenotype [25, 26]. Further analysis of more ACP samples, including adult ACP, in addition to transcriptomic studies of neuropathologically distinct cell subtypes present within ACP tumors will contribute to our understanding of how these tumors form and perhaps how to better treat them.
Current standard therapy for ACP is surgery and radiation, both of which lead to high morbidity in this sensitive region of the brain, especially in children, in whom these morbidities become a lifelong and life-altering disease. Intracystic delivery of therapeutic agents (interferon-alpha, bleomycin or Ytrrium90) has shown some efficacy in treating ACP , but this approach is limited by the requirement of a single cyst in the presenting tumor and requires stereotactic surgery to place a catheter and Ommaya reservoir for delivery. Systemic therapy could more safely and more effectively treat children with ACP. However, progress has been hindered by the absence of in vitro or in vivo models of this tumor that would enable the unbiased screening of drug libraries. This study forms the basis for further studies with rational therapies for ACP. The recent development of ACP xenotransplants in immune deficient mice  will enable pre-clinical testing of these rationally selected targeted therapies, providing further rationale for small studies on efficacy in augmenting surgery and radiation or in treating recurrent ACP. These efforts, combined with further collaborations between centers and consortiums will provide the foundation for a randomized clinical trial using targeted agents to treat ACP in the near future.
This work was supported by the Morgan Adams Foundation (J.M.G., T.C.H., N.F.), Colorado Clinical and Translational Sciences Institute/Children’s Hospital Colorado Research Institute KL2 Research Scholar Award NCATS/NIH UL1 TR001082 (T.C.H.), T32CA082086 (J.M.G.), American Cancer Society Postdoctoral Fellowship (J.M.G.) and the Molecular Pathology and Genomics and Microarray Shared Resources of the University of Colorado’s NIH/NCI Cancer Center support Grant P30CA046934.
We would like to thank Susan Staulcup, MS, for her extensive organizational and administrative support of this work. We also thank the laboratory of Dr. Margaret Wierman for the use of their pituitary microarray data.
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