Somatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case
© Belinsky et al. 2015
Received: 22 July 2015
Accepted: 30 October 2015
Published: 10 November 2015
Approximately 10–15 % of gastrointestinal stromal tumors (GISTs) lack gain of function mutations in the KIT and platelet-derived growth factor receptor alpha (PDGFRA) genes. An alternate mechanism of oncogenesis through loss of function of the succinate-dehydrogenase (SDH) enzyme complex has been identified for a subset of these “wild type” GISTs.
Paired tumor and normal DNA from an SDH-intact wild-type GIST case was subjected to whole exome sequencing to identify the pathogenic mechanism(s) in this tumor. Selected findings were further investigated in panels of GIST tumors through Sanger DNA sequencing, quantitative real-time PCR, and immunohistochemical approaches.
A hemizygous frameshift mutation (p.His2261Leufs*4), in the neurofibromin 1 (NF1) gene was identified in the patient’s GIST; however, no germline NF1 mutation was found. A somatic frameshift mutation (p.Lys54Argfs*31) in the MYC associated factor X (MAX) gene was also identified. Immunohistochemical analysis for MAX on a large panel of GISTs identified loss of MAX expression in the MAX-mutated GIST and in a subset of mainly KIT-mutated tumors.
This study suggests that inactivating NF1 mutations outside the context of neurofibromatosis may be the oncogenic mechanism for a subset of sporadic GIST. In addition, loss of function mutation of the MAX gene was identified for the first time in GIST, and a broader role for MAX in GIST progression was suggested.
KeywordsGastrointestinal stromal tumor (GIST) Wild type KIT PDGFRA Succinate dehydrogenase (SDH) NF1 MAX
Gastrointestinal stromal tumor (GIST) is a mesenchymal neoplasm that originates throughout the GI tract, primarily in the stomach (>50 %) and small intestine (~30 %) . GIST generally presents in older adults, while ~2 % of cases are children [2, 3]. Originally thought to be of smooth muscle origin, immunohistochemical and ultrastructural studies suggest that GIST is related to spindle-shaped cells of the GI tract known as the interstitial cells of Cajal (ICC) [4, 5]. ICC and the majority (95 %) of GIST express the type III receptor tyrosine kinase KIT (CD117), and variably exhibit myoid or neural features. The majority of GISTs exhibit gain of function mutations in KIT or in the related receptor PDGFRA [6, 7]. A subset (~10–15 %) of GISTs in adults lack mutations in the KIT and PDGFRA genes, as do almost all pediatric cases [8, 9]. The commonly used label of “wild type” (WT) GIST belies the epidemiological, clinico-pathological and molecular heterogeneity that define these tumors. WT GIST occurs in the context of several multitumor syndromes, including the inherited Carney-Stratakis Syndrome (CSS) and the non-familial Carney triad (CT). Manifestations of CSS and CT include gastric GIST and paraganglioma (PGL), a neural crest-derived tumor, while the spectrum of CT neoplasms includes pulmonary chondroma and several other neoplasms [10, 11]. CSS results from loss of function mutations in subunit genes of the succinate-dehydrogenase (SDH) enzyme complex, SDHB, SDHC, and SDHD . Inactivation of the SDHA gene subunit has recently been implicated as a causative factor in a subset of apparently sporadic adult WT GIST (reviewed in ). GISTs from CT patients do not manifest SDHX mutations; however, these tumors are also SDH-deficient, and the molecular underpinning of CT GIST has been attributed to epigenetic silencing of the SDHC gene . Pediatric GIST patients share hallmarks of CT-associated GIST, namely early-onset, multi-focal, gastric disease with a predilection towards females , and pediatric GIST cases have also been associated with SDHC epimutation . Thus the identification of SDH-deficient GIST, also referred to as “type 2”, helps distinguish between KIT/PDGFRA mutant, or type I GIST, and a majority of wild type GIST.
SDH-intact WT GISTs with alternate oncogenic events have been described. Mutations in the serine-threonine kinase gene BRAF have recently been identified in approximately 5–15 % of sporadic wild type GIST . These tumors are generally KIT-positive with spindle cell or mixed morphology, and are found primarily in the small intestine in adult cases. Approximately 1–2 % of GISTs occur in the context of neurofibromatosis type I (NF1) , an autosomal dominant disorder with skin and ophthalmologic manifestations that predisposes to a variety of benign and malignant tumors. GIST in NF1 individuals also present typically in the small bowel with spindle-cell morphology, are found in men and women at a younger median age than KIT/PDGFRA mutant GIST, and are often multifocal [17, 18]. Neurofibromatosis is due to germline mutations in neurofibromin 1, a RAS-GAP protein and negative regulator for RAS signaling, and germline NF1 mutations accompanied by somatic events have been identified in NF1 GIST cases .
In this report we describe whole exome sequencing (WES) of a particularly complex, SDH-intact wild type GIST case. The WES analysis identified for the first time the somatic inactivation of NF1 in a GIST outside the context of NF1 syndrome. A novel somatic loss of function mutation in the MYC-associated factor X (MAX) gene was also identified. Immunohistochemical studies of a panel of GISTs identified deficiencies in MAX expression in a number of tumors. Implications for these and other identified mutations are discussed.
Preparation of genomic DNA and total RNA
De-identified tumor samples and normal blood were obtained following written informed consent from the Fox Chase Cancer Center Biosample Repository. The protocol was approved by the Fox Chase Cancer Center Institutional Review Board (#03-848). The isolation and characterization of genomic DNA and total RNA from frozen tumor specimens embedded in optimum-temperature cutting medium has been described .
Whole exome sequencing data analysis
Confirmed somatic mutations
Primers for amplification and sequencing of KIT (exons 9, 11, 13, 17), PDGFRA (exons 12, 14, 18), and BRAF (exons 11,15) have been described , as have primers for SDHA  and SDHB-D . Primer sequences for confirmation of mutations listed in Table 1 and MAX genomic sequencing are shown in Additional file 1: Table S1. Relevant exons were PCR-amplified from genomic DNA and subjected to Sanger sequencing (Beckman Coulter Genomics).
GIST tissue microarrays (TMAs) were constructed in conjunction with the FCCC Biosample Repository. H&E-stained sections from paraffin-embedded tissue blocks were evaluated by a pathologist for tumor content and cellularity, and two cores from each block were selected for the TMA. Each TMA consists of ~ 30 GIST specimens along with normal tissue sections. IHC for MAX was performed with the SC-197 antibody (Santa Cruz Biotechnology, Dallas TX) at a 1:400 dilution with antigen retrieval. Aperio Digital Pathology (Leica Biosystems, Buffalo Grove, IL) was used to capture and quantify MAX-stained TMAs using the nuclear algorithm. MAX-deficient cases were confirmed on whole-tissue sections, as were a subset of MAX-positive cases. IHC for KIT was performed as described .
Gene expression analysis
Random-primed cDNA was prepared from 2 μg total RNA using the High Capacity cDNA Reverse Transcription KIT (Life Technologies). RNA expression was measured by real-time PCR (qRT-PCR) on an ABI PRISM 7900 HT Sequence Detection System using fluorescein phosphoramidite (FAM) primer/probe sets (Applied Biosystems). RNA expression data for MAX were normalized using hypoxanthine guanine phosphoribosyl transferase 1 (HPRT1) and glucuronidase beta (GUSB). Taqmen sets used were Hs99999909_m1 (HPRT1), Hs99999908_m1 (GUSB), and Hs00811069_g1 (MAX).
The patient first presented at the age of 54 with a high-risk GIST of the small bowel. Resections of several local and distant recurrences were documented over several years, and the patient was treated with imatinib, sunitinib, and several additional targeted agents. A locally recurrent 1.5 cm small bowel tumor was resected, and a small portion of flash-frozen tumor and a whole blood sample were provided following informed consent. Formalin-fixed paraffin embedded (FFPE) tissue from an earlier small bowel resection was also available. Histologic evaluation of these specimens indicated a high-cellularity spindle-cell tumor with a high mitotic index (5-10/50 HPF) and no necrosis.
Sanger sequencing of DNA from the flash-frozen tumor indicated that no mutations were present in the “hotspot” exons of KIT, PDGFRA, or BRAF. Exon-based sequencing of the SDH complex subunit genes SDHA-D identified no SDHX mutations, and the tumor was immunohistochemically positive for SDHB expression . These analyses suggested that the case belonged to the small subset of SDH-intact and KIT, PDGFA, BRAF wild-type GIST, for which no clear molecular pathogenic mechanism has been established. DNA from this GIST and from the patient’s blood was therefore subjected to whole-exome sequencing (WES) (see Materials and Methods).
Description of MAX-negative cases
PDGRA exon 18
KIT exon 11
KIT exon 11
KIT exon 11
KIT exon 11
KIT exon 11
KIT exon 11
KIT exon 11, 17
KIT exon 11
KIT exon 11
Table 2 lists the clinico-pathological characteristics of the 10 MAX-deficient cases. Nine cases harbor KIT exon 11 mutations, while one patient’s tumor exhibited a mutation in exon 18 of PDGFRA. The cases are mainly males (7 of 9 available), with an average age of presentation of 56.9 years. Most were of gastric origin, and nine were high- or intermediate-risk GIST. None of these parameters varied significantly however when compared to the rest of the sample set (Additional file 2: Table S2). Exon-based Sanger sequencing of eight of these cases did not identify any mutations in MAX.
Table 1 lists several other confirmed somatic mutations in our index case: two indels and five missense mutations that were predicted to affect protein structure or function. The variant calls represent ~30–60 % of the total reads at these positions, and exon-based Sanger sequencing confirmed that these mutations were at most heterozygous in the tumors. A frameshift deletion in reticulon 4 (RTN4) was identified, along with an in-frame insertion in the coiled-coiled domain-containing protein CCDC66. Missense mutations were identified in 5 genes: the gene encoding the enzyme mevalonate decarboxylase (MVD) that catalyzes an early step in cholesterol synthesis; MAFA (musculoaponeurotic fibrosarcoma oncogene family, protein A), a transcription factor that controls insulin gene expression in the pancreas; the ring-finger protein gene RNF123, which acts as a ubiquitin ligase towards the cyclin-dependent kinase inhibitor KIP1; a member of the spindlin family of chromatin readers (SPIN4); and the SELP (selectin P) gene, encoding a calcium-dependent receptor that mediates the interaction of activated endothelial cells or platelets with leukocytes.
This study is the first report of somatic inactivation of the NF1 gene in a sporadic SDH-intact GIST lacking gain of function mutations in KIT, PDGFR, and BRAF. Although tissue from the primary tumor from this patient was not available for analysis, it is reasonable to suggest that somatic inactivation of NF1 may have been an early causative event in this case. NF1 patients are ~45X more likely to develop GIST than the general population , and it has been estimated that 1–2 % of GIST arise in patients with NF1 . GISTs in NF1 patients commonly lack activating mutations in the KIT and PDGFRA receptors [17, 18, 43], and may owe their incidence to germline NF1 mutation coupled with somatic second hits, as has been demonstrated in some cases [19, 44, 45]. It is perhaps not surprising to find NF1 gene inactivation in a sporadic wild-type GIST, as NF1 somatic mutations have been identified in a number of non-NF1-associated tumor types (reviewed in ). Moreover, while PCCs are known to occur in the context of NF1 , NF1 somatic mutations were also identified in a high percentage (21/61) of sporadic PCC selected for specific gene expression patterns or low levels of NF1 gene expression . The finding of NF1 gene inactivation in sporadic GIST has diagnostic implications, as the molecular identification of mutations in the large and complex NF1 gene is a challenging task. A comprehensive approach combining NF1 transcript and genomic sequencing with multiplex ligation dependent probe amplification and other techniques for detection of gene duplications and deletions has been used to detect mutations in up to 95% of NF1 cases . Immunohistochemical approaches using available anti-NF1 antibodies have been largely unsuccessful in identifying NF1-mutated PCC with a high degree of sensitivity or specificity [47, 49]. Recently, WES approaches have been used to identify the germline and somatic NF1 events in various tumors from an NF1 patient . Whether NF1 inactivation is a common event in sporadic, SDH-intact wild type GIST is an open question. In a recent transcriptome-sequencing study , no NF1 mutations were identified in two SDH intact wild-type GIST, although it has been shown that only a portion of exonic variants are typically captured by RNA-seq approaches . Interestingly, next-generation sequencing of eight SDH-negative GIST cases using a targeted cancer-associated gene capture library identified a low-frequency (8 %) frameshift NF1 mutation in a GIST that also harbored an activating KRAS gene mutation (G12V) .
The identification of a loss of function mutation in the MAX gene is a novel finding in GIST. As a hetero-dimeric partner for MYC, MAX was originally thought to be required for oncogenic pathways initiated by MYC over-expression . However, in MAX-deficient rat PC12 PCC cell lines it has been shown that MAX is dispensable for MYC transcriptional regulation . Intriguingly, MAX inactivation has recently been implicated in both inherited and sporadic PCC and PGL cases [39, 40]. Mutation of MAX is a relatively rare event in these tumors, accounting for 1.12 % of hereditary PCC/PGL lacking mutations in other susceptibility genes and 1.65 % of sporadic cases. In the familial PCC cases preferential transmission of the disease from the paternal allele was observed, along with a tendency towards aggressive behavior. A recent report also describes MAX inactivation in 6 % of primary SCLC specimens . The authors suggest that SCLC, like PCC, may arise from neuroendocrine cells or differentiate towards neural features, which may explain the shared mechanism of MAX-associated oncogenesis. Similarly, sub-populations of GISTs may also variably exhibit neural properties or markers, and in a recent report a set of SDH-intact WT GIST was shown to exhibit high relative expression of neural markers, along with expression of members of the insulin-like growth family network . In SCLC, inactivating MAX mutations were found to be mutually exclusive with amplifications of hetero-dimeric partners MYC, MYCL1, and MYCN, and mutations in BRG1, which encodes an ATPase of the SWI/SNF chromatin -remodeling complex that regulates expression of MYC, MYC target genes, as well as MAX. In GIST, the contributions of the MYC/MAX/MXD network to pathogenesis have not been extensively described. There have been descriptions of amplification of the MYC gene locus on chromosome 8q [57, 58], and reduced mRNA expression of the MAX gene associated with copy number loss of chromosome14q . These secondary chromosome aberrations are common in KIT/PDGFRA-mutated GIST . In this report we used immunohistochemical approaches to identify reduced/absent MAX nuclear staining in 10/78 (~13 %) of GIST cases analyzed, in addition to the index case. We found no additional MAX mutations in these tumors, and MAX RNA expression was only marginally and not significantly reduced (1.3-fold, P = 0.47) compared to the remaining MAX-positive cases. Further investigations into the mechanism(s) of MAX dysregulation and its contribution to pathogenesis in GIST are warranted.
In addition to inactivating NF1 and MAX mutations found in our index case, we also identified a heterozygous 4-base deletion in RTN4 and an in-frame insertion in CCD66, as well as potentially pathogenic substitutions in the MVD, MAFA, RNF123, SPIN4, and SELP genes. Although to our knowledge these genes have not been studied in GIST, a recent systems biological approach to identifying key transcriptional regulators in GIST and leiomyosarcoma identified nine differentially expressed genes, including the MYC gene, the MAF gene which encodes another basic leucine zipper (bZIP)-containing transcription factor closely related to MAFA, and another coiled-coil domain containing transcription factor gene, CCDC6 . The MAF proteins are members of the AP1 family: the large MAF proteins contain transactivation domains and are considered onco-proteins by virtue of their ability to transform primary cells and induce tumors in various animal models (reviewed in ). Interestingly, the Q257L substitution we identified is located in the MAFA bZIP domain, very close to the predicted DNA-binding domain that has been shown to be required for MAFA transformation activity in avian fibroblasts . The substitution we identified may affect the specificity or avidity of MAFA binding to its target sequences.
In conclusion, next-generation sequencing of an SDH-intact, KIT, PDGFR, BRAF wild type GIST identified for the first time somatic loss of function mutations in two tumor-suppressor genes, NF1 and MAX. Somatic inactivation of neurofibromin should be explored as a potential oncogenic mechanism in this subset of GIST. The identification of MAX inactivation provides another etiological link between GIST and PGL/PCC, in addition to mutations of the NF1 gene and mutations in the subunit genes of the SDH complex that have been identified in these tumors.
Availability of supporting data
The data supporting the results of this article are included within the article and its additional files.
gastrointestinal stromal tumors
hematoxylin and eosin
interstitial cells of Cajal
insertions and deletions
Myc-associated factor X
neurofibromatosis type 1
platelet-derived growth factor receptor alpha
quantitative real-time polymerase chain reaction
small-cell lung cancer
single nucleotide variant
single nucleotide polymorphism
whole exome sequencing
We would like to acknowledge Dr. Mark Andrake of the FCCC Molecular Modeling facility, along with the FCCC Biosample Repository, Histopathology Facility, Genotyping and Real-Time PCR facility, and the DNA Sequencing Facility for work contributing to this manuscript. The authors acknowledge support from the Kansas Bioscience Authority Eminent Scholar Program (awarded to A.K. Godwin). Dr. Godwin is the Chancellors Distinguished Chair in Biomedical Sciences endowment at University of Kansas. The authors also acknowledge support from the GIST Cancer Research Fund and the D’Amico family fund.
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