- Open Access
Genomic aberrations in cell cycle genes predict progression of KIT-mutant gastrointestinal stromal tumors (GISTs)
Clinical Sarcoma Research volume 9, Article number: 3 (2019)
Activating mutations of the receptor tyrosine kinase KIT are early events in the development of most gastrointestinal stromal tumors (GISTs). Although GISTs generally remain dependent on oncogenic KIT during tumor progression, KIT mutations alone are insufficient to induce malignant behavior. This is evidenced by KIT-mutant micro-GISTs, which are present in up to one-third of normal individuals, but virtually never progress to malignancy.
We performed whole exome sequencing on 29 tumors obtained from 21 patients with high grade or metastatic KIT-mutant GIST (discovery set). We further validated the frequency and potential prognostic significance of aberrations in CDKN2A/B, RB1, and TP53 in an independent series of 71 patients with primary GIST (validation set).
Using whole exome sequencing we found significant enrichment of genomic aberrations in cell cycle-associated genes (Fisher’s Exact p = 0.001), most commonly affecting CDKN2A/B, RB1, and TP53 in our discovery set. We found a low mutational tumor burden in these 29 advanced GIST samples, a finding with significant implications for the development of immunotherapy for GIST. In addition, we found mutation of spliceosome genes in a minority of cases, implicating dysregulation of splicing as a potential cancer promoting mechanism in GIST. We next assessed the prognostic significance of CDKN2A, RB1 or TP53 mutation/copy loss in an independent cohort of 71 patients with primary GIST. Genetic events (mutation, deletion, and/or LOH) involving at least one of the three genes examined were found in 17% of the very low-risk, 36% of the low-risk, 42% of the intermediate risk, 67% of the high-risk/low mitotic-count, and in 86% of the high-risk/high mitotic-count group. The presence of cell cycle-related events was associated with a significantly shorter relapse-free survival (median 67 months versus not reached; p < 0.0001) and overall survival (Log Rank, p = 0.042).
Our results demonstrate that genomic events targeting cell cycle-related genes are associated with GIST progression to malignant disease. Based on this data, we propose a model for molecular pathogenesis of malignant GIST.
Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. The vast majority of these tumors have activating mutations of the KIT or PDGFRA receptor tyrosine kinases that are considered to be initiating oncogenic events [1, 2]. GISTs lacking KIT or PDGFRA mutations comprise 10–15% of the cases. Alternative oncogenic events in these tumors include activating mutations of BRAF or KRAS or inactivating mutations of NF1 or genes encoding the succinate dehydrogenase (SDH) complex [3,4,5]. The oncogenic reliance of GISTs upon mutated KIT/PDGFRA is emphasized by their sensitivity to imatinib mesylate (IM), a tyrosine kinase inhibitor (TKI) that targets both KIT and PDGFRA kinase activity, leading to substantial tumor shrinkage with durable responses in most patients [6, 7].
However, IM is not a cure for GIST. Most patients will eventually experience tumor progression despite continuous IM treatment [8, 9]. Resistance to IM often arises due to secondary mutations within KIT or PDGFRA. Such mutations are commonly found in tumors removed from patients with clinical IM resistance. Additional kinase inhibitors target these secondary mutations and are used as second-line or later treatment for IM-resistant GISTs [10, 11]. Nevertheless, the progression-free survival with these salvage tyrosine kinase inhibitors is limited, and most patients experience progression from these agents within 6–12 months [6, 12].
Numerous studies have reported small incidental GISTs, less than a centimeter in diameter, that are identified during gastrectomy or at autopsy [13,14,15,16]. Many of these lesions harbor KIT mutations identical to those identified in larger malignant lesions, indicating that additional genetic events are necessary to transform these micro-GISTs into malignant tumors. Detection of genomic events associated with the development of malignant GISTs could therefore identify patients at high risk of recurrence after curative-intent resection of a primary tumor. Here we report that genomic alterations in key cell cycle regulators are recurrent abnormalities in patients with advanced GIST.
Patients and tumor tissues
De-identified samples analyzed by whole exome sequencing (WES) were obtained from participating institutions (Oregon Health and Science University, University of Duisburg-Essen, Brigham and Women`s Hospital and Katholieke Universiteit Leuven and University Hospitals Leuven). This study was approved by the institutional review boards at each of the participating sites. For whole exome sequencing approach, we selected 21 patients with high-risk GISTs, including 20 patients who presented with or eventually developed metastatic disease (discovery set). All tumor samples were obtained from frozen tissues except for one (19A), which was obtained from formalin-fixed paraffin embedded (FFPE) tissue. Paired normal DNA was extracted from frozen normal tissue (32%, 7/22), blood (63%, 14/22), or FFPE tissue (5%, 1/22).
Targeted sequence analysis was performed on a second group of 71 GIST samples representing an independent cohort of clinically characterized patients from prospectively maintained databases of participating institutions (University of Duisburg-Essen, Brigham and Women`s Hospital, and Oregon Health and Science University) and from the Life Raft Group patient database (validation data set) . This cohort study was approved by the institutional review boards at each of the participating sites.
Progression-free survival (PFS) was calculated as the length of time from diagnosis of localized disease to the date of documented recurrence or death from any cause, whichever occurred first. Overall survival (OS) was defined as the length of time from the time of diagnosis of localized disease to death from any cause. PFS and OS estimates and standard errors determined using the Kaplan–Meier method and statistical comparisons were performed using the log-rank test. Two-sided p values less than 0.05 were considered to be statistically significant. The statistical analyses were performed using SPSS 19.0 and R 2.15.2 (http://www.r-project.org/). We conducted a multivariate analysis for PFS using three covariates (mitotic count, size and cell-cycle-related genomic events) using SAS software 9.4 (SAS Institute Inc., Cary, NC, USA).
Whole exome sequencing
The experimental and computational details of these experiments are included in additional methods.
Ion torrent targeted-exome genomic sequencing
In an independent validation cohort of 71 patients, targeted sequence analysis was performed with a custom AmpliSeq panel (Life Technologies, Grand Island, NY) that includes 24 genes (AKT1, AKT2, AKT3, ATM, BRAF, CDKN2A, HRAS, KIT, KRAS, MAP2K1, NF1, NRAS, PDGFRA, PIK3CA, PTEN, PTPN11, RB1, SDHA, SDHAF1, SDHAF2, SDHB, SDHC, SDHD, TP53). Sequencing was carried out on an Ion Torrent PGM instrument (Thermo Fisher Scientific, Inc., Waltham, MA), and Torrent Suite Software v3.2 was used for sequence alignment and variant calling.
Interphase FISH on tumor sections
To detect deletions affecting the CDKN2A/B/9p21.3, RB1/13q14 and TP53/17p13 genes, cut sections (4 µm thick) from paraffin-embedded tumor tissues from 42 patients were subjected to separate interphase FISH assays. FISH assays were performed using the commercially available dual-color probes LSI CDKN2A/B (9p21)-Spectrum Orange (SO)/CEP9-Spectrum Green (SG), LSI RB1-SO/CEPX-SG and LSI TP53-SO/CEP17-SG cocktails (all from Abbott Laboratories, Des Plaines, IL). Probe hybridization and detection were carried out according to standard methods. Slides were analyzed blinded from the clinical data, using a Zeiss microscope (Axioplan 2, Jena, Germany) equipped with the appropriate filters. The numbers of differentially labeled hybridization signals representing the investigated gene and reference centromere chromosomal regions were individually recorded for 100 non-overlapping interphase nuclei in at least two different areas of the section. Zero to 1 green centromeric (green) signals per nucleus in > 60% of cells were defined as a whole chromosome loss. In addition, the ratio of red to green signals was calculated. Heterozygous or homozygous losses were delineated by ratios < 0.6 and < 0.3, respectively.
Multiplex ligation-dependent probe amplification (MLPA)
Gene dosage ratios for 12 CDKN2A/CDKN2B loci and 11 other chromosome 9p genes were determined using the 9p21 MLPA kit (ME024-B1 MRC-Holland, Amsterdam, Netherlands). The probe-mix contains 21 different probes for the CDKN2A/B genes. In addition, it contains 2 probes each for MTAP, CDKN2B-AS1, PAX5 and MIR31, and 4 probes between the MIR31 gene and the 9p telomere. Two digestion control probes and 12 reference probes were included for data analysis. In each set of experiments, one negative control sample (no DNA) and 6 normal control samples (DNA isolated from paraffin sections of normal human intestines from different individuals) were included. Briefly, 50 ng of extracted tumor DNA was denatured and target gene probes were hybridized to the target DNA prior to probe ligation in the presence of Ligase-65 (MRC-Holland). The ligation products were subjected to polymerase chain reaction (PCR) amplification performed on a GeneAmp PCR System 9700 Thermal Cycler (Applied Biosystems, Warrington, UK) with a hot-start PCR program. MLPA fragments were visualized on an ABI 3130XL Automated DNA Sequencer (Applied Biosystems). Peak detection analysis has been automated using ABI PRISM Genescan® Analysis software version 3.1 (Applied Biosystems) and GeneMarker software (Softgenetics, State College, PA, USA).
CDKN2A copy number variation assessment using SNP arrays
CDKN2A homozygous deletions were identified by Affymetrix 250 K Nsp1 SNP arrays (Thermo Fisher Scientific). High-molecular-weight genomic DNA was isolated using the QIAamp DNA Mini kit (Qiagen). DNA was digested with Nsp1, and linkers were ligated to the restriction fragments to permit PCR amplification. PCR products were purified and fragmented by treatment with DNase I, and fragments were then labeled and hybridized to microarray chips. The positions and intensities of fluorescence emissions were analyzed using Chip software. Array intensity values were normalized to the value for the array with median intensity.
Clinical characteristics of GIST patients analyzed by whole exome sequencing (discovery set)
We analyzed 29 high-risk GIST lesions paired with normal tissue obtained from 21 patients (Discovery Set, Table 1). Twenty of these patients presented with, or developed, metastatic disease, and thirteen of these patients had one to ten metastatic lesions that were surgically removed after clinical resistance to one or more tyrosine kinase inhibitors (median of one lesion). Seventeen of the 21 patients had tumor samples collected after one or more lines of TKI therapy. Secondary KIT mutations were identified in 18 of the 25 tumors harvested after TKI therapy (72%). In the other seven tumors, only a primary KIT gain-of-function mutation was identified. As expected, only a primary KIT mutation was found in samples from the four patients whose tumors were collected prior to TKI therapy.
Whole exome sequencing
The average whole exome sequencing read depth for each tumor sample was 88X (75X median) (Additional file 1: Figure S1). Only 4 of the 21 patients had samples with coverage less than 50×, with a 40–49× average (41–48× median) coverage over the targeted panel. Given the high purity of GIST samples (80–90% tumor cells), coverage was deemed adequate for identifying somatic variants of interest and only mutations with a read depth of at least 20 reads were included in our analysis. Across the entire cohort of GIST specimens, we identified a total of 4303 exonic or splice-site, non-synonymous somatic mutations including 1278 missense, 123 nonsense, 82 splice site, and 4 read-through mutations. In addition, we identified 157 deletion and 35 insertion mutations (Additional file 1: Table S1) .
It is well established that detection of larger insertion/deletion mutations (“indels”) by next-generation sequencing is challenging. Therefore, we used Sanger sequencing to identify or verify primary KIT insertion/deletion mutations, especially for KIT exon 9 and 11 mutations. Known primary insertion/deletion mutations not called by our indel detector were verified by visual inspection of whole exome sequencing reads.
GIST mutational signature
An average of 122 somatic mutations were identified in the 29 KIT-mutant GIST samples (Additional file 1: Table S1). Genetic significance was determined based on the frequency of somatic variants with MutSigCV 1.4, which accounts for heterogeneity in mutational rate across the genome . The mutation pattern of KIT-mutant GISTs consists largely of CpG transversions to A/T mutations, occurring at a relative rate of approximately 3.3 mutations per megabase (Mb) (Additional file 1: Table S2) . The mutation signature was assessed by incorporating the sequence context of bases immediately 5′ and 3′ to the mutated base . Percentages of mutations were normalized using the trinucleotide frequency in the human exome to the genome, leading to a decrease of C > T mutations occurring in NpCpG trinucleotides from 3 to 4% to 2% (Fig. 1a). The normalized signature show similarities to several COSMIC Signatures of Mutational Processes in Human Cancer, including Signature 5 (transcriptional strand bias for T > C substitutions at ApTpN context) and Signature 18 (neuroblastoma, breast and stomach carcinoma) . The high frequencies of transition mutations at CpG in GIST are consistent with results of mutation rates of other gastrointestinal malignancies, including colorectal carcinoma, as previously reported . Overall, the tumor mutation burden in these tumors was low (Additional file 1: Table S2), a finding with implications for the development of immunotherapy for GIST . Ranked by q-value (lowest q-value first), the ten most commonly mutated genes in our collection of KIT-mutant GIST were KIT, SF3A2, RB1, FRG1, NFAM1, GRB14, APLF, CELA1, YY1AP1, and ZYX (Fig. 1b).
Somatic copy number alterations
Various recurrent cytogenetic events have been described in GIST including deletions of chromosomes 14q, 22q, 15q, 1p, 9p and gains of chromosome 8q [24,25,26,27,28]. Large copy number events affecting more than 20% of a chromosomal arm were computationally identified using sequencing data (Table 2, Additional file 1: Table S3). Consistent with the above-cited literature, 23 out of 29 samples (16/21 patients) exhibited heterozygous loss of the long arm of chromosome 22q, and 24 of 29 samples (17/21 patients) had heterozygous copy number loss of the long arm of chromosome 14q (encompassing RBM25, HSP90AA1, and MAX).
Additional heterozygous large chromosomal copy number losses were detected for a large region of chromosome 1p (encompassing SF3A3, RBMXL1, and MAD2L2) in 25/29 tumors (18/21 patients), chromosome 15q in 21/29 tumors (13/21 patients), and chromosome 13q (including RB1) in 20/29 tumors (11/21 patients), respectively. These results are consistent with prior studies [29,30,31].
KIT-mutant GISTs had heterozygous copy number gains affecting more than 20% of chromosomes arms 5p (14/29 tumors, 10/21 patients), 8q (10/29 tumors, 7/21 patients), and 7q (8/29 tumors, 6/21 patients) . Heterozygous copy number gains affecting chromosome 5q (including CCNB1, DDX46) were observed in 8/29 GIST samples (6/21 patients; Table 2).
Enrichment for Somatic Mutation of Cell Cycle Pathway-Related Genes in GISTs
Pathway analysis using the list of genes associated with exonic/splice site, non-silent somatic mutations in the KIT-mutant GISTs was performed using KEGGREST v1.8.1. This analysis not only showed significant enrichment in cancer-related pathways and other KIT-associated pathways, but also enrichment for the KEGG cell cycle pathway (hsa04110; Fisher’s Exact p = 0.001, Additional file 2: Table S4) . In addition, gene set enrichment analysis (GSEA) of somatic mutations using MutSigCV against a gene enrichment database, Molecular Signatures Database (MsigDB) v5.1, showed enrichment of genes associated with the cell cycle pathway (Reactome, M543, p = 0.011, Additional file 3: Table S5).
A total of ten KEGG cell cycle-associated genes were found to be significantly mutated by MutSigCV (nominal p < 0.05) in the entire cohort of GIST patients (Additional file 4: Tables S6, Additional file 5: Tables S7) . These mutated cell cycle-related genes had 14 unique somatic exonic or splice site-related non-synonymous point mutation events that were filtered by variant allelic fraction greater than 0.2 to eliminate potential false positive results due to the presence of pseudogenes. The significantly mutated cell cycle genes in our cohort of KIT-mutant GISTs consisted of eight genes: RB1 (p = 1.3e−6), CUL1 (p = 3.1e−4), TP53 (p = 3.7e−4), CDC27 (p = 2.0e−3), ANAPC1 (7.4e−3), E2F3 (2.2e−2), GADD45A (p = 4.9e−2), and MAD2L2 (p = 0.05) (Table 3). Evaluation using STRINGv10 of significantly mutated genes showed significant enrichment for the cell cycle pathway (p = 0.0007) and spliceosome-related genes (p = 0.0008) in KIT-mutant GISTs (Fig. 2) .
Integrated mutation and copy number analysis of cell cycle genes
To delineate the spectrum of molecular mechanisms that inactivate cell cycle genes in advanced GIST, we integrated the data from the somatic variant analysis with the inferred copy number variation data from the sequencing analysis. As shown in Fig. 3, TP53 (9/21 patients, 14/29 tumors), RB1 (12/21 cases, 19/29 tumors), CDKN2A (5/22 cases, 5/29 tumors), and MAX (17/21 patients, 25/29 tumors) were frequently altered by somatic mutation and/or copy number variation. Hemizyous/homozygous inactivating single nucleotide mutations of MAX were previously reported in 8/76 (10.5%) of GIST . We did not any identify any inactivating MAX mutations in our series; this difference may be due to our smaller sample size. As noted above, large heterozygous deletions of chromosome 14 that included MAX were found in 17/21 (81%) patients in our WES cohort. Homozygous inactivation of MAX was previously reported to decrease expression of CDKN2A in GIST . Based on our results, we speculate that haplo insufficiency of MAX may be enough to provide early dysregulation of the cell cycle (CDKN2A) during GIST pathogenesis.
Somatic cell cycle mutations are conserved between individual tumors resected from the same patient
In general, any somatic cell cycle mutation found in one metastasis from a given patient was also found in the other metastases analyzed from that patient. For example, all three metastases analyzed of Patient 1 had the same CDKN2A homozygous deletion, as identified by Affymetrix array. Similarly, both metastases analyzed from Patient 2 had the same TP53 c.(733–735) Ggc > Agc, p.G245S mutation at allelic fractions that were essentially homozygous (0.92 and 0.89, respectively; samples 2A and 2B, Table 3).
Deletion of dystrophin (DMD), a tumor suppressor gene in human cancers with a myogenic program, has been reported as a late genetic event associated with the development of metastatic potential in GIST . In our cohort, DMD copy loss was observed in eleven of the 29 lesions of KIT-mutant GIST (8/21 patients). The majority of the DMD copy loss events occurred in exons 1 through 32 which impacts Dp427 myogenic dystrophin but preserves a ubiquitously-expressed Dp71 dystrophin, as reported previously . Among the patients with multiple tumors sequenced (patients 1, 2, 10, 14, and 16), no DMD copy loss was found in samples from patients 10, 14, or 16. Samples from patient 1 (3 samples) and patient 2 (2 samples) had identical DMD deletions in all analyzed samples.
Loss-of-heterozygosity (LOH) and targeted sequencing of CDKN2A, RB1 and TP53 in a cohort of 71 patients with well-defined GIST (validation data set)
Based on the whole exome sequencing results, we expanded our study to perform a focused genetic screen for mutations and/or LOH of the cell cycle regulators CDKN2A/B, RB1 and TP53 using a combination of a clinically validated next generation sequencing panel, MLPA, and FISH in a cohort of 71 GIST patients from well-defined clinical risk groups with annotated clinical follow up. MAX was excluded from these analyses as we viewed this as an early event that was unlikely to influence prognosis . In addition to the AFIP (Armed Forces Institute of Pathology) criteria for risk of GIST recurrence, we further divided the high-risk group into patients with lower (< 6 mitoses/50 high power fields [HPF]) and those with higher mitotic counts (≥ 6 mitoses/50HPF). Genetic events (mutation, deletion, and/or LOH) involving at least one of the three genes examined (CDKN2A/B, RB1, TP53) were found in 17% (1/6) of the very low-risk, 36% (5/14) of the low-risk, 42% (10/24) of the intermediate risk, 67% (4/6) of the high-risk/low mitotic-count and in 86% (18/21) of the high-risk/high mitotic-count group (Fig. 4a). The presence of cell cycle-related events was associated with a significantly shorter relapse-free survival (median 67 months versus not reached; p < 0.0001; Fig. 4b) and overall survival (Log Rank, p = 0.042; Fig. 4C) in the univariate analysis. Patients who were receiving ongoing adjuvant imatinib treatment were excluded from our analyses. In a multivariate analysis, the proportional hazards assumption was fulfilled for all covariates, and Cox regression analysis revealed a hazard ratio of 3.9, 7.3 and 4.5 for cell cycle-related events, mitotic count, and tumor size, respectively (p = 0.0775; Additional file 6: Table S8).
The dependency of most GIST on oncogenic KIT mutations is indisputable. Consistent with this statement, our current whole exome sequencing studies revealed secondary KIT mutations in 18/29 tumors obtained from 21 patients with malignant KIT-mutant GIST (Table 1). Other recurrent molecular causes of TKI resistance such as acquired mutations of downstream signaling effectors (e.g., KRAS or PIK3CA) were not identified in our discovery sample set. We conclude that secondary KIT mutations are found in most cases of KIT-mutant GIST with acquired resistance to kinase inhibitors. These results are in agreement with prior sequencing studies that analyzed the frequency of secondary kinase mutations in TKI-resistant, KIT-mutant GIST [30, 36].
However, additional events besides primary KIT mutations are needed for GIST cells to evolve into metastatic or resistant disease, as evidenced by similar or identical KIT mutations in cases of micro-GISTs and metastatic tumors . In this study, we provide evidence that mutational dysregulation of the cell cycle is a crucial mechanism in progression from low-risk to malignant GIST. Whole exome sequencing of a set of high grade or metastatic GIST specimens showed significant enrichment of mutations of cell cycle pathway-related genes (Fisher’s Exact p = 0.001). We found further evidence of genomic inactivation of cell cycle control genes when analyzing copy number loss using the whole exome sequencing data. Overall, the most common recurrently copy number loss events were found in MAX (17/21 patients) and the cell cycle-related genes RB1 (13/22 patients), TP53 (12/21 patients), CDKN1B (5/21 cases), and CDKN2A/B (5/21 cases). Samples with somatic mutations of cell cycle genes and/or copy number losses of these same genes are summarized in Fig. 3.
Because the whole exome sequencing results in our present series underscored the importance of genomic inactivation of cell cycle regulator genes in GIST, we performed focused testing of the genomic status (mutation, copy number variation, and LOH) of three of these genes (CDKN2A, RB1, and TP53) in an independent group of GIST patients with annotated long-term clinical follow up (validation data set). We found that mutations and/or copy loss of these cell cycle regulator genes were associated with an increased risk of metastatic recurrence. In this second group of patients, we noted a significantly lower percentage of TP53, CDKN2A/B or RB1 genomic alterations in low-risk compared to high-risk GIST (Fig. 4). All but two of the patients who later experienced recurrence had at least one genomic alteration involving CDKN2A/B, RB1, or TP53. Notably, cell cycle-related genetic events were associated with higher number of mitoses in primary GISTs (Fig. 4a), a well-recognized risk factor for the development of metastatic disease.
Patients with intermediate-risk GISTs are clinically challenging, because there are currently no reliable biomarkers to identify the patients in this risk category who have a higher risk of relapse and might benefit from adjuvant imatinib therapy. Among the 24 intermediate-risk GISTs in our second cohort, ten (42%) had cell cycle-related genetic events. Notably, among these ten patients, seven did not receive adjuvant imatinib and five patients experienced a recurrence of their GIST. By contrast, none of the 14 patients with intermediate-risk GIST lacking a genomic cell cycle event had a recurrence (2-sample proportion test, p = 0.002). Overall, a cell cycle-related genetic event was strongly associated with poor progression-free survival in patients with GIST (p < 0.0001). Notably, the only patient with metastatic relapse in the very low-risk group of six patients had LOH of the CDKN2A/B locus in his gastric primary tumor.
In a multivariate analysis, both mitotic count and tumor size were highly significant prognostic factors. Due to the limitations of sample size, primary tumor site was excluded from the analysis. Nonetheless, multivariate analysis for recurrence-free survival revealed a hazard ratio of 3.9 for GISTs with a cell cycle-related genetic event (p = 0.078) even against the background of a relatively small group of patients. Further assessment of the clinical validity of these genetic events as prognostic factors will require larger numbers of patients with annotated long-term clinical follow-up. Our results are generally concordant with other studies that correlated cell cycle events and risk of GIST recurrence. However, these studies used a variety of techniques, including immunohistochemistry, to identify cell cycle gene dysregulation [37,38,39,40]. As shown in our studies, analysis of both specific cell cycle gene mutation status and CNV are necessary to identify a more complete spectrum of genomic events targeting RB1, CDN2A/B, and TP53 genes. Our experimental methods may not detect all intragenic deletions (e.g. microdeletions). In addition, in some cases of malignant GIST, CDKN2A is inactivated by promoter hypermethylation [41, 42]. Further studies are needed to identify the optimal diagnostic techniques needed to identify all mechanisms of inactivation of cell cycle genes in GIST. If validated in subsequent studies, these cell cycle markers could be used for prognostication in conjunction with standard pathological features that are known to correlate with risk.
In addition to the recurrent genomic events targeting cell cycle control genes, we also discovered evidence for dysregulation of mRNA splicing in the biology of metastatic GIST. Gene set enrichment analysis found KIT-mutant GISTs to also be enriched for mutations of genes involved in spliceosome regulation (p value = 0.026), including SF3A2 (q < 0.001), U2AF2, RBMX, RBMXL3, PRPF18, SNRP200 that were significantly mutated in KIT-mutant GISTs with p < 0.05. SF3A2 and U2AF2 are both associated with spliceosome component U2 small nuclear ribonucleotide proteins (snRNP) . Three lesions from a single patient (samples 14A, 14B, 14C) contained the identical SF3A2 nonsense mutation E177*. Two other tumors from different patients (9A and 17A) contained identical somatic U2AF2 splice site mutations. The remaining mutated genes involved in spliceosome assembly with p < 0.001 were identified in nine other samples from eight different patients. In addition, four KIT-mutant samples contained somatic single nucleotide variants in FRG1 (q < 0.01), a cancer driver gene in follicular thyroid cancer .
Notably, mutations of SF3A2 and FRG1 ranked as the first and third most common somatic mutations (after KIT), respectively in KIT-mutant GIST (Fig. 1b). SF3A2 is part of the U2 snRNP, and another member of this complex (SF3B1) is recurrently mutated in myelodysplastic syndrome, acute myeloid leukemia, and chronic lymphocytic leukemia . We also identified loss of the SF3A3 gene, located on 1p, to be a frequent event in our series (17/21 patients, 25/29 samples). Like SF3A2, the SF3A3 gene encodes a component of the splicing factor 3a complex. In addition, we found mutations of U2AF2, a component of the U2AF complex. U2AF2 mutations leading to spliceosome dysfunction have been reported in other cancers . Notably, mutation of the other member of the U2AF complex (U2AF1) has been reported in the same hematologic malignancies associated with SF3B1 mutations . Further studies are needed to understand how dysregulation of the spliceosome contributes to GIST biology.
Taken together, our study provides evidence that mutational dysregulation of the cell cycle is a crucial mechanism in progression from low-risk to malignant GIST. Based on these observations we propose a model of genetic progression leading to malignant, invasive and metastatic GIST as shown in Fig. 5. Our model depicts chromosome 14q and 22q deletions as early events in GIST progression. KIT-mutant asymptomatic and innocuous micro-GISTs have been found in approximately one-third of the general population. These tumors rarely progress to malignancy, presumably because they require additional mutations to become clinically aggressive. Cytogenetic studies support this hypothesis, demonstrating that early GISTs typically harbor KIT or PDGFRA mutations, often accompanied by chromosome 14q and 22q deletions, but do not yet show evidence of chromosome 9p deletions that potentially target CDKN2A/B . In contrast, inactivation of dystrophin is a late event in GIST progression (Fig. 5). Dystrophin has been shown to behave as a tumor suppressor, and in a large series of GISTs genomic mechanisms of dystrophin inactivation were present in 96% of metastatic GIST, but absent in low-risk GIST . We therefore propose that cell cycle-related events are ubiquitous, intermediate steps in the progression of GIST. Our observations also suggest that clinical assessment of genetic events involving CDKN2A/B, RB1 or TP53 may be a useful addition to existing risk assessment models, with implications for selection of patients for adjuvant treatment and intensified surveillance schedules.
Our studies show that cell cycle dysregulation due to genomic inactivation of cell cycle regulatory genes is a ubiquitous mechanism during the transition from low-risk to high-risk/metastatic GIST. These events might sensitize cells to KIT-independent treatment approaches such as CDK4 or MDM2 inhibitors. Based on this data, we propose a model for molecular pathogenesis of malignant GIST. Further studies are needed to confirm these genomic observations as potential predictors of clinical behavior and to examine the efficacy of imatinib combination therapy with cell cycle inhibitors in GIST. In addition, further studies are needed to understand the role of spliceosome mutations in malignant GIST biology.
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Study design: MCH, JP, MD-R, CLC, AD, BR, TO, MvdR, JC, JAF, SB. Initial draft: MCH, JP, JAF, SB. Provision of tumor samples: MCH, MvDR, CLC, CPR, MvdR, AD, JC, JAF, SB. Data analysis: MCH, JP, CB, JAF, SB. Writing, editing, and final approval of manuscript: all authors. All authors read and approved the final manuscript.
MCH: Novartis consulting and expert testimony, Molecular MD consulting and equity interest, patent on treatment of GIST. SB: Research support from Novartis, Blueprint Medicines, Ariad; Consultant for GSK, Novartis, Pfizer, Bayer, Fresenius, Lilly, Blueprint Medicines, Deciphera; Honoraria (CME) from Pharmamar, GSK, Pfizer, Bayer; Travel support from Pharmamar, Bayer.
Availability of data and materials
The dataset(s) supporting the conclusions of this article are included within the article and its additional file(s). Additional datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request. We are in the process of depositing all of the data in a publically available database.
Consent for publication
Does not apply (all samples were de-identified).
Ethics approval and consent to participate
De-identified samples analyzed by whole exome sequencing (WES) were obtained from participating institutions (Oregon Health and Science University, University of Duisburg-Essen, Brigham and Women`s Hospital and Katholieke Universiteit Leuven and University Hospitals Leuven). These samples included 29 samples from 21 different patients. This portion of our study was approved by the institutional review boards at each of the participating sites.
Targeted sequence analysis was performed on a second group of 71 GIST samples representing an independent cohort of clinically characterized patients from prospectively maintained databases of participating institutions (University of Duisburg-Essen, Brigham and Women`s Hospital, and Oregon Health and Science University) and from the Life Raft Group patient database. This cohort study was approved by the institutional review boards at each of the participating sites.
Life Raft Group (MCH, MD-R, CLC, AD, BR, TO, MvDR, JAF, SB), GIST Cancer Research Fund (MCH, CLC, AD), VA Merit Review Grant (MCH, 2I01BX000338-05), NIH Grant DK058185 (TO), Sarkomtour Fundraising Initiative (SB).
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Heinrich, M.C., Patterson, J., Beadling, C. et al. Genomic aberrations in cell cycle genes predict progression of KIT-mutant gastrointestinal stromal tumors (GISTs). Clin Sarcoma Res 9, 3 (2019) doi:10.1186/s13569-019-0112-7
- GI stromal tumor
- Cell cycle