Methylation changes at the GNAS imprinted locus in pancreatic cystic neoplasms are important for the diagnosis of malignant cysts

Sandra Faias,Marlene Duarte,Luísa Pereira,Paula Chaves,Marília Cravo,Antonio Dias Pereira,Cristina Albuquerque

Sandra Faias,Antonio Dias Pereira,Department of Gastroenterology,Instituto Português de Oncologia de Lisboa Francisco Gentil,EPE,Lisboa 1099-023,Portugal

Sandra Faias,Paula Chaves,Faculty of Health Sciences,University of Beira Interior,Covilh? 6200-506,Portugal

Marlene Duarte,Cristina Albuquerque,Unidade de Investiga??o em Patobiologia Molecular(UIPM),Instituto Português de Oncologia de Lisboa Francisco Gentil,EPE,Lisboa 1099-023,Portugal

Luísa Pereira,Centro de Matemática e Aplica??es(CMA-UBI),Universidade da Beira Interior,Covilh? 6200-506,Portugal

Paula Chaves,Department of Pathology,Instituto Português de Oncologia de Lisboa Francisco Gentil,EPE,Lisboa 1099-023,Portugal

Marília Cravo,Department of Gastroenterology,Hospital Beatriz ?ngelo,Loures 2674-514,Portugal

Abstract BACKGROUND Guanine nucleotide-binding protein,alpha stimulating(GNAS)mutations are characteristic of intraductal papillary mucinous neoplasms(IPMNs).Pancreatic ductal adenocarcinomas(PDACs)harboring GNAS mutations originate in IPMNs.GNAS is a complex imprinted locus that produces five transcripts regulated by differential methylated regions,NESP55,GNASAS,GNASXL,GNAS1A,and GNAS.AIM To evaluate if methylation changes in the differential methylated regions of GNAS locus contributed to malignant progression of pancreatic cysts.METHODS GNAS locus methylation was analyzed in archival pancreatic cyst fluid(PCF)obtained by endoscopic ultrasound with fine-needle aspiration by methylation specific–multiplex ligation dependent probe amplification.Results were normalized and analyzed using Coffalyser.Net software.RESULTS Fifty-two PCF samples obtained by endoscopic ultrasound with fine-needle aspiration and previously characterized for KRAS and GNAS mutations were studied.The final diagnoses were surgical(11)and clinicopathological(41),including 30 benign cysts,14 pre-malignant cyst,and eight malignant cysts.Methylation changes at NESP55,GNASAS,GNAS1A,and especially GNASXL were more frequent in malignant cysts,and NESP55 and GNASAS were useful for diagnosis.A combined variable defined as “GNAS locus methylation changes”was significantly associated with malignancy(6/8 malignant cysts and only 2/20 benign cysts)and improved classification.Hypermethylation in both maternally(NESP55)and paternally(GNASXL)derived promoters was found in 3/3 PDACs.CONCLUSION This is the first study to identify methylation changes in the GNAS locus,improving the diagnosis of malignant pancreatic cysts and suggesting a role in progression to PDAC.

Key Words:Intraductal papillary mucinous neoplasms;Pancreas cyst;Methylation;Biomarker;GNAS locus;Pancreatic neoplasm

INTRODUCTION

Pancreatic cystic lesions(PCLs)constitute a clinical dilemma due to indeterminate risk of malignancy,including benign cysts(BCs),pre-malignant cysts(PMCs),and malignant cysts(MCs)[1].Intraductal papillary mucinous neoplasms(IPMNs)and mucinous cystic neoplasms(MCNs)are cystic precursors of pancreatic ductal adenocarcinoma(PDAC),allowing early diagnosis[2].

Somatic mutations in guanine nucleotide-binding protein,alpha stimulating(GNAS)are characteristic of IPMNs[3,4],but their role in carcinogenesis is unclear,with early occurrence precluding prediction of dysplasia[5,6].However,if detected in PDACs,somatic mutations inGNASare specific for an IPMN origin[3].

GNASis a complex imprinted locus in the long arm of chromosome 20(20q13.32)[7],which encodes the α-subunit of the stimulatory heterotrimeric G protein(Gsα),a ubiquitous signaling protein translated fromGNASexons 1-13.This locus encodes four monoallelic(NESP55,AS,XL,1A)and one biallelic(Gsα)transcript,due to differentially methylated regions(DMRs)in paternal and maternal alleles,denominated imprinting[8,9].Paternal methylation ofNESP55and maternal methylation ofAS,XL,and1Alead,respectively,to maternal and paternal allele expressions,with Gsα biallelically expressed in most tissues,due to absent methylation[10].

Epigenetic alterations in theGNASlocus have not been previously evaluated in PCLs.Methylation of DMRs may occur at the somatic level and modulate Gsα expression[10,11],leading us to hypothesize that methylation changes in DMRs at theGNASlocus could contribute to tumor progression of PCLs.To test our hypothesis,we performed a longitudinal cohort pilot study of PCLs and analyzedGNASlocus methylation in pancreatic cyst fluid(PCF)samples.

MATERIALS AND METHODS

Case selection

All patients gave informed consent,and the study was approved by the Ethics Committee and Institutional Scientific Board(UIC/1143).

For this study we performed molecular analysis in samples of 52 patients with more than 1 mL of PCF stored in the biorepository of our hospital,with sample processing and storage described in a previous publication[12].Clinical data,including demographics,cyst characteristics,and treatment decision,have been prospectively registered.

After undergoing endoscopic ultrasound with fine needle aspiration,patients were evaluated in clinics,and referred for surgery(surgical cohort,surgical pathology diagnosis)or imaging surveillance,palliation,or endoscopic drainage(clinical cohort,clinico-cytological diagnosis)when surgery was not clinically indicated and a surgical pathology specimen was not available for diagnosis.The diagnostic criteria for the clinical cohort were determineda prioriby one of the investigators(SF)after reviewing imaging features,PCF levels of CEA,and cytology analysis of PCLs,all with a prolonged imaging and clinical follow-up(of at least 24 mo).To evaluateGNASlocus methylation distribution and the performance of methylation analysis for cyst diagnosis,PCLs were further classified into one of three groups:Group 1)Benign cysts(BCs),including neoplastic benign and inflammatory cysts(serous cystadenomas(SCAs),pseudocysts,and lymphangiomas);Group 2)Mucinous pre-malignant cysts(PMCs),including IPMNs and MCNs with low grade atypia(LG);Group 3)Highrisk/malignant cysts(MCs),including cystic PDACs,IPMNs with adenocarcinoma(ADC)or high grade atypia(HG),MCN-HG,and neuroendocrine cystic tumors(NETs).

Patients and specimens

The samples studied were predominantly from female patients(35/52,67%)with a mean age of 59 ± 15 years(29-91);22 PCLs were in the head,20 in the body,nine in the tail,and one case of multiple pancreatic locations.The mean cyst size was 3.9 ± 2.3 cm(1-10),CEA level in PCF was >192 ng/mL in 17/52(33%),and malignant/atypical cytology was present in 11/52(21%)PCF samples,as shown in Table 1.

These 52 PCF samples obtained by endoscopic ultrasound with fine-needle aspiration(EUS-FNA)have been previously characterized forKRASandGNASmutations[12],which were present in nine and two samples,respectively.

The final diagnoses,11 surgical and 41 clinicopathological,encompassed 30 BCs(SCAs,pseudocysts,and lymphangiomas),14 PMCs(IPMNs and MCNs),and eight MCs(one cystic PDAC,one IPMN-ADC,one NET,and five mucinous-malignant).

Methylation analysis and categorization

For this study,DNA was extracted from 0.250 mL of archival PCF.Methylation analysis of theGNASlocus was performed by methylation specific–multiplex ligation dependent probe amplification(MS-MLPA)(SALSA MS-MLPA ME031-B1,MRCHolland?,Amsterdam,The Netherlands),according with the manufacturer’s instructions.MS-MLPA fragments were analyzed on the Applied Biosystems?3130 Genetic Analyzer(ThermoFisher Scientific,Waltham,MA,United States)using the GeneMapper?software.Results were normalized and analyzed using Coffalyser.Net software(MRC-Holland?).

We studied methylation in four DMRs,NESP55,GNASAS,GNASXL,andGNAS1A,and in the biallelic expressedGsα,including two exonic regions.DMRs were classified as hypermethylated or hypomethylated,according to the percentage of methylation obtained using the Coffalyser.net software recommended by the manufacturer,if methylation percentage was,respectively,above or below the reference values plus or minus twice the standard deviation(SD).The normal methylation ofNESP55is approximately 50%,as only the paternal allele is methylated,similarly to the percentage of methylation inGNASXL,GNASAS,andGNAS1A,as only the maternal alleles are expected to be methylated.The methylation ofGsα exon 1 is usually absent,as neither maternal nor paternal allele is methylated.Methylation ofGsα exonic regions(exons 9 and 13)is usually near 100%,as both maternal and paternal alleles are methylated.The MS-MLPA kit comprised three methylation sensitive probes forNESP55,three forGNASAS,five forGNASXL,two forGNAS1A,and four forGsα methylation evaluation.

Table 1 Demographics and clinical characteristics of the study population

Statistical analysis

The methylation levels obtained for each of the individual DMRs and for each individual MS-MLPA probe were calculated and converted into a categorical variable defined as:(1)Hypomethylated if methylation level obtained was below the cut-off level minus twice the SD;(2)Hypermethylated if the methylation level obtained was above the cut-off level plus twice the SD;and(3)Normally methylated if neither criteria(1)or(2)were met.A combined variable,including hypermethylation at upstream DMRs or intragenic hypomethylation ofGNASlocus,defining “GNASlocus methylation changes” pattern was created.For(epi)genotype-phenotype associations,Fisher’s exact test and chi-square test were performed as well as Kendall’s rank correlation adjusted for age and gender,using partial correlation.Methylation analysis in mucinous and malignant cysts was also represented by boxplot,and Mann-Whitney was used to assess the difference of median methylation values.The diagnostic accuracy of PCF biomarkers was assessed by receiver operating characteristics curve analysis.Statistics were performed using SPSS Statistical software,version 23(Armonk,NY,United States),with aPvalue <0.05 considered as statistically significant.

RESULTS

GNASlocus methylation was informative in 38/52(73%)PCF samples,with the remaining(14/52)non-informative due to inadequate quality/quantity of DNA and rarely,to copy-number variation(probe ratios below 0.7 or above 1.3,regarded as indicative of heterozygous deletion or duplication,respectively,according with the manufacturer(Coffalyser.Net software,MRC-Holland?).Methylation changes atNESP55,GNASAS,GNAS1A,and especiallyGNASXLwere more frequent in MCs(Table 2),presenting wider methylation levels of these DMRs compared to nonmalignant cysts,which showed methylation levels around 50% in imprinted alleles(Figure 1).

Based on the influence of methylation changes at DMRs in the modulation ofGNAStranscription[10,11]and on the suggested role for hypomethylated exons in transcription regulation and its overlap with predicted enhancers[13],we defined a combined variable documenting “GNASlocus methylation changes”:(1)Presence of hypermethylation in at least two DMRs or in one DMR for all MLPA probes;or(2)Presence of intragenic hypomethylation ofGNASin at least two exonic regions.Notably,“GNASlocus methylation changes” was significantly associated with malignancy(6/8 MCs and only 2/20 BCs)(Table 2),and it is of note that one of these two BCs was later diagnosed as pancreatic cancer.

We further analyzed the correlation between methylation changes and malignancy,while controlling for gender and age.We found a strong significant positive rank correlation between malignancy andGNASmethylation changes(r= 0.837,P<0.001)and a moderate rank correlation withGNASAShypermethylation(r= 0.431,P= 0.015),GNASXLhypermethylation(r= 0.434,P= 0.011),andNESP55hypermethylation(r=0.539,P= 0.003),which was sustained after controlling for gender and age using partial correlation analysis(Table 3).

Moreover,the “GNASlocus methylation changes” variable improved MCs classification in samples with clinicopathological diagnosis(possible diagnostic uncertainty)as well as surgical diagnosis(definitive diagnosis but limited number of cases),further supporting our results.

Interestingly,simultaneous hypermethylation inNESP55andGNASXLDMRs was detected exclusively in 3/3 PDACs.Hypomethylation in two exonicGNASregions(exons 9 and 13)was detected in the only NET in this series.

Additionally,“GNASlocus methylation changes” was associated with symptoms,KRAS/GNASmutations,and malignant/atypical cytology but not with patient gender,age,or CEA level in PCF(Table 4),with the area under the curve analysis revealing better performance than cytology for diagnosis of MCs(Table 5).

DISCUSSION

Aberrant DNA methylation in PCF of IPMNs progressing to high-grade dysplasia and carcinoma has been described[14],butGNASlocus methylation was not studied therein.We report for the first time methylation changes in theGNASlocus,namely hypermethylation ofGNASXL,NESP55,GNASAS,andGNAS1Ain PCLs.Notably,hypermethylation ofGNASXL,and especially the combined variable “GNASlocus methylation changes”,was associated with malignancy,suggesting the potential to be used for diagnosis of MCs and for monitoring cancer progression,if confirmed in larger series.Indeed,hypermethylation ofGNASXLhas been associated toGNASlocus gain of function[10],and although its possible association with malignant progression remains poorly understood,GNASoncogenic potential appears to be unquestionable[3-5,10,15].Moreover,somatic DNA methylation has been shown to drivetranscription within the imprintedGNAScluster[11],further supporting our results.NESP55also appears to regulate imprinting at theGNAScomplex locus,and its hypermethylation in the maternal allele may lead,similarly to maternal deletion,as previously described,to subsequent modulation ofGNAS[10].

Table 2 Frequency of GNAS locus methylation changes in malignant,mucinous,and benign cysts,n(%)

Table 3 Correlation between methylation status and malignancy with partial correlation controlling for patients’ gender and age

Table 4 Frequencies of distinct clinical features and pancreatic cystic fluid analysis in the two groups,with or without GNAS locus methylation changes

Herein,hypermethylation in both maternally(NESP55)and paternally(GNASXL)derived promoters,and therefore overall increase of methylation in these two DMRs,was detected exclusively in PDAC,further suggesting a role ofGNASin malignant progression of PCL.Interestingly,the detection of exonicGNAShypomethylation in the pancreatic NET is in agreement with the recent findings showing that pancreatic NETs are genetically and phenotypically related to pancreatic ductal adenocarcinoma,having a closer relationship to ductal adenocarcinomas than to neuroendocrine tumors G3[16].In agreement with the role ofGNASin the progression to PDAC is also the recent finding that overexpression of mutantGNAS,resulting in constitutive activation ofGsα,in a mouse model ofKrasG12D-driven pancreatic cancer,led to the formation of moderately differentiated PDAC that were locally invasive and increased mitogenactivated protein kinase activation[17].

Table 5 Area under the curve for diagnosis of mucinous and malignant cysts

Figure 1 Methylation analysis of non-malignant and malignant cysts.GNAS:Guanine nucleotide-binding protein,alpha stimulating.

Although copy-number alterations,which could in part explain some of the methylation changes found,were detected in only one case,we cannot exclude the presence of uniparental disomy(UPD)associated copy-neutral loss of heterozygosity(LOH),as previously described by Bastepeet al[18]to explainGNASmethylation changes.An analysis of LOH in theGNASlocus would be needed to evaluate uniparental disomy(UPD)associated copy-neutral LOH(which can often be segmental)and investigate if some of these methylation alterations may indeed reflect epigenetic alterations or could instead be explained(at least in part)by acquired UPD.Nevertheless,independent of their cause(epigenetic or acquired UPD),the resulting methylation alterations detected in theGNASlocus DMRs appear to be related to malignant progression and may improve MCs diagnosis.Our study may contribute to the current epigenetic landscape of PCs,similar to recent studies documenting a role for methylation markers in discriminating pancreatic neoplasia[19,20],possibly offering an opportunity for early diagnosis for pancreatic cancer.

Ultimately,the significant association ofGNASlocus methylation changes to malignant behavior suggests a role for modulation ofGNASexpression in the malignant progression of PCs,which may be relevant for the development of novel therapeutic approaches for pancreatic cancer.Due to small sample size and poor DNA yield,the final analysis was based on eight samples with HGD/cancer.Although the small sample size and lack of validation in an independent sample are significant limits regarding the present study,our pilot data may be the basis for exploringGNASmethylation in larger,well-characterized sets of samples that may represent future validation studies.Finally,as gene methylation may affect gene expression,additional evaluation ofGNAStranscripts in PCF may elucidate their function in PCLs.

ARTICLE HIGHLIGHTS

Research background

Pancreatic cystic lesions(PCLs)constitute a clinical dilemma due to indeterminate risk of malignancy.Intraductal papillary mucinous neoplasms(IPMNs)and mucinous cystic neoplasms are cystic precursors of pancreatic ductal adenocarcinoma(PDAC),possibly allowing early diagnosis.Somatic mutations inGNASare characteristic of IPMNs,but their role in carcinogenesis is unclear.GNASis a complex imprinted locus that encodes the α-subunit of the stimulatory heterotrimeric G protein(Gsα),an ubiquitous signaling protein.This locus encodes four monoallelic(NESP55,AS,XL,1A)and one biallelic(Gsα)transcript(s),due to differentially methylated regions(DMRs)in paternal and maternal alleles,denominated imprinting.Paternal methylation ofNESP55and maternal methylation ofAS,XL,and1Alead,respectively,to maternal and paternal allele expressions,with Gsα biallelically expressed in most tissues,due to absent methylation.

Research motivation

GNASsomatic mutations are characteristic of IPMNs,although epigenetic alterations in theGNASlocus have not been previously evaluated in PCLs.Methylation of DMRs at theGNASlocus may occur at the somatic level and modulate Gsα expression.

Research objectives

In this study,we evaluate if methylation changes in DMRs at theGNASlocus could contribute to tumor progression of PCLs.

Research methods

We performed a longitudinal cohort study of PCLs withGNASlocus methylation analysis performed in PCF samples obtained by endoscopic ultrasound with fine needle aspiration.

Research results

Fifty-two PCF samples obtained by endoscopic ultrasound with fine needle aspiration and previously characterized forKRASandGNASmutations were studied.The final diagnoses were surgical(11)and clinicopathological(41),including 30 benign cysts,14 pre-malignant cyst,and eight malignant cysts.Methylation changes atNESP55,GNASAS,GNAS1A,and especiallyGNASXLwere more frequent in malignant cysts and were useful for their diagnosis.A combined variable defined as “GNASlocus methylation changes” was significantly associated with malignancy(6/8 malignant cysts and only 2/20 benign cysts)and improved classification.Hypermethylation in both maternally(NESP55)and paternally(GNASXL)derived promoters was found in 3/3 PDACs.

Research conclusions

This is the first study to identify methylation changes in theGNASlocus that improved the diagnosis of malignant PCs and suggest a role in progression to PDAC.

Research perspectives

Although the small sample size and lack of validation in an independent sample are significant limits regarding the present study,our pilot data may be the basis for exploringGNASmethylation in larger,well-characterized sets of samples.As methylation status may impact gene expression,additional evaluation ofGNAStranscripts in PCF may elucidate their function in pancreatic cystic neoplasms.