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International Journal of Biological Sciences logoLink to International Journal of Biological Sciences
. 2014 Aug 30;10(9):957–965. doi: 10.7150/ijbs.9773

KRAS and DAXX/ATRX Gene Mutations Are Correlated with the Clinicopathological Features, Advanced Diseases, and Poor Prognosis in Chinese Patients with Pancreatic Neuroendocrine Tumors

Fei Yuan 3,*, Min Shi 1,*, Jun Ji 1, Hailong Shi 1, Chenfei Zhou 1, Yingyan Yu 1, Bingya Liu 1, Zhenggang Zhu 1,2, Jun Zhang 1,2,
PMCID: PMC4159686  PMID: 25210493

Abstract

Background and Aim: Pancreatic neuroendocrine tumor (pNET) is a clinically rare and heterogeneous group of tumors; its pharmacogenetic characteristics are not fully understood. This study was designed to examine the relationship between key gene variations and disease development and prognosis among Chinese patients with pNET.

Methods: Various pNET associated genes such as DAXX/ATRX, KRAS, MEN1, PTEN, TSC2, SMAD4/DPC, TP53 and VHL were analyzed in high-throughput sequencing. The links between the gene mutations and the clinicopathological features and prognosis of the patients were determined.

Results: The somatic mutation frequencies of the DAXX/ATRX, KRAS, MEN1, mTOR pathway genes (PTEN and TSC2), SMAD4/DPC, TP53, and VHL in Chinese pNET patients were 54.05%, 10.81%, 35.14%, 54.05%, 2.70%, 13.51%, and 40.54%, respectively, while the same figures in Caucasians pNET patients were 43%, 0%, 44%, 15%, 0%, 3%, and 0%, respectively. The numbers of mutated genes were from 0 to 6; 4 patients with more than 3 mutated genes had higher proliferation (Ki-67) index or nerve vascular invasion or organ involvement, but only 9 of 27 patients with 3 or few mutated genes had such features. Mutations in KRAS and DAXX/ATRX, but not other genes analyzed, were associated with a shortened survival.

Conclusion: The mutation rates of these genes in Chinese pNET patients are different from those in Caucasians. A higher number of gene mutations and the DAXX/ATRX and KRAS gene mutations are correlated with a poor prognosis of patients with pNET.

Keywords: pancreatic neuroendocrine tumor, gene mutation, prognosis, KRAS, DAXX/ATRX.

Introduction

Pancreatic neuroendocrine tumors (pNETs) include a heterogeneous group of tumors and account for about 3%-5% of all pancreatic malignancies, with an incidence estimated to range from 0.3 to 0.4 per 100,000 in the United States 1-3. The incidence and prevalence of pNETs have increased about five-fold in the last three decades, partly due to the improvement of diagnostic standards and early detection of asymptomatic lesions 3. The pNETs can be divided into functional and nonfunctional tumors. Functional tumors, such as insulinomas and gastrinomas, can secrete hormones and lead to corresponding clinical symptoms, whereas nonfunctional tumors cause non-specific symptoms, such as pain, an abdominal mass, pernicious vomiting, and anemia 4, 5.

The mainstay of treatment for pNETs is surgery. However, most patients are contraindicated for resection, because 65% of patients have unresectable or metastatic disease at the time of diagnosis 6. Unresectable pNETs are associated with a poor prognosis, with a median overall survival (mOS) of 24 months 3. The 10-year survival rate is only 40% and has not changed significantly over the last 30 years 2. Newer chemotherapeutic agents and molecular targeted therapy have recently been developed to treat the unresectable pNETs, but their efficacy has been modest 7.

The genetic background of pNETs has not been fully understood. One study has revealed that there are multiple genetic mutations in nonfamilial pNETs, including mutations in multiple endocrine neoplasias type 1 (MEN1), DAXX (death domain-associated protein)/ATRX (α-thalassemia/mental retardation syndrome X-linked), and genes in the mammalian target of rapamycin (mTOR) pathway 8. Interestingly, the mutations in the MEN1 and DAXX/ATRX genes are associated with a better prognosis of pNET patients in that study. Furthermore, the investigators suggest that the identification of mutations in genes in the mTOR pathway could be used to stratify pNET patients for treatment with mTOR inhibitors 8.

We have been interested in elucidating the genetic mechanisms for the development and progression of pNETs and believe patients' pharmacogenetic characgteristics could be used to guide their diagnosis and treatment. Additionally, it has been well documented that there are significant differences in genetic/genomic variations for many diseases among various ethnic groups. In the present study, we analyzed the gene mutations of Chinese pNET patients. Considering that all of the published studies had focused on Caucasian and Western populations and no studies have been conducted in Chinese populations, we compared the mutations in our patients with those of the previous studies in Westerners and examined the relationship between the key gene mutations and the clinic-pathological features and prognosis of our pNET patients.

Materials and Methods

Ethics Statement

The study was reviewed and approved by the Institutional Review Board (IRB) of Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China. Informed written consent to participate in the study was obtained from each of the patients before the entry of the study.

Patient Characteristics, Tissue Samples, and Follow-Up

This was a retrospective study. From 2005 to 2011, 43 consecutive pNET patients underwent surgical resections of their tumors and had a definite pathological diagnosis of pNET in the Department of Surgery, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China. Six cases also had pancreatic adenocarcinoma and were excluded from the present study; therefore, 37 patients were finally enrolled in the study. All tumor specimens were formalin-fixed and paraffin-embedded. The tumors were classified into three groups according to the 2010 World Health Organization (WHO) classification criteria 9. The clinic-pathological data are shown in Table 1. Patients were followed up, and the overall survival time was analyzed.

Table 1.

Characteristics of the 37 patients with pNETs from Ruijin Hospital.

Sample Age Gender Function WHO classification TNM(A7) Ki-67
pNET1 41 Male NF G1 Ib ≤2%
pNET2 37 Female NF G1 Ib ≤2%
pNET3 54 Male NF G2 Ib ≤2%
pNET4 18 Male NF G2 IV 3-20%
pNET6 61 Male NF G1 Ib ≤2%
pNET7 58 Female NF G1 IIb ≤2%
pNET9 32 Female Insulinoma G1 Ia ≤2%
pNET10 66 Male NF G1 IIa ≤2%
pNET11 64 Female NF G1 Ib ≤2%
pNET13 51 Female NF G1 Ia ≤2%
pNET14 48 Male NF G1 IIb ≤2%
pNET15 47 Male NF G1 Ib ≤2%
pNET16 48 Male NF G1 Ib ≤2%
pNET17 61 Female NF G1 Ib ≤2%
pNET18 47 Male NF G3 IIb >20%
pNET20 38 Female NF G2 Ia ≤2%
pNET21 65 Female Insulinoma G2 IV 3-20%
pNET22 67 Female NF G2 Ia ≤2%
pNET23 54 Male NF G2 Ia ≤2%
pNET24 62 Female NF G1 Ib ≤2%
pNET25 47 Male NF G3 IIa >20%
pNET28 57 Female NF G1 Ib ≤2%
pNET29 61 Female Insulinoma G1 Ia ≤2%
pNET30 61 Female NF G1 Ib ≤2%
pNET31 45 Male NF G1 Ia ≤2%
pNET32 55 Female NF G1 Ia ≤2%
pNET33 59 Female Insulinoma G1 Ia ≤2%
pNET34 47 Male NF G2 IIa ≤2%
pNET35 62 Female NF G1 Ia ≤2%
pNET36 67 Female NF G1 Ib ≤2%
pNET37 72 Male NF G1 Ib ≤2%
pNET38 47 Female NF G2 Ib 3-20%
pNET39 57 Male NF G3 IIa >20%
pNET40 37 Male NF G3 IIb >20%
pNET41 64 Male NF G3 IIa >20%
pNET42 61 Female NF G3 IV >20%
pNET43 35 Female NF G2 Ib 3-20%

DNA Extraction and Gene Sequencing

Cellular DNA was extracted from formalin-fixed paraffin-embedded (FFPE) tumor tissues using the QIAamp DNA FFPE Tissue Kit (QIAGEN, China). DNA was extracted only from samples with more than 80% tumor cell content. Target gene amplification was accomplished using Unicorn PCR per-mix kit (Shenzhen, China); the gene sequence and data analyses were applied under the guideline of HYKGENE sequence reagents kit or operation guide (Shenzhen, China). The sequencing flux requirement by a single locus was higher than that of 300×, and the quality requirement of the single locus sequence number was higher than 100× base number accounts for more than 95% of the total length. In somatic mutation selection criteria, the sequencing depth was more than 100, which had on different reads and distribution in different positions. The SNP/somatic mutations of the candidate loci were compared with the SNP database on the HapMap to confirm whether they were reported. Finally, filters were used to remove coding-synon, eventually forming the somatic mutation data of the Chinese pNET patients.

Literature Review: Inclusion Criteria, Search Strategies, and Data Extraction

In the present study, we also conducted a systemic review on pNET clinical studies. Studies were selected according to the following inclusion criteria: 1) studies must explore the genetic alterations of pNETs; and 2) studies must be published in English in a peer-reviewed journal. We performed a search of the National Center for Biotechnology Information (NCBI) PubMed database using the search terms “Pancreatic endocrine tumors OR Pancreatic neuroendocrine tumors OR pancreatic islet cell tumor OR gastrinoma OR insulinoma OR glucagonoma OR vasoactive intestinal peptide tumor OR somatostatinoma OR nfpets OR growth hormone tumor OR acth tumor OR pancreatic polypeptide tumor OR pets causing carcinoid syndrome OR pets causing hypercalcemia AND mutation”. This search yielded 2278 articles published as of November 1, 2013. After manually screening the studies, we selected 178 articles for data mining, based on the aforementioned criteria. The data were extracted by two investigators independently to avoid any bias due to personal preference. When the two investigators were not in agreement, a third person was consulted to reach a final agreement regarding whether the article was suitable. The following information, if presented, was extracted and tabulated from each article: first author, year of publication, journal, genotype, gene, mutation type, chromosomal location, number of cases, number of mutation cases, population, family history, pNET type, gender, and any other important information.

Statistical Analysis

The chi-squared test was used to analyze the categorical variables. The log-rank test for the Kaplan-Meier method and the Cox regression test were used to assess the patients' outcomes and the prognostic factors. All statistical analyses were performed using the SPSS 17.0 software program. A two-tailed value of P<0.05 was considered statistically significant.

Results

Literature search results

Based on the literature search, 178 papers were included in the analysis of the mutation frequency after manually screening the full text. These reports described 551 mutations in 11 different genes (SMAD4/DPC4, KRAS, TP53, VHL, PTEN, TSC2, DAXX/ATRX, MEN1, BRAF, BRCA2 and PIK3CA). The mutations and the gene functions were summarized as a table (Supplementary Table 1).

Mutation Frequency in pNET Tissue Samples

By using Sanger sequencing, we identified 133 somatic mutations in eight different genes in our cases (Table 2). The somatic mutation frequency of the DAXX/ATRX, KRAS, MEN1, mTOR pathway genes (PTEN and TSC2), SMAD4/DPC, TP53 and VHL were 54.05%, 10.81%, 35.14%, 54.05%, 2.70%, 13.51%, and 40.54%, respectively.

Table 2.

The mutations in SMAD4/DPC4. KRAS, TP53, VHL, PTEN, TSC2, DAXX, ATRX, and MEN1 in pNETs.

Sample Gene Nucleotide (genomic) Amino acid change Mutation type
pNET4 ATRX chrx:76778854 CAG(Q)>CCG(P) missense
ATRX chrx:76907608 AGA(R)>ATA(I) missense
ATRX chrx:76814262 GCT(A)>ACT(T) missense
ATRX chrx:76814186 CGC(R)>CAC(H) missense
pNET9 ATRX chrx:76907836-76907837 indel
pNET15 ATRX chrx:76907741 Gly(GGA)->Arg(AGA) missense
pNET17 ATRX chrx:76907744 Pro(CCT)->Ser(TCT) missense
pNET25 ATRX chrx:76874303 CTC(L)>GTC(V) missense
pNET28 ATRX chrx:76907645 CGT(R)>GGT(G) missense
pNET31 ATRX chrx:76778855 CAG(Q)>TAG(Stop) nonsense
pNET34 ATRX chrx:76874303 CTC(L)>GTC(V) missense
pNET37 ATRX chrx:76778844 AAA(K)>AAT(N) missense
pNET40 ATRX chrx:76939403 CCT(P)>GCT(A) missense
ATRX chrx:76907612 TTG(L)>ATG(M) missense
ATRX chrx:76907660 GAA(E)>AAA(K) missense
pNET41 ATRX chrx:76907663 GAG(E)>CAG(Q) missense
ATRX chrx:76907840 AAT(N)>TAT(Y) missense
pNET42 ATRX chrx:76909619 AAG(K)>AGG(R) missense
ATRX chrx:76907840 AAT(N)>TAT(Y) missense
pNET43 ATRX chrx:76907660 GAA(E)>AAA(K) missense
pNET1 DAXX chr6:33287895 Glu(GAA)->Gly(GGA) missense
pNET3 DAXX chr6:33288158 Glu(GAG)->Val(GTG) missense
pNET4 DAXX chr6:33287895 Glu(GAA)->Gly(GGA) missense
pNET6 DAXX chr6:33287869 Glu(GAA)->Lys(AAA) missense
pNET15 DAXX chr6:33289268 Ala(GCC)->Val(GTC) missense
pNET20 DAXX chr6:33289256-33289256 indel
pNET22 DAXX chr6:33289256-33289256 indel
pNET25 DAXX chr6:33286925 TCC(S)>TTC(F) missense
pNET29 DAXX chr6:33288170 L-Stop 413 nonsense
pNET30 DAXX chr6:33287844 ATG(M)>AGG(R) missense
pNET31 DAXX chr6:33287902 GAG(E)>CAG(Q) missense
DAXX chr6:33287844 ATG(M)>AGG(R) missense
pNET15 KRAS chr12:25398299 Val(GTG)->Ala(GCG) missense
pNET25 KRAS chr12:25398284 rs121913529 missense
Gly(GGT)->Asp(GAT)
pNET31 KRAS chr12:25398266 Ala(GCC)->Val(GTC) missense
pNET40 KRAS chr12:25398284 rs121913529 missense
Gly(GGT)->Asp(GAT)
pNET1 MEN1 chr11:64577464 Val(GTG)->Leu(TTG) missense
MEN1 chr11:64577355 T->I 76 missense
pNET3 MEN1 chr11:64577526 Val(GTG)->Glu(GAG) missense
pNET4 MEN1 chr11:64574502 Pro(CCA)->Leu(CTA) missense
MEN1 chr11:64577391 CAG(Q)>CGG(R) missense
MEN1 chr11:64577182 TTC(F)>CTC(L) missense
pNET9 MEN1 chr11:64577397 Thr(ACC)->Ile(ATC) missense
pNET13 MEN1 chr11:64574514 Gly(GGC)->Asp(GAC) missense
pNET14 MEN1 chr11:64577307 R->H 92 missense
MEN1 chr11:64577397 Thr(ACC)->Ile(ATC) missense
pNET15 MEN1 chr11:64577185 Y->H 133 missense
pNET17 MEN1 chr11:64574502 Pro(CCA)->Leu(CTA) missense
pNET30 MEN1 chr11:64574565 CCC(P)>CTC(L) missense
pNET33 MEN1 chr11:64577389 CCC(P)>ACC(T) missense
CCC(P)>TCC(S) missense
pNET34 MEN1 chr11:64577316 Leu(CTC)->Arg(CGC) missense
MEN1 chr11:64577389 CCC(P)>ACC(T) missense
CCC(P)>TCC(S)
pNET35 MEN1 chr11:64574671 Tyr(TAT)->Stop(TAG) nonsense
pNET38 MEN1 chr11:64574502 Pro(CCA)->Leu(CTA) missense
pNET3 TP53 chr17:7579424 Ala(GCC)->Asp(GAC) missense
pNET25 TP53 chr17:7579387 Q->H 100 missense
pNET36 TP53 chr17:7577509-7577509 indel
pNET37 TP53 chr17:7579293-7579294 indel
pNET41 TP53 chr17:7578481 ACA(T)>AAA(K) missense
pNET3 PTEN chr10:89720826 Asp(GAC)->Ala(GCC) missense
pNET18 PTEN chr10:89720870 Phe(TTT)->Val(GTT) missense
pNET21 PTEN chr10:89720870 Phe(TTT)->Val(GTT) missense
pNET24 PTEN chr10:89720826 Asp(GAC)->Ala(GCC) missense
pNET25 PTEN chr10:89720853 CGA(R)>CAA(Q) missense
pNET32 PTEN chr10:89720870 Phe(TTT)->Val(GTT) missense
pNET34 PTEN chr10:89685307 TAC(Y)>CAC(H) missense
PTEN chr10:89720816-89720817 rs121913291 indel
pNET22 SMAD4/DPC4 chr18:48593423 Lys(AAA)->Gln(CAA) missense
pNET1 TSC2 chr16:2134968 Leu(CTC)->Val(GTC) missense
pNET4 TSC2 chr16:2130258 GCG(A)>ACG(T) missense
pNET7 TSC2 chr16:2134973-2134974 rs137854017 indel
pNET10 TSC2 chr16:2134973-2134974 rs137854017 indel
pNET15 TSC2 chr16:2134994 D->E 151 missense
TSC2 chr16:2135013 L->M 1519 missense
pNET16 TSC2 chr16:2134994 D->E 151 missense
TSC2 chr16:2135013 L->M 1519 missense
TSC2 chr16:2136843 G->S 1654 missense
pNET20 TSC2 chr16:2136843 G->S 1654 missense
pNET24 TSC2 chr16:2134992 D->N 1512 missense
TSC2 chr16:2136873-2136873 rs137854005 indel
pNET25 TSC2 chr16:2130168-2130169 rs137854314 indel
pNET28 TSC2 chr16:2134961-2134962 rs137854160 indel
pNET29 TSC2 chr16:2130168-2130169 rs137854314 indel
pNET30 TSC2 chr16:2134329 CGG(R)>CAG(Q) missense
pNET31 TSC2 chr16:2134328 rs45517328 1369 missense
TSC2 chr16:2134391 GAG(E)>CAG(Q) missense
pNET33 TSC2 chr16:2134961-2134962 rs137854160 indel
TSC2 chr16:2130259 rs45448801 missense
GCG(A)>GAG(E)
pNET34 TSC2 chr16:2134961-2134962 rs137854160 indel
pNET35 TSC2 chr16:2134961-2134962 rs137854160 indel
TSC2 chr16:2130168-2130169 rs137854314 indel
TSC2 chr16:2130266-2130266 rs137854340 indel
pNET1 VHL chr3:10183775 Arg(CGC)->Cys(TGC) missense
VHL chr3:10188212 F->I 119 missense
VHL chr3:10188218 D->H 121 missense
VHL chr3:10183734 Ser(TCG)->Leu(TTG) missense
pNET3 VHL chr3:10183737 Arg(CGC)->His(CAC) missense
VHL chr3:10188304-10188305 indel
pNET7 VHL chr3:10191563 Glu(GAA)->Lys(AAA) missense
pNET10 VHL chr3:10183841 Gly(GGC)->Ser(AGC) missense
pNET13 VHL chr3:10188307-10188308 rs5030624 indel
pNET14 VHL chr3:10183736 Arg(CGC)->Cys (TGC) missense
VHL chr3:10183734 Ser(TCG)->Leu(TTG) missense
pNET15 VHL chr3:10183736 Arg(CGC)->Cys (TGC) missense
pNET17 VHL chr3:10183826 Pro(CCA)->Ser(TCA) missense
pNET20 VHL chr3:10183734 Ser(TCG)->Leu(TTG) missense
VHL chr3:10188304-10188305 indel
pNET22 VHL chr3:10183734 Ser(TCG)->Leu(TTG) missense
pNET25 VHL chr3:10183736 Arg(CGC)->Cys (TGC) missense
VHL chr3:10183682 Glu(GAG)->Stop(TAG) nonsense
pNET28 VHL chr3:10183704 CGG(R)>CAG(Q) missense
pNET33 VHL chr3:10183802 Phe(TTC)->Leu(CTC) missense
pNET34 VHL chr3:10188304-10188305 indel
pNET38 VHL chr3:10183809 GGC(G)>GAC(D) missense
VHL chr3:10188230 CAC(H)>TAC(Y) missense

There were some obvious differences between our findings and the results reported by Jiao et al 8, in which similar genes were investigated. In our study, the KRAS, TP53, mTOR pathway genes (PTEN and TSC2), and VHL genes had significantly higher mutation rates than those in their study (Table 3). The potential reasons for these differences are not clear by may be associated with the following: 1) most of the subjects in their study were Caucasian (85%), while in our study, all of the patients were Chinese; and 2) there were only three patients with Grade 3 (poorly differentiated) tumors in their study (5%), but there were six cases (16.2%) with of poorly differentiated tumors in our study.

Table 3.

Comparison of the most commonly mutated genes in pNETs between Chinese and Caucasians.

Genes pNETs (Chinese) pNETs (Caucasian) a
KRAS 10.81% 0%
TP53 13.51% 3%
mTOR (PTEN and TSC2) 54.05% 15%
VHL 40.54% 0%
SMAD4/DPC4 2.70% 0%
DAXX/ATRX 54.05% 43%
MEN1 35.14% 44%

a The data are from Science 2011;331:1199-203.

Gene Mutations in KRAS, TP53, TSC2, and VHL in pNET Tissue Samples

The mutation frequencies of the KRAS, TP53, TSC2, and VHL genes in our study were different from those in Caucasians, so we subjected these genes to a more detailed mutation analysis (Table 2). We detected four cases with KRAS mutations, all of which were missense mutations. There were two G-to-A transitions and one T-to-C transition and one C-to-T transition. All of the mutations were in the GTPase domain. Fifteen of the 30 cases examined for VHL gene mutations were positive, including 23 different mutant sites, among which were 18 missense mutations, four indels, and one nonsense mutations. C-to-T transitions and C-to-A transitions were responsible for 55.6% and 27.8%, respectively, of the missense mutations. The mutations occurred mainly in the β domain and its nearby regions.

Fifteen cases were identified that had TSC2 gene mutations, among which 25 different mutant sites containing 14 missense mutations and 11 indels were found. There were two G-to-A transitions, one G-to-C, one C-to-G, and one C-to-A transition. The TSC2 mutations mainly occurred in or near the RAP-GAP domain. We detected five cases with TP53 mutations, three of which were missense mutations and two of which were indels. Two C-to-A transitions were detected in the missense mutations. One patient had an indel mutation at the 258 region, which is located at the center of the TP53 DNA binding domain (102-292 region). This patient had a higher degree of differentiation and an earlier clinical stage compared to the other patients. His overall survival time was also longer than the average of the remaining patients (45.8 vs. 26.7 months, P<0.05). This suggested that patients with the TP53 indel mutation in the 258 region may have a lower level of malignancy and a better prognosis.

Relationships between Gene Mutations and the Clinico-pathological Characteristics of pNETs

The three most frequently mutated genes found in our study were DAXX/ATRX (54.1%), TSC2 (43.2%) and VHL (40.5%). Missense mutations were the most common type of mutation in DAXX/ATRX and VHL (comprising 82.1% and 78.3% of mutations, respectively), while in TSC2, missense and indel mutations comprised 54.2% and 45.8% of the mutations, respectively (Table 4). The number of mutations among these well-differentiated samples are from 0 to 6 and we cutoff at the median 3, there were 27 patients have 3 or less genes occur mutations and only 9 patients in them have higher Ki-67 index or associated with the nerve vascular invasion or organ involvement. Otherwise in other 4 patients with more than 3 mutated genes all have these features (Table 5). This difference may indicates that well-differentiated patients with mutations of multiple genes tend tumor invasion. Specifically, one patient (No. 25) had six gene mutations, with a Ki-67 index of 80%, with neurological vascular invasion and spleen metastasis. These findings suggested that the number of mutated genes may be correlated with the pNETs' growth and progression.

Table 4.

All gene mutations identified in the 37 Chinese pNETs patients.

Sample SMAD4/DPC4 KRAS TP53 VHL PTEN TSC2 DAXX/ATRX MEN1
pNET1 missense missense missense missense
pNET2
pNET3 missense missense/ indel indel missense missense
pNET4 missense missense missense
pNET6 missense
pNET7 missense Indel
pNET9 indel missense
pNET10 missense Indel
pNET11
pNET13 indel missense
pNET14 missense missense
pNET15 missense missense missense missense missense
pNET16 missense
pNET17 missense missense missense
pNET18 missense
pNET20 missense/ indel missense indel
pNET21 missense
pNET22 Missense missense indel
pNET23
pNET24 missense missense/ indel
pNET25 missense missense missense/ nonsense missense indel missense
pNET28 missense indel missense
pNET29 indel nonsense
pNET30 missense missense missense
pNET31 missense missense missense/ nonsense
pNET32 missense
pNET33 missense indel missense
pNET34 indel missense/ indel indel missense missense
pNET35 indel nonsense
pNET36 indel
pNET37 indel missense
pNET38 missense missense
pNET39
pNET40 missense missense
pNET41 missense missense
pNET42 missense
pNET43 missense

Table 5.

The relationship between the number of mutated genes and the Ki-67 index or TNM stage of well-differentiated pNETs patients.

Ki-67 index or TNM stage
Number of mutated genes Cases (n=31) High Low P value
≤ 3 27 9 18 0.012
> 3 4 4 0

The KRAS and DAXX/ATRX Gene Mutations Predict a Poor Prognosis in Patients With pNETs

We assessed whether the mutations in KRAS, TP53, mTOR pathway genes (PTEN and TSC2), VHL, SMAD4/DPC4, DAXX/ATRX, and MEN1 were associated with the patient survival. A Kaplan-Meier survival analysis was performed for the 37 pNET patients. Mutations in KRAS and DAXX/ATRX were found to be associated with a shortened survival (Figure 1), while mutations in TP53, mTOR pathway genes (PTEN and TSC2), VHL, SMAD4/DPC4, and MEN1 did not predict the pNET patients' survival (Figure 2). To our knowledge, this is the first report that the presence of KRAS gene mutations was confirmed in pNETs, and furthermore, provides the first evidence that KRAS gene mutations may predict a poor survival.

Figure 1.

Figure 1

The Kaplan-Meier curves of the overall survival of pNET patients, stratified by the status of gene mutations. A: DAXX/ATRX; B: KRAS. Mutations in DAXX/ATRX and KRAS were found to be associated with a shortened survival (n=37; all p<0.05).

Figure 2.

Figure 2

The Kaplan-Meier curves of the overall survival of pNET patients, stratified by the status of gene mutations. A: TP53; B: PTEN; C: TSC2; D: VHL; E: SMAD4/DPC4; and F: MEN1. These mutations analyzed were not associated with survivals of the pNET patients (n=37; all p>0.05).

Interestingly, the result that mutations of DAXX/ATRX were associated with a shortened survival was inconsistent with the report by Jiao et al.8 Their results showed that mutations in MEN1, DAXX/ATRX, or the combination of both MEN1 and DAXX/ATRX were associated with prolonged survival relative to that of the patients whose tumors lacked these mutations. The results reported by Marinoni et al. 10 are in agreement with our results. In their report, the mutations found in the DAXX/ATRX genes correlated with the loss of the corresponding protein expression in pNETs, and loss of DAXX/ATRX expression was significantly correlated with both a shortened relapse-free survival and tumor-specific survival.

Discussion

In the present study with 37 Chinese pNET patients, we identified 133 somatic mutations in eight different genes, including KRAS, TP53, PTEN, TSC2, VHL, SMAD4/DPC4, DAXX/ATRX, and MEN1. Compared to the results from Caucasians, there were several remarkable differences: 1) the KRAS, TP53, mTOR pathway genes (PTEN and TSC2), and VHL genes had significantly higher mutation rates in Chinese patients than in Caucasian patients; 2) the number of gene mutations was correlated with the growth and progression of well-differentiated PNETs patients; and 3) KRAS and DAXX/ATRX gene mutations were associated with a shortened survival in Chinese pNET patients.

The mutations of such genes may be involved in the development and progression of pNETs. The VHL protein contains two structural domains, called α and β. The α domain can bind to Elongin B or C, while the β domain can interact with hypoxia-inducible factor-1α (HIF-1α). Fifteen of the 30 cases that were evaluated were identified to have VHL gene mutations, and the mutations occurred mainly in or near the β domain. This may have caused VHL to fail to interact with HIF-1α, which would lead to a decrease in HIF-1α ubiquitination and degradation. As a result, the subsequent downstream genes of HIF-1α, such as VEGF, TGF-α and various cytokines, would exhibit sustained activation, which could promote tumor development and progression 11, 12.

It has been demonstrated that pNETs exhibit overexpression of VEGF, its receptor, VEGFR, and platelet-derived growth factor receptor (PDGFR) 13, 14. Sunitinib malate, an oral tyrosine kinase inhibitor, has activity against VEGFRs, PDGFRs, stem-cell factor (KIT) receptor, glial cell line-derived neurotrophic factor, and FMS-like tyrosine kinase-3 15. Recently, several phase II and phase III trials have demonstrated that the administration of sunitinib can significantly improve the progression-free survival and overall survival, and that it shows an acceptable safety profile in patients with advanced pNETs 16-18.

During the process of pNET development, the receptor tyrosine kinase (RTK)-PI3K/PTEN-AKT-TSC1/2-mTOR signaling pathway plays an important role in the control of cell growth, proliferation, survival, and differentiation 19, 20. TSC2 and TSC1 can form a dimer and inhibit the GTPase activity of Rheb, a critical activator of mTOR signaling 21. TSC2 contains two structural domains: one is necessary for the binding to TSC1, but the deletion of this domain has no effect on its GAP activity; another is the RAP-GAP domain. When this domain is mutated, the GTPase activity of Rheb is enhanced, resulting in the activation of mTOR 22. In our study, TSC2 mutations mainly occurred in or near the RAP-GAP domain. Everolimus is an mTOR inhibitor, and many studies have shown the efficacy and safety of everolimus in the treatment of advanced pNETs 23-25. Based on these findings, the results of our study are consistent with the previous reports, and may help predict the response of pNETs to molecular targeted therapies 8.

Mutations in DAXX or ATRX have been detected in about 40% of pNETs. DAXX is an H3.3-specific histone chaperone, while ATRX encodes a protein that has an ADD (ATRX-DNMTT3-DNMT3L) domain at the amino-terminus and a carboxy-terminal helicase domain 10, 26. The interaction between DAXX and ATRX is required for H3.3 incorporation at the telomeres, and ATRX, but not DAXX, could suppress the telomeric repeat-containing RNA expression. Furthermore, ATRX was also found to target CpG islands and G-rich tandem repeats, which exist close to telomeric regions 27-30. In our study, the relationship between DAXX/ATRX mutations and the poor prognosis of pNET patients was inconsistent with the findings of a previous report. In that report, Jiao et al. showed that DAXX/ATRX mutations were associated with prolonged survival in pNET patients. In contrast, Marinoni et al. showed that the loss of DAXX/ATRX expression caused by a DAXX/ATRX gene mutation was significantly correlated with both a shortened relapse-free and tumor-specific survival. The reasons for these differences may include the following: 1) The DAXX/ATRX mutation rate in our study was higher than that in the other studies; 2) The patients in our study were all Chinese, while those in the other studies were mostly Caucasian; and 3) The mutated regions of DAXX/ATRX in our study were different from those in the other studies.

KRAS, a member of the rat sarcoma viral oncogene homolog (RAS) proto-oncogene family, is a key protein in the EGFR pathway, and plays an important role in the activation of various downstream proteins, including Raf, MEK and ERK 31. The mutant status of KRAS may inhibit GTP enzymatic activity, resulting in sustained activation of the EGRF signaling pathway. Codons 12, 13, and 61 are the most common mutation sites in KRAS 32, 33. The mutation rate of KRAS in pancreatic cancer is about 90%, and there is a major region of mutation in codon 12. However, the KRAS mutation rate in pNETs has rarely been reported. In our study, the mutation rate of KRAS was 10.81%, while there were no KRAS mutations reported by Jiao et al. The KARS mutations in our study were found in codons 7, 12, and 18. Interestingly, our study suggests that the presence of a KRAS gene mutation may predict a poorer survival. This was a novel finding, but needs to be further analyzed in a larger number of patients.

In conclusion, the significance of our study is the first to report the gene mutations of pNETs in Chinese patients. Our data indicated that DAXX/ATRX and KRAS gene mutations were correlated with a poor prognosis of pNET patients, and the patients bearing a larger number of gene mutations had a worse prognosis. The limitation of this study may be associated with the small sample size and the sequence methods; thus, future studies enrolling a larger number of pNET patients should be performed, and whole exome sequencing should be conducted to further explore the role of newly identified gene mutations in pNET development and progression.

Supplementary Material

Supplementary Table 1

Acknowledgments

The study was supported by National Science Foundation of China (81372645) and Shanghai Natural Science Foundation from Municipal Government (13ZR1425900) and Shanghai Jiao Tong University School of Medicine Science and Technology Foundation (13XJ10035) and FONG SHU FOOK TONG Foundation.

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Supplementary Materials

Supplementary Table 1

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