Somatic VHLgene alterations in MEN2-associated medullary thyroid carcinoma
© Koch et al; licensee BioMed Central Ltd. 2006
Received: 13 March 2006
Accepted: 17 May 2006
Published: 17 May 2006
Germline mutations in RET are responsible for multiple endocrine neoplasia type 2 (MEN2), an autosomal dominantly inherited cancer syndrome that is characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and parathyroid hyperplasia/adenoma. Recent studies suggest a "second hit" mechanism resulting in amplification of mutant RET. Somatic VHL gene alterations are implicated in the pathogenesis of MEN2 pheochromocytomas. We hypothesized that somatic VHL gene alterations are also important in the pathogenesis of MEN2-associated MTC.
We analyzed 6 MTCs and 1 C-cell hyperplasia (CCH) specimen from 7 patients with MEN2A and RET germline mutations in codons 609, 618, 620, or 634, using microdissection, microsatellite analysis, phosphorimage densitometry, and VHL mutation analysis.
First, we searched for allelic imbalance between mutant and wild-type RET by using the polymorphic markers D10S677, D10S1239, and RET on thyroid tissue from these patients. Evidence for RET amplification by this technique could be demonstrated in 3 of 6 MTCs. We then performed LOH analysis using D3S1038 and D3S1110 which map to the VHL gene locus at 3p25/26. VHL gene deletion was present in 3 MTCs. These 3 MTCs also had an allelic imbalance between mutant and wild-type RET. Mutation analysis of the VHL gene showed a somatic frameshift mutation in 1 MTC that also demonstrated LOH at 3p25/26. In the 2 other MTCs with allelic imbalance of RET and somatic VHL gene deletion, no somatic VHL mutation could be detected. The CCH specimen did neither reveal RET imbalance nor somatic VHL gene alterations.
These data suggest that a RET germline mutation is necessary for development of CCH, that allelic imbalance between mutant and wild-type RET may set off tumorigenesis, and that somatic VHL gene alterations may not play a major role in tumorigenesis of MEN2A-associated MTC.
Medullary thyroid carcinoma (MTC) develops from the parafollicular C cells in the thyroid gland and occurs sporadically as well as in the hereditary syndrome multiple endocrine neoplasia type 2 (MEN2). The gene responsible for MEN2 is the RET protooncogene, located at chromosome 10q11.2 [1, 2]. Patients with germline mutations in RET invariably develop MTC, although there are some patients with RET germline mutations who have lived beyond age 70 without MTC [3, 4]. Therefore, patients with germline mutations in RET usually are divided into different risk groups (low, intermediate, and high risk for developing MTC). So-called low-risk or level I mutations include those at codons 609, 768, 790, 791, 804, and 891 [1, 5–8]. Hyperplasia of the parafollicular C cells has been regarded as the precursor lesion for MTC [9, 10]. Accumulating evidence suggests that a 'second hit' or additional genetic events may be required to set off tumorigenesis in susceptible cells of patients with RET germline mutations. An allelic imbalance between mutant and wild-type RET may represent the decisive step of tumorigenesis for MTC and pheochromocytoma [11–15]. Somatic VHL gene alterations are implicated in the pathogenesis of MEN2-associated pheochromocytomas, possibly through accumulation of RET protein . Therefore, we hypothesized that somatic VHL gene alterations may also play a role in the pathogenesis of MEN2-associated MTC.
Patients and tissues
Somatic VHL gene deletion and mutation in MEN 2A-associated medullary thyroid carcinomas/CCH with germline mutations of RET
LOH at the VHLlocus
Allelic imbalance of RET
Codon 620 TGC/CGC
del C nt 389 Exon 1
Codon 618 TGC/AGC
Codon 609 TGC/CGC
Codon 609 TGC/CGC
Codon 609 TGC/CGC
Codon 609 TGC/CGC
Codon 634 TGC/CGC
Plasma calcitonin (pg/ml, normal: < 100)
Age at thyroidectomy
Codon 620 TGC/CGC
Codon 618 TGC/AGC
Codon 609 TGC/CGC
Codon 609 TGC/CGC
No, but HTN
Codon 609 TGC/CGC
No, but HTN
Codon 609 TGC/CGC
Codon 634 TGC/CGC
Frozen or paraffin-embedded tissue was microdissected and analyzed for loss of heterozygosity (LOH) by polymorphic markers mapping to the VHL gene locus, as previously described .
Tissue was obtained from these 7 patients under an Internal Review Board (IRB)-approved protocol at the National Institutes of Health. All of them had MEN 2A with a germline mutation in RET. Blood was drawn for DNA extraction. Thyroid specimens including MTC were removed at the time of surgery and frozen at -80°C. DNA was extracted from lymphoblasts and tumor tissue by standard methods.
Six-micron sections were obtained from frozen tumor and briefly stained with hematoxylin and eosin (H & E). If no frozen tumor was available, paraffin-embedded tissue was prepared for microdissection. Under direct light microscopic visualization using a 30-gauge needle, a modified microdissection procedure was performed, as previously described . In all cases, we obtained also samples of nontumor control tissue from the same slides.
Allelic imbalance of the RET gene locus and loss of heterozygosity of the VHL gene locus
We performed imbalance analyses of RET, using polymorphic markers/primers D10S677, D10S1239, and RET for the RET locus, and loss of heterozygosity studies using markers D3S1038 and D3S1110 which map to the VHL gene locus 3p25/26 in the presence of [alpha-32P] dCTP (0.1 μCi/μl) (Dupont). PCR conditions using AmpliTaq Gold DNA polymerase (Perkin Elmer Roche) in a Hybaid Omnigene thermal cycler were as follows: initial denaturation at 95°C for 10 min, then 35 cycles, each with 1 min of denaturation at 95°C, 1 min of annealing at 55°C for RET markers, at 60°C for VHL markers, and 1 min of extension at 72°C; PCR was completed with a final extension at 72°C for 10 min. The amplicons were resolved on a 6% polyacrylamide gel. Gels were dried and exposed to Kodak XAR film. All PCR reactions were performed in triplicate.
VHL gene mutation analysis
Exons 1–3 of the VHL gene were amplified from genomic DNA using polymerase chain reaction conditions described elsewhere . Mutation scanning by conformation sensitive gel electrophoresis (CSGE) was performed on the PCR products as described by Ganguly et al. . DNA sequence analysis was performed using a cycle sequencing kit with dye-labeled terminators (PE Advanced Biosystems, Inc., Foster City, CA). Sequences were analyzed on an ABI 377 automated DNA sequencer.
In this study, we show that somatic VHL mutation and deletion are involved in tumor progression rather than tumor initiation of MEN 2A-related MTC. In both sporadic and familial forms of MTC, allelic losses at 1p, 3, 4, 9q, 10q, 13q, and 22q have been reported [20–24]. Specific tumor suppressor genes or oncogenes at these chromosomal loci, however, have rarely been analyzed.
In sporadic pheochromocytomas, somatic mutations of VHL or RET are found in less than 10% of tumors, suggesting a possible role in tumorigenesis, whereas the prevalence and role of such mutations in hereditary pheochromocytomas such as those occurring in MEN 2 is not known. In a recent study, we detected inactivating somatic mutations of VHL and LOH at 3p25/26 in several MEN 2A-related pheochromocytomas . In all of these MEN 2A-associated pheochromocytomas as well as in the present study of thyroid C cell specimens, regular wild-type VHL alleles were detected in normal control tissue confirming the presence of two wild-type alleles and excluding the presence of VHL disease.
VHL disease consists of a variety of tumors including pheochromocytoma [25, 26]. However, MTC is not part of VHL syndrome, although MTC was found (likely coincidentally) in 2 patients with VHL germline mutation . Mutations in the VHL gene lead to constitutive expression of many hypoxia-inducible genes, in part related to increasing levels of hypoxia-inducible transcription factor (HIF) 1-alpha which in normal cells is rapidly ubiquitinated and degraded . VHL protein, a ubiquitinase adapter, plays a role in cell-cycle control, differentiation, extracellular matrix formation and turnover, and angiogenesis. Therefore, mutations in VHL may lead to an absent or reduced VHL protein function with reduced degradation of proteins including RET protein. In addition to other events, RET protein accumulation secondary to absent or reduced VHL protein, may then cause further transformation of selected parafollicular C-cells.
Although a 'second hit' which usually consists of deletion in the wild-type VHL allele, is necessary for initiation of tumor growth in patients with VHL germline mutations, it may not be sufficient [26, 29, 30]. Similarly, in patients with MEN2, a RET germline mutation is necessary for formation of MTC and pheochromocytoma, but may not be sufficient, as there are patients who have never developed MTC or pheochromocytoma during their life or developed MTC late in their lifetime [3, 4, 31–33]. Here, we detected somatic VHL gene alterations in 3 of 6 MTCs from MEN2A patients and no somatic VHL gene alteration in 1 patient with MEN2A and CCH. In addition, all 3 MTCs with LOH at the VHL gene also had allelic imbalance of RET. However, in only one of these MTCs, a somatic VHL mutation was found in addition to LOH at the VHL gene. In our single case of CCH, no imbalance between mutant and wild-type RET has been detected and no somatic VHL gene alteration. Therefore, additional somatic mutational events including the VHL gene may be required to set off tumorigenesis in patients with RET germline mutations. CCH foci have heterogeneous DNA deletions including LOH of TP53, RB1, and WT1 . Polymorphisms G691S/S904S of RET have recently been found to affect the development of MTC and the age at onset of MEN2A in patients with a RET germline mutation [35–37]. Elisei et al.  found a statistically significant higher allelic frequency of G691S polymorphism in MTCs than that found in normal controls. Cebrian et al.  carried out an association study in 135 sporadic MTC patients and 533 controls and discovered a strong association between the disease and specific haplotypes of RET. Somatic RET mutations such as M918T in MTC or pheochromocytoma of patients with a RET germline mutation appear to represent a phenomenon of tumor progression [38–43]. Chromosomal imbalances in MTC include deletions of chromosomes 1p, 3q26.3-q27, 4, 9q13-q22, 13 q, and 22q . Marsh et al.  found loss of whole or partial chromosome 3 including the region of the VHL locus as the predominant imbalance (40% of cases). Biallelic inactivation of VHL should lead to loss of VHL protein. Using immunohistochemistry, VHL protein is detectable in thyroid follicles and differentiated tumors derived from follicular epithelium, but is weakly or not detectable in nonneoplastic and neoplastic C cells . Since, in our study, neither allelic imbalance of RET nor somatic VHL gene alterations occurred in the CCH specimen (presumably the precursor lesion of MTC), we suggest that such somatic VHL gene alterations rather play a role in tumor progression than in tumor formation of MEN2-related MTC. This interpretation is based on a single case of CCH and would require confirmation in studies of larger size.
Tumor formation in these selected MEN 2A-related MTCs may have occurred by first, a RET germline mutation, leading to hyperplasia of C cells and second, an amplification event of mutant RET which, however, could not be consistently detected by the methods used by us (polymorphic marker analysis). Subsequent somatic VHL gene deletion and mutation in selected C cells may lead to further transformation and tumor progression. However, given the small sample size, it is possible that tumor formation and progression in a significant number of tumors may occur by other mechanisms.
medullary thyroid carcinoma
c cell hyperplasia
multiple endocrine neoplasia type 2
loss of heterozygosity
von Hippel Lindau
We thank Jeffrey Moley, MD, from the Washington University in St. Louis, for providing MTC samples (here: cases 1 and 2), and Catherine Stolle, PhD, from the University of Pennsylvania School of Medicine, for analyzing samples for VHL mutations. We also thank Celso Gomez-Sanchez, MD, from the University of Mississippi, for technical support.
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