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(American Journal of Pathology. 2000;156:433-437.)
© 2000 American Society for Investigative Pathology

Short Communications

APC Mutations in Sporadic Medulloblastomas

Huatao Huang^*, Betania M. Mahler-Araujo^*, Anna Sankila^*, Leila Chimelli, Yasuhiro Yonekawa, Paul Kleihues^* and Hiroko Ohgaki^*

From the International Agency for Research on Cancer,^*
Lyon, France; the Department of Pathology,
University Hospital, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil; and the Department of Neurosurgery,
University Hospital Zurich, Zurich, Switzerland

	Abstract

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The cerebellar medulloblastoma (WHO Grade IV) is a highly malignant, invasive embryonal tumor with preferential manifestation in children. Several molecular alterations appear to be involved, including isochromosome 17q and the p53, PTCH, and ß-catenin gene mutations. In this study, 46 sporadic medulloblastomas were screened for the presence of mutations in genes of the Wnt signaling pathway (APC and ß-catenin). Single-strand conformational polymorphism (SSCP) analysis followed by direct DNA sequencing revealed 3 miscoding APC mutations in 2 (4.3%) medulloblastomas. One case contained a GCAGTA mutation at codon 1296 (AlaVal), and another case had double point mutations at codons 1472 (GTAATA, ValIle) and 1495 (AGTGGT, SerGly). Miscoding ß-catenin mutations were detected in 4 tumors (8.7%). Three of these were located at codon 33 (TCT TTT, SerPhe) and another at codon 37 (TCTGCT, SerAla). Adenomatous polyposis coli (APC) gene and ß-catenin mutations were mutually exclusive and occurred in a total of 6 of 46 cases (13%). Although germline APC mutations are a well established cause of familial colon and brain tumors (Turcot syndrome), this study provides the first evidence that APC mutations are also operative in a subset of sporadic medulloblastomas.

	Introduction

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The medulloblastoma (WHO Grade IV) is a malignant, invasive embryonal tumor of the cerebellum with a preferential manifestation in children.¹⁰ Although the majority of medulloblastomas occur sporadically, some manifest within familial cancer syndromes including the naevoid basal cell carcinoma (Gorlin) syndrome¹⁰ and Turcot syndrome, which is defined as manifestation of colorectal cancer and malignant brain tumor in the same patient. Turcot syndrome is heterogeneous, encompassing at least two subtypes.¹¹ One of these is characterized by the occurrence of glioblastoma in patients with hereditary non-polyposis colon cancer (HNPCC) and is caused by germline mutations in one of the DNA mismatch repair genes, such as hPSM2 or hMLH1.¹⁰ A second Turcot subtype is characterized by medulloblastoma in the setting of FAP and APC germline mutations. This raises the question of whether sporadic medulloblastomas also contain APC mutations. Previous attempts to identify APC mutations by an RNase protection assay failed.¹² Furthermore, loss of heterozygosity (LOH) on chromosome 5q, on which the APC gene is located, was not detected in 23 sporadic medulloblastomas.¹³ However, a recent study showed that ß-catenin mutations are present in 4% of cases,¹⁴ suggesting the involvement of the Wnt signaling pathway in the development of sporadic medulloblastomas. In this study, we screened 46 sporadic medulloblastomas for APC and ß-catenin mutations using SSCP followed by direct DNA sequencing, and show that APC mutations occur in a small fraction of sporadic medulloblastomas that lack a ß-catenin mutation.

	Materials and Methods

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Tumor Samples

Thirty-four medulloblastomas were obtained from the Department of Pathology, University Hospital Zurich (Zurich, Switzerland) and twelve from the Department of Pathology, School of Medicine of Ribeirao Preto, University of Sao Paulo (Sao Paulo, Brazil). The mean age of patients was 15.6 ± 13.5 years (range, 0.5–60 years). Twenty-seven patients were males and 19 were females. Tumors were fixed in buffered formalin and embedded in paraffin. DNA was extracted from paraffin sections as described previously.¹⁵

SSCP Analysis and Direct DNA Sequencing for ß-Catenin Mutations

Pre-screening for mutations in exon 3 of human ß-catenin gene, which contains the four potential GSK-3ß phosphorylation sites,¹⁶ was carried out by polymerase chain reaction (PCR)-SSCP analysis. Briefly, PCR was performed in a total volume of 10 µl, consisting of 2 µl of DNA solution, 0.5 U of Taq DNA polymerase (Sigma, St. Louis, MO), 0.5 µCi of [-³³P]-dCTP (ICN Biomedicals, Inc., Costa Mesa, CA; specific activity, 3000 Ci/mmol), 1.5 mmol/L MgCl₂, 0.2 mmol/L of each dNTP, 0.4 µmol/L of both sense and antisense primers, 10 mmol/L Tris-HCl, pH 8.3, and 50 mmol/L KCl in the RoboCycler Gradient 96 (Stratagene, La Jolla, CA), with an initial denaturing step at 95°C for 5 minutes, followed by 35 cycles of denaturation at 95°C for 1 minute, annealing at 53°C for 1 minute, and polymerization at 72°C for 1 minute, and a final extension of 5 minutes at 72°C. After amplification, 5 µl of PCR products were mixed with 12.5 µl loading buffer (95% formamide, 20 mmol/L EDTA, 0.05% xylene cyanol, and bromophenol blue), denatured at 95°C for 10 minutes, and quenched on ice. Four microliters of the above mixture were run on a 6% polyacrylamide nondenaturing gel containing 8% glycerol at 4 W for 14 hours at room temperature and/or on a 6% polyacrylamide nondenaturing gel containing 6% glycerol at 40 W for 3.5 hours with cooling by fan. Gels were dried at 80°C and autoradiographed for 12 to 48 hours. Primer sequences used were 5'-ATGGAACCAGACAGAAAAG-3' (nt 254–272) and 5'-TACAGGACTTGGGAGGTATC-3' (nt 386–405).

Samples that showed mobility shifts in the SSCP analysis were further analyzed by direct DNA sequencing. PCR was carried out as described above in the absence of [-³³P]-dCTP. Five microliters of PCR products were digested with 1 U of shrimp alkaline phosphatase and 5 U of exonuclease I at 37°C for 15 minutes. After inactivation of these enzymes at 80°C for 15 minutes, primers (the same primers for PCR, 15 pmol) and 2 µl of 5x sequenase buffer (200 mmol/L Tris-HCl, pH 7.5, 100 mmol/L MgCl₂, 250 mmol/L NaCl) were added. Template-primer mixture was heated at 100°C for 5 minutes and then placed in ice-cold water. 0.1 mol/L dithiothreitol, 3 U Sequenase version 2.0 (USB, Cleveland, OH), and 0.5 µCi [-³³P]-dATP or [-³³P]-dCTP were added to samples, which were then divided into four wells, each containing termination mixture. Samples were incubated at 42°C for 6 minutes and mixed with 5 µl of stop solution (USB). After heating at 80°C for 3 minutes, samples were loaded onto a 6% polyacrylamide/7 mol/L urea gel and run at 70 W for 1.5 to 3 hours. Gels were dried at 80°C and autoradiographed for 12 to 48 hours. Samples were considered mutated only if the mutations were confirmed on two independent PCRs.

SSCP Analysis and Direct DNA Sequencing for APCMutations

Codons 1255–1513 in exon 15 of the APC gene, which corresponds to the mutation cluster region and covers about two-thirds of all APC somatic mutations in colon tumors in FAP and non-FAP patients,^6,17 were screened for mutations by SSCP-direct DNA sequencing. The following primers were used for PCR amplification: 5'-AACCAAGAAACAATACAGA-3' (sense) and (5'-CACTTTTGGAGGGAGATTT-3' (antisense) to amplify codons 1255–1363 (fragment A), 5'-AGAATCAGCCAGGCACAAAG-3' (sense) and 5'-GCTTGGTGGCATGGTTTGT-3' (antisense) to amplify codons 1342–1433 (fragment B), and 5'-GCAGTGGAATGGTAAGTGG-3' (sense) and 5'-TCATCGAGGCTCAGAGCA-3' (antisense) to amplify codons 1410–1513 (fragment C). PCR was carried out in a total volume of 10 µl, consisting of 1 µl of DNA solution, 0.5 U of Taq DNA polymerase (Sigma), 0.5 µCi of [-³³P]-dCTP (ICN Biomedicals; specific activity, 3000 Ci/mmol), 2.0 mmol/L (for fragment A) or 1.5 mmol/L (for fragments B and C) MgCl₂, 0.2 mmol/L of each dNTP, 0.4 µmol/L of both sense and antisense primers, 10 mmol/L Tris-HCl, pH 8.3, and 50 mmol/L KCl in the RoboCycler Gradient 96 (Stratagene), with an initial denaturation step at 95°C for 5 minutes, followed by 40 cycles of denaturation at 95°C for 60 sec, annealing at 47°C (for fragment A), 57°C (for fragment B) or 55°C (for fragment C) for 70 seconds, and polymerization at 72°C for 70 seconds, followed by a final extension of 5 minutes at 72°C. Five microliters of PCR products were mixed with 12.5 µl loading buffer (95% formamide, 20 mmol/L EDTA, 0.05% xylene cyanol, and bromophenol blue), denatured at 95°C for 10 minutes, and quenched on ice. Four microliters of this mixture were run on a 6% polyacrylamide nondenaturing gel containing 6% glycerol at 40 W for 5 hours with cooling by fan. Gels were dried at 80°C and autoradiographed for 12 to 48 hours.

Samples that showed mobility shifts in two independent SSCP analyses were further analyzed by direct DNA sequencing. For this, PCR amplifications were repeated as described above in the absence of [-³³P]-dCTP. DNA sequencing was carried out using the same protocol as described above for sequencing of ß-catenin mutations. The following internal primers were used: 5'-AATCAGACGACACAGGAAG-3' (nt 3886–3904) and 5'-GGAACTTCGCTCACAGGAT-3' (nt 3971–3989) for fragment A, and 5'-AAAACACCTCCACCACCTC-3' (nt 4327–4345) and 5'-CTGGAAGAACCTGGACCCT-3' (nt 4450–4468) for fragment C.

A polymorphism at codon 1493 (exon 15) of the APC gene (ACG/ACA, Thr/Thr) was detected in this study. To assess whether particular alleles are overrepresented in medulloblastomas, we also analyzed blood DNAs obtained from 50 healthy individuals in the United States for this polymorphism.

Statistical Analysis

Fisher’s exact test was carried out to analyze the significance of allelic frequency difference in APC codon 1493 polymorphism between medulloblastoma patients and healthy individuals and to compare the frequencies of ß-catenin and APC mutations in tumors developed in adults (older than 16 years) and in children.

	Results

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SSCP followed by direct DNA sequencing revealed 3 miscoding APC mutations in 2 medulloblastomas. One case (case 236) contained a GCAGTA mutation at codon 1296 (AlaVal) and another case (case 331) had double point mutations at codons 1472 (GTAATA, ValIle) and 1495 (AGTGGT, SerGly). Another biopsy (case 325) contained a silent mutation at codon 1443 (CCTCCA, ProPro). In all cases, the respective wild-type bases were also detectable. For case 236, adjacent nontumorous brain tissue was also analyzed and was shown to be wild-type, indicating that the APC mutation in this tumor was somatic (Table 1 and Figure 1 ). Patient 331 had no familial history of cancer at any site over three generations.

View larger version (51K): [in this window] [in a new window]   Figure 1. Representative DNA sequencing autoradiographs of ß-catenin and APC mutations in sporadic medulloblastomas. Note that wild-type bases are detectable in all cases. The case numbers on the top correspond to those in Table 1 .

A polymorphism at codon 1493 of the APC gene (ACG/ACA, Thr/Thr) was detected in this study. The frequency of A/A (14/44, 32%), G/G (6/44, 14%), and G/A (24/44, 54%) in medulloblastomas was similar to that in DNA from healthy Caucasian individuals: 20/50 (40%) for A/A, 3/50 (6%) for G/G, and 27/50 (54%) for G/A (P = 0.2904).

	Discussion

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The molecular basis of the development of medulloblastomas is still poorly understood. Isochromosome 17q, the most frequent genetic alteration, occurs in up to 50% of cases^18,19 and appears to be the cause of LOH at 17p, which is found in 30 to 45% of medulloblastomas.²⁰ The smallest deletions were observed at 17p13, which includes the p53 locus, but the frequency of p53 mutations in medulloblastomas is below 10%,^15,21 suggesting the presence of another tumor suppressor gene in this chromosomal region. The mapping to 17p13.3 of the hypermethylated in cancer (HIC-1) gene, which encodes a zinc-finger transcription factor, has raised the possibility that this gene may be involved in the development of medulloblastomas.²² Translocation, deletions, and duplications of chromosome 1 were also frequently observed in medulloblastomas.^18,19 Rearrangements of chromosome 1 often result in trisomy 1q without loss of 1p. Mutations of the Patched gene (PTCH) are present in approximately 10% of medulloblastomas, with a preferential tendency for the desmoplastic variant.^23-25

The present study provides the first evidence that APC mutations occur in sporadic medulloblastomas, albeit infrequently (4.3%). As observed in colon cancer,⁷ ß-catenin and APC mutations were mutually exclusive, suggesting that one of these alterations is sufficient to activate the Wnt signaling pathway. The failure in a previous study to detect APC mutations¹² may be due to the sensitivity of RNase protection assay used, which efficiently detects small deletions or insertions that lead to truncated protein but does not detect all point mutations.^6,17

The APC mutations detected in sporadic medulloblastomas in this study were all missense mutations, whereas those in medulloblastoma patients with Turcot syndrome were trunctations.^12,26 Similarly, the majority of APC germline and somatic mutations in colon carcinomas are nonsense or frameshift mutations, leading to truncation of the APC protein.^6,7,27 However, 90% of mutations found in hepatoblastomas were missense mutations and only one was a frameshift mutation.²⁸ In gastric carcinomas, 30 to 50% of APC mutations found were missense mutations.^29-31 One APC mutation found in 39 pancreatic carcinomas³² and both APC mutations found in 31 breast carcinomas³³ were missense mutations. It is of interest to note that all of the APC missense mutations detected in medulloblastomas in the present study (codons 1296, 1472, and 1495), as well as those in breast carcinomas (codons 1081 and 1096),³³ gastric carcinomas (codons 1120–1495),^29-31 hepatoblastomas (codons 1306–1534),²⁸ and pancreatic carcinomas (codon 1321),³² were located in regions with three 15-amino acid consensus sequences (ß-catenin binding sites) or seven 20-amino acid repeats (ß-catenin and axin binding sites).^34,35 This suggests that APC missense mutations may affect the APC protein structure and impair its binding to ß-catenin and/or axin.

In all cases with APC mutations, the respective wild-type bases were present (Figure 1) . This is consistent with the previous studies showing that LOH involving the APC locus on chromosome 5q is a rare event in both familial (Turcot syndrome) and sporadic medulloblastmas.^12,13,26,36 Only 1 out of 7 medulloblastomas with a germline APC mutation in Turcot patients had lost the wild-type allele.^12,26 Similarly, none of 55 sporadic medulloblastomas showed LOH at the APC gene locus.^13,36 Truncated mutant APC proteins retaining the first 171 amino acids may oligomerize in vivo with wild-type proteins and inactivate them in a dominant negative manner.³⁷ It remains to be shown whether mutant APC proteins, due to missense mutations, act in a similar fashion to impair normal APC function.

In the present study, ß-catenin mutations in exon 3 occurred in 4 of 46 (9%) sporadic medulloblastomas. Three of these were located at codon 33 and another was at codon 37. It is noteworthy that of the three mutations detected by Zurawel et al¹⁴ in 67 sporadic medulloblastomas, two were also located at codon 33 and one at codon 37. This suggests that codons 33 and 37 are hot spots for ß-catenin mutations in medulloblastomas. A similar clustering of mutations in codon 37 was observed in human bladder carcinomas.³⁸ In contrast, ß-catenin mutations were randomly distributed at several serine/threonine residues in hepatocellular,¹⁶ colorectal,⁷ prostate,³⁹ and uterine carcinomas.⁴⁰

The majority of medulloblastomas (70%) occur in children.¹⁰ The histopathology of medulloblastoma in adults and in children is similar, but a tendency for longer survival of adult patients has been observed.⁴¹ It is notable that in this study, 5 of 26 (19%) medulloblastomas in children (<16 years) carried a ß-catenin or APC mutation but only 1 of 20 (5%) medulloblastomas in adults had a ß-catenin mutation. This difference was not significant (P = 0.2122) and it remains to be shown in larger studies whether pediatric medulloblastomas carry genetic alterations different from those manifested in adults.

More than 20 polymorphisms have been identified in the APC gene. Among these, the I1307K polymorphism has been studied in detail and has been related to predisposition to colorectal cancer in Ashkenazi Jewish populations.⁴² Little is known about the significance of other polymorphisms. In this study, we did not observe any I1307K polymorphism, but detected an APC polymorphism at codon 1493 (ACA/ACG), as previously reported.¹⁷ DNA from medulloblastomas showed allelic patterns similar to those from healthy individuals, indicating that this polymorphism confers no risk for medulloblastoma.

In summary, the present study provides the first evidence that APC mutations are present in a subset of sporadic medulloblastomas. APC and ß-catenin mutations were mutually exclusive and occurred in 6 of 46 (13%) cases, suggesting the involvement of the Wnt pathway in a subset of sporadic medulloblastomas. Codons 33 and 37 of the ß-catenin gene constitute mutational hot spots in medulloblastomas.

	Footnotes

 
Address reprint requests to Dr. Hiroko Ohgaki, Unit of Molecular Pathology, International Agency for Research on Cancer, 150 cours Albert Thomas, 69372 Lyon Cedex 08, France. E-mail: ohgaki{at}iarc.fr

Supported by a grant from the Foundation for Promotion of Cancer Research, Japan. A. Sankila is a recipient of a grant from the Academy of Finland. M. B. Mahler-Araujo was supported by a grant from the Conselho National de Desenvolvimento Científico e Tecnológico, Brazil.

Accepted for publication October 19, 1999.

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