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(American Journal of Pathology. 1999;155:1879-1884.)
© 1999 American Society for Investigative Pathology

Regular Articles

Malignant Transformation of Neurofibromas in Neurofibromatosis 1 Is Associated with CDKN2A/p16 Inactivation

Gunnlaugur P. Nielsen*, Anat O. Stemmer-Rachamimov*, Yasushi Ino*, Michael B. Møller{dagger}, Andrew E. Rosenberg* and David N. Louis*

From the Molecular Neuro-Oncology Laboratory and the James Homer Wright Pathology Laboratories,*
Department of Pathology and Neurosurgical Service, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts; and the Department of Pathology,{dagger}
University of Southern Denmark, Odense University, Odense, Denmark


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Patients with neurofibromatosis 1 (NF1) are predisposed to develop multiple neurofibromas (NFs) and are at risk for transformation of NFs to malignant peripheral nerve sheath tumors (MPNSTs). Little is known, however, about the biological events involved in the malignant transformation of NFs. We examined the CDKN2A/p16 gene and p16 protein in NFs and MPNSTs from patients with NF1. On immunohistochemical analysis, all NFs expressed p16 protein. The MPNSTs, however, were essentially immunonegative for p16, with striking transitions in cases that contained both benign and malignant elements. None of the benign tumors had CDKN2A/p16 deletions, whereas three of six MPNSTs appeared to have homozygous CDKN2A/p16 deletions. Methylation analysis and mutation analysis of CDKN2A/p16 in MPNSTs did not reveal any abnormalities. These results show that malignant transformation of NF is associated with loss of p16 expression, which is often secondary to homozygous deletion of the CDKN2A/p16 gene. The findings suggest that CDKN2A/p16 inactivation occurs during the malignant transformation of NFs in NF1 patients and raises the possibility that p16 immunohistochemistry may provide ancillary information in the distinction of NF from MPNST.


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Neurofibromatosis 1 (NF1; von Recklinghausen neurofibromatosis) is one of the most common autosomal dominant disorders, affecting approximately one in 3000 individuals.1,2 Diagnostic criteria for NF1 include two or more neurofibromas (NFs) of any type or one plexiform NF, café-au-lait macules, axillary or inguinal freckles, optic glioma, Lisch nodules, distinctive osseous lesions, and/or a first-degree relative with NF1.3 Patients with NF1 have an increased risk of developing malignant tumors, in particular a tendency for some NFs to undergo malignant transformation to a malignant peripheral nerve sheath tumor (MPNST).2,4 At the present time, however, there are no clinical or pathological means of identifying or predicting which NFs will progress to MPNST.

Patients with NF1 have a defect in the NF1 gene, which is located on the long arm of chromosome 17 (17q11.2).5 Given the predilection of NF1 patients to develop NFs, it is likely that inactivation of the NF1 gene predisposes patients to the formation of benign NFs. Indeed, biallelic inactivation of the NF1 gene has been documented in some NFs from NF1 patients.6 The subsequent genetic changes that underlie the transformation of NFs into MPNSTs in patients with NF1 are poorly understood. Cytogenetic analysis of MPNSTs in patients with NF1 have revealed complex but not always consistent karyotypic changes. Such changes sometimes involve chromosomes 17 and 22, where the NF1, p53, and NF2 tumor suppressor genes are located.7-9 In particular, mutations of the p53 gene have been documented in the progression of NF to MPNST in patients with NF1.10-17

The p16 protein, encoded by the CDKN2A/p16 gene on the short arm of chromosome 9 (9p21), is a tumor suppressor that inhibits the function of cdk4- and cdk6-cyclin D complexes. These cdk-cyclin complexes in turn regulate the retinoblastoma protein (pRb), thus controlling the G1-S phase checkpoint of the cell cycle. CDKN2A/p16 inactivation thereby results in cellular proliferation.18-28 CDKN2A/p16 inactivation is known to occur in a wide variety of human tumors, including carcinomas, glioblastoma, leukemia, and some sarcomas.29-39 Immunohistochemical studies have shown frequent aberrant p16 expression in various types of sarcomas.39,40 In addition, p16-null mice are prone to develop malignancies, particularly fibrosarcoma and lymphomas.41 Thus p16 alterations characterize some human and experimental sarcomas. Given the need to identify molecular events associated with the sarcomatous transition of NFs to MPNSTs, we therefore evaluated the role of the CDKN2A/p16 gene and p16 protein in NFs and MPNSTs from patients with NF1.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Materials

Formalin-fixed, paraffin-embedded tumors were retrieved from the files of the Department of Pathology of the Massachusetts General Hospital. Eighteen tumors from 16 patients were examined; 13 of the patients carried a diagnosis of NF1. Of the 13 NF1 patients, seven had an MPNST arising in association with a NF; three had MPNST unassociated with identifiable NF; one had a NF and an MPNST resected at different times; and two patients had carried the diagnosis of "atypical" NFs. Three tumors (one schwannoma and two NFs) were from three patients who were not diagnosed with NF1. The study population consisted of 16 patients (seven males and nine females) that ranged in age from 9 to 57 (mean 29) years. DNA was extracted from formalin-fixed, paraffin-embedded tissue according to standard procedure.42 Before DNA extraction, all tumor tissues were examined histologically to determine benign and malignant areas and to ensure that they contained viable tumor.

Homozygous Deletions of CDKN2A

To assay for homozygous deletions of the CDKN2A/p16 gene, we used a comparative multiplex polymerase chain reation (PCR) technique that amplifies a 168-bp fragment of the 5' end of CDKN2A/p16 exon 2 and a 187-bp sequence of the APEX nuclease gene on chromosome 14q, a site not frequently altered in sarcomas.27,28,38 The products were separated by electrophoresis on 2% agarose gels and visualized under ultraviolet light by ethidium bromide staining. This assay has been titrated to detect homozygous CDKN2A/p16 deletions in tumors with less than 30% contaminating nonneoplastic cells and has been confirmed by Southern blotting of selected gliomas.27,28 Each PCR assay was repeated at least three times to confirm the ratios between the CDKN2A/p16 band and the control band.

p16 Immunohistochemistry

p16 immunohistochemistry was performed with the JC8 mouse monoclonal IgG2a antibody, generated in the Massachusetts General Hospital Cancer Center. JC8 antibody is directed against the first ankyrin repeat (amino acids 1–32) of the p16 protein and has been characterized and described elsewhere.31,39,43

Single-Strand Conformation Polymorphism Analysis

Single-strand conformation polymorphism (SSCP) analysis was performed on all three coding exons of the CDKN2A/p16 gene, as previously described.44,45

Methylation-Specific PCR of the CDKN2A/p16 Promoter

The methylation status of the CDKN2A/p16 promoter region was studied in two tumors that lacked CDKN2A/p16 deletion but also showed loss of p16 expression. Methylation was assessed by methylation-specific PCR according to a published protocol,46 with minor modification of the PCR cycle to include a touchdown of the annealing temperature from 67°C to 60°C, followed by 20 cycles at 60°C. The procedure entails bisulfite modification of DNA followed by amplification with primer pairs specific for methylated and unmethylated DNA. DNA samples from the colon carcinoma cell lines HT-29 and CaCo2 were used as positive controls for methylated DNA. The PCR products were run on a 2% agarose gel, stained with ethidium bromide, and visualized under ultraviolet light.


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
Immunohistochemical staining for p16 protein in the two NFs from non-NF1 patients showed nuclear and faint cytoplasmic staining of most of the neoplastic cells. The one schwannoma showed an unusual staining pattern, in which staining was prominent in Antoni B regions and less extensive in the cellular Antoni A regions. Neurofibromas from the NF1 patients had prominent p16 immunopositivity, with most (60–100%) tumor cells displaying strong nuclear and lighter cytoplasmic staining (Figure 1, A and B) . Two "atypical" NFs contained areas of increased cellularity and scattered cells with "degenerative" nuclear atypia and rare mitoses; these had been considered histologically benign. On immunohistochemical analysis, these two cases also showed nuclear and light cytoplasmic staining of most tumor cells, including the "atypical" cells (Figure 1, C and D) .



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  		Figure 1. A and B: Neurofibroma from a patient with NF1, showing bland-looking spindle cells separated by a myxoid and collagenous background (A). Immunohistochemical staining illustrates diffuse nuclear and faint cytoplasmic staining for p16 (DAB chromogen with hematoxylin counterstain) (B). C and D: "Atypical" neurofibroma showing increased cellularity and nuclear atypia (C). No mitotic figures are present. Immunohistochemical staining for p16 demonstrates nuclear and faint cytoplasmic staining of the neoplastic cells, including "atypical" cells (D). E and F: MPNST (E) showing marked increased cellularity, fasicular and herringbone growth pattern, nuclear atypia, and marked mitotic activity. Immunohistochemical staining shows no immunoreactivity for p16 (F). G and H: MPNST arising in association with a neurofibroma (G). An abrupt transition from the neurofibroma (right) to MPNST (left) is seen. Immunohistochemical staining of the same tumor (H) shows that the benign neurofibromatous component (right) stains for p16 protein, whereas the malignant component (left) is immunonegative for p16 protein.

 
With the exception of one case, all 11 MPNSTs were conspicuously negative for p16 on immunohistochemistry (Figure 1, E and F) . One tumor, which arose in association with a benign NF and did not demonstrate any unusual histological features, had scattered (<5%) p16-immunopositive malignant-appearing cells. For the cases in which benign and malignant elements were both present in a single section, the difference in staining was striking between the benign and malignant areas, with the p16-immunopositive NF highlighted against the p16-immunonegative MPNST (Figure 1, G and H) .

DNA was extracted from 15 cases (the three tumors from the non-NF1 patients and 12 tumors (six NFs and six MPNSTs) from patients with NF1). None of the benign tumors (including the "atypical" NFs) had CDKN2A/p16 deletions. Three of the six MPNSTs, however, had comparative multiplex PCR results that were consistent with homozygous CDKN2A/p16 deletions (Figure 2) . Although MPNSTs may have complex cytogenetic aberrations, chromosome 14q (the location of the APEX control gene) is not a common site of amplification47 ; this argues against the possibility that the comparative multiplex results reflect multiple copies of chromosome 14q rather than deletion of CDKN2A/p16. On the other hand, chromosome 14q can be lost in approximately 20% of MPNSTs,47 raising the possibility that the three p16 immunonegative MPNSTs without demonstrable CDKN2A/p16 homozygous deletions represent false negative results from coincident 14q and 9p loss. Methylation analysis of the CDKN2A/p16 promoter and mutation analysis of the CDKN2A/p16 coding region in two of the three MPNSTs without deletions did not reveal any alterations.



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  		Figure 2. Comparative multiplex analysis of the CDKN2A/p16 gene. Homozygous deletion (HD) is present in three tumors (lanes 3, 5, and 10), as evidenced by preferential amplification of the control amplicon (top band) with minimal amplification of the CDKN2A/p16 amplicon (bottom band). M, pUC18/HaeIII digest size marker. Lane 0: Negative control ("no DNA"). Lane 1: Normal control DNA. Lanes 2 and 3: DNA from the same tumor, showing the benign (NF) component (lane 2) and the malignant component (MPNST; lane 3), the latter showing HD for the CDKN2A/p16 gene. Lanes 4 and 5 show findings similar to those of lanes 2 and 3, with DNA from the different areas in another tumor (lane 4, NF; lane 5, MPNST). Lane 5 shows HD for the CDKN2A/p16 gene. Lane 6: Neurofibroma from a patient with NF1. Lanes 7–10: MPNSTs from four different NF1 patients. Lanes 7–9 do not show HD, whereas the MPNST in lane 10 shows HD for the CDKN2A/p16 gene.

 

   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
Tumorigenesis in NF1 patients is a multistep process. Although changes in the NF1 gene are likely initiating events, other genetic alterations must occur for benign tumors such as NFs to progress to malignancy. Because of the clinical importance of understanding the transition of NFs to MPNSTs, we have collected a series of NF-MPNST cases from NF1 patients to evaluate the genetic changes associated with this progression.

In the present study, NFs from NF1 patients, including NFs that had given rise to MPNSTs and "atypical NFs," all expressed p16 protein. Benign nerve sheath tumors from non-NF patients also expressed p16 protein. Thus p16 is expressed in benign nerve sheath tumors, consistent with a role for p16 in controlling cell proliferation in these lesions. Significantly, however, with the exception of one tumor that showed staining of only scattered tumor cells, MPNSTs did not express p16 protein. For tumors in which NF and MPNST coexisted, the difference in staining between benign and malignant areas was striking, with loss of p16 noted only in the malignant components. These results demonstrate that loss of p16 expression is associated with the malignant transition of NF to MPNST in NF1 patients.

In half of the evaluable cases, the genetic mechanism for loss of p16 expression appeared to be homozygous deletion of the CDKN2A/p16 gene. For the other cases, we did not detect CDKN2A/p16 homozygous deletions, promoter methylation, or coding region mutations. Nonetheless, deletions not involving exon 2, methylation outside of the assayed region of the promoter, or point mutations in noncoding regions could all potentially affect protein expression and would not be detected with our analyses. Given the absence of p16 expression in the MPNSTs studied, the finding of gene abnormalities in half of the studied MPNSTs, and the chance of false negative comparative multiplex PCR findings (see Results section), it is possible that all of the MPNSTs harbor CDKN2A/p16 gene alterations.

Only a few studies have examined the role of CDKN2A/p16 in MPNSTs. Cohen et al40 studied p16 and pRB expression immunohistochemically in 59 sarcomas, including six "neurofibrosarcomas," all of which showed normal p16 expression. Schneider-Stock et al48 found loss of heterozygosity (LOH) at the CDKN2A/p16 gene in only one of 14 "malignant schwannomas" (MPNSTs), but such LOH assays will often miss homozygous deletions. Importantly, neither of these studies indicated whether the MPNSTs were from NF1 patients. In a comparative genomic hybridization study47 of sporadic and NF1-associated MPNSTs, three of seven NF1-associated MPNSTs and one of three sporadic MPNSTs showed allelic loss of chromosome 9p, consistent with inactivation of CDKN2A/p16. Recently Kourea et al49 reported, in abstract form, deletion of the CDKN2A/p16 gene in 60% of MPNSTs, with no cases demonstrating CDKN2A/p16 methylation. These results are similar to the present findings, and it would be interesting to know if any of the patients studied by Kourea et al had NF1. These studies leave open the possibility that different mechanisms might be involved in the tumorigenesis of sporadic versus NF1-associated MPNSTs. The definition of sporadic MPNSTs also introduces a problem, because poorly differentiated spindle cell sarcomas may be diagnosed in different ways by different pathologists. The present study overcomes this potential problem by limiting the study to NF1-associated MPNSTs, by assuming that these tumors represent a homogeneous group of neoplasms that are derived from nerve sheath elements.

The association of CDKN2A/p16 inactivation with the transition from NF to MPNST parallels that of p53, because p53 alterations have been documented in MPNSTs but not in NFs. For p53, it has been suggested that immunohistochemical demonstration of p53, most likely indicating mutant protein, supports a diagnosis of MPNST.16,17 However, results for p53 staining have not been consistent in MPNSTs, and some p53 mutants do not lead to immunohistochemically detectable protein. Our findings raise the possibility that p16 immunostaining may provide ancillary information in the distinction of NF from MPNST. In this regard, it is interesting that the atypical NFs maintained p16 staining; if this proves true on larger series of cases, p16 immunopositivity would argue against a diagnosis of MPNST in difficult cases, perhaps allowing a patient to avoid overly aggressive therapies. On the other hand, at the present time such assays are unlikely to provide information for predicting which NFs are likely to progress to MPNSTs, although the absence of staining may strengthen the argument that such a transition has already occurred.


   Footnotes
 
Address reprint requests to Dr. Gunnlaugur P. Nielsen, Department of Pathology, Massachusetts General Hospital, Fruit Street, Boston, MA 02114. E-mail: gnielsen{at}partners.org

The first two authors contributed equally to this work.

Accepted for publication August 1, 1999.


   References
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 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Karnes PS: Neurofibromatosis: a common neurocutaneous disorder. Mayo Clin Proc 1998, 73:1071-1076[Medline]
  2. Zöller MET, Rembeck B, Odén A, Samuelsson M, Angervall L: Malignant and benign tumors in patients with neurofibromatosis type 1 in a defined Swedish population. Cancer 1997, 79:2125-2131[Medline]
  3. : National Institutes of Health Consensus Development Conference: Neurofibromatosis Conference Statement. Arch Neurol 1988, 45:575-578[Medline]
  4. Ducatman BS, Scheithauer BW, Piepgras DG, Reiman HM, Ilstrup DM: Malignant peripheral nerve sheath tumors. A clinicopathlogic study of 120 cases. Cancer 1986, 57:2006-2021[Medline]
  5. von Deimling A, Krone W, Menon AG: Neurofibromatosis type 1: pathology, clinical features and molecular genetics. Brain Pathol 1995, 5:153-162[Medline]
  6. Colman SD, Williams CA, Wallace MR: Benign neurofibroma in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene. Nature Genet 1995, 11:90-92[Medline]
  7. Jhanwar SC, Chen Q, Li FP, Brennan MF, Woodruff JM: Cytogenetic analysis of soft tissue sarcomas. Cancer Genet Cytogenet 1994, 78:138-144[Medline]
  8. Mertens F, Rydholm A, Bauer HFC, Limon J, Nedoszytko B, Szadowska A, Willén H, Heim S, Mitelman F, Mandahl N: Cytogenetic findings in malignant peripheral nerve sheath tumors. Int J Cancer 1995, 61:793-798[Medline]
  9. Fletcher JA, Kozakewich HP, Hoffer FA, Lage JM, Weidner N, Tepper R, Pinkus GS, Morton CC, Corson JM: Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors. N Engl J Med 1991, 324:436-443[Abstract]
  10. Menon AG, Anderson KM, Riccardi VM, Chung RY, Whaley JM, Yandell DW, Farmer GE, Freiman RN, Lee JK, Li FP, Barker DF, Ledbetter DH, Kleider A, Martuza RL, Gusella JF, Seizinger BR: Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis. Proc Natl Acad Sci USA 1990, 87:5435-5439[Abstract/Free Full Text]
  11. Halling KC, Scheithauer BW, Halling AC, Nascimento AG, Ziesmer SC, Roche PC, Wollan PC: p53 expression in neurofibroma and malignant peripheral nerve sheath tumor: an immunohistochemical study of sporadic and NF1-associated tumors. Am J Clin Pathol 1996, 106:282-288[Medline]
  12. Skuse GR, Kosciolek BA, Rowley RT: Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis. Loss of heterozygosity for chromosome 17. Genes Chromosom Cancer 1989, 1:36-41[Medline]
  13. Rey JA, Bello MJ, Kusak ME, de Campos JM, Pestaña A: Involvement of 22q12 in a neurofibrosarcoma in neurofibromatosis type 1. Cancer Genet Cytogenet 1993, 66:28-32[Medline]
  14. Donner LR: Cytogenetics of tumors of soft tissue and bone. Implication for pathology. Cancer Genet Cytogenet 1994, 78:115-126[Medline]
  15. Lothe RA, Sæter G, Danielsen HE, Stenwig AE, Høyheim B, O’Connell PO, Børresen AL: Gentetic alterations in a malignant schwannoma from a patient with neurofibromatosis (NF1). Pathol Res Pract 1993, 189:465-471[Medline]
  16. McCarron KF, Goldblum JR: Plexiform neurofibroma with and without associated malignant peripheral nerve sheath tumor. A clinicopathologic and immunohistochemical analysis of 54 cases. Mod Pathol 1998, 11:612-617[Medline]
  17. Kindblom LG, Ahldén M, Meis-Kinbblom JM, Stenman G: Immunohistochemical and molecular analysis of p53, MDM2, proliferating cell nuclear antigen and Ki67 in benign and malignant peripheral nerve sheath tumors. Virchows Arch 1995, 427:19-26[Medline]
  18. Serrano M, Hannon GJ, Beach D: A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature 1993, 366:704-707[Medline]
  19. Hall M, Peters G: Genetic alterations of cyclins, cyclin-dependent kinases, and Cdk inhibitors in human cancer. Adv Cancer Res 1996, 68:67-108[Medline]
  20. Medema RH, Herrera RE, Lam F, Weinberg RA: Growth suppression by p16ink4 requires functional retinoblastoma protein. Proc Natl Acad Sci USA 1995, 92:6289-6293[Abstract/Free Full Text]
  21. Mao L, Merlo A, Bedi G, Shapiro GI, Edwards CD, Rollins BJ, Sidransky D: A novel p16INK4A transcript. Cancer Res 1995, 55:2995-2997[Abstract/Free Full Text]
  22. Lukas J, Aagaard L, Strauss M, Bartek J: Oncogenic aberrations of p16INK4/CDKN2 and cyclin D1 cooperate to deregulate G1 control. Cancer Res 1995, 55:4818-4823[Abstract/Free Full Text]
  23. Tam SW, Shay JW, Pagano M: Differential expression and cell cycle regulation of cyclin-dependent kinase 4 inhibitor p16Ink4. Cancer Res 1994, 54:5816-5820[Abstract/Free Full Text]
  24. Wiman KG: The retinoblastoma gene: role in cell cycle control and cell differentiation. FASEB J 1993, 7:841-845[Abstract]
  25. Li Y, Nichols MA, Shay JW, Xiong Y: Transcriptional repression of the D-type cyclin-dependent kinase inhibitor p16 by the retinoblastoma susceptibility gene product pRb. Cancer Res 1994, 54:6078-6082[Abstract/Free Full Text]
  26. Cordon-Cardo C: Mutation of cell cycle regulators. Biological and clinical implications for human neoplasia. Am J Pathol 1995, 147:545-560[Abstract]
  27. Ono Y, Tamiya T, Ichikawa T, Kunishio K, Matsumoto K, Furuta T, Ohmoto T, Ueki K, Louis DN: Malignant astrocytomas with homozygous CDKN2/p16 gene deletions have higher Ki-67 proliferation indices. J Neuropathol Exp Neurol 1996, 55:1026-1031[Medline]
  28. Ueki K, Ono Y, Henson JW, Efird JT, von Deimling A, Louis DN: CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated. Cancer Res 1996, 56:150-153[Abstract/Free Full Text]
  29. Schutte M, Hruban RH, Geradts J, Maynard R, Hilgers W, Rabindran SK, Moskaluk CA, Hahn SA, Schwarte-Waldhoff I, Schmiegel W, Baylin SB, Kern SE, Herman JG: Abrogation of the Rb/p16 tumor-suppressive pathway in virtually all pancreatic carcinomas. Cancer Res 1997, 57:3125-3130
  30. Liew CT, Li HM, Lo KW, Leow CK, Chan JY, Lau WY, Lai PB, Lim BK, Huang J, Leung WT, Wu S, Lee JC: High frequency of p16INK4A gene alterations in hepatocellular carcinoma. Oncogene 1999, 18:789-795[Medline]
  31. Burns KL, Ueki K, Jhung SL, Koh J, Louis DN: Molecular genetic correlates of p16, cdk4 and pRb immunohistochemistry in glioblastomas. J Neuropathol Exp Neurol 1998, 57:122-130[Medline]
  32. Hussussian CJ, Struewing JP, Goldstein AM, Higgins PA, Ally DS, Sheahan MD, Clark WH, Tucker MA, Dracopoli NC: Germline p16 mutations in familial melanoma. Nature Genet 1994, 8:15-21[Medline]
  33. Mori T, Miura K, Aoki T, Nishihira T, Mori S, Nakamura Y: Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma. Cancer Res 1994, 54:3396-3397[Abstract/Free Full Text]
  34. Caldas C, Hahn SA, da Costa LT, Redston MS, Schutte M, Seymour AB, Weinstein CL, Hruban RH, Yeo CJ, Kern SE: Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nature Genet 1994, 8:27-32[Medline]
  35. Hebert J, Cayuela JM, Berkeley J, Sigaux F: Candidate tumor-suppressor genes MTS1 (p16INK4A) and MTS2 (p15INK4B) display frequent homozygous deletions in primary cells from T- but not from B-cell lineage acute lymphoblastic leukemias. Blood 1994, 84:4038-4044[Abstract/Free Full Text]
  36. Takeuchi S, Bartram CR, Seriu T, Miller CW, Tobler A, Janssen JW, Reiter A, Ludwig WD, Zimmermann M, Schwaller J, Lee E, Miyoshi I, Koeffler HP: Analysis of a family of cyclin-dependent kinase inhibitors: p15/MTS2/INK4B, p16/MTS1/INK4A, and p18 genes in acute lymphoblastic leukemia of childhood. Blood 1995, 86:755-760[Abstract/Free Full Text]
  37. Cayuela JM, Hebert J, Sigaux F: Homozygous MTS1 (p16INK4A) deletion in primary tumor cells of 163 leukemic patients. Blood 1995, 85:854[Free Full Text]
  38. Goldstein AM, Fraser MC, Struewing JP, Hussussian CJ, Ranade K, Zametkin KP, Fontaine LS, Organic SM, Dracopoli NC, Clark WH, Tucker MA: Increased risk of pancreatic cancer in melanoma-prone kindreds with p16/INK4 mutations. N Engl J Med 1995, 333:970-974[Abstract/Free Full Text]
  39. Nielsen GP, Burns KL, Rosenberg AE, Louis DN: CDKN2A gene deletion and loss of p16 expression occur in osteosarcomas that lack RB alterations. Am J Pathol 1998, 153:159-163[Abstract/Free Full Text]
  40. Cohen JA, Geradts J: Loss of RB and MTS1/CDKN2 (p16) expression in human sarcomas. Hum Pathol 1997, 28:893-898[Medline]
  41. Serrano M, Lee H, Chin L, Cordon-Cardo C, Beach D, DePinho RA: Role of the INK4A locus in tumor suppression and cell mortality. Cell 1996, 85:27-37[Medline]
  42. Louis DN, von Deimling A, Seizinger BR: A(CA)n dinucleotide repeat assay for detection of allelic chromosomal loss in small or archival brain tumor specimens. Am J Pathol 1992, 141:777-782[Abstract]
  43. Nielsen GP, Stemmer-Rachamimov AO, Shaw J, Roy JE, Koh J, Louis DN: Immunohistochemical survey of p16INK4A expression in normal human adult and infant tissue. Lab Invest 1999, 79:1137-1143[Medline]
  44. Ueki K, Rubio MP, Ramesh V, Correa KM, Rutter JL, von Deimling A, Buckler AJ, Gusella JF, Louis DN: MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p. Hum Mol Genet 1994, 3:1841-1845[Abstract/Free Full Text]
  45. Rubio MP, von Deimling A, Yandell DW, Wiestler OD, Gusella JF, Louis DN: Accumulation of wild-type p53 protein in human astrocytomas. Cancer Res 1993, 53:3465-3467[Abstract/Free Full Text]
  46. Herman JG, Graff JR, Myohanen S, Nelkin BD, Baylin SB: Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands. Proc Natl Acad Sci USA 1996, 93:9821-9826[Abstract/Free Full Text]
  47. Lothe RA, Karhu R, Mandahl N, Mertens F, Sæter G, Heim S, Börresen-Dale AL, Kallioniemi OP: Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen’s neurofibromatosis. Cancer Res 1996, 56:4778-4781[Abstract/Free Full Text]
  48. Schneider-Stock R, Radig K, Roessner A: Loss of heterozygosity on chromosome 9q21 (p16 gene) uncommon in soft-tissue sarcomas. Mol Carcinog 1997, 18:63-65[Medline]
  49. Kourea HP, Orlow I, Woodruff JM, Cordon-Cardo C: Alterations of the INK4A gene in malignant peripheral nerve sheath tumors (MPNSTs). Mod Pathol 1999, 12:12A



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Transcriptional Repression of the Neurofibromatosis-1 Tumor Suppressor by the t(8;21) Fusion Protein
Mol. Cell. Biol., July 15, 2005; 25(14): 5869 - 5879.
[Abstract] [Full Text] [PDF]

Home page
 Proc. Natl. Acad. Sci. USAHome page
S. Berghmans, R. D. Murphey, E. Wienholds, D. Neuberg, J. L. Kutok, C. D. M. Fletcher, J. P. Morris, T. X. Liu, S. Schulte-Merker, J. P. Kanki, et al.
tp53 mutant zebrafish develop malignant peripheral nerve sheath tumors
PNAS, January 11, 2005; 102(2): 407 - 412.
[Abstract] [Full Text] [PDF]

Home page
 J. Clin. Pathol.Home page
R S Bridge Jr, J A Bridge, J R Neff, S Naumann, P Althof, and L A Bruch
Recurrent chromosomal imbalances and structurally abnormal breakpoints within complex karyotypes of malignant peripheral nerve sheath tumour and malignant triton tumour: a cytogenetic and molecular cytogenetic study
J. Clin. Pathol., November 1, 2004; 57(11): 1172 - 1178.
[Abstract] [Full Text] [PDF]

Home page
 JCOHome page
R. I. Skotheim, A. Kallioniemi, B. Bjerkhagen, F. Mertens, H. R. Brekke, O. Monni, S. Mousses, N. Mandahl, G. Soeter, J. M. Nesland, et al.
Topoisomerase-II{alpha} Is Upregulated in Malignant Peripheral Nerve Sheath Tumors and Associated With Clinical Outcome
J. Clin. Oncol., December 15, 2003; 21(24): 4586 - 4591.
[Abstract] [Full Text] [PDF]

Home page
 Neuro OncolHome page
K. Tada, M. Kochi, H. Saya, J.-i. Kuratsu, S. Shiraishi, T. Kamiryo, N. Shinojima, and Y. Ushio
Preliminary observations on genetic alterations in pilocytic astrocytomas associated with neurofibromatosis 1
Neuro-oncol, October 1, 2003; 5(4): 228 - 234.
[Abstract] [PDF]

Home page
 Clin. Cancer Res.Home page
F. Perrone, S. Tabano, F. Colombo, G. Dagrada, S. Birindelli, A. Gronchi, M. Colecchia, M. A. Pierotti, and S. Pilotti
p15INK4b, p14ARF, and p16INK4a Inactivation in Sporadic and Neurofibromatosis Type 1-related Malignant Peripheral Nerve Sheath Tumors
Clin. Cancer Res., September 15, 2003; 9(11): 4132 - 4138.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
R. P. H. Huijbregts, K. A. Roth, R. E. Schmidt, and S. L. Carroll
Hypertrophic Neuropathies and Malignant Peripheral Nerve Sheath Tumors in Transgenic Mice Overexpressing Glial Growth Factor {beta}3 in Myelinating Schwann Cells
J. Neurosci., August 13, 2003; 23(19): 7269 - 7280.
[Abstract] [Full Text] [PDF]

Home page
 Clin. Cancer Res.Home page
B. Govindarajan, M. C. Mizesko, M. S. Miller, H. Onda, M. Nunnelly, K. Casper, D. Brat, C. Cohen, and J. L Arbiser
Tuberous Sclerosis-associated Neoplasms Express Activated p42/44 Mitogen-activated Protein (MAP) Kinase, and Inhibition of MAP Kinase Signaling Results in Decreased in Vivo Tumor Growth
Clin. Cancer Res., August 1, 2003; 9(9): 3469 - 3475.
[Abstract] [Full Text] [PDF]

Home page
 NeurologyHome page
Plexiform neurofibromas in NF1: Toward biologic-based therapy
Neurology, May 28, 2002; 58(10): 1461 - 1470.


Home page
 Cancer Res.Home page
R. E. Ferner and D. H. Gutmann
International Consensus Statement on Malignant Peripheral Nerve Sheath Tumors in Neurofibromatosis 1
Cancer Res., March 1, 2002; 62(5): 1573 - 1577.
[Abstract] [Full Text] [PDF]

Home page
 NeurologyHome page
J. Li, A. Perry, C. D. James, and D. H. Gutmann
Cancer-related gene expression profiles in NF1-associated pilocytic astrocytomas
Neurology, April 10, 2001; 56(7): 885 - 890.
[Abstract] [Full Text] [PDF]

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