The Mutational Profile of Unicystic Ameloblastoma

被引:65
作者
Heikinheimo, K. [1 ,2 ]
Huhtala, J. -M. [1 ,2 ]
Thiel, A. [3 ]
Kurppa, K. J. [4 ,5 ]
Heikinheimo, H. [6 ]
Kovac, M. [7 ,8 ]
Kragelund, C. [9 ]
Warfvinge, G. [10 ]
Dawson, H. [11 ]
Elenius, K. [4 ,5 ]
Ristimaki, A. [3 ,12 ,13 ]
Baumhoer, D. [7 ,8 ]
Morgan, P. R. [14 ]
机构
[1] Univ Turku, Inst Dent, Dept Oral & Maxillofacial Surg, Lemminkaisenkatu 2, FI-20520 Turku, Finland
[2] Turku Univ Hosp, Turku, Finland
[3] Univ Helsinki, Res Programs Unit, Genome Scale Biol, Helsinki, Finland
[4] Univ Turku, Dept Med Biochem & Genet, Turku, Finland
[5] Univ Turku, MediC Res Labs, Turku, Finland
[6] Chief Chief Technol, Helsinki, Finland
[7] Univ Hosp Basel, Inst Pathol, Bone Tumour Reference Ctr, Basel, Switzerland
[8] Univ Basel, Basel, Switzerland
[9] Dept Oral Pathol & Med, Copenhagen, Denmark
[10] Malmo Univ, Dept Oral Pathol, Malmo, Sweden
[11] Univ Bern, Inst Pathol, Bern, Switzerland
[12] Univ Helsinki, Cent Hosp, HUSLAB, Dept Pathol, Helsinki, Finland
[13] Univ Helsinki, Medicum, Helsinki, Finland
[14] Kings Coll London, Guys Hosp, Head & Neck Pathol, London, England
关键词
drug therapy; genetic markers; odontogenic tumors; mitogen-activated protein kinase kinases; jaw neoplasms; survival analysis; BRAF V600E MUTATION; COLORECTAL-CANCER; BRAFV600E;
D O I
10.1177/0022034518798810
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BRAF V600E is the most common mutation in conventional ameloblastoma (AM) of the mandible. In contrast, maxillary AMs appear to harbor more frequently RAS, FGFR2, or SMO mutations. Unicystic ameloblastoma (UAM) is considered a less aggressive variant of ameloblastoma, amenable to more conservative treatment, and classified as a distinct entity. The aim of this study was to characterize the mutation profile of UAM (n = 39) and to compare it to conventional AM (n = 39). The associations between mutation status and recurrence probability were also analyzed. In the mandible, 94% of UAMs (29/31, including 8/8 luminal, 6/8 intraluminal, and 15/15 mural subtypes) and 74% of AMs (28/38) revealed BRAF V600E mutations. Among the BRAF wild-type cases, 1 UAM showed a missense SMO mutation (p.L412F), whereas 2 NRAS (p.Q61R), 2 HRAS (p.Q61R), and 2 FGFR2 (p.C383R) activating mutations were identified in AM. Of the 3 maxillary UAMs, only 1 revealed a BRAF V600E mutation. Taken together, our findings demonstrate high frequency of activating BRAF V600E mutations in both UAM and AM of the mandible. In maxillary UAMs, the BRAF V600E mutation prevalence appears to be lower as was shown for AM previously. It could therefore be argued that UAM and AM are part of the spectrum of the same disease. AMs without BRAF V600E mutations were associated with an increased rate of local recurrence (P = 0.0003), which might indicate that routine mutation testing also has an impact on prognosis.
引用
收藏
页码:54 / 60
页数:7
相关论文
共 29 条
  • [1] [Anonymous], PACKAGE SURVIVAL
  • [2] Detection of BRAF V600E mutation in colorectal cancer:: Comparison of automatic sequencing and real-time chemistry methodology
    Benlloch, Susana
    Paya, Artemio
    Alenda, Cristina
    Bessa, Xavier
    Andreu, Montserrat
    Jover, Rodrigo
    Castells, Antoni
    Llor, Xavier
    Aranda, F. Ignacio
    Massuti, Bartomeu
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (05) : 540 - 543
  • [3] Statistics notes - The odds ratio
    Bland, JM
    Altman, DG
    [J]. BRITISH MEDICAL JOURNAL, 2000, 320 (7247) : 1468 - 1468
  • [4] Activating FGFR2-RAS-BRAF Mutations in Ameloblastoma
    Brown, Noah A.
    Rolland, Delphine
    McHugh, Jonathan B.
    Weigelin, Helmut C.
    Zhao, Lili
    Lim, Megan S.
    Elenitoba-Johnson, Kojo S. J.
    Betz, Bryan L.
    [J]. CLINICAL CANCER RESEARCH, 2014, 20 (21) : 5517 - 5526
  • [5] Allosteric modulation of Ras positions Q61 for a direct role in catalysis
    Buhrman, Greg
    Holzapfel, Genevieve
    Fetics, Susan
    Mattos, Carla
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (11) : 4931 - 4936
  • [6] Assessment of BRAFV600E and SMOF412E mutations in epithelial odontogenic tumours
    Diniz, Marina Goncalves
    Gomes, Carolina Cavalieri
    Antonini Guimaraes, Bruna Viana
    Castro, Wagner Henriques
    Tanos Lacerda, Jlio Cesar
    Cardoso, Sergio Vitorino
    de Faria, Paulo Rogerio
    Dias, Fernando Luiz
    Amaral Eisenberg, Ana Lucia
    Loyola, Adriano Mota
    Gomez, Ricardo Santiago
    [J]. TUMOR BIOLOGY, 2015, 36 (07) : 5649 - 5653
  • [7] Progress towards personalized medicine for ameloblastoma
    Gomes, Carolina C.
    Diniz, Marina G.
    Gomez, Ricardo S.
    [J]. JOURNAL OF PATHOLOGY, 2014, 232 (05) : 488 - 491
  • [8] Novel Targets for the Treatment of Ameloblastoma
    Heikinheimo, K.
    Kurppa, K. J.
    Elenius, K.
    [J]. JOURNAL OF DENTAL RESEARCH, 2015, 94 (02) : 237 - 240
  • [9] Early Dental Epithelial Transcription Factors Distinguish Ameloblastoma from Keratocystic Odontogenic Tumor
    Heikinheimo, K.
    Kurppa, K. J.
    Laiho, A.
    Peltonen, S.
    Berdal, A.
    Bouattour, A.
    Ruhin, B.
    Caton, J.
    Thesleff, I.
    Leivo, I.
    Morgan, P. R.
    [J]. JOURNAL OF DENTAL RESEARCH, 2015, 94 (01) : 101 - 111
  • [10] HEIKINHEIMO K, 1991, LAB INVEST, V65, P688