Non-syndromic supernumerary teeth and association with a self-reported family history of cancer

Fortschritte der Kieferorthopädie
Andrea Lips1, Érika Calvano Küchler2, Isabela Ribeiro Madalena1, Patrícia Nivoloni Tannure3, Leonardo Santos Antunes4, Leonardo Santos Antunes4, Marcelo C. Costa5, Peter Proff6, Christian Kirschneck2, Flares Baratto‐Filho7
1Department of Dentistry, University of Joinville Region, Joinville, SC, Brazil
2Department of Orthodontics, Medical Faculty, University Hospital Bonn, Welschnonnenstr. 17, 53111, Bonn, Germany
3Department of Pediatric Dentistry, University of Veiga de Almeida, Rio de Janeiro, RJ, Brazil
4Postgraduate Program in Dentistry, Health Institute of Nova Friburgo, Fluminense Federal University, Nova Friburgo, RJ, Brazil
5Department of Orthodontics, University of Regensburg, Regensburg, Germany
6Department of Pediatric Dentistry and Orthodontics, Rio de Janeiro Federal University, Rio de Janeiro, RJ, Brazil
7School of Dentistry, Tuiuti University from Parana, Curitiba, PR, Brazil

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D’Souza RN, Klein OD (2007) Unraveling the molecular mechanisms that lead to supernumerary teeth in mice and men: current concepts and novel approaches. Cells Tissues Organs 186(1):60–69. https://doi.org/10.1159/000102681

Küchler EC, Costa AG, Costa MC, Vieira AR, Granjeiro JM (2011) Supernumerary teeth vary depending on gender. Braz oral res 25(1):76–79. https://doi.org/10.1590/S1806-83242011000100013

Acikgoz A, Acikgoz G, Tunga U, Otan F (2006) Characteristics and prevalence of non-syndrome multiple supernumerary teeth: a retrospective study. Dentomaxillofac Radiol 35(3):185–190. https://doi.org/10.1259/dmfr/21956432

Ata-Ali F, Ata-Ali J, Peñarrocha-Oltr D, Peñarrocha-Diago M (2014) Prevalence, etiology, diagnosis, treatment and complications of supernumerary teeth. J Clin Exp Dent 6(4):e414–18. https://doi.org/10.4317/jced.51499

Azzaldeen A, Watted N, Mai A, Borbély P, Abu-Hussein M (2017) Tooth agenesis; aetiological factors. IOSR-JDMS 16(1):75–85. https://doi.org/10.9790/0853-1601057585

Bonczek O, Krejci P, Izakovicova-Holla L, Cernochova P, Kiss I, Vojtesek B (2021) Tooth agenesis: What do we know and is there a connection to cancer? Clin Genet 99(4):493–502. https://doi.org/10.1111/cge.13892

Chalothorn LA, Beeman CS, Ebersole JL, Kluemper GT, Hicks EP, Kryscio RJ, Desimone CP, Modesitt SC 2008 Hypodontia as a risk marker for epithelial ovarian cancer: a case-controlled study. J Am Dent Assoc 139(2):163–9. https://doi.org/10.14219/jada.archive.2008.0132.

Küchler EC, Lips A, Tannure PN, Ho B, Costa MC, Granjeiro JM, Vieira AR (2013) Tooth agenesis association with self-reported family history of cancer. J Dent Res 92(2):149–155. https://doi.org/10.1177/0022034512468750

Bonds J, Pollan-White S, Xiang L, Mues G, D’souza R (2014) Is there a link between ovarian cancer and tooth agenesis? Eur J Med Gene 57(5):235–239. https://doi.org/10.1016/j.ejmg.2014.02.013

Williams MA, Biguetti C, Romero-Bustillos M, Maheshwari K, Dinckan N, Cavalla F, Liu X, Silva R, Akyyalcin S, Uyguner ZO, Vieira AR, Amendt BA, Fakhouri WD, Letra A (2018) Colorectal cancer-associated genes are associated with tooth agenesis and may have a role in tooth development. Sci Rep 8(1):2979. https://doi.org/10.1038/s41598-018-21368-z

Gawron-Jakubek W, Spaczynska J, Pitynski K, Loster BW (2019) Coexistence of tooth agenesis and ovarian cancer—a systematic literature review. Ginekol Pol 90(12):707–710. https://doi.org/10.5603/GP.2019.0121

Medina MCG, Bastos RTDRM, Mecenas P, Pinheiro JJV, Normando D (2021) Association between tooth agenesis and cancer: a systematic review. J Appl Oral Sci 29:e20200955. https://doi.org/10.1590/1678-7757-2020-0955

Al-Muzian M, Mohammed H, Ulhaq A, Keightley AJ (2021) Are developmentally missing teeth a predictive risk marker of malignant diseases in non-syndromic individuals? A systematic review. J Orthod 48(3):221–230. https://doi.org/10.1177/1465312520984166

Howe LJ, Hemani G, Lesseur C, Gaborieau V, Ludwig KU, Mangold E, Brennam P, Ness AR, Pourcain BS, Smith GD, Lewis SJ (2020) Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms. Genet Epidemiol 44(8):924–933. https://doi.org/10.1002/gepi.22343

Assis IO, Lacerda RHW, Cavalcante BGN, Bezamat M, Modesto A, Vieira AR (2021) IRE1 less common homozygous genotype in families with positive history of cancer and individuals born with cleft lip/palate. J Craniofac Surg 32(5):e407–11. https://doi.org/10.1097/SCS.0000000000007169

Fonseca CAD, Martelli DRB, Almeida ILF, Mesquita LGM, Dias VO, Martelli-Júnior H (2022) Are dental agenesis and oral clefts clinical markers of ovarian or uterine cancer? Oral Dis 28(1):443–444. https://doi.org/10.1111/odi.13720

Half E, Bercovich D, Rozen P (2009) Familial adenomatous polyposis. Orphanet J Rare Dis 4(22):22. https://doi.org/10.1186/1750-1172-4-22

Gallas MM, Garcia A (2000) Retention of permanent incisors by mesiodens: A family affair. Br Dent J 188(2):63–64. https://doi.org/10.1038/sj.bdj.4800390

Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K (2022) Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations. Am J Hum Genet 71(4):724–738. https://doi.org/10.1086/342717

Zhang S, Qin H, Lv W, Luo S, Wang J, Fu C, Ma R, Shen Y, Chen S, Wu L (2016) Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis. Gene 577(2):187–192. https://doi.org/10.1016/j.gene.2015.11.034

Premalatha S, Sarveswari KN, Lahiri K (2010) Reverse-Namaskar: A new sign in Ehlers-Danlos syndrome: A family pedigree study of four generations. Indian J Dermatol 55(1):86–91. https://doi.org/10.4103/0019-5154.60360

Hibbert S (2005) A previously unreported association between Nance-Horan syndrome and spontaneous dental abscesses. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 99(2):207–211. https://doi.org/10.1016/j.tripleo.2004.07.004

Garvey MT, Barry HJ, Blake M (1999) Supernumerary teeth—An overview of classification, diagnosis, and management. J Can Dent Assoc 65(11):612–616

Kantaputra P, Miletich I, Ludecke HJ, Suzuki EY, Praphanphoj V, Shivdasani R, Wuelling M, Vortkamp A, Napierala D, Sharpe PT (2008) Tricho-rhino-phalangeal syndrome with supernumerary teeth. J Dent Res 87(11):1027–1031. https://doi.org/10.1177/154405910808701102

Afzal AR, Jeffery S (2003) One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B. Hum Mutat 22(1):1–11. https://doi.org/10.1002/humu.10233

Fekonja A, Cretnik A, Zerdoner D, Takac I (2015) Hypodontia phenotype in patients with epithelial ovarian cancer. Radiol Oncol 49(1):65–70. https://doi.org/10.2478/raon-2014-0034

Sorosky JI (2012) Endometrial cancer. Obstet Gynecol 120(2Pt1):383–397. https://doi.org/10.1097/AOG.0b013e3182605bf1

Altman DG, Bland JM (2007) Missing data. BMJ 334:424. https://doi.org/10.1136/bmj.38977.682025.2C

Ozaki T, Yu M, Yin D, Sun D, Zhu Y, Bu Y, Sang M (2018) Impact of RUNX2 on drug-resistant human pancreatic cancer cells with p53 mutations. Bmc Cancer 18:309. https://doi.org/10.1186/s12885-018-4217-9

Camilleri S, McDonald F (2006) Runx2 and dental development. Eur J Oral Sci 114(5):361–373. https://doi.org/10.1111/j.1600-0722.2006.00399.x

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