Tooth agenesis: What do we know and is there a connection to cancer?
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F21%3A73611772" target="_blank" >RIV/61989592:15110/21:73611772 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00159816:_____/21:00074092 RIV/00216224:14110/21:00121356 RIV/00209805:_____/21:00078498
Výsledek na webu
<a href="https://onlinelibrary.wiley.com/doi/epdf/10.1111/cge.13892" target="_blank" >https://onlinelibrary.wiley.com/doi/epdf/10.1111/cge.13892</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/cge.13892" target="_blank" >10.1111/cge.13892</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Tooth agenesis: What do we know and is there a connection to cancer?
Popis výsledku v původním jazyce
Like all developmental processes, odontogenesis is highly complex and dynamically regulated, with hundreds of genes co-expressed in reciprocal networks. Tooth agenesis (missing one or more/all teeth) is a common human craniofacial anomaly and may be caused by genetic variations and/or environmental factors. Variants in PAX9, MSX1, AXIN2, EDA, EDAR, and WNT10A genes are associated with tooth agenesis. Currently, variants in ATF1, DUSP10, CASC8, IRF6, KDF1, GREM2, LTBP3, and components and regulators of WNT signaling WNT10B, LRP6, DKK, and KREMEN1 are at the forefront of interest. Due to the interconnectedness of the signaling pathways of carcinogenesis and odontogenesis, tooth agenesis could be a suitable marker for early detection of cancer predisposition. Variants in genes associated with tooth agenesis could serve as prognostic or therapeutic targets in cancer. This review aims to summarize existing knowledge of development and clinical genetics of teeth. Concurrently, the review proposes possible approaches for future research in this area, with particular attention to roles in monitoring, early diagnosis and therapy of tumors associated with defective tooth development.
Název v anglickém jazyce
Tooth agenesis: What do we know and is there a connection to cancer?
Popis výsledku anglicky
Like all developmental processes, odontogenesis is highly complex and dynamically regulated, with hundreds of genes co-expressed in reciprocal networks. Tooth agenesis (missing one or more/all teeth) is a common human craniofacial anomaly and may be caused by genetic variations and/or environmental factors. Variants in PAX9, MSX1, AXIN2, EDA, EDAR, and WNT10A genes are associated with tooth agenesis. Currently, variants in ATF1, DUSP10, CASC8, IRF6, KDF1, GREM2, LTBP3, and components and regulators of WNT signaling WNT10B, LRP6, DKK, and KREMEN1 are at the forefront of interest. Due to the interconnectedness of the signaling pathways of carcinogenesis and odontogenesis, tooth agenesis could be a suitable marker for early detection of cancer predisposition. Variants in genes associated with tooth agenesis could serve as prognostic or therapeutic targets in cancer. This review aims to summarize existing knowledge of development and clinical genetics of teeth. Concurrently, the review proposes possible approaches for future research in this area, with particular attention to roles in monitoring, early diagnosis and therapy of tumors associated with defective tooth development.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30101 - Human genetics
Návaznosti výsledku
Projekt
<a href="/cs/project/EF16_019%2F0000868" target="_blank" >EF16_019/0000868: Molekulární, buněčný a klinický přístup ke zdravému stárnutí</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
CLINICAL GENETICS
ISSN
0009-9163
e-ISSN
—
Svazek periodika
99
Číslo periodika v rámci svazku
4
Stát vydavatele periodika
DK - Dánské království
Počet stran výsledku
10
Strana od-do
493-502
Kód UT WoS článku
000618548500001
EID výsledku v databázi Scopus
2-s2.0-85101440781