NITA, Alexandru, Sara POOVAKULATHU ABRAHAM, Pavel KREJČÍ and Michaela BOSÁKOVÁ. Oncogenic FGFR Fusions Produce Centrosome and Cilia Defects by Ectopic Signaling. Cells. Basel: MDPI, 2021, vol. 10, No 6, p. 1-25. ISSN 2073-4409. Available from: https://dx.doi.org/10.3390/cells10061445.
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Basic information
Original name Oncogenic FGFR Fusions Produce Centrosome and Cilia Defects by Ectopic Signaling
Authors NITA, Alexandru (642 Romania, belonging to the institution), Sara POOVAKULATHU ABRAHAM (356 India, belonging to the institution), Pavel KREJČÍ (203 Czech Republic, belonging to the institution) and Michaela BOSÁKOVÁ (203 Czech Republic, guarantor, belonging to the institution).
Edition Cells, Basel, MDPI, 2021, 2073-4409.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 7.666
RIV identification code RIV/00216224:14110/21:00122060
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3390/cells10061445
UT WoS 000667840600001
Keywords in English FGFR; fibroblast growth factor receptor; FGFR fusion; cancer; oncogenic driver; neoplastic transformation; primary cilia; cilia; centrosome; centrosome cycle
Tags 14110513, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 21/2/2022 13:13.
Abstract
A single primary cilium projects from most vertebrate cells to guide cell fate decisions. A growing list of signaling molecules is found to function through cilia and control ciliogenesis, including the fibroblast growth factor receptors (FGFR). Aberrant FGFR activity produces abnormal cilia with deregulated signaling, which contributes to pathogenesis of the FGFR-mediated genetic disorders. FGFR lesions are also found in cancer, raising a possibility of cilia involvement in the neoplastic transformation and tumor progression. Here, we focus on FGFR gene fusions, and discuss the possible mechanisms by which they function as oncogenic drivers. We show that a substantial portion of the FGFR fusion partners are proteins associated with the centrosome cycle, including organization of the mitotic spindle and ciliogenesis. The functions of centrosome proteins are often lost with the gene fusion, leading to haploinsufficiency that induces cilia loss and deregulated cell division. We speculate that this complements the ectopic FGFR activity and drives the FGFR fusion cancers.
Links
EF19_073/0016943, research and development projectName: Interní grantová agentura Masarykovy univerzity
MUNI/A/1325/2020, interní kód MUName: Biomedicínské vědy
Investor: Masaryk University
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