Detailed Information on Publication Record
2021
RNF43 inhibits WNT5A-driven signaling and suppresses melanoma invasion and resistance to the targeted therapy
RADASZKIEWICZ, Tomasz Witold, Michaela NOSKOVÁ, Kristína GÖMÖRYOVÁ, Olga VONDÁLOVÁ BLANÁŘOVÁ, Katarzyna Anna RADASZKIEWICZ et. al.Basic information
Original name
RNF43 inhibits WNT5A-driven signaling and suppresses melanoma invasion and resistance to the targeted therapy
Authors
RADASZKIEWICZ, Tomasz Witold (616 Poland, belonging to the institution), Michaela NOSKOVÁ (203 Czech Republic, belonging to the institution), Kristína GÖMÖRYOVÁ (703 Slovakia, belonging to the institution), Olga VONDÁLOVÁ BLANÁŘOVÁ (203 Czech Republic, belonging to the institution), Katarzyna Anna RADASZKIEWICZ (616 Poland, belonging to the institution), Markéta PÍCKOVÁ (203 Czech Republic, belonging to the institution), Ráchel VÍCHOVÁ, Tomáš GYBEĽ (703 Slovakia, belonging to the institution), Karol KAISER (703 Slovakia, belonging to the institution), Lucia DEMKOVÁ, Lucia KUČEROVÁ, Tomáš BÁRTA (203 Czech Republic, belonging to the institution), David POTĚŠIL (203 Czech Republic, belonging to the institution), Zbyněk ZDRÁHAL (203 Czech Republic, belonging to the institution), Karel SOUČEK (203 Czech Republic, belonging to the institution) and Vítězslav BRYJA (203 Czech Republic, guarantor, belonging to the institution)
Edition
eLife, eLife Sciences Publications Ltd, 2021, 2050-084X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 8.713
RIV identification code
RIV/00216224:14310/21:00119379
Organization unit
Faculty of Science
UT WoS
000712036700001
Keywords in English
RNF43; WNT5A; melanoma; ROR1; VANGL1; BRAF V600E; Human; Mouse
Tags
International impact, Reviewed
Změněno: 10/10/2024 14:47, Ing. Martina Blahová
Abstract
V originále
RNF43 is an E3 ubiquitin ligase and known negative regulator of WNT/beta-catenin signaling. We demonstrate that RNF43 is also a regulator of noncanonical WNT5A-induced signaling in human cells. Analysis of the RNF43 interactome using BioID and immunoprecipitation showed that RNF43 can interact with the core receptor complex components dedicated to the noncanonical Wnt pathway such as ROR1, ROR2, VANGL1, and VANGL2. RNF43 triggers VANGL2 ubiquitination and proteasomal degradation and clathrin-dependent internalization of ROR1 receptor and inhibits ROR2 activation. These activities of RNF43 are physiologically relevant and block pro-metastatic WNT5A signaling in melanoma. RNF43 inhibits responses to WNT5A, which results in the suppression of invasive properties of melanoma cells. Furthermore, RNF43 prevented WNT5A-assisted development of resistance to BRAF V600E and MEK inhibitors. Next, RNF43 acted as melanoma suppressor and improved response to targeted therapies in vivo. In line with these findings, RNF43 expression decreases during melanoma progression and RNF43-low patients have a worse prognosis. We conclude that RNF43 is a newly discovered negative regulator of WNT5A-mediated biological responses that desensitizes cells to WNT5A.
Links
GX19-28347X, research and development project |
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LM2018127, research and development project |
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LM2018140, research and development project |
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90127, large research infrastructures |
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