Regulation of the Hippo signaling pathway by ubiquitin modification
The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause for multiple types of human cancers. Since the awareness of the importance of the Hippo signaling in a wide range of biological fields has bee...
Saved in:
Published in | BMB reports Vol. 51; no. 3; pp. 143 - 150 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Society for Biochemistry and Molecular Biology
01.03.2018
생화학분자생물학회 |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause for multiple types of human cancers. Since the awareness of the importance of the Hippo signaling in a wide range of biological fields has been continually grown, it is also understood that a thorough and well-rounded comprehension of the precise dynamics could provide fundamental insights for therapeutic applications. Several components in the Hippo signaling pathway are known to be targeted for proteasomal degradation via ubiquitination by E3 ligases. β-TrCP is a well-known E3 ligase of YAP/TAZ, which leads to the reduction of YAP/TAZ levels. The Hippo signaling pathway can also be inhibited by the E3 ligases (such as ITCH) which target LATS1/2 for degradation. Regulation via ubiquitination involves not only complex network of E3 ligases but also deubiquitinating enzymes (DUBs), which remove ubiquitin from its targets. Interestingly, non-degradative ubiquitin modifications are also known to play important roles in the regulation of Hippo signaling. Although there has been much advanced progress in the investigation of ubiquitin modifications acting as regulators of the Hippo signaling pathway, research done to date still remains inadequate due to the sheer complexity and diversity of the subject. Herein, we review and discuss recent developments that implicate ubiquitin-mediated regulatory mechanisms at multiple steps of the Hippo signaling pathway. [BMB Reports 2018; 51(3): 143-150]. |
---|---|
AbstractList | The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause for multiple types of human cancers. Since the awareness of the importance of the Hippo signaling in a wide range of biological fields has been continually grown, it is also understood that a thorough and well-rounded comprehension of the precise dynamics could provide fundamental insights for therapeutic applications.
Several components in the Hippo signaling pathway are known to be targeted for proteasomal degradation via ubiquitination by E3 ligases. β-TrCP is a well-known E3 ligase of YAP/TAZ, which leads to the reduction of YAP/TAZ levels. The Hippo signaling pathway can also be inhibited by the E3 ligases (such as ITCH) which target LATS1/2 for degradation. Regulation via ubiquitination involves not only complex network of E3 ligases but also deubiquitinating enzymes (DUBs), which remove ubiquitin from its targets. Interestingly, non-degradative ubiquitin modifications are also known to play important roles in the regulation of Hippo signaling. Although there has been much advanced progress in the investigation of ubiquitin modifications acting as regulators of the Hippo signaling pathway, research done to date still remains inadequate due to the sheer complexity and diversity of the subject. Herein, we review and discuss recent developments that implicate ubiquitin-mediated regulatory mechanisms at multiple steps of the Hippo signaling pathway. KCI Citation Count: 5 The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause for multiple types of human cancers. Since the awareness of the importance of the Hippo signaling in a wide range of biological fields has been continually grown, it is also understood that a thorough and well-rounded comprehension of the precise dynamics could provide fundamental insights for therapeutic applications. Several components in the Hippo signaling pathway are known to be targeted for proteasomal degradation via ubiquitination by E3 ligases. β-TrCP is a well-known E3 ligase of YAP/TAZ, which leads to the reduction of YAP/TAZ levels. The Hippo signaling pathway can also be inhibited by the E3 ligases (such as ITCH) which target LATS1/2 for degradation. Regulation via ubiquitination involves not only complex network of E3 ligases but also deubiquitinating enzymes (DUBs), which remove ubiquitin from its targets. Interestingly, non-degradative ubiquitin modifications are also known to play important roles in the regulation of Hippo signaling. Although there has been much advanced progress in the investigation of ubiquitin modifications acting as regulators of the Hippo signaling pathway, research done to date still remains inadequate due to the sheer complexity and diversity of the subject. Herein, we review and discuss recent developments that implicate ubiquitin-mediated regulatory mechanisms at multiple steps of the Hippo signaling pathway. The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause for multiple types of human cancers. Since the awareness of the importance of the Hippo signaling in a wide range of biological fields has been continually grown, it is also understood that a thorough and well-rounded comprehension of the precise dynamics could provide fundamental insights for therapeutic applications. Several components in the Hippo signaling pathway are known to be targeted for proteasomal degradation via ubiquitination by E3 ligases. β-TrCP is a well-known E3 ligase of YAP/TAZ, which leads to the reduction of YAP/TAZ levels. The Hippo signaling pathway can also be inhibited by the E3 ligases (such as ITCH) which target LATS1/2 for degradation. Regulation via ubiquitination involves not only complex network of E3 ligases but also deubiquitinating enzymes (DUBs), which remove ubiquitin from its targets. Interestingly, non-degradative ubiquitin modifications are also known to play important roles in the regulation of Hippo signaling. Although there has been much advanced progress in the investigation of ubiquitin modifications acting as regulators of the Hippo signaling pathway, research done to date still remains inadequate due to the sheer complexity and diversity of the subject. Herein, we review and discuss recent developments that implicate ubiquitin-mediated regulatory mechanisms at multiple steps of the Hippo signaling pathway. [BMB Reports 2018; 51(3): 143-150]. |
Author | Jho, Eek-Hoon Kim, Youngeun |
Author_xml | – sequence: 1 givenname: Youngeun surname: Kim fullname: Kim, Youngeun organization: Department of Life Science, University of Seoul, Seoul 02504, Korea – sequence: 2 givenname: Eek-Hoon surname: Jho fullname: Jho, Eek-Hoon organization: Department of Life Science, University of Seoul, Seoul 02504, Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29366444$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002328491$$DAccess content in National Research Foundation of Korea (NRF) |
BookMark | eNpVkEtLw0AUhQep2Fr7D0Rm6yJxHplHNkIpagsFoVRwF2Yyk3RoMol5KP33htaKrs6Be75vca_ByFfeAnCLUcgiSR90qRtbhwRhGTIc0hBhcQEmOBY84AK9j86dx3wMZm3rNGKUCi5kfAXGJKacR1E0AYuNzftCda7ysMpgt7Nw6eq6gq3LvSqcz2Gtut2XOkB9gL12H73rnIdlZVzm0iN4Ay4zVbR29pNT8Pb8tF0sg_Xry2oxXwcpQ7ILuLEk04YaGqE4zQhXRGNkOTJKKMsYlgxhI6zMUkosNUxqEnGDiKA4EkbRKbg_eX2TJfvUJZVyx8yrZN8k8812lVAkMZFs2D6etnWvS2tS67tGFUnduFI1hyP5_-LdbvB8JkxKQggeBHd_Bb_k-XX0G9p9doc |
CitedBy_id | crossref_primary_10_1016_j_mbm_2024_100085 crossref_primary_10_1242_dev_179069 crossref_primary_10_1038_s41420_024_01943_2 crossref_primary_10_1016_j_biopha_2020_110956 crossref_primary_10_1016_j_critrevonc_2023_103964 crossref_primary_10_1038_s41419_023_06130_2 crossref_primary_10_1126_sciadv_abg2106 crossref_primary_10_3390_jcm8122131 crossref_primary_10_3390_ijms231710119 crossref_primary_10_1016_j_canlet_2024_216861 crossref_primary_10_1038_s41388_020_1318_0 crossref_primary_10_1096_fj_201901278R crossref_primary_10_7554_eLife_49439 crossref_primary_10_1007_s00018_020_03579_8 crossref_primary_10_1002_JPER_20_0176 crossref_primary_10_1248_bpb_b19_00795 crossref_primary_10_3389_fcell_2020_00161 crossref_primary_10_3892_ijo_2024_5656 crossref_primary_10_1016_j_arr_2024_102536 crossref_primary_10_1016_j_bbrc_2019_03_015 crossref_primary_10_1016_j_biocel_2024_106646 crossref_primary_10_1016_j_yexcr_2021_112646 crossref_primary_10_1073_pnas_1822155116 crossref_primary_10_1016_j_bbadis_2020_165839 crossref_primary_10_1016_j_oraloncology_2018_08_020 crossref_primary_10_1016_j_pharmthera_2021_107881 crossref_primary_10_1007_s12032_019_1290_0 crossref_primary_10_1038_s41418_022_01040_w crossref_primary_10_1002_mco2_340 crossref_primary_10_1016_j_vetmic_2019_108564 crossref_primary_10_3390_ijms23010430 crossref_primary_10_1016_j_jbc_2021_100599 crossref_primary_10_1371_journal_ppat_1008231 crossref_primary_10_3389_fcimb_2020_603457 crossref_primary_10_3390_biomedicines10112834 crossref_primary_10_3390_cancers12113090 crossref_primary_10_1016_j_gendis_2019_06_004 crossref_primary_10_1002_jcb_30606 crossref_primary_10_3390_cells10092462 crossref_primary_10_1016_j_bbrc_2020_07_008 crossref_primary_10_1016_j_biocel_2024_106559 crossref_primary_10_1038_s41419_022_04816_7 crossref_primary_10_1186_s13287_022_02811_5 crossref_primary_10_4103_jpbs_jpbs_134_24 |
ContentType | Journal Article |
Copyright | Copyright © 2018 by the The Korean Society for Biochemistry and Molecular Biology 2018 |
Copyright_xml | – notice: Copyright © 2018 by the The Korean Society for Biochemistry and Molecular Biology 2018 |
DBID | CGR CUY CVF ECM EIF NPM 5PM ACYCR |
DOI | 10.5483/bmbrep.2018.51.3.017 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed PubMed Central (Full Participant titles) Korean Citation Index |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) |
DatabaseTitleList | MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1976-670X |
EndPage | 150 |
ExternalDocumentID | oai_kci_go_kr_ARTI_3081285 PMC5882221 29366444 |
Genre | Journal Article Review |
GroupedDBID | .UV ALMA_UNASSIGNED_HOLDINGS CGR CUY CVF ECM EIF NPM --- 23N 2WC 5GY 5PM 5VS 87B 9ZL AAFWJ ACGFO ACYCR ADBBV AENEX AFPKN AOIJS BAWUL BCNDV DIK E3Z F5P GROUPED_DOAJ GX1 HH5 HYE HZB JDI KQ8 OVT RNS RPM TR2 53G 85H IPNFZ M~E OK1 RIG |
ID | FETCH-LOGICAL-c508t-6de2fbd3d3409cf26a2b10e60da7ae5518501d7e8fc32e3d58b246d0273147da3 |
ISSN | 1976-6696 |
IngestDate | Tue Nov 21 21:43:11 EST 2023 Thu Aug 21 14:03:49 EDT 2025 Fri Feb 23 03:43:48 EST 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 3 |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c508t-6de2fbd3d3409cf26a2b10e60da7ae5518501d7e8fc32e3d58b246d0273147da3 |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC5882221 |
PMID | 29366444 |
PageCount | 8 |
ParticipantIDs | nrf_kci_oai_kci_go_kr_ARTI_3081285 pubmedcentral_primary_oai_pubmedcentral_nih_gov_5882221 pubmed_primary_29366444 |
PublicationCentury | 2000 |
PublicationDate | 20180301 |
PublicationDateYYYYMMDD | 2018-03-01 |
PublicationDate_xml | – month: 3 year: 2018 text: 20180301 day: 1 |
PublicationDecade | 2010 |
PublicationPlace | Korea (South) |
PublicationPlace_xml | – name: Korea (South) |
PublicationTitle | BMB reports |
PublicationTitleAlternate | BMB Rep |
PublicationYear | 2018 |
Publisher | Korean Society for Biochemistry and Molecular Biology 생화학분자생물학회 |
Publisher_xml | – name: Korean Society for Biochemistry and Molecular Biology – name: 생화학분자생물학회 |
SSID | ssib053376789 ssj0061272 |
Score | 2.3915122 |
SecondaryResourceType | review_article |
Snippet | The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause... |
SourceID | nrf pubmedcentral pubmed |
SourceType | Open Website Open Access Repository Index Database |
StartPage | 143 |
SubjectTerms | Animals Deubiquitinating Enzymes - metabolism Humans Invited Mini Review Protein-Serine-Threonine Kinases - metabolism Signal Transduction - physiology Ubiquitin - metabolism Ubiquitin-Protein Ligases - metabolism 화학 |
Title | Regulation of the Hippo signaling pathway by ubiquitin modification |
URI | https://www.ncbi.nlm.nih.gov/pubmed/29366444 https://pubmed.ncbi.nlm.nih.gov/PMC5882221 https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002328491 |
Volume | 51 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
ispartofPNX | BMB Reports, 2018, 51(3), , pp.143-150 |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELeq8QAviG_KAEWIN5SS2ImdPrJqUCZ1mtAm9S2yY4dG1ZJQJULbX8_5o4mL9gB7cSu3dVLf5fw7--53CH1kiqc8pXN40mQWJjgR4RxTGYqCCQDkjDFTeW51TpdXydk6XU8mrRe11HdiVtzemVdyH6lCH8hVZ8n-h2SHQaED3oN8oQUJQ_tPMv5hC8k7zKch5LJq2-aTDsrgNs8cAN5vfqNBZi-qX33VVbWufqMDhEaZDIe6J_szhPFo3uiLsQmqHxTpbGN2WE_VNtw0bhC3dRBnY-yUDcRvdnq33w8PPal0nS5baM5GeuyL9LramJ59igHJhJTOHZO118eitW9gHaNs5fvfxlrGlqHJLbyxZaD926aDS6W5JWAKwCXRsXjZLI1nZBbZnE9PzO21kTMAGAooLxlXuCHu8GK1SDMNicBffoDBsdA1L76tBwsH2JdRw79v13KAf6b81_BXbfKlvqXPd92QppZ2VwesUu9KD9ccxtx6IObyCXrsvI_gi1Wlp2ii6mfo4WIvi-doMapU0JQBqFRgVCoYVCpwKhWIm2BQqcBXqRfo6uvp5WIZujobYQHwvAupVLgUkkgCzn5RYsqxiCNFI8kZV5qyL41iyVRWFgQrItNM4IRKzYQUJ0xy8hId1U2tXqOAFrFURFChMp4IClgHF4pFeC4yQTiRU_QBZiXfFlWuec31688m3-5y8N6-5wTwKc7SKXpl5ypvLeNKvp_UKWIHszh8QQ92-EldbQxZupP3m3v_8hg9Gp-dt-io2_XqHQDRTrw3ugPt-cXqD7eTio0 |
linkProvider | Geneva Foundation for Medical Education and Research |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Regulation+of+the+Hippo+signaling+pathway+by+ubiquitin+modification&rft.jtitle=BMB+reports&rft.au=Kim%2C+Youngeun&rft.au=Jho%2C+Eek-hoon&rft.date=2018-03-01&rft.pub=Korean+Society+for+Biochemistry+and+Molecular+Biology&rft.issn=1976-6696&rft.eissn=1976-670X&rft.volume=51&rft.issue=3&rft.spage=143&rft.epage=150&rft_id=info:doi/10.5483%2FBMBRep.2018.51.3.017&rft_id=info%3Apmid%2F29366444&rft.externalDocID=PMC5882221 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1976-6696&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1976-6696&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1976-6696&client=summon |