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Items: 1 to 20 of 97

1.
Human tankyrases are aberrantly expressed in colon tumors and contain multiple epitopes that induce humoral and cellular immune responses in cancer patients
Yuriy V. Shebzukhov, Inna N. Lavrik, Julia Karbach, Svetlana V. Khlgatian, Ekaterina P. Koroleva, Pavel V. Belousov, Kirill N. Kashkin, Alexander Knuth, Elke Jager, Nai-Wen Chi, Dmitry V. Kuprash, Sergei A. Nedospasov
Cancer Immunol Immunother. 2008 Jun; 57(6): 871–881. Published online 2007 Nov 20. doi: 10.1007/s00262-007-0423-z
PMCID:
PMC11030928
AbstractArticlePDF–587K
2.
Tankyrase inhibition interferes with junction remodeling, induces leakiness, and disturbs YAP1/TAZ signaling in the endothelium
Nan Ma, Yohanes Cakrapradipta Wibowo, Phillip Wirtz, Doris Baltus, Thomas Wieland, Sepp Jansen
Naunyn Schmiedebergs Arch Pharmacol. 2024; 397(3): 1763–1789. Published online 2023 Sep 23. doi: 10.1007/s00210-023-02720-1
PMCID:
PMC10858845
AbstractArticlePDF–9.4M
3.
Chr21 protein–protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer’s disease
Julia Viard, Yann Loe-Mie, Rachel Daudin, Malik Khelfaoui, Christine Plancon, Anne Boland, Francisco Tejedor, Richard L Huganir, Eunjoon Kim, Makoto Kinoshita, Guofa Liu, Volker Haucke, Thomas Moncion, Eugene Yu, Valérie Hindie, Henri Bléhaut, Clotilde Mircher, Yann Herault, Jean-François Deleuze, Jean-Christophe Rain, Michel Simonneau, Aude-Marie Lepagnol-Bestel
Life Sci Alliance. 2022 Dec; 5(12): e202101205. Published online 2022 Aug 1. doi: 10.26508/lsa.202101205
PMCID:
PMC9348576
AbstractArticlePDF–3.0M
4.
Proteomic analysis of ubiquitination substrates reveals a CTLH E3 ligase complex‐dependent regulation of glycolysis
Matthew E. R. Maitland, Miljan Kuljanin, Xu Wang, Gilles A. Lajoie, Caroline Schild‐Poulter
FASEB J. 2021 Sep; 35(9): e21825. Published online 2021 Aug 12. doi: 10.1096/fj.202100664R
PMCID:
PMC9292413
AbstractArticlePDF–1.5M
5.
Tankyrases inhibit innate antiviral response by PARylating VISA/MAVS and priming it for RNF146-mediated ubiquitination and degradation
Yan-Ran Xu, Meng-Ling Shi, Yu Zhang, Na Kong, Cong Wang, Yi-Feng Xiao, Shi-Shen Du, Qi-Yun Zhu, Cao-Qi Lei
Proc Natl Acad Sci U S A. 2022 Jun 28; 119(26): e2122805119. Published online 2022 Jun 21. doi: 10.1073/pnas.2122805119
PMCID:
PMC9245648
AbstractArticlePDF–2.6M
6.
Deubiquitination of TNKS1 Regulates Wnt/β-Catenin to Affect the Expression of USP25 to Promote the Progression of Glioma
Bin Tang, Hai Luo, Shenhao Xie, Chengbing Pan, Jun Fu
Dis Markers. 2022; 2022: 9087190. Published online 2022 Apr 11. doi: 10.1155/2022/9087190
PMCID:
PMC9017575
AbstractArticlePDF–1.2M
7.
Proteome‐scale mapping of binding sites in the unstructured regions of the human proteome
Caroline Benz, Muhammad Ali, Izabella Krystkowiak, Leandro Simonetti, Ahmed Sayadi, Filip Mihalic, Johanna Kliche, Eva Andersson, Per Jemth, Norman E Davey, Ylva Ivarsson
Mol Syst Biol. 2022 Jan; 18(1): e10584. Published online 2022 Jan 19. doi: 10.15252/msb.202110584
PMCID:
PMC8769072
AbstractArticlePDF–2.9M
8.
Tankyrase-1-mediated degradation of Golgin45 regulates glycosyltransferase trafficking and protein glycosylation in Rab2-GTP-dependent manner
Xihua Yue, Neeraj Tiwari, Lianhui Zhu, Hai Dang Truong Ngo, Jae-Min Lim, Bopil Gim, Shuaiyang Jing, Yijing Wang, Yi Qian, Intaek Lee
Commun Biol. 2021; 4: 1370. Published online 2021 Dec 7. doi: 10.1038/s42003-021-02899-0
PMCID:
PMC8651787
AbstractArticlePDF–12M
9.
Discovery of a Novel Triazolopyridine Derivative as a Tankyrase Inhibitor
Hwani Ryu, Ky-Youb Nam, Hyo Jeong Kim, Jie-Young Song, Sang-Gu Hwang, Jae Sung Kim, Joon Kim, Jiyeon Ahn
Int J Mol Sci. 2021 Jul; 22(14): 7330. Published online 2021 Jul 8. doi: 10.3390/ijms22147330
PMCID:
PMC8303674
AbstractArticlePDF–4.6M
10.
Tankyrase regulates epithelial lumen formation via suppression of Rab11 GEFs
Arun A. Chandrakumar, Étienne Coyaud, Christopher B. Marshall, Mitsuhiko Ikura, Brian Raught, Robert Rottapel
J Cell Biol. 2021 Jul 5; 220(7): e202008037. Published online 2021 Jun 15. doi: 10.1083/jcb.202008037
PMCID:
PMC8221736
AbstractArticlePDF–4.4M
11.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
12.
Arpin Regulates Migration Persistence by Interacting with Both Tankyrases and the Arp2/3 Complex
Gleb Simanov, Irene Dang, Artem I. Fokin, Ksenia Oguievetskaia, Valérie Campanacci, Jacqueline Cherfils, Alexis M. Gautreau
Int J Mol Sci. 2021 Apr; 22(8): 4115. Published online 2021 Apr 16. doi: 10.3390/ijms22084115
PMCID:
PMC8073056
AbstractArticlePDF–4.6M
13.
Evaluation of AXIN1 and AXIN2 as targets of tankyrase inhibition in hepatocellular carcinoma cell lines
Wenhui Wang, Pengyu Liu, Marla Lavrijsen, Shan Li, Ruyi Zhang, Shanshan Li, Wesley S. van de Geer, Harmen J. G. van de Werken, Maikel P. Peppelenbosch, Ron Smits
Sci Rep. 2021; 11: 7470. Published online 2021 Apr 2. doi: 10.1038/s41598-021-87091-4
PMCID:
PMC8018973
AbstractArticlePDF–2.0M
14.
Dissecting the molecular determinants of clinical PARP1 inhibitor selectivity for tankyrase1
Kevin Ryan, Ben Bolaňos, Marissa Smith, Prakash B. Palde, Paulina Delgado Cuenca, Todd L. VanArsdale, Sherry Niessen, Lianglin Zhang, Douglas Behenna, Martha A. Ornelas, Khanh T. Tran, Stephen Kaiser, Lawrence Lum, Al Stewart, Ketan S. Gajiwala
J Biol Chem. 2021 Jan-Jun; 296: 100251. Published online 2021 Jan 9. doi: 10.1074/jbc.RA120.016573
PMCID:
PMC7948648
AbstractArticlePDF–2.3M
15.
circ5615 functions as a ceRNA to promote colorectal cancer progression by upregulating TNKS
Zhifei Ma, Chencheng Han, Wenjia Xia, Siwei wang, Xiang Li, Panqi Fang, Rong Yin, Lin Xu, Liu Yang
Cell Death Dis. 2020 May; 11(5): 356. Published online 2020 May 11. doi: 10.1038/s41419-020-2514-0
PMCID:
PMC7214456
AbstractArticlePDF–2.5M
16.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
17.
Biological Functions of TNKS1 and Its Relationship with Wnt/β-Catenin Pathway in Astrocytoma
Min Chen, Bin Tang, Shenhao Xie, Jian Yan, Le Yang, Xinhui Zhou, Erming Zeng
Onco Targets Ther. 2019; 12: 10841–10850. Published online 2019 Dec 11. doi: 10.2147/OTT.S206142
PMCID:
PMC6912014
AbstractArticlePDF–7.1M
18.
Structural and functional analysis of parameters governing tankyrase-1 interaction with telomeric repeat-binding factor 1 and GDP-mannose 4,6-dehydratase
Travis Eisemann, Marie-France Langelier, John M. Pascal
J Biol Chem. 2019 Oct 4; 294(40): 14574–14590. Published online 2019 Aug 2. doi: 10.1074/jbc.RA119.009200
PMCID:
PMC6779445
AbstractArticlePDF–4.7M
19.
Tankyrase disrupts metabolic homeostasis and promotes tumorigenesis by inhibiting LKB1-AMPK signalling
Nan Li, Yifan Wang, Shinya Neri, Yuanli Zhen, Lon Wolf R. Fong, Yawei Qiao, Xu Li, Zhen Chen, Clifford Stephan, Weiye Deng, Rui Ye, Wen Jiang, Shuxing Zhang, Yonghao Yu, Mien-Chie Hung, Junjie Chen, Steven H. Lin
Nat Commun. 2019; 10: 4363. Published online 2019 Sep 25. doi: 10.1038/s41467-019-12377-1
PMCID:
PMC6761205
AbstractArticlePDF–2.2M
20.
Tankyrase Promotes Aerobic Glycolysis and Proliferation of Ovarian Cancer through Activation of Wnt/β-Catenin Signaling
Hong-Yi Yang, Jin-Xing Shen, Yi Wang, Yu Liu, Dong-Yan Shen, Song Quan
Biomed Res Int. 2019; 2019: 2686340. Published online 2019 Feb 20. doi: 10.1155/2019/2686340
PMCID:
PMC6402242
AbstractArticlePDF–5.1M

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