The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
KIBRA Regulates Hippo Signaling Activity via Interactions with Large Tumor Suppressor Kinases
Open accessAbstract
The Hippo pathway controls tissue growth and tumorigenesis by inhibiting cell proliferation and promoting apoptosis. Recent genetic studies in Drosophila identified Kibra as a novel regulator of Hippo signaling. Human KIBRA has been associated with memory performance and cell migration. However, it is unclear whether or how KIBRA is connected to the Hippo pathway in mammalian cells. Here, we show that KIBRA associates with and activates Lats (large tumor suppressor) 1 and 2 kinases by stimulating their phosphorylation on the hydrophobic motif. KIBRA overexpression stimulates the phosphorylation of Yes-associated protein (YAP), the Hippo pathway effector. Conversely, depletion of KIBRA by RNA interference reduces YAP phosphorylation. Furthermore, KIBRA stabilizes Lats2 by inhibiting its ubiquitination. We also found that KIBRA mRNA is induced by YAP overexpression in both murine and human cells, suggesting the evolutionary conservation of KIBRA as a transcriptional target of the Hippo signaling pathway. Thus, our study revealed a new connection between KIBRA and mammalian Hippo signaling.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“KIBRA can induce activation of LATS1/2 kinases and phosphorylation of the downstream effector YAP1 in the Hippo pathway (Xiao et al. 2011)”
From The Serine/Threonine Kinase NDR2 Regulates Integrin Signaling, Synapse Formation, and Synaptic Plasticity in the Hippocampus (2025) · cites this paper as Xiao et al. 2011
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Zhao, B., Wei, X., Li, W., Udan, R. S., Yang, Q., Kim, J., Xie, J., Ikenoue, T., Yu, J., Li, L., et al. (2007) · Genes & Development · doi:10.1101/gad.1602907 · Cited by 3,092
TEAD mediates YAP-dependent gene induction and growth control
Zhao, B., Ye, X., Yu, J., Li, L., Li, W., Li, S., Yu, J., Lin, J. D., Wang, C.-Y., Chinnaiyan, A. M., et al. (2008) · Genes & Development · doi:10.1101/gad.1664408 · Cited by 2,498
Elucidation of a universal size-control mechanism in Drosophila and mammals
Dong, J., Feldmann, G., Huang, J., Wu, S., Zhang, N., Comerford, S. A., Gayyed, M. F., Anders, R. A., Maitra, A., & Pan, D. (2007) · Cell · doi:10.1016/j.cell.2007.07.019 · Cited by 2,370
Self-citationThe Hippo Signaling Pathway in Development and Cancer
Pan, D. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.09.011 · Cited by 2,317
Huang, J., Wu, S., Barrera, J. A., Matthews, K. A., & Pan, D. (2005) · Cell · doi:10.1016/j.cell.2005.06.007 · Cited by 1,917
YAP1 increases organ size and expands undifferentiated progenitor cells
Camargo, F. D., Gokhale, S., Johnnidis, J. B., Fu, D., Bell, G. W., Jaenisch, R., & Brummelkamp, T. R. (2007) · Current Biology · doi:10.1016/j.cub.2007.10.039 · Cited by 1,252
The Hippo–YAP pathway in organ size control and tumorigenesis: an updated versionPreprint
Zhao, B., Li, L., Lei, Q., & Guan, K. (2010) · Genes & Development · doi:10.1101/gad.1909210 · Cited by 1,173
Wu, S., Huang, J., Dong, J., & Pan, D. (2003) · Cell · doi:10.1016/s0092-8674(03)00549-x · Cited by 1,120
Self-citationThe Drosophila Mst Ortholog, hippo, Restricts Growth and Cell Proliferation and Promotes Apoptosis
Harvey, K. F., Pfleger, C. M., & Hariharan, I. K. (2003) · Cell · doi:10.1016/s0092-8674(03)00557-9 · Cited by 1,007
Zhou, D., Conrad, C. H., Xia, F., Park, J.-S., Payer, B., Yin, Y., Lauwers, G. Y., Thasler, W. E., Lee, J. T., Avruch, J., et al. (2009) · Cancer Cell · doi:10.1016/j.ccr.2009.09.026 · Cited by 937
Research works printed but not linked: 1
- Schneider, 2010, Front. Aging. Neurosci., 2, 4
Cited by
Sorted by citations
The Biology of YAP/TAZ: Hippo Signaling and Beyond
Piccolo, S., Dupont, S., & Cordenonsi, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00005.2014 · Cited by 1,873
Yin, F., Yu, J., Zheng, Y., Chen, Q., Zhang, N., & Pan, D. (2013) · Cell · doi:10.1016/j.cell.2013.08.025 · Cited by 520
YAP1 Exerts Its Transcriptional Control via TEAD-Mediated Activation of Enhancers
Stein, C., Bardet, A. F., Roma, G., Bergling, S., Clay, I., Ruchti, A., Agarinis, C., Schmelzle, T., Bouwmeester, T., Schübeler, D., et al. (2015) · PLOS Genetics · doi:10.1371/journal.pgen.1005465 · Cited by 414
The LATS1 and LATS2 tumor suppressors: beyond the Hippo pathway
Furth, N., & Aylon, Y. (2017) · Cell Death and Differentiation · doi:10.1038/cdd.2017.99 · Cited by 262
KIBRA controls exosome secretion via inhibiting the proteasomal degradation of Rab27a
Song, L., Tang, S. H., Han, X., Jiang, Z., Dong, L., Liu, C., Liang, X., Dong, J., Qiu, C., Wang, Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09720-x · Cited by 249
Self-citationAngiomotin family proteins are novel activators of the LATS2 kinase tumor suppressor
Paramasivam, M., Sarkeshik, A., Yates, J. R., Fernandes, M. J., & McCollum, D. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-04-0300 · Cited by 216
The Hippo signaling pathway in development and regeneration
Zhong, Z., Jiao, Z., & Yu, F. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113926 · Cited by 223
PTPN14 interacts with and negatively regulates the oncogenic function of YAP
Liu, X., Yang, N., Figel, S. A., Wilson, K. E., Morrison, C. D., Gelman, I. H., & Zhang, J. (2013) · Oncogene · doi:10.1038/onc.2012.147 · Cited by 196
Rewiring cell polarity signaling in cancer
Halaoui, R., & McCaffrey, L. M. (2014) · Oncogene · doi:10.1038/onc.2014.59 · Cited by 183
The Hippo pathway and apico–basal cell polarity
Genevet, A., & Tapon, N. (2011) · Biochemical Journal · doi:10.1042/bj20110217 · Cited by 172
The Hippo pathway in normal development and cancer
Maugeri‐Saccà, M., & Maria, R. D. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2017.12.011 · Cited by 169
Zhang, L., Yang, S., Chen, X., Stauffer, S., Yu, F., Lele, S. M., Fu, K., Datta, K., Palermo, N. Y., Chen, Y., et al. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00102-15 · Cited by 162
Self-citationCellular Organization and Cytoskeletal Regulation of the Hippo Signaling Network
Sun, S., & Irvine, K. D. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.05.003 · Cited by 133
Stephens, R., Lim, K., Portela, M., Kvansakul, M., Humbert, P. O., & Richardson, H. E. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.01.011 · Cited by 132
Defining the Protein–Protein Interaction Network of the Human Hippo Pathway
Wang, W., Li, X., Huang, J., Feng, L., Dolinta, K., & Chen, J. (2013) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.030049 · Cited by 134
Integrating developmental signals: a Hippo in the (path)way
Mauviel, A., Nallet-Staub, F., & Varelas, X. (2011) · Oncogene · doi:10.1038/onc.2011.363 · Cited by 139
KIBRA exhibits MST-independent functional regulation of the Hippo signaling pathway in mammals
Moleirinho, S., Chang, N., Sims, A. H., Tilston-Lünel, A., Angus, L., Steele, A., Boswell, V., Barnett, S. C., Ormandy, C. J., Faratian, D., et al. (2012) · Oncogene · doi:10.1038/onc.2012.196 · Cited by 131
Yang, S., Zhang, L., Liu, M., Chong, R., Ding, S., Chen, Y., & Dong, J. (2013) · Cancer Research · doi:10.1158/0008-5472.can-13-2049 · Cited by 122
Self-citationThe Angiomotins – From discovery to function
Moleirinho, S., Guerrant, W., & Kissil, J. L. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.02.006 · Cited by 112
WWC proteins mediate LATS1/2 activation by Hippo kinases and imply a tumor suppression strategy
Qi, S., Zhu, Y., Liu, X., Li, P., Wang, Y., Zeng, Y. J., Yu, A., Wang, Y., Sha, Z., Zhong, Z., et al. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.03.027 · Cited by 122
Zyxin-Siah2–Lats2 axis mediates cooperation between Hippo and TGF-β signalling pathways
Ma, B., Cheng, H., Gao, R., Mu, C., Chen, L., Wu, S., Chen, Q., & Zhu, Y. (2016) · Nature Communications · doi:10.1038/ncomms11123 · Cited by 111
Multiphase coalescence mediates Hippo pathway activation
Wang, L., Choi, K., Su, T., Li, B., Wu, X., Zhang, R., Driskill, J. H., Li, H., Lei, H., Guo, P., et al. (2022) · Cell · doi:10.1016/j.cell.2022.09.036 · Cited by 109
Regulation and functions of mammalian LATS/NDR kinases: looking beyond canonical Hippo signalling
Hergovich, A. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-32 · Cited by 109
The mammalian Hippo pathway: regulation and function of YAP1 and TAZ
Kodaka, M., & Hata, Y. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1742-9 · Cited by 115
Yang, S., Zhang, L., Purohit, V., Shukla, S. K., Chen, X., Yu, F., Fu, K., Chen, Y., Solheim, J. C., Singh, P. K., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5935 · Cited by 106
Self-citationCoordinating developmental signaling: novel roles for the Hippo pathway
Varelas, X., & Wrana, J. L. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.10.002 · Cited by 109
Drosophila Pez Acts in Hippo Signaling to Restrict Intestinal Stem Cell Proliferation
Poernbacher, I., Baumgartner, R., Marada, S., Edwards, K. A., & Stocker, H. (2012) · Current Biology · doi:10.1016/j.cub.2012.01.019 · Cited by 99
Orr, B., & Compton, D. A. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00164 · Cited by 109
Hippo‐YAP signaling pathway: A new paradigm for cancer therapy
Ma, Y., Yang, Y., Wang, F., Wei, Q., & Qin, H. (2014) · International Journal of Cancer · doi:10.1002/ijc.29073 · Cited by 100
Wilson, K. E., Li, Y.-W., Yang, N., Shen, H., Orillion, A. R., & Zhang, J. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.534701 · Cited by 92
WWP1 E3 Ligase Targets LATS1 for Ubiquitin-Mediated Degradation in Breast Cancer Cells
Yeung, B., Ho, K. C., & Yang, X. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061027 · Cited by 90
Frassanito, M. A., Desantis, V., Marzo, L. D., Craparotta, I., Beltrame, L., Marchini, S., Annese, T., Visino, F., Arciuli, M., Saltarella, I., et al. (2018) · The Journal of Pathology · doi:10.1002/path.5187 · Cited by 91
NEDD4 E3 ligase inhibits the activity of the Hippo pathway by targeting LATS1 for degradation
Salah, Z., Cohen, S., Itzhaki, E., & Aqeilan, R. I. (2013) · Cell Cycle · doi:10.4161/cc.26672 · Cited by 89
The Hippo Signaling Pathway in Cancer: A Cell Cycle Perspective
Xiao, Y., & Dong, J. (2021) · Cancers · doi:10.3390/cancers13246214 · Cited by 84
Self-citationMokhtari, R. B., Ashayeri, N., Baghaie, L., Sambi, M., Satari, K., Baluch, N., Bosykh, D. A., Szewczuk, M. R., & Chakraborty, S. (2023) · Cancers · doi:10.3390/cancers15133468 · Cited by 92
Zhang, X., Liu, X., Luo, J., Xiao, W. L., Ye, X., Chen, M., Li, Y., & Zhang, G.-J. (2016) · Oncogenesis · doi:10.1038/oncsis.2016.67 · Cited by 84
Mammalian Hippo signalling: a kinase network regulated by protein–protein interactions
Hergovich, A. (2012) · Biochemical Society Transactions · doi:10.1042/bst20110619 · Cited by 82
WW domain interactions regulate the Hippo tumor suppressor pathway
Salah, Z., & Aqeilan, R. I. (2011) · Cell Death and Disease · doi:10.1038/cddis.2011.53 · Cited by 77
Han, Q., Lin, X., Zhang, X., Jiang, G., Zhang, Y., Miao, Y., Rong, X., Zheng, X., Han, Y., Han, X., et al. (2017) · The Journal of Pathology · doi:10.1002/path.4919 · Cited by 76
KIBRA (KIdney/BRAin protein) regulates learning and memory and stabilizes Protein kinase Mζ
Vogt-Eisele, A. K., Krüger, C., Duning, K., Weber, D., Spoelgen, R., Pitzer, C., Plaas, C., Eisenhardt, G., Meyer, A., Vogt, G., et al. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12480 · Cited by 71
Hippo signaling: A hub of growth control, tumor suppression and pluripotency maintenance
Yin, M.-X., & Zhang, L. (2011) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2011.09.009 · Cited by 70
Evolutionary and Molecular Facts Link the WWC Protein Family to Hippo Signaling
Wennmann, D. O., Schmitz, J., Wehr, M. C., Krahn, M. P., Koschmal, N., Gromnitza, S., Schulze, U., Weide, T., Chekuri, A., Skryabin, B. V., et al. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu115 · Cited by 66
Liu, Y., Lu, J., Zhang, Z., Zhu, L., Dong, S., Guo, G., Li, R., Yang, N., Yu, K., Zhong, Y., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.396 · Cited by 69
mRNA Expression in Papillary and Anaplastic Thyroid Carcinoma: Molecular Anatomy of a Killing Switch
Hébrant, A., Dom, G., Dewaele, M., Andry, G., Trésallet, C., Leteurtre, E., Dumont, J. E., & Maenhaut, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037807 · Cited by 67
Hippo pathway and breast cancer stem cells
Maugeri‐Saccà, M., & Maria, R. D. (2015) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2015.12.004 · Cited by 70
Song, H., Pu, J., Wang, L., Wu, L., Xiao, J., Liu, Q., Chen, J., Zhang, M., Liu, Y., Ni, M., et al. (2015) · Autophagy · doi:10.1080/15548627.2015.1060386 · Cited by 64
NEDD4 controls intestinal stem cell homeostasis by regulating the Hippo signalling pathway
Bae, S. J., Kim, M., Kim, S.-H., Kwon, Y. E., Lee, J.-H., Kim, J., Chung, C. H., Lee, W., & Seol, J. H. (2015) · Nature Communications · doi:10.1038/ncomms7314 · Cited by 66
Hippo signaling in mammalian stem cells
Tremblay, A., & Camargo, F. D. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.08.001 · Cited by 66
KIBRA: In the brain and beyond
Zhang, L., Yang, S., Wennmann, D. O., Chen, Y., Kremerskothen, J., & Dong, J. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.02.023 · Cited by 64
Self-citationThe expanding family of FERM proteins
Moleirinho, S., Tilston-Lünel, A., Angus, L., Gunn‐Moore, F. J., & Reynolds, P. A. (2013) · Biochemical Journal · doi:10.1042/bj20121642 · Cited by 68
KIBRA Protein Phosphorylation Is Regulated by Mitotic Kinase Aurora and Protein Phosphatase 1
Xiao, L., Chen, Y., Ji, M. H., Volle, D. J., Lewis, R. E., Tsai, M.-Y., & Dong, J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.246850 · Cited by 62
Self-citationZhou, J., Zeng, Y., Cui, L., Chen, X., Stauffer, S., Wang, Z., Yu, F., Lele, S. M., Talmon, G. A., Black, A. R., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800621115 · Cited by 61
Self-citationRegulators of mammalian Hippo pathway in cancer
Liu, A. M., Wong, K., Jiang, X., Qiao, Y., & Luk, J. M. (2012) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2012.05.006 · Cited by 61
Morgan, J. T., Murphy, C. J., & Russell, P. (2013) · Experimental Eye Research · doi:10.1016/j.exer.2013.06.012 · Cited by 61
YAP/TAZ in Bone and Cartilage Biology
Zarka, M., Haÿ, E., & Cohen-Solal, M. E. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.788773 · Cited by 64
Ajuba Phosphorylation by CDK1 Promotes Cell Proliferation and Tumorigenesis
Chen, X., Stauffer, S., Chen, Y., & Dong, J. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.722751 · Cited by 54
Self-citationKnight, J. F., Sung, V. Y. C., Kuzmin, E., Couzens, A. L., de Verteuil, D. A., Ratcliffe, C. D. H., Coelho, P. P., Johnson, R. M., Samavarchi‐Tehrani, P., Gruosso, T., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.02.095 · Cited by 54
CRB3 regulates contact inhibition by activating the Hippo pathway in mammary epithelial cells
Mao, X., Li, P., Wang, Y., Liang, Z., Liu, J., Li, J., Jiang, Y., Bao, G., Li, L., Zhu, B., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2016.478 · Cited by 52
Zhang, L., Iyer, J., Chowdhury, A., Ji, M. H., Xiao, L., Yang, S., Chen, Y., Tsai, M.-Y., & Dong, J. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.385518 · Cited by 52
Self-citationZhou, P.-J., Xue, W., Peng, J., Wang, Y., Wei, L., Yang, Z., Zhu, H. H., Fang, Y., & Gao, W. (2017) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-017-0609-y · Cited by 51
Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity
Lin, Z., Yang, Z., Xie, R., Ji, Z., Guan, K., & Zhang, M. (2019) · eLife · doi:10.7554/elife.49439 · Cited by 54
Targeting the Hippo pathway in heart repair
Meng, F., Xie, B., & Martin, J. F. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab291 · Cited by 52
Yang, S., Ji, M. H., Zhang, L., Chen, Y., Wennmann, D. O., Kremerskothen, J., & Dong, J. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.11.012 · Cited by 51
Self-citationGrieve, S., Hao, Y., & Yang, X. (2011) · Oncogene · doi:10.1038/onc.2011.318 · Cited by 51
Hermann, A., Wennmann, D. O., Gromnitza, S., Edeling, M., Marck, V. V., Sudol, M., Schaefer, L., Duning, K., Weide, T., Pavenstädt, H. J., et al. (2017) · Hepatology · doi:10.1002/hep.29647 · Cited by 50
Two Hippo signaling modules orchestrate liver size and tumorigenesis
Qi, S., Zhong, Z., Zhu, Y., Wang, Y., Ma, M., Wang, Y., Liu, X., Jin, R., Jiao, Z., Zhu, R., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2022112126 · Cited by 48
Interaction of the Hippo Pathway and Phosphatases in Tumorigenesis
Emami, S. S., Zhang, D., & Yang, X. (2020) · Cancers · doi:10.3390/cancers12092438 · Cited by 47
Tian, Y., Bachman, J. F., & Lai, Z.-C. (2014) · Protein & Cell · doi:10.1007/s13238-014-0122-4 · Cited by 46
Targeting the Hippo pathway: Clinical implications and therapeutics
Ye, S., & Eisinger‐Mathason, T. S. K. (2015) · Pharmacological Research · doi:10.1016/j.phrs.2015.11.025 · Cited by 46
Chen, N., Uddin, B., Voit, R., & Schiebel, E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1515605113 · Cited by 44
Stauffer, S., Zeng, Y., Zhou, J., Chen, X., Chen, Y., & Dong, J. (2017) · Cellular Signalling · doi:10.1016/j.cellsig.2017.08.001 · Cited by 43
Self-citationMukund, A. X., Tycko, J., Allen, S. J., Robinson, S. A., Andrews, C. J., Sinha, J., Ludwig, C., Spees, K., Bassik, M. C., & Bintu, L. (2023) · Cell Systems · doi:10.1016/j.cels.2023.07.001 · Cited by 41
WWC Proteins: Important Regulators of Hippo Signaling in Cancer
Höffken, V., Hermann, A., Pavenstädt, H. J., & Kremerskothen, J. (2021) · Cancers · doi:10.3390/cancers13020306 · Cited by 41
Phospho-regulation of KIBRA by CDK1 and CDC14 phosphatase controls cell-cycle progression
Ji, M. H., Yang, S., Chen, Y., Xiao, L., Zhang, L., & Dong, J. (2012) · Biochemical Journal · doi:10.1042/bj20120751 · Cited by 38
Self-citationThe Tumor Suppressor BAP1 Regulates the Hippo Pathway in Pancreatic Ductal Adenocarcinoma
Lee, H.-J., Pham, T., Chang, M. T., Barnes, D., Cai, A. G., Noubade, R., Tótpál, K., Chen, X., Tran, C., Hagenbeek, T. J., et al. (2020) · Cancer Research · doi:10.1158/0008-5472.can-19-1704 · Cited by 38
The Role of the Hippo Pathway in Melanocytes and Melanoma
Kim, J. E., Finlay, G. J., & Baguley, B. C. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00123 · Cited by 40
Zeng, Y., Stauffer, S., Zhou, J., Chen, X., Chen, Y., & Dong, J. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.796284 · Cited by 35
Self-citationYAP ping about and not forgetting TAZ
Callus, B. A., Finch‐Edmondson, M., Fletcher, S., & Wilton, S. D. (2018) · FEBS Letters · doi:10.1002/1873-3468.13318 · Cited by 37
The Role of Noncoding RNAs in the Regulation of Anoikis and Anchorage-Independent Growth in Cancer
Lee, H. Y., Son, S. W., Moeng, S., Choi, S. Y., & Park, J. K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020627 · Cited by 35
Yuan, T., Annamalai, K., Naik, S., Lupše, B., Geravandi, S., Pal, A., Dobrowolski, A., Ghawali, J., Ruhlandt, M., Gorrepati, K. D. D., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25145-x · Cited by 40
CDK1 phosphorylation of TAZ in mitosis inhibits its oncogenic activity
Zhang, L., Chen, X., Stauffer, S., Yang, S., Chen, Y., & Dong, J. (2015) · Oncotarget · doi:10.18632/oncotarget.5189 · Cited by 33
Self-citationKIBRA promotes prostate cancer cell proliferation and motility
Stauffer, S., Chen, X., Zhang, L., Chen, Y., & Dong, J. (2016) · FEBS Journal · doi:10.1111/febs.13718 · Cited by 32
Self-citationDeng, L., Jiang, L., Lin, X., Tseng, K., Lu, Z., & Wang, X. (2017) · Oncology Letters · doi:10.3892/ol.2017.5597 · Cited by 32
The Regulatory Role of KIBRA and PTPN14 in Hippo Signaling and Beyond
Wilson, K. E., Yang, N., Mussell, A. L., & Zhang, J. (2016) · Genes · doi:10.3390/genes7060023 · Cited by 32
Yang, S., Zhang, L., Chen, X., Chen, Y., & Dong, J. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.624411 · Cited by 31
Self-citationZhang, Y., Yan, S., Chen, J., Gan, C., Chen, D., Li, Y., Wen, J., Kremerskothen, J., Chen, S., Zhang, J., et al. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13281 · Cited by 31
WWC3 Inhibits Glioma Cell Proliferation Through Suppressing the Wnt/β-Catenin Signaling Pathway
Wang, Y., Jiang, M., Yao, Y., & Cai, Z. (2017) · DNA and Cell Biology · doi:10.1089/dna.2017.3931 · Cited by 30
Schelleckes, K., Schmitz, B., Ciarimboli, G., Lenders, M., Pavenstädt, H. J., Herrmann, E., Brand, S., & Brand, E. (2017) · Clinical Epigenetics · doi:10.1186/s13148-017-0415-6 · Cited by 31
The Regulation of the Hippo Pathway by Intercellular Junction Proteins
Ahmad, U. S., Uttagomol, J., & Wan, H. (2022) · Life · doi:10.3390/life12111792 · Cited by 30
Yoshihama, Y., Chida, K., & Ohno, S. (2012) · Communicative & Integrative Biology · doi:10.4161/cib.18849 · Cited by 29
Hippo Signaling Pathway as a Central Mediator of Receptors Tyrosine Kinases (RTKs) in Tumorigenesis
Azad, T., Rezaei, R., Surendran, A., Singaravelu, R., Boulton, S., Dave, J., Bell, J. C., & Ilkow, C. S. (2020) · Cancers · doi:10.3390/cancers12082042 · Cited by 29
G protein-coupled receptors: bridging the gap from the extracellular signals to the Hippo pathway
Zhou, X., Wang, Z., Huang, W., & Lei, Q. (2014) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmu108 · Cited by 28
Hippo Stabilises Its Adaptor Salvador by Antagonising the HECT Ubiquitin Ligase Herc4
Aerne, B. L., Gailite, I., Sims, D., & Tapon, N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0131113 · Cited by 27
Wasinski, B. D., Sohail, A., Bonfil, R. D., Kim, S., Saliganan, A. D., Polin, L., Bouhamdan, M., Kim, H.-R. C., Prunotto, M., & Fridman, R. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-59028-w · Cited by 28
Ubiquitin-Dependent Regulation of the Mammalian Hippo Pathway: Therapeutic Implications for Cancer
Nguyen, T., & Kugler, J. (2018) · Cancers · doi:10.3390/cancers10040121 · Cited by 24
Moleirinho, S., Calum, P., Tilston-Lünel, A., Higginson, J. R., Angus, L., Antkowiak, M. K., Barnett, S. C., Prystowsky, M. B., Reynolds, P. A., & Gunn‐Moore, F. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060028 · Cited by 26
Mechanical Properties of Glioblastoma: Perspectives for YAP/TAZ Signaling Pathway and Beyond
Pontes, B., & Mendes, F. A. (2023) · Diseases · doi:10.3390/diseases11020086 · Cited by 27
Transcriptomic and Epigenetic Analysis of Breast Cancer Stem Cells
Li, G., Wang, D., Ma, W., An, K., Liu, Z. Z., Wang, X., Yang, C., Du, F., Han, X., Chang, S., et al. (2018) · Epigenomics · doi:10.2217/epi-2018-0008 · Cited by 24
Stauffer, S., Zeng, Y., Santos, M., Zhou, J., Chen, Y., & Dong, J. (2019) · Journal of Cell Science · doi:10.1242/jcs.236000 · Cited by 25
Self-citationMendoza, M. L., Quigley, L. D., Dunham, T., & Volk, L. J. (2022) · iScience · doi:10.1016/j.isci.2022.105623 · Cited by 21
Metadata
- Authors
- Xiao, L., Chen, Y., Ji, M., & Dong, J.
- Affiliations
- University of Nebraska Medical Center (US)
- Corresponding author
- Ji, Ming
- Dong, Jixin
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2011-03
- Volume
- 286
- Issue
- 10
- Pages
- 7788-7796
- ISSN
- 0021-9258 (ISSN-L)
- PMC
- PMC3048666
- OpenAlex
- W2000662094
- Cited by
- 190
- References
- 47
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 7 · 2023: 12 · 2022: 13 · 2021: 14 · 2020: 12 · 2019: 11 · 2018: 14 · 2017: 17 · 2016: 11 · 2015: 14 · 2014: 13 · 2013: 19 · 2012: 11
- FWCI
- 7.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Health and Human Services
- University of Nebraska Medical Center
- Johns Hopkins University
- Nebraska Department of Health and Human Services
- National Institutes of Health
- National Center for Research Resources (5P20-RR018759-07, P20RR018759)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hippo pathway signaling and YAP/TAZ
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Keywords
- KIBRA, Hippo signaling pathway, LATS1, LATS2, YAP, YAP phosphorylation, hydrophobic motif, kinase activation, ubiquitination, protein stability, transcriptional regulation, cell proliferation, apoptosis, tissue growth, carcinogenesis
- MeSH terms
- YAP-Signaling Proteins, Animals, Carrier Proteins, Drosophila melanogaster, Humans, Phosphoproteins, Phosphorylation, Proteins, Transcription Factors, Signal Transduction, Protein Serine-Threonine Kinases, Amino Acid Motifs, Tumor Suppressor Proteins, Cell Line, Tumor, Intracellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, Mice, Ubiquitination, HEK293 Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review