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The Role of WAVE2 Signaling in Cancer
Open accessAbstract
The Wiskott-Aldrich syndrome protein (WASP) and WASP family verprolin-homologous protein (WAVE)-WAVE1, WAVE2 and WAVE3 regulate rapid reorganization of cortical actin filaments and have been shown to form a key link between small GTPases and the actin cytoskeleton. Upon receiving upstream signals from Rho-family GTPases, the WASP and WAVE family proteins play a significant role in polymerization of actin cytoskeleton through activation of actin-related protein 2/3 complex (Arp2/3). The Arp2/3 complex, once activated, forms actin-based membrane protrusions essential for cell migration and cancer cell invasion. Thus, by activation of Arp2/3 complex, the WAVE and WASP family proteins, as part of the WAVE regulatory complex (WRC), have been shown to play a critical role in cancer cell invasion and metastasis, drawing significant research interest over recent years. Several studies have highlighted the potential for targeting the genes encoding either part of or a complete protein from the WASP/WAVE family as therapeutic strategies for preventing the invasion and metastasis of cancer cells. WAVE2 is well documented to be associated with the pathogenesis of several human cancers, including lung, liver, pancreatic, prostate, colorectal and breast cancer, as well as other hematologic malignancies. This review focuses mainly on the role of WAVE2 in the development, invasion and metastasis of different types of cancer. This review also summarizes the molecular mechanisms that regulate the activity of WAVE2, as well as those oncogenic pathways that are regulated by WAVE2 to promote the cancer phenotype. Finally, we discuss potential therapeutic strategies that target WAVE2 or the WAVE regulatory complex, aimed at preventing or inhibiting cancer invasion and metastasis.
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“The seven subunit ARP2/3 complex is responsible for creating branched actin networks through polymerization of actin”
From SHARPIN S146 phosphorylation mediates ARP2/3 interaction, cancer cell invasion and metastasis (2022) · cites this paper as Rana, Alkrekshi et al., 2021
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Yeatman, T. J. (2004) · Nature Reviews Cancer · doi:10.1038/nrc1366 · Cited by 1,113
Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck
Eden, S., Rohatgi, R., Podtelejnikov, A. V., Mann, M., & Kirschner, M. W. (2002) · Nature · doi:10.1038/nature00859 · Cited by 835
Takenawa, T., & Miki, H. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.10.1801 · Cited by 604
Structure and control of the actin regulatory WAVE complex
Chen, Z., Borek, D., Padrick, S. B., Gomez, T. S., Metlagel, Z., Ismail, A. M., Umetani, J., Billadeau, D. D., Otwinowski, Z., & Rosen, M. K. (2010) · Nature · doi:10.1038/nature09623 · Cited by 500
Kunda, P., Craig, G., Dominguez, V., & Baum, B. (2003) · Current Biology · doi:10.1016/j.cub.2003.10.005 · Cited by 341
Interaction of WASP/Scar proteins with actin and vertebrate Arp2/3 complex
Marchand, J.-B., Kaiser, D. A., Pollard, T. D., & Higgs, H. N. (2001) · Nature Cell Biology · doi:10.1038/35050590 · Cited by 331
Flagged first, then by citations
Research works printed but not linked: 130
- Rana, P.S., Kurokawa, M., and Model, M.A. (2020). Evidence for macromolecular crowding as a direct apoptotic stimulus. J. Cell Sci., 133. · DOI
- Rana, 2020, A Reverse-Osmosis Model of Apoptotic Shrinkage, Front. Cell Dev. Biol., 8, 588721, 10.3389/fcell.2020.588721 · DOI
- Tarin, 2011, Cell and tissue interactions in carcinogenesis and metastasis and their clinical significance, Semin. Cancer Biol., 21, 72, 10.1016/j.semcancer.2010.12.006 · DOI
- Chambers, 2002, Dissemination and growth of cancer cells in metastatic sites, Nat. Rev. Cancer, 2, 563, 10.1038/nrc865 · DOI
- Fidler, 2003, The pathogenesis of cancer metastasis: The “seed and soil” hypothesis revisited, Nat. Rev. Cancer, 3, 453, 10.1038/nrc1098 · DOI · Paper page
- Welch, 2019, Defining the Hallmarks of Metastasis, Cancer Res., 79, 3011, 10.1158/0008-5472.CAN-19-0458 · DOI
- Friedl, 2010, Plasticity of cell migration: A multiscale tuning model, J. Cell Biol., 188, 11, 10.1083/jcb.200909003 · DOI
- Polacheck, 2012, Tumor cell migration in complex microenvironments, Cell. Mol. Life Sci., 70, 1335, 10.1007/s00018-012-1115-1 · DOI
- Yamaguchi, 2007, Regulation of the actin cytoskeleton in cancer cell migration and invasion, Biochim. Biophys. Acta, 1773, 642, 10.1016/j.bbamcr.2006.07.001 · DOI
- Mullins, 1996, Actin’ like actin?, Trends Cell Biol., 6, 208, 10.1016/0962-8924(96)20017-0 · DOI
- Welch, 1997, The human Arp2/3 complex is composed of evolutionarily conserved subunits and is localized to cellular regions of dynamic actin filament assembly, J. Cell Biol., 138, 375, 10.1083/jcb.138.2.375 · DOI
- Blundell, 2010, The Wiskott-Aldrich syndrome: The actin cytoskeleton and immune cell function, Dis. Markers, 29, 157, 10.1155/2010/781523 · DOI
- Blanchoin, 2000, Direct observation of dendritic actin filament networks nucleated by Arp2/3 complex and WASP/Scar proteins, Nat. Cell Biol., 404, 1007
- Machesky, 1999, Scar, a WASp-related protein, activates nucleation of actin filaments by the Arp2/3 complex, Proc. Natl. Acad. Sci. USA, 96, 3739, 10.1073/pnas.96.7.3739 · DOI · Paper page
- Mullins, 1998, The interaction of Arp2/3 complex with actin: Nucleation, high affinity pointed end capping, and formation of branching networks of filaments, Proc. Natl. Acad. Sci. USA, 95, 6181, 10.1073/pnas.95.11.6181 · DOI
- Welch, 2002, Cellular control of actin nucleation, Annu. Rev. Cell Dev. Biol., 18, 247, 10.1146/annurev.cellbio.18.040202.112133 · DOI
- Padrick, 2010, Physical mechanisms of signal integration by WASP family proteins, Annu. Rev. Biochem., 79, 707, 10.1146/annurev.biochem.77.060407.135452 · DOI
- Paunola, 2002, WH2 domain: A small, versatile adapter for actin monomers, FEBS Lett., 513, 92, 10.1016/S0014-5793(01)03242-2 · DOI
- Miki, 1998, WAVE, a novel WASP-family protein involved in actin reorganization induced by Rac, EMBO J., 17, 6932, 10.1093/emboj/17.23.6932 · DOI
- Kelly, 2006, Actin binding to the central domain of WASP/Scar proteins plays a critical role in the activation of the Arp2/3 complex, J. Biol. Chem., 281, 10589, 10.1074/jbc.M507470200 · DOI
- Kurisu, 2009, The WASP and WAVE family proteins, Genome Biol., 10, 226, 10.1186/gb-2009-10-6-226 · DOI
- Stradal, 2004, Regulation of actin dynamics by WASP and WAVE family proteins, Trends Cell Biol., 14, 303, 10.1016/j.tcb.2004.04.007 · DOI · Paper page
- Millard, 2004, Signalling to actin assembly via the WASP (Wiskott-Aldrich syndrome protein)-family proteins and the Arp2/3 complex, Biochem. J., 380, 1, 10.1042/bj20040176 · DOI
- Miki, 1996, N-WASP, a novel actin-depolymerizing protein, regulates the cortical cytoskeletal rearrangement in a PIP2-dependent manner downstream of tyrosine kinases, EMBO J., 15, 5326, 10.1002/j.1460-2075.1996.tb00917.x · DOI
- Massaad, 2013, Wiskott-Aldrich syndrome: A comprehensive review, Ann. N. Y. Acad. Sci., 1285, 26, 10.1111/nyas.12049 · DOI
- Tsuboi, 2006, Wiskott–Aldrich syndrome protein is involved in αIIbβ3-mediated cell adhesion, EMBO Rep., 7, 506, 10.1038/sj.embor.7400665 · DOI
- Semple, 1997, Flow cytometric analysis of platelets from childrenwith the Wiskott-Aldrich syndrome reveals defects in platelet development, activation and structure, Br. J. Haematol., 97, 747, 10.1046/j.1365-2141.1997.1132938.x · DOI
- Baldini, 1972, Nature of the platelet DEFECT in the Wiskott-Aldrich Syndrome, Ann. N. Y. Acad. Sci., 201, 437, 10.1111/j.1749-6632.1972.tb16316.x · DOI
- Hovig, 1969, Wiskott—Aldrich Syndrome: Qualitative Platelet Defects and Short Platelet Survival, Br. J. Haematol., 17, 373, 10.1111/j.1365-2141.1969.tb01383.x · DOI
- Shcherbina, 1999, WASP levels in platelets and lymphocytes of wiskott-aldrich syndrome patients correlate with cell dysfunction, J. Immunol., 163, 6314, 10.4049/jimmunol.163.11.6314 · DOI
- Prislovsky, 2013, Platelets from WAS patients show an increased susceptibility toex vivophagocytosis, Platelets, 24, 288, 10.3109/09537104.2012.693991 · DOI
- Marathe, 2009, Antiplatelet antibodies in WASP (-) mice correlate with evidence of increased in vivo platelet consumption, Exp. Hematol., 37, 1353, 10.1016/j.exphem.2009.08.007 · DOI
- Prislovsky, 2008, Rapid platelet turnover in WASP (-) mice correlates with increased ex vivo phagocytosis of opsonized WASP (-) platelets, Exp. Hematol., 36, 609, 10.1016/j.exphem.2007.12.019 · DOI
- Rottner, 2017, Actin assembly mechanisms at a glance, J. Cell Sci., 130, 3427, 10.1242/jcs.206433 · DOI
- Lebensohn, 2009, Activation of the WAVE Complex by Coincident Signals Controls Actin Assembly, Mol. Cell, 36, 512, 10.1016/j.molcel.2009.10.024 · DOI · Paper page
- Suetsugu, 2006, Optimization of WAVE2 complex–induced actin polymerization by membrane-bound IRSp53, PIP3, and Rac, J. Cell Biol., 173, 571, 10.1083/jcb.200509067 · DOI
- Miki, 2000, IRSp53 is an essential intermediate between Rac and WAVE in the regulation of membrane ruffling, Nat. Cell Biol., 408, 732
- Dahl, 2003, Characterization of the WAVE1 Knock-Out Mouse: Implications for CNS Development, J. Neurosci., 23, 3343, 10.1523/JNEUROSCI.23-08-03343.2003 · DOI · Paper page
- Yan, 2003, WAVE2 deficiency reveals distinct roles in embryogenesis and Rac-mediated actin-based motility, EMBO J., 22, 3602, 10.1093/emboj/cdg350 · DOI · Paper page
- Qin, 2019, Wasf3 Deficiency Reveals Involvement in Metastasis in a Mouse Model of Breast Cancer, Am. J. Pathol., 189, 2450, 10.1016/j.ajpath.2019.08.012 · DOI
- Innocenti, 2004, Abi1 is essential for the formation and activation of a WAVE2 signalling complex, Nat. Cell Biol., 6, 319, 10.1038/ncb1105 · DOI
- Mendoza, M.C. (2013). Phosphoregulation of the WAVE regulatory complex and signal integration. Seminars in Cell & Developmental Biology, Academic Press. · DOI · Paper page
- Campellone, 2010, A nucleator arms race: Cellular control of actin assembly, Nat. Rev. Mol. Cell Biol., 11, 237, 10.1038/nrm2867 · DOI
- Pollard, 2007, Regulation of actin filament assembly by Arp2/3 complex and formins, Annu. Rev. Biophys. Biomol. Struct., 36, 451, 10.1146/annurev.biophys.35.040405.101936 · DOI
- Chen, 2017, Rac1 GTPase activates the WAVE regulatory complex through two distinct binding sites, eLife, 6, e29795, 10.7554/eLife.29795 · DOI · Paper page
- Takahashi, 2010, WAVE2 targeting to phosphatidylinositol 3,4,5-triphosphate mediated by insulin receptor substrate p53 through a complex with WAVE, Cell. Signal., 22, 1708, 10.1016/j.cellsig.2010.06.011 · DOI
- Oikawa, 2004, PtdIns(3,4,5)P3 binding is necessary for WAVE2-induced formation of lamellipodia, Nat. Cell Biol., 6, 420, 10.1038/ncb1125 · DOI · Paper page
- Head, 2003, Genomic organization and expression profile of the human and mouse WAVE gene family, Mamm. Genome, 14, 314, 10.1007/s00335-002-2247-7 · DOI · Paper page
- 2012, Surfing the big WAVE: Insights into the role of WAVE3 as a driving force in cancer progression and metastasis, Semin. Cell Dev. Biol., 24, 287
- Kurisu, 2004, Rac-WAVE2 signaling is involved in the invasive and metastatic phenotypes of murine melanoma cells, Oncogene, 24, 1309, 10.1038/sj.onc.1208177 · DOI
- Ranalli, 2005, WAVE3 promotes cell motility and invasion through the regulation of MMP-1, MMP-3, and MMP-9 expression, Exp. Cell Res., 308, 135, 10.1016/j.yexcr.2005.04.011 · DOI
- Wang, 2020, WAVE3 phosphorylation regulates the interplay between PI3K, TGF-β, and EGF signaling pathways in breast cancer, Oncogenesis, 9, 1, 10.1038/s41389-020-00272-0 · DOI
- Siegel, 2021, Cancer Statistics, CA Cancer J. Clin., 71, 7, 10.3322/caac.21654 · DOI · Paper page
- Park, 2016, TGFβ1-Mediated SMAD3 Enhances PD-1 Expression on Antigen-Specific T Cells in Cancer, Cancer Discov., 6, 1366, 10.1158/2159-8290.CD-15-1347 · DOI · Paper page
- Xing, 2017, Dicer suppresses cytoskeleton remodeling and tumorigenesis of colorectal epithelium by miR-324-5p mediated suppression of HMGXB3 and WASF-2, Oncotarget, 8, 55776, 10.18632/oncotarget.18218 · DOI
- Iwaya, 2007, Correlation between liver metastasis of the colocalization of actin-related protein 2 and 3 complex and WAVE2 in colorectal carcinoma, Cancer Sci., 98, 992, 10.1111/j.1349-7006.2007.00488.x · DOI · Paper page
- Tan, 2020, WAVE2 Enhanced Hepatic Stellate Cells Activity in Colorectal Liver Metastases, Cancer Manag. Res., 12, 7671, 10.2147/CMAR.S259125 · DOI
- Li, 2021, Abelson interactor 1 splice isoform-L plays an anti-oncogenic role in colorectal carcinoma through interactions with WAVE2 and full-length Abelson interactor 1, World J. Gastroenterol., 27, 1595, 10.3748/wjg.v27.i15.1595 · DOI
- Wang, 2018, SH3BP1-induced Rac-Wave2 pathway activation regulates cervical cancer cell migration, invasion, and chemoresistance to cisplatin, J. Cell. Biochem., 119, 1733, 10.1002/jcb.26334 · DOI
- Taniuchi, 2018, WAVE2 is associated with poor prognosis in pancreatic cancers and promotes cell motility and invasiveness via binding to ACTN4, Cancer Med., 7, 5733, 10.1002/cam4.1837 · DOI
- Taniuchi, 2019, Efficient delivery of small interfering RNAs targeting particular mRNAs into pancreatic cancer cells inhibits invasiveness and metastasis of pancreatic tumors, Oncotarget, 10, 2869, 10.18632/oncotarget.26880 · DOI
- Kitagawa, 2019, Circulating pancreatic cancer exosomal RNA s for detection of pancreatic cancer, Mol. Oncol., 13, 212, 10.1002/1878-0261.12398 · DOI
- Kato, T., Kawai, K., Egami, Y., Kakehi, Y., and Araki, N. (2014). Rac1-dependent lamellipodial motility in prostate cancer PC-3 cells revealed by Optogenetic control of rac1 activity. PLoS ONE, 9. · DOI
- Sung, 2021, Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries, CA Cancer J. Clin., 71, 209, 10.3322/caac.21660 · DOI · Paper page
- Thike, 2009, Triple-negative breast cancer: Clinicopathological characteristics and relationship with basal-like breast cancer, Mod. Pathol., 23, 123, 10.1038/modpathol.2009.145 · DOI
- Welch, 1997, Actin polymerization is induced by Arp 2/3 protein complex at the surface of Listeria monocytogenes, Nat. Cell Biol., 385, 265
- Machesky, 1994, Purification of a cortical complex containing two unconventional actins from Acanthamoeba by affinity chromatography on profilin-agarose, J. Cell Biol., 127, 107, 10.1083/jcb.127.1.107 · DOI
- Ko, 2014, Urokinase-type plasminogen activator expression and Rac1/WAVE-2/Arp2/3 pathway are blocked by pterostilbene to suppress cell migration and invasion in MDA-MB-231 cells, Bioorg. Med. Chem. Lett., 24, 1176, 10.1016/j.bmcl.2013.12.115 · DOI
- Bryce, N.S., Reynolds, A.B., Koleske, A.J., and Weaver, A.M. (2013). WAVE2 Regulates Epithelial Morphology and Cadherin Isoform Switching through Regulation of Twist and Abl. PLoS ONE, 8. · DOI
- Takahashi, 2011, WAVE2, N-WASP, and mena facilitate cell invasion via phosphatidylinositol 3-kinase-dependent local accumulation of actin filaments, J. Cell. Biochem., 112, 3421, 10.1002/jcb.23276 · DOI
- Yokotsuka, 2010, Overexpression of HER2 signaling to WAVE2–Arp2/3 complex activates MMP-independent migration in breast cancer, Breast Cancer Res. Treat., 126, 311, 10.1007/s10549-010-0896-x · DOI
- Yamazaki, 2003, WAVE2 is required for directed cell migration and cardiovascular development, Nat. Cell Biol., 424, 452
- Suetsugu, 2003, Differential roles of WAVE1 and WAVE2 in dorsal and peripheral ruffle formation for fibroblast cell migration, Dev. Cell, 5, 595, 10.1016/S1534-5807(03)00297-1 · DOI
- Yeh, 1996, Characterization and cloning of a 58/53-kDa substrate of the insulin receptor tyrosine kinase, J. Biol. Chem., 271, 2921, 10.1074/jbc.271.6.2921 · DOI
- Zhao, 2011, I-BAR domain proteins: Linking actin and plasma membrane dynamics, Curr. Opin. Cell Biol., 23, 14, 10.1016/j.ceb.2010.10.005 · DOI
- Mattila, 2007, Missing-in-metastasis and IRSp53 deform PI(4,5)P2-rich membranes by an inverse BAR domain–like mechanism, J. Cell Biol., 176, 953, 10.1083/jcb.200609176 · DOI
- Ismail, 2009, The WAVE regulatory complex is inhibited, Nat. Struct. Mol. Biol., 16, 561, 10.1038/nsmb.1587 · DOI
- Takahashi, 2012, WAVE2 protein complex coupled to membrane and microtubules, J. Oncol., 2012, 1, 10.1155/2012/590531 · DOI
- Yuan, 2008, PI3K pathway alterations in cancer: Variations on a theme, Oncogene, 27, 5497, 10.1038/onc.2008.245 · DOI · Paper page
- Vuori, 2007, GEF what? Dock180 and related proteins help Rac to polarize cells in new ways, Trends Cell Biol., 17, 383, 10.1016/j.tcb.2007.05.001 · DOI
- Rossman, 2005, GEF means go: Turning on RHO GTPases with guanine nucleotide-exchange factors, Nat. Rev. Mol. Cell Biol., 6, 167, 10.1038/nrm1587 · DOI · Paper page
- Leng, 2005, Abelson-interactor-1 promotes WAVE2 membrane translocation and Abelson-mediated tyrosine phosphorylation required for WAVE2 activation, Proc. Natl. Acad. Sci. USA, 102, 1098, 10.1073/pnas.0409120102 · DOI · Paper page
- Salgia, 1997, BCR/ABL induces multiple abnormalities of cytoskeletal function, J. Clin. Investig., 100, 46, 10.1172/JCI119520 · DOI
- Huang, 2008, The c-Abl tyrosine kinase regulates actin remodeling at the immune synapse, Blood, 112, 111, 10.1182/blood-2007-10-118232 · DOI
- 1999, Cycling, stressed-out and nervous: Cellular functions of c-Abl, Trends Cell Biol., 9, 179, 10.1016/S0962-8924(99)01549-4 · DOI
- Zhuang, 2011, CDK1-mediated phosphorylation of abi1 attenuates Bcr-Abl-induced F-actin assembly and tyrosine phosphorylation of WAVE complex during mitosis, J. Biol. Chem., 286, 38614, 10.1074/jbc.M111.281139 · DOI
- Stuart, 2006, c-Abl interacts with the WAVE2 signaling complex to induce membrane ruffling and cell spreading, J. Biol. Chem., 281, 31290, 10.1016/S0021-9258(19)84041-3 · DOI
- Li, 2007, Bcr-Abl induces abnormal cytoskeleton remodeling, β1 integrin clustering and increased cell adhesion to fibronectin through the Abl interactor 1 pathway, J. Cell Sci., 120, 1436, 10.1242/jcs.03430 · DOI
- Ardern, 2006, Src-dependent phosphorylation of Scar1 promotes its association with the Arp2/3 complex, Cell Motil. Cytoskelet., 63, 6, 10.1002/cm.20101 · DOI
- Frame, 2002, Src in cancer: Deregulation and consequences for cell behaviour, Biochim. Biophys. Acta, 1602, 114
- Guarino, 2010, Src signaling in cancer invasion, J. Cell. Physiol., 223, 14, 10.1002/jcp.22011 · DOI
- Miyamoto, 2008, Cdk5 phosphorylation of WAVE2 regulates oligodendrocyte precursor cell migration through nonreceptor tyrosine kinase fyn, J. Neurosci., 28, 8326, 10.1523/JNEUROSCI.1482-08.2008 · DOI · Paper page
- Ortega, C.E., Seidner, Y., and Dominguez, I. (2014). Mining CK2 in cancer. PLoS ONE, 9. · DOI
- Pocha, 2009, WAVE2 is regulated by multiple phosphorylation events within its VCA domain, Cell Motil. Cytoskelet., 66, 36, 10.1002/cm.20323 · DOI · Paper page
- Ura, 2012, Pseudopod growth and evolution during cell movement is controlled through SCAR/WAVE dephosphorylation, Curr. Biol., 22, 553, 10.1016/j.cub.2012.02.020 · DOI · Paper page
- Danson, 2007, Phosphorylation of WAVE2 by MAP kinases regulates persistent cell migration and polarity, J. Cell Sci., 120, 4144, 10.1242/jcs.013714 · DOI · Paper page
- Mendoza, 2011, ERK-MAPK Drives Lamellipodia Protrusion by Activating the WAVE2 Regulatory Complex, Mol. Cell, 41, 661, 10.1016/j.molcel.2011.02.031 · DOI · Paper page
- Nakanishi, 2006, Effect of WAVE2 phosphorylation on activation of the Arp2/3 complex, J. Biochem., 141, 319, 10.1093/jb/mvm034 · DOI · Paper page
- Ceglia, 2010, Signaling pathways controlling the phosphorylation state of WAVE1, a regulator of actin polymerization, J. Neurochem., 114, 182, 10.1111/j.1471-4159.2010.06743.x · DOI · Paper page
- Yamashita, 2011, WAVE2 forms a complex with PKA and is involved in PKA enhancement of membrane protrusions, J. Biol. Chem., 286, 3907, 10.1074/jbc.M110.145409 · DOI
- Westphal, 2000, Scar/WAVE-1, a Wiskott-Aldrich syndrome protein, assembles an actin-associated multi-kinase scaffold, EMBO J., 19, 4589, 10.1093/emboj/19.17.4589 · DOI · Paper page
- Hao, 2019, Expression of miR-335 in triple-negative breast cancer and its effect on chemosensitivity, J. Buon, 24, 1526
- Wang, 2014, miR-206 inhibits cell migration through direct targeting of the actin-binding protein Coronin 1C in triple-negative breast cancer, Mol. Oncol., 8, 1690, 10.1016/j.molonc.2014.07.006 · DOI
- Damiano, 2017, Epigenetic silencing of miR-200c in breast cancer is associated with aggressiveness and is modulated by ZEB1, Genes Chromosom. Cancer, 56, 147, 10.1002/gcc.22422 · DOI
- Meng, 2020, miR-200c/PAI-2 promotes the progression of triple negative breast cancer via M1/M2 polarization induction of macrophage, Int. Immunopharmacol., 81, 106028, 10.1016/j.intimp.2019.106028 · DOI
- Han, 2019, The microRNA miR-181c enhances chemosensitivity and reduces chemoresistance in breast cancer cells via down-regulating osteopontin, Int. J. Biol. Macromol., 125, 544, 10.1016/j.ijbiomac.2018.12.075 · DOI
- Hong, 2019, MicroRNA-126-3p inhibits the proliferation, migration, invasion, and angiogenesis of triple-negative breast cancer cells by targeting RGS3, Oncol. Rep., 42, 1569
- Yu, 2019, MiR-140-5p inhibits cell proliferation and metastasis by regulating MUC1 via BCL2A1/MAPK pathway in triple negative breast cancer, Cell Cycle, 18, 2641, 10.1080/15384101.2019.1653107 · DOI
- Weihua, 2020, MiR-33a functions as a tumor suppressor in triple-negative breast cancer by targeting EZH2, Cancer Cell Int., 20, 1, 10.1186/s12935-020-1160-z · DOI
- Kawaguchi, 2017, Overexpression of suppressive microRNAs, miR-30a and miR-200c are associated with improved survival of breast cancer patients, Sci. Rep., 7, 15945, 10.1038/s41598-017-16112-y · DOI
- Derivery, E., Fink, J., Martin, D., Houdusse, A., Piel, M., Stradal, T.E., Louvard, D., and Gautreau, A. (2008). Free Brick1 is a trimeric precursor in the assembly of a functional wave complex. PLoS ONE, 3. · DOI
- Escobar, 2010, Brick1 is an essential regulator of actin cytoskeleton required for embryonic development and cell transformation, Cancer Res., 70, 9349, 10.1158/0008-5472.CAN-09-4491 · DOI
- Cai, 2009, Metastatic potential of lung squamous cell carcinoma associated with HSPC300 through its interaction with WAVE2, Lung Cancer, 65, 299, 10.1016/j.lungcan.2009.06.001 · DOI
- Wang, 2018, MiR-133b targets Sox9 to control pathogenesis and metastasis of breast cancer, Cell Death Dis., 9, 752, 10.1038/s41419-018-0715-6 · DOI
- Takenawa, 2007, The WASP-WAVE protein network: Connecting the membrane to the cytoskeleton, Nat. Rev. Mol. Cell. Biol., 8, 37, 10.1038/nrm2069 · DOI · Paper page
- Insall, 2009, Actin Dynamics at the Leading Edge: From Simple Machinery to Complex Networks, Dev. Cell, 17, 310, 10.1016/j.devcel.2009.08.012 · DOI
- Derivery, 2010, Generation of branched actin networks: Assembly and regulation of the N-WASP and WAVE molecular machines, Bioessays, 32, 119, 10.1002/bies.200900123 · DOI
- Bellacosa, 2005, Activation of AKT kinases in cancer: Implications for therapeutic targeting, Adv. Cancer Res., 94, 29, 10.1016/S0065-230X(05)94002-5 · DOI
- Liu, 2018, Satb1 promotes Schwann cell viability and migration via activation of PI3K/AKT pathway, Eur. Rev. Med. Pharmacol. Sci., 22, 4268
- Moraes, 2017, ABI3, a component of the WAVE2 complex, is potentially regulated by PI3K/AKT pathway, Oncotarget, 8, 67769, 10.18632/oncotarget.18840 · DOI · Paper page
- Tian, 2009, The TGFβ paradox in human cancer: An update, Future Oncol., 5, 259, 10.2217/14796694.5.2.259 · DOI
- Ferrari, 2009, Transforming growth factor-beta 1 (TGF-β1) induces angiogenesis through vascular endothelial growth factor (VEGF)-mediated apoptosis, J. Cell. Physiol., 219, 449, 10.1002/jcp.21706 · DOI
- Carmeliet, 2005, VEGF as a key mediator of angiogenesis in cancer, Oncology, 69, 4, 10.1159/000088478 · DOI
- Tao, 2016, SH3-domain binding protein 1 in the tumor microenvironment promotes hepatocellular carcinoma metastasis through WAVE2 pathway, Oncotarget, 7, 18356, 10.18632/oncotarget.7786 · DOI
- Holmqvist, 2004, The adaptor protein Shb binds to tyrosine 1175 in vascular endothelial growth factor (VEGF) receptor-2 and regulates VEGF-dependent cellular migration, J. Biol. Chem., 279, 22267, 10.1074/jbc.M312729200 · DOI
- Kim, 2014, Rhapontigenin suppresses cell migration and invasion by inhibiting the PI3K-dependent Rac1 signaling pathway in MDA-MB-231 human breast cancer cells, J. Nat. Prod., 77, 1135, 10.1021/np401078g · DOI
- Wewer, 2012, Regulation of ROCK Activity in Cancer, J. Histochem. Cytochem., 61, 185
- Gadea, 2008, Rac Activation and Inactivation Control Plasticity of Tumor Cell Movement, Cell, 135, 510, 10.1016/j.cell.2008.09.043 · DOI
- Uehata, 1997, Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension, Nat. Cell Biol., 389, 990
- Asano, 1987, Mechanism of action of a novel antivasospasm drug, HA1077, J. Pharmacol. Exp. Ther., 241, 1033
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- Rana, P. S., Alkrekshi, A., Wang, W., Markovic, V., & Sossey-Alaoui, K.
- Affiliations
- MetroHealth Medical Center (US)
- MetroHealth Medical Center, Cleveland, OH 44109, USA
- Department of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA
- Venue
- Biomedicines
- Publisher
- MDPI AG
- Published
- 2021-09-14
- Volume
- 9
- Issue
- 9
- Pages
- 1217
- ISSN
- 2227-9059 (ISSN-L)
- PMC
- PMC8464821
- OpenAlex
- W3199192392
- Cited by
- 25
- References
- 6
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 4 · 2023: 10 · 2022: 2
- FWCI
- 0.50
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Biomedicines (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Cancer Institute (R01CA226921)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
- Keywords
- WAVE2, WAVE regulatory complex, WASP family proteins, Arp2/3 complex, actin cytoskeleton remodeling, Rho GTPases, tumor invasion, metastasis, cell migration, oncogenic signaling
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.
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