References
- Allahverdian, S., Chaabane, C., Boukais, K., Francis, G.A., and Bochaton-Piallat, M.L. (2018). Smooth muscle cell fate and plasticity in atherosclerosis. Cardiovasc. Res. 114, 540-550. https://doi.org/10.1093/cvr/cvy022
- Bamburg, J.R. (1999). Proteins of the ADF/cofilin family: essential regulators of actin dynamics. Annu. Rev. Cell Dev. Biol. 15, 185-230. https://doi.org/10.1146/annurev.cellbio.15.1.185
- Bravo-Cordero, J.J., Magalhaes, M.A., Eddy, R.J., Hodgson, L., and Condeelis, J. (2013). Functions of cofilin in cell locomotion and invasion. Nat. Rev. Mol. Cell Biol. 14, 405-415. https://doi.org/10.1038/nrm3609
- Cervero, P., Himmel, M., Kruger, M., and Linder, S. (2012). Proteomic analysis of podosome fractions from macrophages reveals similarities to spreading initiation centres. Eur. J. Cell Biol. 91, 908-922. https://doi.org/10.1016/j.ejcb.2012.05.005
- Chang, Q., Bournazou, E., Sansone, P., Berishaj, M., Gao, S.P., Daly, L., Wels, J., Theilen, T., Granitto, S., Zhang, X., et al. (2013). The IL-6/JAK/Stat3 feedforward loop drives tumorigenesis and metastasis. Neoplasia 15, 848-862. https://doi.org/10.1593/neo.13706
- Cimica, V., Chen, H.C., Iyer, J.K., and Reich, N.C. (2011). Dynamics of the STAT3 transcription factor: nuclear import dependent on Ran and importin-beta1. PLoS One 6, e20188. https://doi.org/10.1371/journal.pone.0020188
- Collazo, J., Zhu, B., Larkin, S., Martin, S.K., Pu, H., Horbinski, C., Koochekpour, S., and Kyprianou, N. (2014). Cofilin drives cell-invasive and metastatic responses to TGF-beta in prostate cancer. Cancer Res. 74, 2362-2373. https://doi.org/10.1158/0008-5472.CAN-13-3058
- Cooper, J.A. and Schafer, D.A. (2000). Control of actin assembly and disassembly at filament ends. Curr. Opin. Cell Biol. 12, 97-103. https://doi.org/10.1016/S0955-0674(99)00062-9
- Dzau, V.J., Braun-Dullaeus, R.C., and Sedding, D.G. (2002). Vascular proliferation and atherosclerosis: new perspectives and therapeutic strategies. Nat. Med. 8, 1249-1256. https://doi.org/10.1038/nm1102-1249
- Fu, Y., Zhao, Y., Liu, Y., Zhu, Y., Chi, J., Hu, J., Zhang, X., and Yin, X. (2012). Adenovirus-mediated tissue factor pathway inhibitor gene transfer induces apoptosis by blocking the phosphorylation of JAK-2/STAT-3 pathway in vascular smooth muscle cells. Cell. Signal. 24, 1909-1917. https://doi.org/10.1016/j.cellsig.2012.06.001
- Gomez, D. and Owens, G.K. (2012). Smooth muscle cell phenotypic switching in atherosclerosis. Cardiovasc. Res. 95, 156-164. https://doi.org/10.1093/cvr/cvs115
- Hirano, T., Ishihara, K., and Hibi, M. (2000). Roles of STAT3 in mediating the cell growth, differentiation and survival signals relayed through the IL-6 family of cytokine receptors. Oncogene 19, 2548-2556. https://doi.org/10.1038/sj.onc.1203551
- Hu, J., Shi, Y., Xia, M., Liu, Z., Zhang, R., Luo, H., Zhang, T., Yang, Z., and Yuan, B. (2018). WDR1-regulated actin dynamics is required for outflow tract and right ventricle development. Dev. Biol. 438, 124-137. https://doi.org/10.1016/j.ydbio.2018.04.004
- Huang, X., Li, Z., Hu, J., Yang, Z., Liu, Z., Zhang, T., Zhang, C., and Yuan, B. (2019). Knockout of Wdr1 results in cardiac hypertrophy and impaired cardiac function in adult mouse heart. Gene 697, 40-47. https://doi.org/10.1016/j.gene.2019.02.023
- Intengan, H.D. and Schiffrin, E.L. (2000). Structure and mechanical properties of resistance arteries in hypertension: role of adhesion molecules and extracellular matrix determinants. Hypertension 36, 312-318. https://doi.org/10.1161/01.HYP.36.3.312
- Jackson, N.M. and Ceresa, B.P. (2017). EGFR-mediated apoptosis via STAT3. Exp. Cell Res. 356, 93-103. https://doi.org/10.1016/j.yexcr.2017.04.016
- Johnson, D.E., O'Keefe, R.A., and Grandis, J.R. (2018). Targeting the IL-6/ JAK/STAT3 signalling axis in cancer. Nat. Rev. Clin. Oncol. 15, 234-248. https://doi.org/10.1038/nrclinonc.2018.8
- Jonasson, L., Holm, J., and Hansson, G.K. (1988). Cyclosporin A inhibits smooth muscle proliferation in the vascular response to injury. Proc. Natl. Acad. Sci. U. S. A. 85, 2303-2306. https://doi.org/10.1073/pnas.85.7.2303
- Kou, X., Qi, S., Dai, W., Luo, L., and Yin, Z. (2011). Arctigenin inhibits lipopolysaccharide-induced iNOS expression in RAW264.7 cells through suppressing JAK-STAT signal pathway. Int. Immunopharmacol. 11, 1095-1102. https://doi.org/10.1016/j.intimp.2011.03.005
- Kovacic, J.C., Gupta, R., Lee, A.C., Ma, M., Fang, F., Tolbert, C.N., Walts, A.D., Beltran, L.E., San, H., Chen, G., et al. (2010). Stat3-dependent acute Rantes production in vascular smooth muscle cells modulates inflammation following arterial injury in mice. J. Clin. Invest. 120, 303-314. https://doi.org/10.1172/JCI40364
- Kumar, A. and Lindner, V. (1997). Remodeling with neointima formation in the mouse carotid artery after cessation of blood flow. Arterioscler. Thromb. Vasc. Biol. 17, 2238-2244. https://doi.org/10.1161/01.ATV.17.10.2238
- Lee, J.H., Kim, J.E., Kim, B.G., Han, H.H., Kang, S., and Cho, N.H. (2016). STAT3-induced WDR1 overexpression promotes breast cancer cell migration. Cell. Signal. 28, 1753-1760. https://doi.org/10.1016/j.cellsig.2016.08.006
- Lee, S.H. and Dominguez, R. (2010). Regulation of actin cytoskeleton dynamics in cells. Mol. Cells 29, 311-325. https://doi.org/10.1007/s10059-010-0053-8
- Li, Y.L., Ding, K., Hu, X., Wu, L.W., Zhou, D.M., Rao, M.J., Lin, N.M., and Zhang, C. (2019). DYRK1A inhibition suppresses STAT3/EGFR/Met signalling and sensitizes EGFR wild-type NSCLC cells to AZD9291. J. Cell. Mol. Med. 23, 7427-7437. https://doi.org/10.1111/jcmm.14609
- Limagne, E., Thibaudin, M., Euvrard, R., Berger, H., Chalons, P., Vegan, F., Humblin, E., Boidot, R., Rebe, C., Derangere, V., et al. (2017). Sirtuin-1 activation controls tumor growth by impeding Th17 differentiation via STAT3 deacetylation. Cell Rep. 19, 746-759. https://doi.org/10.1016/j.celrep.2017.04.004
- Marrero, M.B., Schieffer, B., Li, B., Sun, J., Harp, J.B., and Ling, B.N. (1997). Role of Janus kinase/signal transducer and activator of transcription and mitogen-activated protein kinase cascades in angiotensin II- and plateletderived growth factor-induced vascular smooth muscle cell proliferation. J. Biol. Chem. 272, 24684-24690. https://doi.org/10.1074/jbc.272.39.24684
- Marx, S.O. and Marks, A.R. (2001). Bench to bedside: the development of rapamycin and its application to stent restenosis. Circulation 104, 852-855. https://doi.org/10.1161/01.CIR.104.8.852
- Minakhina, S., Myers, R., Druzhinina, M., and Steward, R. (2005). Crosstalk between the actin cytoskeleton and Ran-mediated nuclear transport. BMC Cell Biol. 6, 32. https://doi.org/10.1186/1471-2121-6-32
- Ni, Z., Deng, J., Potter, C.M.F., Nowak, W.N., Gu, W., Zhang, Z., Chen, T., Chen, Q., Hu, Y., Zhou, B., et al. (2019). Recipient c-Kit lineage cells repopulate smooth muscle cells of transplant arteriosclerosis in mouse models. Circ. Res. 125, 223-241. https://doi.org/10.1161/CIRCRESAHA.119.314855
- O'Brien, E.R., Ma, X., Simard, T., Pourdjabbar, A., and Hibbert, B. (2011). Pathogenesis of neointima formation following vascular injury. Cardiovasc. Hematol. Disord. Drug Targets 11, 30-39. https://doi.org/10.2174/187152911795945169
- Owens, G.K., Kumar, M.S., and Wamhoff, B.R. (2004). Molecular regulation of vascular smooth muscle cell differentiation in development and disease. Physiol. Rev. 84, 767-801. https://doi.org/10.1152/physrev.00041.2003
- Qi, Z., Qi, S., Ling, L., Lv, J., and Feng, Z. (2016). Salidroside attenuates inflammatory response via suppressing JAK2-STAT3 pathway activation and preventing STAT3 transfer into nucleus. Int. Immunopharmacol. 35, 265-271. https://doi.org/10.1016/j.intimp.2016.04.004
- Schwartz, S.M., deBlois, D., and O'Brien, E.R. (1995). The intima. Soil for atherosclerosis and restenosis. Circ. Res. 77, 445-465. https://doi.org/10.1161/01.RES.77.3.445
- Seki, Y., Kai, H., Shibata, R., Nagata, T., Yasukawa, H., Yoshimura, A., and Imaizumi, T. (2000). Role of the JAK/STAT pathway in rat carotid artery remodeling after vascular injury. Circ. Res. 87, 12-18. https://doi.org/10.1161/01.RES.87.1.12
- Souissi, I., Najjar, I., Ah-Koon, L., Schischmanoff, P.O., Lesage, D., Le Coquil, S., Roger, C., Dusanter-Fourt, I., Varin-Blank, N., Cao, A., et al. (2011). A STAT3-decoy oligonucleotide induces cell death in a human colorectal carcinoma cell line by blocking nuclear transfer of STAT3 and STAT3-bound NF-kappaB. BMC Cell Biol. 12, 14. https://doi.org/10.1186/1471-2121-12-14
- Tripathi, S.K., Chen, Z., Larjo, A., Kanduri, K., Nousiainen, K., Aijo, T., Ricano-Ponce, I., Hrdlickova, B., Tuomela, S., Laajala, E., et al. (2017). Genome-wide analysis of STAT3-mediated transcription during early human Th17 cell differentiation. Cell Rep. 19, 1888-1901. https://doi.org/10.1016/j.celrep.2017.05.013
- Watanabe, S., Mu, W., Kahn, A., Jing, N., Li, J.H., Lan, H.Y., Nakagawa, T., Ohashi, R., and Johnson, R.J. (2004). Role of JAK/STAT pathway in IL-6-induced activation of vascular smooth muscle cells. Am. J. Nephrol. 24, 387-392. https://doi.org/10.1159/000079706
- Weintraub, W.S. (2007). The pathophysiology and burden of restenosis. Am. J. Cardiol. 100, 3K-9K. https://doi.org/10.1016/j.amjcard.2007.06.002
- Wu, Z., Liu, J., Hu, S., Zhu, Y., and Li, S. (2018). Serine/threonine kinase 35, a target gene of STAT3, regulates the proliferation and apoptosis of osteosarcoma cells. Cell. Physiol. Biochem. 45, 808-818. https://doi.org/10.1159/000487172
- Xiang, Y., Liao, X.H., Yao, A., Qin, H., Fan, L.J., Li, J.P., Hu, P., Li, H., Guo, W., Li, J.Y., et al. (2017). MRTF-A-miR-206-WDR1 form feedback loop to regulate breast cancer cell migration. Exp. Cell Res. 359, 394-404. https://doi.org/10.1016/j.yexcr.2017.08.023
- Xie, C., Ritchie, R.P., Huang, H., Zhang, J., and Chen, Y.E. (2011). Smooth muscle cell differentiation in vitro: models and underlying molecular mechanisms. Arterioscler. Thromb. Vasc. Biol. 31, 1485-1494. https://doi.org/10.1161/ATVBAHA.110.221101
- Xie, N., Chen, M., Dai, R., Zhang, Y., Zhao, H., Song, Z., Zhang, L., Li, Z., Feng, Y., Gao, H., et al. (2017). SRSF1 promotes vascular smooth muscle cell proliferation through a Delta133p53/EGR1/KLF5 pathway. Nat. Commun. 8, 16016. https://doi.org/10.1038/ncomms16016
- Xu, J., Wan, P., Wang, M., Zhang, J., Gao, X., Hu, B., Han, J., Chen, L., Sun, K., Wu, J., et al. (2015). AIP1-mediated actin disassembly is required for postnatal germ cell migration and spermatogonial stem cell niche establishment. Cell Death Dis. 6, e1818. https://doi.org/10.1038/cddis.2015.182
- Yuan, B., Wan, P., Chu, D., Nie, J., Cao, Y., Luo, W., Lu, S., Chen, J., and Yang, Z. (2014). A cardiomyocyte-specific Wdr1 knockout demonstrates essential functional roles for actin disassembly during myocardial growth and maintenance in mice. Am. J. Pathol. 184, 1967-1980. https://doi.org/10.1016/j.ajpath.2014.04.007
- Yuan, B., Zhang, R., Hu, J., Liu, Z., Yang, C., Zhang, T., and Zhang, C. (2018). WDR1 promotes cell growth and migration and contributes to malignant phenotypes of non-small cell lung cancer through ADF/cofilin-mediated actin dynamics. Int. J. Biol. Sci. 14, 1067-1080. https://doi.org/10.7150/ijbs.23845
- Zhang, L., Shao, J., Zhou, Y., Chen, H., Qi, H., Wang, Y., Chen, L., Zhu, Y., Zhang, M., Chen, L., et al. (2018). Inhibition of PDGF-BB-induced proliferation and migration in VSMCs by proanthocyanidin A2:Involvement of KDR and Jak-2/STAT-3/cPLA2 signaling pathways. Biomed. Pharmacother. 98, 847-855. https://doi.org/10.1016/j.biopha.2018.01.010
- Zhang, S.M., Zhu, L.H., Chen, H.Z., Zhang, R., Zhang, P., Jiang, D.S., Gao, L., Tian, S., Wang, L., Zhang, Y., et al. (2014). Interferon regulatory factor 9 is critical for neointima formation following vascular injury. Nat. Commun. 5, 5160. https://doi.org/10.1038/ncomms6160
- Zulkifli, A.A., Tan, F.H., Putoczki, T.L., Stylli, S.S., and Luwor, R.B. (2017). STAT3 signaling mediates tumour resistance to EGFR targeted therapeutics. Mol. Cell. Endocrinol. 451, 15-23. https://doi.org/10.1016/j.mce.2017.01.010