Siah1 in cancer and nervous system diseases (Review)
- Authors:
- Hui Zhang
- Jie Wang
- Yidong Ge
- Meng Ye
- Xiaofeng Jin
-
Affiliations: Department of Oncology, The Affiliated Hospital of School of Medicine, Ningbo University, Ningbo, Zhejiang 315020, P.R. China - Published online on: December 23, 2021 https://doi.org/10.3892/or.2021.8246
- Article Number: 35
This article is mentioned in:
Abstract
Hershko A and Ciechanover A: The ubiquitin system. Ann Rev Biochem. 67:425–479. 1998. View Article : Google Scholar : PubMed/NCBI | |
Mani RS: The emerging role of speckle-type POZ protein (SPOP) in cancer development. Drug Discov Today. 19:1498–1502. 2014. View Article : Google Scholar : PubMed/NCBI | |
Zou T and Zhang J: Diverse and pivotal roles of neddylation in metabolism and immunity. FEBS J. 288:3884–3912. 2020. View Article : Google Scholar : PubMed/NCBI | |
Chen RH: Cullin 3 and its role in tumorigenesis. Adv Exp Med Biol. 1217:187–210. 2020. View Article : Google Scholar : PubMed/NCBI | |
Nandi D, Tahiliani P, Kumar A and Chandu D: The ubiquitin-proteasome system. J Biosci. 31:137–155. 2006. View Article : Google Scholar : PubMed/NCBI | |
Cuneo MJ and Mittag T: The ubiquitin ligase adaptor SPOP in cancer. FEBS J. 286:3946–3958. 2019. View Article : Google Scholar : PubMed/NCBI | |
Wang D, Ma L, Wang B, Liu J and Wei W: E3 ubiquitin ligases in cancer and implications for therapies. Cancer Metastasis Rev. 36:683–702. 2017. View Article : Google Scholar : PubMed/NCBI | |
Wang Z, Song Y, Ye M, Dai X, Zhu X and Wei W: The diverse roles of SPOP in prostate cancer and kidney cancer. Nat Rev Urol. 17:339–350. 2020. View Article : Google Scholar : PubMed/NCBI | |
Morreale F and Walden H: Types of ubiquitin ligases. Cell. 165:248. 2016. View Article : Google Scholar : PubMed/NCBI | |
Yun S, Möller A, Chae SK, Hong WP, Bae YJ, Bowtell DD, Ryu SH and Suh PG: Siah proteins induce the epidermal growth factor-dependent degradation of phospholipase Cepsilon. J Biol Chem. 283:1034–1042. 2008. View Article : Google Scholar : PubMed/NCBI | |
Qi J, Kim H, Scortegagna M and Ronai ZA: Regulators and effectors of Siah ubiquitin ligases. Cell Biochem Biophys. 67:15–24. 2013. View Article : Google Scholar : PubMed/NCBI | |
Garrison JB, Correa RG, Gerlic M, Yip KW, Krieg A, Tamble CM, Shi R, Welsh K, Duggineni S, Huang Z, et al: ARTS and Siah collaborate in a pathway for XIAP degradation. Mol Cell. 41:107–116. 2011. View Article : Google Scholar : PubMed/NCBI | |
Santelli E, Leone M, Li C, Fukushima T, Preece NE, Olson AJ, Ely KR, Reed JC, Pellecchia M, Liddington RC and Matsuzawa SI: Structural analysis of Siah1-Siah-interacting protein interactions and insights into the assembly of an E3 ligase multiprotein complex. J Biol Chem. 280:34278–34287. 2005. View Article : Google Scholar : PubMed/NCBI | |
Zhang Q, Wang Z, Hou F, Harding R, Huang X, Dong A, Walker JR and Tong Y: The substrate binding domains of human SIAH E3 ubiquitin ligases are now crystal clear. Biochim Biophys Acta Gen Subj. 1861:3095–3105. 2017. View Article : Google Scholar : PubMed/NCBI | |
Knauer SK, Mahendrarajah N, Roos WP and Krämer OH: The inducible E3 ubiquitin ligases SIAH1 and SIAH2 perform critical roles in breast and prostate cancers. Cytokine Growth Factor Rev. 26:405–413. 2015. View Article : Google Scholar : PubMed/NCBI | |
Nakayama K and Ronai Z: Siah: New players in the cellular response to hypoxia. Cell Cycle. 3:1345–1347. 2004. View Article : Google Scholar : PubMed/NCBI | |
Famulski JK, Trivedi N, Howell D, Yang Y, Tong Y, Gilbertson R and Solecki DJ: Siah regulation of Pard3A controls neuronal cell adhesion during germinal zone exit. Science. 330:1834–1838. 2010. View Article : Google Scholar : PubMed/NCBI | |
Wong CS and Möller A: Siah: A promising anticancer target. Cancer Res. 73:2400–2406. 2013. View Article : Google Scholar : PubMed/NCBI | |
House CM, Möller A and Bowtell DD: Siah proteins: Novel drug targets in the Ras and hypoxia pathways. Cancer Res. 69:8835–8838. 2009. View Article : Google Scholar : PubMed/NCBI | |
Matsuzawa S, Li C, Ni CZ, Takayama S, Reed JC and Ely KR: Structural analysis of Siah1 and its interactions with Siah-interacting protein (SIP). J Biol Chem. 278:1837–1840. 2003. View Article : Google Scholar : PubMed/NCBI | |
Topolska-Woś AM, Chazin WJ and Filipek A: CacyBP/SIP-structure and variety of functions. Biochim Biophys Acta. 1860:79–85. 2016. View Article : Google Scholar : PubMed/NCBI | |
Yan S, Li A and Liu Y: CacyBP/SIP inhibits the migration and invasion behaviors of glioblastoma cells through activating Siah1 mediated ubiquitination and degradation of cytoplasmic p27. Cell Biol Int. 42:216–226. 2018. View Article : Google Scholar : PubMed/NCBI | |
Wen YY, Yang ZQ, Song M, Li BL, Yao XH, Chen XL, Zhao J, Lu YY, Zhu JJ and Wang EH: The expression of SIAH1 is downregulated and associated with Bim and apoptosis in human breast cancer tissues and cells. Mol Carcinog. 49:440–449. 2010. View Article : Google Scholar : PubMed/NCBI | |
Briant DJ, Ceccarelli DF and Sicheri F: I Siah substrate! Structure. 14:627–628. 2006. View Article : Google Scholar : PubMed/NCBI | |
Czechowicz JS, Nagel CH, Voges M, Spohn M, Eibl MM and Hauber J: Interaction between the cellular E3 ubiquitin ligase SIAH-1 and the viral immediate-early protein ICP0 enables efficient replication of herpes simplex virus type 2 in vivo. PLoS One. 13:e02018802018. View Article : Google Scholar : PubMed/NCBI | |
Shi H, Zheng B, Wu Y, Tang Y, Wang L, Gao Y, Gong H, Du J and Yu R: Ubiquitin ligase Siah1 promotes the migration and invasion of human glioma cells by regulating HIF-1α signaling under hypoxia. Oncol Rep. 33:1185–1190. 2015. View Article : Google Scholar : PubMed/NCBI | |
Krämer OH, Stauber RH, Bug G, Hartkamp J and Knauer SK: SIAH proteins: Critical roles in leukemogenesis. Leukemia. 27:792–802. 2013. View Article : Google Scholar : PubMed/NCBI | |
Sim HW and Knox J: Hepatocellular carcinoma in the era of immunotherapy. Curr Probl Cancer. 42:40–48. 2018. View Article : Google Scholar : PubMed/NCBI | |
Matsuo K, Satoh S, Okabe H, Nomura A, Maeda T, Yamaoka Y and Ikai I: SIAH1 inactivation correlates with tumor progression in hepatocellular carcinomas. Genes Chromosomes Cancer. 36:283–291. 2003. View Article : Google Scholar : PubMed/NCBI | |
Yoshibayashi H, Okabe H, Satoh S, Hida K, Kawashima K, Hamasu S, Nomura A, Hasegawa S, Ikai I and Sakai Y: SIAH1 causes growth arrest and apoptosis in hepatoma cells through beta-catenin degradation-dependent and -independent mechanisms. Oncol Rep. 17:549–556. 2007.PubMed/NCBI | |
Yao H, Ashihara E and Maekawa T: Targeting the Wnt/β-catenin signaling pathway in human cancers. Expert Opin Ther Targets. 15:873–887. 2011. View Article : Google Scholar : PubMed/NCBI | |
Clevers H and Nusse R: Wnt/β-catenin signaling and disease. Cell. 149:1192–1205. 2012. View Article : Google Scholar : PubMed/NCBI | |
Arend RC, Londoño-Joshi AI, Straughn JM Jr and Buchsbaum DJ: The Wnt/β-catenin pathway in ovarian cancer: A review. Gynecol Oncol. 131:772–779. 2013. View Article : Google Scholar : PubMed/NCBI | |
Taciak B, Pruszynska I, Kiraga L, Bialasek M and Krol M: Wnt signaling pathway in development and cancer. J Physiol Pharmacol. 69:doi: 10.26402. 2018.PubMed/NCBI | |
Steinhart Z and Angers S: Wnt signaling in development and tissue homeostasis. Development. 145:dev1465892018. View Article : Google Scholar : PubMed/NCBI | |
Huang P, Yan R, Zhang X, Wang L, Ke X and Qu Y: Activating Wnt/β-catenin signaling pathway for disease therapy: Challenges and opportunities. Pharmacol Ther. 196:79–90. 2019. View Article : Google Scholar : PubMed/NCBI | |
Kim E, Lisby A, Ma C, Lo N, Ehmer U, Hayer KE, Furth EE and Viatour P: Promotion of growth factor signaling as a critical function of β-catenin during HCC progression. Nat Commun. 10:19092019. View Article : Google Scholar : PubMed/NCBI | |
Ji L, Jiang B, Jiang X, Charlat O, Chen A, Mickanin C, Bauer A, Xu W, Yan X and Cong F: The SIAH E3 ubiquitin ligases promote Wnt/β-catenin signaling through mediating wnt-induced axin degradation. Genes Dev. 31:904–915. 2017. View Article : Google Scholar : PubMed/NCBI | |
Yang Y, Zhang J, Wu T, Xu X, Cao G, Li H and Chen X: Histone deacetylase 2 regulates the doxorubicin (Dox) resistance of hepatocarcinoma cells and transcription of ABCB1. Life Sci. 216:200–206. 2019. View Article : Google Scholar : PubMed/NCBI | |
Cheng C, Li C, Zhu X, Han W, Li J and Lv Y: Doxorubicin-loaded Fe(3)O(4)-ZIF-8 nano-composites for hepatocellular carcinoma therapy. J Biomater Appl. 33:1373–1381. 2019. View Article : Google Scholar : PubMed/NCBI | |
Long L, Xiang H, Liu J, Zhang Z and Sun L: ZEB1 mediates doxorubicin (Dox) resistance and mesenchymal characteristics of hepatocarcinoma cells. Exp Mol Pathol. 106:116–122. 2019. View Article : Google Scholar : PubMed/NCBI | |
Li LY, Yang CC, Yang JF, Li HD, Zhang BY, Zhou H, Hu S, Wang K, Huang C, Meng XM, et al: ZEB1 regulates the activation of hepatic stellate cells through Wnt/β-catenin signaling pathway. Eur J Pharmacol. 865:1727872019. View Article : Google Scholar : PubMed/NCBI | |
Qin Y, Yu J, Zhang M, Qin F and Lan X: ZEB1 promotes tumorigenesis and metastasis in hepatocellular carcinoma by regulating the expression of vimentin. Mol Med Rep. 19:2297–2306. 2019.PubMed/NCBI | |
Han X, Liu F, Zhang C, Ren Z, Li L and Wang G: SIAH1/ZEB1/IL-6 axis is involved in doxorubicin (Dox) resistance of osteosarcoma cells. Biol Chem. 400:545–553. 2019. View Article : Google Scholar : PubMed/NCBI | |
Abshire CF, Carroll JL and Dragoi AM: FLASH protects ZEB1 from degradation and supports cancer cells' epithelial-to-mesenchymal transition. Oncogenesis. 5:e2542016. View Article : Google Scholar : PubMed/NCBI | |
Wu Y, Yang X, Chen Z, Tian L, Jiang G, Chen F, Li J, An P, Lu L, Luo N, et al: m6 A-induced lncRNA RP11 triggers the dissemination of colorectal cancer cells via upregulation of Zeb1. Mol Cancer. 18:872019. View Article : Google Scholar : PubMed/NCBI | |
Brauckhoff A, Malz M, Tschaharganeh D, Malek N, Weber A, Riener MO, Soll C, Samarin J, Bissinger M and Schmidt J: Nuclear expression of the ubiquitin ligase seven in absentia homolog (SIAH)-1 induces proliferation and migration of liver cancer cells. J Hepatol. 55:1049–1057. 2011. View Article : Google Scholar : PubMed/NCBI | |
Veronesi U, Boyle P, Goldhirsch A, Orecchia R and Viale G: Breast cancer. Lancet. 365:1727–1741. 2005. View Article : Google Scholar : PubMed/NCBI | |
Woolston C: Breast cancer. Nature. 527:S1012015. View Article : Google Scholar : PubMed/NCBI | |
DeSantis C, Siegel R, Bandi P and Jemal A: Breast cancer statistics, 2011. CA Cancer J Clin. 61:409–418. 2011. View Article : Google Scholar : PubMed/NCBI | |
Ullah MF: Breast cancer: Current perspectives on the disease status. Adv Exp Med Biol. 1152:51–64. 2019. View Article : Google Scholar : PubMed/NCBI | |
Tsang JYS and Tse GM: Molecular classification of breast cancer. Adv Anat Pathol. 27:27–35. 2020. View Article : Google Scholar : PubMed/NCBI | |
Barzaman K, Karami J, Zarei Z, Hosseinzadeh A, Kazemi MH, Moradi-Kalbolandi S, Safari E and Farahmand L: Breast cancer: Biology, biomarkers, and treatments. Int Immunopharmacol. 84:1065352020. View Article : Google Scholar : PubMed/NCBI | |
Bruzzoni-Giovanelli H, Faille A, Linares-Cruz G, Nemani M, Deist FL, Germani A, Chassoux D, Millot G, Roperch JP, Amson R, et al: SIAH-1 inhibits cell growth by altering the mitotic process. Oncogene. 18:7101–7109. 1999. View Article : Google Scholar : PubMed/NCBI | |
Medhioub M, Vaury C, Hamelin R and Thomas G: Lack of somatic mutation in the coding sequence of SIAH1 in tumors hemizygous for this candidate tumor suppressor gene. Int J Cancer. 87:794–797. 2000. View Article : Google Scholar : PubMed/NCBI | |
Germani A, Bruzzoni-Giovanelli H, Fellous A, Gisselbrecht S, Varin-Blank N and Calvo F: SIAH-1 interacts with alpha-tubulin and degrades the kinesin Kid by the proteasome pathway during mitosis. Oncogene. 19:5997–6006. 2000. View Article : Google Scholar : PubMed/NCBI | |
Wen YY, Yang ZQ, Song M, Li BL, Zhu JJ and Wang EH: SIAH1 induced apoptosis by activation of the JNK pathway and inhibited invasion by inactivation of the ERK pathway in breast cancer cells. Cancer Sci. 101:73–79. 2010. View Article : Google Scholar : PubMed/NCBI | |
Nedeljković M and Damjanović A: Mechanisms of chemotherapy resistance in triple-negative breast cancer-how we can rise to the challenge. Cells. 8:9572019. View Article : Google Scholar : PubMed/NCBI | |
Zhang L, Ma P, Sun LM, Han YC, Li BL, Mi XY, Wang EH and Song M: MiR-107 down-regulates SIAH1 expression in human breast cancer cells and silencing of miR-107 inhibits tumor growth in a nude mouse model of triple-negative breast cancer. Mol Carcinog. 55:768–777. 2016. View Article : Google Scholar : PubMed/NCBI | |
Hong HC, Chuang CH, Huang WC, Weng SL, Chen CH, Chang KH, Liao KW and Huang HD: A panel of eight microRNAs is a good predictive parameter for triple-negative breast cancer relapse. Theranostics. 10:8771–8789. 2020. View Article : Google Scholar : PubMed/NCBI | |
Sahlberg KK, Bottai G, Naume B, Burwinkel B, Calin GA, Børresen-Dale AL and Santarpia L: A serum microRNA signature predicts tumor relapse and survival in triple-negative breast cancer patients. Clin Cancer Res. 21:1207–1214. 2015. View Article : Google Scholar : PubMed/NCBI | |
Flores-Pérez A, Marchat LA, Rodríguez-Cuevas S, Bautista VP, Fuentes-Mera L, Romero-Zamora D, Maciel-Dominguez A, de la Cruz OH, Fonseca-Sánchez M, Ruíz-García E, et al: Suppression of cell migration is promoted by miR-944 through targeting of SIAH1 and PTP4A1 in breast cancer cells. BMC Cancer. 16:3792016. View Article : Google Scholar : PubMed/NCBI | |
Ren H, Mi X, Zhao P, Zhao X, Wei N, Huang H, Meng Z, Kou J, Sun M, Liu Y, et al: TRAF4, a new substrate of SIAH1, participates in chemotherapy resistance of breast cancer cell by counteracting SIAH1-mediated downregulation of β-catenin. Breast Cancer Res Treat. 183:275–289. 2020. View Article : Google Scholar : PubMed/NCBI | |
Butti R, Gunasekaran VP, Kumar TVS, Banerjee P and Kundu GC: Breast cancer stem cells: Biology and therapeutic implications. Int J Biochem Cell Biol. 107:38–52. 2019. View Article : Google Scholar : PubMed/NCBI | |
Fisusi FA and Akala EO: Drug combinations in breast cancer therapy. Pharm Nanotechnol. 7:3–23. 2019. View Article : Google Scholar : PubMed/NCBI | |
Tang Y, Wang Y, Kiani MF and Wang B: Classification, treatment strategy, and associated drug resistance in breast cancer. Clin Breast Cancer. 16:335–343. 2016. View Article : Google Scholar : PubMed/NCBI | |
Zhou J, Li W, Ming J, Yang W, Lu L, Zhang Q, Ruan S and Huang T: High expression of TRAF4 predicts poor prognosis in tamoxifen-treated breast cancer and promotes tamoxifen resistance. Anticancer Drugs. 31:558–566. 2020. View Article : Google Scholar : PubMed/NCBI | |
Zhang X, Wen Z and Mi X: Expression and anti-apoptotic function of TRAF4 in human breast cancer MCF-7 cells. Oncol Lett. 7:411–414. 2014. View Article : Google Scholar : PubMed/NCBI | |
Wang A, Wang J, Ren H, Yang F, Sun L, Diao K, Zhao Z, Song M, Cui Z, Wang E, et al: TRAF4 participates in wnt/β-catenin signaling in breast cancer by upregulating β-catenin and mediating its translocation to the nucleus. Mol Cell Biochem. 395:211–219. 2014. View Article : Google Scholar : PubMed/NCBI | |
Liu M, Hsu J, Chan C, Li Z and Zhou Q: The ubiquitin ligase Siah1 controls ELL2 stability and formation of super elongation complexes to modulate gene transcription. Mol Cell. 46:325–334. 2012. View Article : Google Scholar : PubMed/NCBI | |
de Thé H, Pandolfi PP and Chen Z: Acute promyelocytic leukemia: A paradigm for oncoprotein-targeted cure. Cancer Cell. 32:552–560. 2017. View Article : Google Scholar : PubMed/NCBI | |
De Braekeleer E, Douet-Guilbert N and De Braekeleer M: RARA fusion genes in acute promyelocytic leukemia: A review. Expert Rev Hematol. 7:347–357. 2014. View Article : Google Scholar : PubMed/NCBI | |
Liquori A, Ibañez M, Sargas C, Sanz MA, Barragán E and Cervera J: Acute promyelocytic leukemia: A constellation of molecular events around a single PML-RARA Fusion Gene. Cancers (Basel). 12:6242020. View Article : Google Scholar : PubMed/NCBI | |
Pietschmann K, Buchwald M, Müller S, Knauer SK, Kögl M, Heinzel T and Krämer OH: Differential regulation of PML-RARα stability by the ubiquitin ligases SIAH1/SIAH2 and TRIAD1. Int J Biochem Cell Biol. 44:132–138. 2012. View Article : Google Scholar : PubMed/NCBI | |
Bug G, Ritter M, Wassmann B, Schoch C, Heinzel T, Schwarz K, Romanski A, Kramer OH, Kampfmann M, Hoelzer D, et al: Clinical trial of valproic acid and all-trans retinoic acid in patients with poor-risk acute myeloid leukemia. Cancer. 104:2717–2725. 2005. View Article : Google Scholar : PubMed/NCBI | |
Bursen A, Moritz S, Gaussmann A, Moritz S, Dingermann T and Marschalek R: Interaction of AF4 wild-type and AF4.MLL fusion protein with SIAH proteins: Indication for t(4;11) pathobiology? Oncogene. 23:6237–6249. 2004. View Article : Google Scholar : PubMed/NCBI | |
Krämer OH, Müller S, Buchwald M, Reichardt S and Heinzel T: Mechanism for ubiquitylation of the leukemia fusion proteins AML1-ETO and PML-RARalpha. Faseb J. 22:1369–1379. 2008. View Article : Google Scholar : PubMed/NCBI | |
Luo Z, Lin C and Shilatifard A: The super elongation complex (SEC) family in transcriptional control. Nat Rev Mol Cell Biol. 13:543–547. 2012. View Article : Google Scholar : PubMed/NCBI | |
Dahl NA, Danis E, Balakrishnan I, Wang D, Pierce A, Walker FM, Gilani A, Serkova NJ, Madhavan K, Fosmire S, et al: Super elongation complex as a targetable dependency in diffuse midline glioma. Cell Rep. 31:1074852020. View Article : Google Scholar : PubMed/NCBI | |
Yu D, Liu R, Yang G and Zhou Q: The PARP1-Siah1 axis controls HIV-1 transcription and expression of Siah1 substrates. Cell Rep. 23:3741–3749. 2018. View Article : Google Scholar : PubMed/NCBI | |
Wu J, Xue Y, Gao X and Zhou Q: Host cell factors stimulate HIV-1 transcription by antagonizing substrate-binding function of Siah1 ubiquitin ligase to stabilize transcription elongation factor ELL2. Nucleic Acids Res. 48:7321–7332. 2020.PubMed/NCBI | |
Nagel CH, Albrecht N, Milovic-Holm K, Mariyanna L, Keyser B, Abel B, Weseloh B, Hofmann TG, Eibl MM and Hauber J: Herpes simplex virus immediate-early protein ICP0 is targeted by SIAH-1 for proteasomal degradation. J Virol. 85:7644–7657. 2011. View Article : Google Scholar : PubMed/NCBI | |
Abe T, Umeki I, Kanno SI, Inoue SI, Niihori T and Aoki Y: LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases. Cell Death Differ. 27:1023–1035. 2020. View Article : Google Scholar : PubMed/NCBI | |
Frattini V, Trifonov V, Chan JM, Castano A, Lia M, Abate F, Keir ST, Ji AX, Zoppoli P, Niola F, et al: The integrated landscape of driver genomic alterations in glioblastoma. Nat Genet. 45:1141–1149. 2013. View Article : Google Scholar : PubMed/NCBI | |
Wirsching HG, Galanis E and Weller M: Glioblastoma. Handb Clin Neurol. 134:381–397. 2016. View Article : Google Scholar : PubMed/NCBI | |
He Y, Roos WP, Wu Q, Hofmann TG and Kaina B: The SIAH1-HIPK2-p53ser46 damage response pathway is involved in temozolomide-induced glioblastoma cell death. Mol Cancer Res. 17:1129–1141. 2019. View Article : Google Scholar : PubMed/NCBI | |
Fan Z, Li Z, Yang Y, Liu S, Guo J and Xu Y: HIF-1α coordinates epigenetic activation of SIAH1 in hepatocytes in response to nutritional stress. Biochim Biophys Acta Gene Regul Mech. 1860:1037–1046. 2017. View Article : Google Scholar : PubMed/NCBI | |
Matsui-Hasumi A, Sato Y, Uto-Konomi A, Yamashita S, Uehori J, Yoshimura A, Yamashita M, Asahara H, Suzuki S and Kubo M: E3 ubiquitin ligases SIAH1/2 regulate hypoxia-inducible factor-1 (HIF-1)-mediated Th17 cell differentiation. Int Immunol. 29:133–143. 2017. View Article : Google Scholar : PubMed/NCBI | |
Ke Q and Costa M: Hypoxia-inducible factor-1 (HIF-1). Mol Pharmacol. 70:1469–1480. 2006. View Article : Google Scholar : PubMed/NCBI | |
Semenza GL: Targeting HIF-1 for cancer therapy. Nat Rev Cancer. 3:721–732. 2003. View Article : Google Scholar : PubMed/NCBI | |
You L, Wu W, Wang X, Fang L, Adam V, Nepovimova E, Wu Q and Kuca K: The role of hypoxia-inducible factor 1 in tumor immune evasion. Med Res Rev. 41:1622–1643. 2021. View Article : Google Scholar : PubMed/NCBI | |
Peng S, Zhang J, Tan X, Huang Y, Xu J, Silk N, Zhang D, Liu Q and Jiang J: The VHL/HIF axis in the development and treatment of pheochromocytoma/paraganglioma. Front Endocrinol (Lausanne). 11:5868572020. View Article : Google Scholar : PubMed/NCBI | |
Gopalsamy A, Hagen T and Swaminathan K: Investigating the molecular basis of Siah1 and Siah2 E3 ubiquitin ligase substrate specificity. PLoS One. 9:e1065472014. View Article : Google Scholar : PubMed/NCBI | |
Kim SY, Choi DW, Kim EA and Choi CY: Stabilization of HIPK2 by escape from proteasomal degradation mediated by the E3 ubiquitin ligase Siah1. Cancer Lett. 279:177–184. 2009. View Article : Google Scholar : PubMed/NCBI | |
Choi DW and Choi CY: HIPK2 modification code for cell death and survival. Mol Cell Oncol. 1:e9559992014. View Article : Google Scholar : PubMed/NCBI | |
Feng Y, Zhou L, Sun X and Li Q: Homeodomain-interacting protein kinase 2 (HIPK2): A promising target for anti-cancer therapies. Oncotarget. 8:20452–20461. 2017. View Article : Google Scholar : PubMed/NCBI | |
Moll UM and Petrenko O: The MDM2-p53 interaction. Mol Cancer Res. 1:1001–1008. 2003.PubMed/NCBI | |
Krastev DB and Buchholz F: Ribosome biogenesis and p53: Who is regulating whom? Cell Cycle. 10:3417–3418. 2011. View Article : Google Scholar : PubMed/NCBI | |
Chao CC: Mechanisms of p53 degradation. Clin Chim Acta. 438:139–147. 2015. View Article : Google Scholar : PubMed/NCBI | |
Kanapathipillai M: Treating p53 mutant aggregation-associated cancer. Cancers (Basel). 10:1542018. View Article : Google Scholar : PubMed/NCBI | |
Feng L, Hollstein M and Xu Y: Ser46 phosphorylation regulates p53-dependent apoptosis and replicative senescence. Cell Cycle. 5:2812–2819. 2006. View Article : Google Scholar : PubMed/NCBI | |
Liebl MC and Hofmann TG: Cell fate regulation upon DNA damage: p53 serine 46 kinases pave the cell death road. Bioessays. 41:e19001272019. View Article : Google Scholar : PubMed/NCBI | |
Winter M, Sombroek D, Dauth I, Moehlenbrink J, Scheuermann K, Crone J and Hofmann TG: Control of HIPK2 stability by ubiquitin ligase Siah-1 and checkpoint kinases ATM and ATR. Nat Cell Biol. 10:812–824. 2008. View Article : Google Scholar : PubMed/NCBI | |
Moehlenbrink J, Bitomsky N and Hofmann TG: Hypoxia suppresses chemotherapeutic drug-induced p53 Serine 46 phosphorylation by triggering HIPK2 degradation. Cancer Lett. 292:119–124. 2010. View Article : Google Scholar : PubMed/NCBI | |
Chen D, Li M, Luo J and Gu W: Direct interactions between HIF-1 alpha and Mdm2 modulate p53 function. J Biol Chem. 278:13595–13598. 2003. View Article : Google Scholar : PubMed/NCBI | |
Wang P, Guan D, Zhang XP, Liu F and Wang W: Modeling the regulation of p53 activation by HIF-1 upon hypoxia. FEBS Lett. 593:2596–2611. 2019. View Article : Google Scholar : PubMed/NCBI | |
Fukuba H, Yamashita H, Nagano Y, Jin HG, Hiji M, Ohtsuki T, Takahashi T, Kohriyama T and Matsumoto M: Siah-1 facilitates ubiquitination and degradation of factor inhibiting HIF-1alpha (FIH). Biochem Biophys Res Commun. 353:324–329. 2007. View Article : Google Scholar : PubMed/NCBI | |
Xiao Z, Wei Z, Deng D, Zheng Z, Zhao Y, Jiang S, Zhang D, Zhang LJ, Fan M, Chen S, et al: Downregulation of Siah1 promotes colorectal cancer cell proliferation and migration by regulating AKT and YAP ubiquitylation and proteasome degradation. Cancer Cell Int. 20:502020. View Article : Google Scholar : PubMed/NCBI | |
Wu W, Liu X, Wei L, Li T, Zang Y, Qian Y, Bai T, Li J, Xie M, Zhu Y, et al: Tp53 mutation inhibits ubiquitination and degradation of WISP1 via down-regulation of siah1 in pancreatic carcinogenesis. Front Pharmacol. 9:8572018. View Article : Google Scholar : PubMed/NCBI | |
Ascherio A and Schwarzschild M: The epidemiology of Parkinson's disease: Risk factors and prevention. Lancet Neurol. 15:1257–1272. 2016. View Article : Google Scholar : PubMed/NCBI | |
Bloem BR, Okun MS and Klein C: Parkinson's disease. Lancet. 397:2284–2303. 2021. View Article : Google Scholar : PubMed/NCBI | |
Lees A, Hardy J and Revesz T: Parkinson's disease. Lancet. 373:2055–2066. 2009. View Article : Google Scholar : PubMed/NCBI | |
Franck T, Krueger R, Woitalla D, Müller T, Engelender S and Riess O: Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's disease. J Neural Transm (Vienna). 113:1903–1908. 2006. View Article : Google Scholar : PubMed/NCBI | |
Nagano Y, Yamashita H, Takahashi T, Kishida S, Nakamura T, Iseki E, Hattori N, Mizuno Y, Kikuchi A and Matsumoto M: Siah-1 facilitates ubiquitination and degradation of synphilin-1. J Biol Chem. 278:51504–51514. 2003. View Article : Google Scholar : PubMed/NCBI | |
Liani E, Eyal A, Avraham E, Shemer R, Szargel R, Berg D, Bornemann A, Riess O, Ross CA, Rott R and Engelender S: Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease. Proc Natl Acad Sci USA. 101:5500–5505. 2004. View Article : Google Scholar : PubMed/NCBI | |
Burchell VS, Nelson DE, Sanchez-Martinez A, Delgado-Camprubi M, Ivatt RM, Pogson JH, Randle SJ, Wray S, Lewis PA, Houlden H, et al: The Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagy. Nat Neurosci. 16:1257–1265. 2013. View Article : Google Scholar : PubMed/NCBI | |
Yamamura Y, Kuzuhara S, Kondo K, Yanagi T, Uchida M, Matsumine H and Mizuno Y: Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation. Parkinsonism Relat Disord. 4:65–72. 1998. View Article : Google Scholar : PubMed/NCBI | |
Shahnawaz M, Mukherjee A, Pritzkow S, Mendez N, Rabadia P, Liu X, Hu B, Schmeichel A, Singer W, Wu G, et al: Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy. Nature. 578:273–277. 2020. View Article : Google Scholar : PubMed/NCBI | |
Lövestam S, Schweighauser M, Matsubara T, Murayama S, Tomita T, Ando T, Hasegawa K, Yoshida M, Tarutani A, Hasegawa M, et al: Seeded assembly in vitro does not replicate the structures of α-synuclein filaments from multiple system atrophy. FEBS Open Bio. 11:999–1013. 2021. View Article : Google Scholar : PubMed/NCBI | |
Schweighauser M, Shi Y, Tarutani A, Kametani F, Murzin AG, Ghetti B, Matsubara T, Tomita T, Ando T, Hasegawa K, et al: Structures of α-synuclein filaments from multiple system atrophy. Nature. 585:464–469. 2020. View Article : Google Scholar : PubMed/NCBI | |
Szargel R, Shani V, Elghani FA, Mekies LN, Liani E, Rott R and Engelender S: The PINK1, synphilin-1 and SIAH-1 complex constitutes a novel mitophagy pathway. Hum Mol Genet. 25:3476–3490. 2016. View Article : Google Scholar : PubMed/NCBI | |
Subramaniam SR and Chesselet MF: Mitochondrial dysfunction and oxidative stress in Parkinson's disease. Prog Neurobiol. 106–107. 17–32. 2013.PubMed/NCBI | |
Pickrell AM and Youle RJ: The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease. Neuron. 85:257–273. 2015. View Article : Google Scholar : PubMed/NCBI | |
Ganguly G, Chakrabarti S, Chatterjee U and Saso L: Proteinopathy, oxidative stress and mitochondrial dysfunction: Cross talk in Alzheimer's disease and Parkinson's disease. Drug Des Devel Ther. 11:797–810. 2017. View Article : Google Scholar : PubMed/NCBI | |
Rocha EM, De Miranda B and Sanders LH: Alpha-synuclein: Pathology, mitochondrial dysfunction and neuroinflammation in Parkinson's disease. Neurobiol Dis. 109:249–257. 2018. View Article : Google Scholar : PubMed/NCBI | |
Macdonald R, Barnes K, Hastings C and Mortiboys H: Mitochondrial abnormalities in Parkinson's disease and Alzheimer's disease: Can mitochondria be targeted therapeutically? Biochem Soc Trans. 46:891–909. 2018. View Article : Google Scholar : PubMed/NCBI | |
Wang T, Zhang J, Hu M, Zhang Y, Cui P, Li X, Li J, Vestin E, Brännström M, Shao LR and Billig H: Differential expression patterns of glycolytic enzymes and mitochondria-dependent apoptosis in PCOS patients with endometrial hyperplasia, an early hallmark of endometrial cancer, in vivo and the impact of metformin in vitro. Int J Biol Sci. 15:714–725. 2019. View Article : Google Scholar : PubMed/NCBI | |
Buratti J, Ji L, Keren B, Lee Y, Booke S, Erdin S, Kim SY, Palculict TB, Meiner V, Chae JH, et al: De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features. J Med Genet. 58:205–212. 2021. View Article : Google Scholar : PubMed/NCBI | |
Khan I and Leventhal BL: Developmental delay. StatPearls StatPearls Publishing. Copyright © 2021, StatPearls Publishing LLC.; Treasure Island, FL: 2021 | |
Oberklaid F and Efron D: Developmental delay - identification and management. Aust Fam Physician. 34:739–742. 2005.PubMed/NCBI | |
Martiniuk AL, Vujovich-Dunn C, Park M, Yu W and Lucas BR: Plagiocephaly and developmental delay: A systematic review. J Dev Behav Pediatr. 38:67–78. 2017. View Article : Google Scholar : PubMed/NCBI | |
Zhou T, Chen Y, Zhao B, Hu S, Li J, Liu M, Liang S, Bao Z and Wu X: Characterization and functional analysis of SIAH1 during skin and hair follicle development in the angora rabbit (Oryctolagus cuniculus). Hereditas. 157:102020. View Article : Google Scholar : PubMed/NCBI | |
Farmanullah Hosseini SM, Liang A, Hua G, Rehman ZU, Talpur HS, Salim M, Ahmad S, Abulaiti A, Khan M, et al: Adaptive molecular evolution of AKT3 gene for positive diversifying selection in mammals. Biomed Res Int. 2020:25846272020. View Article : Google Scholar : PubMed/NCBI | |
Alcantara D, Timms AE, Gripp K, Baker L, Park K, Collins S, Cheng C, Stewart F, Mehta SG, Saggar A, et al: Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly. Brain. 140:2610–2622. 2017. View Article : Google Scholar : PubMed/NCBI | |
Ko HR, Jin E, Lee SB, Kim CK, Yun T, Cho SW, Park KW and Ahn JY: SIAH1 ubiquitin ligase mediates ubiquitination and degradation of Akt3 in neural development. J Biol Chem. 294:15435–15445. 2019. View Article : Google Scholar : PubMed/NCBI | |
Taoufik E and Probert L: Ischemic neuronal damage. Curr Pharm Des. 14:3565–3573. 2008. View Article : Google Scholar : PubMed/NCBI | |
Bruce-Keller AJ: Microglial-neuronal interactions in synaptic damage and recovery. J Neurosci Res. 58:191–201. 1999. View Article : Google Scholar : PubMed/NCBI | |
Huo J, Zhu XL, Ma R, Dong HL and Su BX: GAPDH/Siah1 cascade is involved in traumatic spinal cord injury and could be attenuated by sivelestat sodium. Neuroscience. 330:171–180. 2016. View Article : Google Scholar : PubMed/NCBI | |
Huo J, Ma R, Chai X, Liang HJ, Jiang P, Zhu XL, Chen X and Su BX: Inhibiting a spinal cord signaling pathway protects against ischemia injury in rats. J Thoracic Cardiovascular Surg. 157:494–503. 2019. View Article : Google Scholar : PubMed/NCBI | |
Hara MR, Thomas B, Cascio MB, Bae BI, Hester LD, Dawson VL, Dawson TM, Sawa A and Snyder SH: Neuroprotection by pharmacologic blockade of the GAPDH death cascade. Proc Natl Acad Sci USA. 103:3887–3889. 2006. View Article : Google Scholar : PubMed/NCBI | |
Bangaru ML, Park F, Hudmon A, McCallum JB and Hogan QH: Quantification of gene expression after painful nerve injury: Validation of optimal reference genes. J Mol Neurosci. 46:497–504. 2012. View Article : Google Scholar : PubMed/NCBI | |
Chuang DM and Ishitani R: A role for GAPDH in apoptosis and neurodegeneration. Nat Med. 2:609–610. 1996. View Article : Google Scholar : PubMed/NCBI | |
Su BX, Chen X, Huo J, Guo SY, Ma R and Liu YW: The synthetic cannabinoid WIN55212-2 ameliorates traumatic spinal cord injury via inhibition of GAPDH/Siah1 in a CB2-receptor dependent manner. Brain Res. 1671:85–92. 2017. View Article : Google Scholar : PubMed/NCBI | |
Zhai D, Chin K, Wang M and Liu F: Disruption of the nuclear p53-GAPDH complex protects against ischemia-induced neuronal damage. Mol Brain. 7:202014. View Article : Google Scholar : PubMed/NCBI | |
Li C, Feng JJ, Wu YP and Zhang GY: Cerebral ischemia-reperfusion induces GAPDH S-nitrosylation and nuclear translocation. Biochemistry (Mosc). 77:671–678. 2012. View Article : Google Scholar : PubMed/NCBI | |
Jiang X and Shen X: Knockdown of miR-299-5p inhibits the progression of hepatocellular carcinoma by targeting SIAH1. Bull Cancer. 105:873–883. 2018. View Article : Google Scholar : PubMed/NCBI | |
Hui Z, Zhijun Y, Yushan Y, Liping C, Yiying Z, Difan Z, Chunglit CT and Wei C: The combination of acyclovir and dexamethasone protects against Alzheimer's disease-related cognitive impairments in mice. Psychopharmacology (Berl). 237:1851–1860. 2020. View Article : Google Scholar : PubMed/NCBI | |
Vogel J, Young A, Oxtoby N, Smith R, Ossenkoppele R, Strandberg OT, Joie RL, Aksman LM, Grothe MJ, Iturria-Medina Y, et al: Four distinct trajectories of tau deposition identified in Alzheimer's disease. Nat Med. 27:871–881. 2021. View Article : Google Scholar : PubMed/NCBI | |
Knopman DS, Amieva H, Petersen RC, Chételat G, Holtzman DM, Hyman BT, Nixon RA and Jones DT: Alzheimer disease. Nat Rev Dis Primers. 7:332021. View Article : Google Scholar : PubMed/NCBI | |
Wasik U, Schneider G, Mietelska-Porowska A, Mazurkiewicz M, Fabczak H, Weis S, Zabke C, Harrington CR, Filipek A and Niewiadomska G: Calcyclin binding protein and Siah-1 interacting protein in Alzheimer's disease pathology: Neuronal localization and possible function. Neurobiol Aging. 34:1380–1388. 2013. View Article : Google Scholar : PubMed/NCBI | |
Chen Y, Lian YJ, Ma YQ, Wu CJ, Zheng YK and Xie NC: LncRNA SNHG1 promotes α-synuclein aggregation and toxicity by targeting miR-15b-5p to activate SIAH1 in human neuroblastoma SH-SY5Y cells. Neurotoxicology. 68:212–221. 2018. View Article : Google Scholar : PubMed/NCBI | |
Pang RT, Liu WM, Leung CO, Ye TM, Kwan PC, Lee KF and Yeung WS: miR-135A regulates preimplantation embryo development through down-regulation of E3 ubiquitin ligase seven in absentia homolog 1A (SIAH1A) expression. PLoS One. 6:e278782011. View Article : Google Scholar : PubMed/NCBI | |
Schafer AR, Smith JL, Pryke KM, DeFilippis VR and Hirsch AJ: The E3 ubiquitin ligase SIAH1 targets MyD88 for proteasomal degradation during dengue virus infection. Front Microbiol. 11:242020. View Article : Google Scholar : PubMed/NCBI | |
Zhou Y, Li L, Liu Q, Xing G, Kuai X, Sun J, Yin X, Wang J, Zhang L and He F: E3 ubiquitin ligase SIAH1 mediates ubiquitination and degradation of TRB3. Cell Signal. 20:942–948. 2008. View Article : Google Scholar : PubMed/NCBI | |
Nagano Y, Fukushima T, Okemoto K, Tanaka K, Bowtell DD, Ronai Z, Reed JC and Matsuzawa SI: Siah1/SIP regulates p27(kip1) stability and cell migration under metabolic stress. Cell Cycle. 10:2592–2602. 2011. View Article : Google Scholar : PubMed/NCBI | |
Hara MR and Snyder SH: Nitric oxide-GAPDH-Siah: A novel cell death cascade. Cell Mol Neurobiol. 26:527–538. 2006. View Article : Google Scholar : PubMed/NCBI | |
Song Y, Xu Y, Pan C, Yan L, Wang ZW and Zhu X: The emerging role of SPOP protein in tumorigenesis and cancer therapy. Mol Cancer. 19:22020. View Article : Google Scholar : PubMed/NCBI | |
Shah M, Stebbins JL, Dewing A, Qi J, Pellecchia M and Ronai ZA: Inhibition of Siah2 ubiquitin ligase by vitamin K3 (menadione) attenuates hypoxia and MAPK signaling and blocks melanoma tumorigenesis. Pigment Cell Melanoma Res. 22:799–808. 2009. View Article : Google Scholar : PubMed/NCBI | |
Zhang H, Cao X, Wang J, Li Q, Zhao Y and Jin X: LZTR1: A promising adaptor of the CUL3 family. Oncol Lett. 22:5642021. View Article : Google Scholar : PubMed/NCBI |