Wnt/beta-Catenin Signaling Contributes to Vincristine-Induced Neuropathic Pain
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32584132
PubMed Central
PMC8549884
DOI
10.33549/physiolres.934314
PII: 934314
Knihovny.cz E-zdroje
- MeSH
- beta-katenin metabolismus MeSH
- fytogenní protinádorové látky škodlivé účinky farmakologie MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- nádory farmakoterapie metabolismus patologie MeSH
- neuralgie chemicky indukované metabolismus patologie MeSH
- proteiny Wnt metabolismus MeSH
- signální dráha Wnt * MeSH
- signální transdukce MeSH
- vinkristin škodlivé účinky farmakologie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- beta-katenin MeSH
- CTNNB1 protein, mouse MeSH Prohlížeč
- fytogenní protinádorové látky MeSH
- proteiny Wnt MeSH
- vinkristin MeSH
Chemotherapy-induced neuropathic pain (CNP) is the major dose-limiting factor in cancer chemotherapy. However, the mechanisms underlying CNP remain elusive. In the present study, CNP was induced by repeated intraperitoneal injection of vincristine (VCR) into male C57BL/6J mice. VCR administration caused significant activation of Wnt/beta-catenin signaling, which led to the activation of astrocytes, microglia, the release of inflammatory cytokines tumour necrosis factor (TNF)-alpha, monocyte chemoattractant protein-1 (MCP-1) and the activation of subsequent mitogen-activated protein kinase (MAPK)/extracellular signal-regulated protein kinase (ERK) signaling pathway in CNP mice. Blocking Wnt/beta-catenin signaling by intrathecal administration of the inhibitors of Wnt response (IWR) effectively attenuated VCR-induced neuropathic pain. Furthermore, IWR inhibited the activation of astrocytes, microglia, TNF-alpha, MCP-1 and MAPK/ERK signaling in the spinal cord, which was triggered by VCR-induced Wnt/beta-catenin signaling upregulation. These results suggest that Wnt/beta-catenin signaling plays a critical role in VCR-induced neuropathic pain and provides evidence for potential interfering with Wnt/beta-catenin signaling to ameliorate VCR-induced neuropathic pain.
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BIKKAVILLI RK, MALBON CC. Mitogen-activated protein kinases and Wnt/beta-catenin signaling: Molecular conversations among signaling pathways. Commun Integr Biol. 2009:246–249. doi: 10.4161/cib.2.1.7503. PubMed DOI PMC
CARICASOLE A, COPANI A, CARACI F, ARONICA E, ROZEMULLER AJ, CARUSO A, STORTO M, GAVIRAGHI G, TERSTAPPEN GC, NICOLETTI F. Induction of Dickkopf-1, a negative modulator of the Wnt pathway, is associated with neuronal degeneration in Alzheimer’s brain. J Neurosci. 2004;24:6021–6027. doi: 10.1523/JNEUROSCI.1381-04.2004. PubMed DOI PMC
CHAPLAN SR, BACH FW, POGREL JW, CHUNG JM, YAKSH TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods. 1994;53:55–63. doi: 10.1016/0165-0270(94)90144-9. PubMed DOI
CIANI L, SALINAS PC. WNTs in the vertebrate nervous system: from patterning to neuronal connectivity. Nat Rev Neurosci. 2005;6:351–362. doi: 10.1038/nrn1665. PubMed DOI
DOUGHERTY PM, CATA JP, BURTON AW, VU K, WENG HR. Dysfunction in multiple primary afferent fiber subtypes revealed by quantitative sensory testing in patients with chronic vincristine-induced pain. J Pain Symptom Manage. 2007;33:166–179. doi: 10.1016/j.jpainsymman.2006.08.006. PubMed DOI
ELLIS A, BENNETT DL. Neuroinflammation and the generation of neuropathic pain. Br J Anaesth. 2013;111:26–37. doi: 10.1093/bja/aet128. PubMed DOI
FTOUH S, AKBAR MT, HIRSCH SR, de BELLEROCHE JS. Down-regulation of Dickkopf 3, a regulator of the Wnt signalling pathway, in elderly schizophrenic subjects. J Neurochem. 2005;94:520–530. doi: 10.1111/j.1471-4159.2005.03239.x. PubMed DOI
FUERER C, NUSSE R, TEN BERGE D. Wnt signalling in development and disease. Max Delbruck Center for Molecular Medicine meeting on Wnt signaling in Development and Disease. EMBO Rep. 2008;9:134–138. doi: 10.1038/sj.embor.7401159. PubMed DOI PMC
GAO YJ, JI RR. Targeting astrocyte signaling for chronic pain. Neurotherapeutics. 2010;7:482–493. doi: 10.1016/j.nurt.2010.05.016. PubMed DOI PMC
GAO YJ, XU ZZ, LIU YC, WEN YR, DECOSTERD I, JI RR. The c-Jun N-terminal kinase 1 (JNK1) in spinal astrocytes is required for the maintenance of bilateral mechanical allodynia under a persistent inflammatory pain condition. Pain. 2010;148:309–319. doi: 10.1016/j.pain.2009.11.017. PubMed DOI PMC
GRIGORYAN T, WEND P, KLAUS A, BIRCHMEIER W. Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of beta-catenin in mice. Genes Dev. 2008;22:2308–2341. doi: 10.1101/gad.1686208. PubMed DOI PMC
HU CY, ZHANG GP, ZHAO YT. Fucoidan attenuates the existing allodynia and hyperalgesia in a rat model of neuropathic pain. Neurosci Lett. 2014;571:66–71. doi: 10.1016/j.neulet.2014.04.030. PubMed DOI
ITOKAZU T, HAYANO Y, TAKAHASHI R, YAMASHITA T. Involvement of Wnt/beta-catenin signaling in the development of neuropathic pain. Neurosci Res. 2014;79:34–40. doi: 10.1016/j.neures.2013.12.002. PubMed DOI
JHA MK, SUK K. Management of glia-mediated neuroinflammation and related patents. Recent Pat Inflamm Allergy Drug Discov. 2014;8:118–124. doi: 10.2174/1872213X08666140619105915. PubMed DOI
JI XT, QIAN NS, ZHANG T, LI JM, LI XK, WANG P, ZHAO DS, HUANG G, ZHANG L, FEI Z, JIA D, NIU L. Spinal astrocytic activation contributes to mechanical allodynia in a rat chemotherapy-induced neuropathic pain model. PloS one. 2013;8:e60733. doi: 10.1371/journal.pone.0060733. PubMed DOI PMC
KIGUCHI N, MAEDA T, KOBAYASHI Y, KISHIOKA S. Up-regulation of tumor necrosis factor-alpha in spinal cord contributes to vincristine-induced mechanical allodynia in mice. Neurosci Lett. 2008;445:140–143. doi: 10.1016/j.neulet.2008.09.009. PubMed DOI
LIU D, SUN M, XU D, MA X, GAO D, YU H. Inhibition of TRPA1 and IL-6 signal alleviates neuropathic pain following chemotherapeutic bortezomib. Physiol Res. 2019;68:845–855. doi: 10.33549/physiolres.934015. PubMed DOI
LIU Y, WANG X, LU CC, KERMAN R, STEWARD O, XU XM, ZOU Y. Repulsive Wnt signaling inhibits axon regeneration after CNS injury. J Neurosci. 2008;28:8376–8382. doi: 10.1523/JNEUROSCI.1939-08.2008. PubMed DOI PMC
MacDONALD BT, TAMAI K, HE X. Wnt/beta-catenin signaling: components, mechanisms, and diseases. Dev Cell. 2009;17:9–26. doi: 10.1016/j.devcel.2009.06.016. PubMed DOI PMC
MARCHETTI B, PLUCHINO S. Wnt your brain be inflamed? Yes, it Wnt! Trends Mol Med. 2013;19:144–156. doi: 10.1016/j.molmed.2012.12.001. PubMed DOI PMC
NISHIMURA M, YU G, LEVESQUE G, ZHANG DM, RUEL L, CHEN F, MILMAN P, HOLMES E, LIANG Y, KAWARAI T, JO E, SUPALA A, ROGAEVA E, XU DM, JANUS C, LEVESQUE L, BI Q, DUTHIE M, OZMAHEL RR, MATTILA K, LANNFELT L, WESTAWAY D, MOUNT HT, WOODGETT J, ST GEORGE-HYSLOP P, et al. Presenilin mutations associated with Alzheimer disease cause defective intracellular trafficking of beta-catenin, a component of the presenilin protein complex. Nat Med. 1999;5:164–169. doi: 10.1038/5526. PubMed DOI
PACKARD M, KOO ES, GORCZYCA M, SHARPE J, CUMBERLEDGE S, BUDNIK V. The Drosophila Wnt, wingless, provides an essential signal for pre- and postsynaptic differentiation. Cell. 2002;111:319–330. doi: 10.1016/S0092-8674(02)01047-4. PubMed DOI PMC
PARK M, SHEN K. WNTs in synapse formation and neuronal circuitry. EMBO J. 2012;31:2697–2704. doi: 10.1038/emboj.2012.145. PubMed DOI PMC
RESHAM K, SHARMA SS. Pharmacologic inhibition of porcupine, disheveled, and beta-catenin in Wnt signaling pathway ameliorates diabetic peripheral neuropathy in rats. J Pain. 2019;19:30717–30725. doi: 10.1016/j.jpain.2019.04.010. PubMed DOI
SHEN DY, ZHANG W, ZENG X, LIU CQ. Inhibition of Wnt/beta-catenin signaling downregulates P-glycoprotein and reverses multi-drug resistance of cholangiocarcinoma. Cancer Sci. 2013;104:1303–1308. doi: 10.1111/cas.12223. PubMed DOI PMC
SHEN Y, ZHANG ZJ, ZHU MD, JIANG BC, YANG T, GAO YJ. Exogenous induction of HO-1 alleviates vincristine-induced neuropathic pain by reducing spinal glial activation in mice. Neurobiol Dis. 2015;79:100–110. doi: 10.1016/j.nbd.2015.04.012. PubMed DOI
SHI Y, SHU J, GELMAN BB, LISINICCHIA JG, TANG SJ. Wnt signaling in the pathogenesis of human HIV-associated pain syndromes. J Neuroimmune Pharmacol. 2013;8:956–964. doi: 10.1007/s11481-013-9474-4. PubMed DOI PMC
SPEESE SD, BUDNIK V. Wnts: up-and-coming at the synapse. Trends Neurosci. 2007;30:268–275. doi: 10.1016/j.tins.2007.04.003. PubMed DOI PMC
SVENSSON CI, MARSALA M, WESTERLUND A, CALCUTT NA, CAMPANA WM, FRESHWATER JD, CATALANO R, FENG Y, PROTTER AA, SCOTT B, YAKSH TL. Activation of p38 mitogen-activated protein kinase in spinal microglia is a critical link in inflammation-induced spinal pain processing. J Neurochem. 2003;86:1534–1544. doi: 10.1046/j.1471-4159.2003.01969.x. PubMed DOI
TANG J, JI Q, JIN L, TIAN M, ZHANG LD, LIU XY. Secreted frizzled-related protein 1 regulates the progression of neuropathic pain in mice following spinal nerve ligation. J Cell Physiol. 2018;233:5815–5822. doi: 10.1002/jcp.26358. PubMed DOI
VALLEJO R, TILLEY DM, VOGEL L, BENYAMIN R. The role of glia and the immune system in the development and maintenance of neuropathic pain. Pain Pract. 2010;10:167–184. doi: 10.1111/j.1533-2500.2010.00367.x. PubMed DOI
WATKINS LR, MILLIGAN ED, MAIER S. Glial proinflammatory cytokines mediate exaggerated pain states: implications for clinical pain. Adv Exp Med Biol. 2003;521:1–21. PubMed
WEYERBACHER AR, XU Q, TAMASDAN C, SHIN SJ, INTURRISI CE. N-Methyl-D-aspartate receptor (NMDAR) independent maintenance of inflammatory pain. Pain. 2010;148:237–246. doi: 10.1016/j.pain.2009.11.003. PubMed DOI PMC
WICKSTROM M, DYBERG C, MILOSEVIC J, EINVIK C, CALERO R, SVEINBJORNSSON B, SANDEN E, DARABI A, SIESJO P, KOOL M, KOGNER P, BARYAWNO N, JOHNSEN JI. Wnt/beta-catenin pathway regulates MGMT gene expression in cancer and inhibition of Wnt signalling prevents chemoresistance. Nat Commun. 2015;6:8904. doi: 10.1038/ncomms9904. PubMed DOI PMC
WU WP, XU XJ, HAO JX. Chronic lumbar catheterization of the spinal subarachnoid space in mice. J Neurosci Methods. 2004;133:65–69. doi: 10.1016/j.jneumeth.2003.09.015. PubMed DOI
YUAN S, SHI Y, TANG SJ. Wnt signaling in the pathogenesis of multiple sclerosis-associated chronic pain. J Neuroimmune Pharmacol. 2012;7:904–913. doi: 10.1007/s11481-012-9370-3. PubMed DOI
YUN MS, KIM SE, JEON SH, LEE JS, CHOI KY. Both ERK and Wnt/beta-catenin pathways are involved in Wnt3a-induced proliferation. J Cell Sci. 2005;118:313–322. doi: 10.1242/jcs.01601. PubMed DOI
ZHANG H, YOON SY, DOUGHERTY PM. Evidence that spinal astrocytes but not microglia contribute to the pathogenesis of Paclitaxel-induced painful neuropathy. J Pain. 2012;13:293–303. doi: 10.1016/j.jpain.2011.12.002. PubMed DOI PMC
ZHANG W, SHI Y, PENG Y, ZHONG L, ZHU S, ZHANG W, TANG SJ. Neuron activity-induced Wnt signaling up-regulates expression of brain-derived neurotrophic factor in the pain neural circuit. J Biol Chem. 2018;293:15641–15651. doi: 10.1074/jbc.RA118.002840. PubMed DOI PMC
ZHANG YK, HUANG ZJ, LIU S, LIU YP, SONG AA, SONG XJ. WNT signaling underlies the pathogenesis of neuropathic pain in rodents. J Clin Invest. 2013;123:2268–2286. doi: 10.1172/JCI65364. PubMed DOI PMC
ZHOU X, TAO L, ZHAO M, WU S, OBENG E, WANG D, ZHANG W. Wnt/beta-catenin signaling regulates brain-derived neurotrophic factor release from spinal microglia to mediate HIV1 gp120-induced neuropathic pain. Mol pain. 2020;16:1744806920922100. doi: 10.1177/1744806920922100. PubMed DOI PMC