2007
DOI: 10.1016/j.ceca.2006.11.005
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A novel function of capsaicin-sensitive TRPV1 channels: Involvement in cell migration

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Cited by 137 publications
(107 citation statements)
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References 58 publications
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“…In this context, previous studies provided evidence for tonic activation of NK-1 receptors, through NK-1 receptor antagonist SR14033 administration, which blocked the second phase of the orofacial formalin test in rat (Henry et al, 1999;Luccarini et al, 2003). Waning et al (2007) demonstrated that capsaicin-sensitive transient receptor potential vaniloid 1 (TRPV1) is one of the Ca +2 influx channels involved in cell migration, which plays an important role in pain transduction. Moreover, Honda et al (2008) suggest that TRPV1 receptor mechanisms in rat facial skin influence nociceptive responses to noxious cutaneous thermal and mechanical stimuli by inducing neuroplastic changes in subnucleus caudalis (Vc) and C1-C2 neurons.…”
Section: Discussionmentioning
confidence: 95%
“…In this context, previous studies provided evidence for tonic activation of NK-1 receptors, through NK-1 receptor antagonist SR14033 administration, which blocked the second phase of the orofacial formalin test in rat (Henry et al, 1999;Luccarini et al, 2003). Waning et al (2007) demonstrated that capsaicin-sensitive transient receptor potential vaniloid 1 (TRPV1) is one of the Ca +2 influx channels involved in cell migration, which plays an important role in pain transduction. Moreover, Honda et al (2008) suggest that TRPV1 receptor mechanisms in rat facial skin influence nociceptive responses to noxious cutaneous thermal and mechanical stimuli by inducing neuroplastic changes in subnucleus caudalis (Vc) and C1-C2 neurons.…”
Section: Discussionmentioning
confidence: 95%
“…However, with respect to TRPV1 channel diverging results have been reported, suggesting that its role in malignant motility and invasion may be cancer cell-specific. Indeed, activation of the TRPV1 channel was shown to promote migration of human hepatoblastoma cells in response to hepatocyte growth factor treatment [74]. On the other hand, in urothelial cancer TRPV1 downregulation rather than enhancement was found to correlate with more aggressive and invasive tumour phenotype suggesting that such downregulation may present an independent negative prognostic factor for bladder cancer patients [81].…”
Section: Ca 2þ Remodelling In Promotion Cell Migration and Metastasismentioning
confidence: 99%
“…The following Ca 2þ permeable channels have been implicated in the enhanced migration of various types of cancer cells (figure 3): TRPC1 [64], TRPM7 [65 -71], TRPM8 [43,72,73], TRPV1 [74], TRPV2 [75], TRPV6 [40], STIM1 and ORAI1 SOC constituents [13,[76][77][78][79], some types of VGCCs [35,80]. Owing to the presence of mechanical stimulusdependent and Mg-ATP-dependent modes of activation TRPM7 was especially implicated in providing spatially restricted Ca 2þ entry in response to local membrane stretch in front of migrating cells [66,69] as well as promoting m-calpain-mediated disassembly of peripheral adhesions under decreased intracellular Mg-ATP levels [65] typically found in hypoxic tumour conditions.…”
Section: Ca 2þ Remodelling In Promotion Cell Migration and Metastasismentioning
confidence: 99%
“…Interesting candidates are members of the transient receptor potential (TRP) family of cation channels. We have recently shown that activation of the TRP vanilloid 1 channel (TRPVA) accelerates migration of human hepatoblastoma cells [44]. Here, we study the effect of TRP cation channel subfamily C member 1 (TRPC1) on migration of transformed renal epithelial (Madin-Darby canine kidney-focus (MDCK-F)) cells.…”
Section: Introductionmentioning
confidence: 99%