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      Targeting calcium signaling in cancer therapy.

      Acta Pharmaceutica Sinica. B
      Elsevier BV
      TRIM, 1-(2-(trifluoromethyl) phenyl) imidazole, OSCC, oral squamous cell carcinoma cells, SPCA, secretory pathway Ca2+-ATPase, CPZ, capsazepine, CBD, cannabidiol, MLCK, myosin light-chain kinase, RyR, ryanodine receptor, MICU (1, 2, 3), mitochondrial calcium uptake (type 1, type 2, type 3), CBG, cannabigerol, CRAC, Ca2+ release-activated Ca2+ channel, Ca2+ channels, MCUR1, MCU uniporter regulator 1, CaM, calmodulin, ROS, reactive oxygen species, PM, plasma membrane, MCU, mitochondrial Ca2+ uniporter, TEA, tetraethylammonium, VGCC, voltage-gated Ca2+ channel, Apoptosis, NSCLC, non-small cell lung cancer, IP3R (1, 2, 3), IP3 receptor (type 1, type 2, type 3), SOCE, store-operated Ca2+ entry, 20-GPPD, 20-O-β-D-glucopyranosyl-20(S)-protopanaxadiol, IP3, inositol 1,4,5-trisphosphate, mAb, monoclonal antibody, PTP, permeability transition pore, TPC2, two-pore channel 2, Cell proliferation, HCX, H+/Ca2+ exchangers, TG, thapsigargin, CTL, cytotoxic T cells, Channel blockers;, ER/SR, endoplasmic/sarcoplasmic reticulum, SERCA, SR/ER Ca2+-ATPase, PMCA, plasma membrane Ca2+-ATPase, NFAT, nuclear factor of activated T cells, CaMKII, calmodulin-dependent protein kinase II, Store-operated Ca2+ entry, Cancer therapy, PKC, protein kinase C, TRP (A, C, M, ML, N, P, V), transient receptor potential (ankyrin, canonical, melastatin, mucolipin, no mechanoreceptor potential C, polycystic, vanilloid), NF-κB, nuclear factor-κB, NCX, Na+/Ca2+ exchanger, Migration, CYP3A4, cytochrome P450 3A4

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          Abstract

          The intracellular calcium ions (Ca2+) act as second messenger to regulate gene transcription, cell proliferation, migration and death. Accumulating evidences have demonstrated that intracellular Ca2+homeostasis is altered in cancer cells and the alteration is involved in tumor initiation, angiogenesis, progression and metastasis. Targeting derailed Ca2+signaling for cancer therapy has become an emerging research area. This review summarizes some important Ca2+channels, transporters and Ca2+-ATPases, which have been reported to be altered in human cancer patients. It discusses the current research effort toward evaluation of the blockers, inhibitors or regulators for Ca2+channels/transporters or Ca2+-ATPase pumps as anti-cancer drugs. This review is also aimed to stimulate interest in, and support for research into the understanding of cellular mechanisms underlying the regulation of Ca2+signaling in different cancer cells, and to search for novel therapies to cure these malignancies by targeting Ca2+channels or transporters.

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          Author and article information

          Journal
          28119804
          5237760
          10.1016/j.apsb.2016.11.001

          TRIM, 1-(2-(trifluoromethyl) phenyl) imidazole,OSCC, oral squamous cell carcinoma cells,SPCA, secretory pathway Ca2+-ATPase,CPZ, capsazepine,CBD, cannabidiol,MLCK, myosin light-chain kinase,RyR, ryanodine receptor,MICU (1, 2, 3), mitochondrial calcium uptake (type 1, type 2, type 3),CBG, cannabigerol,CRAC, Ca2+ release-activated Ca2+ channel,Ca2+ channels,MCUR1, MCU uniporter regulator 1,CaM, calmodulin,ROS, reactive oxygen species,PM, plasma membrane,MCU, mitochondrial Ca2+ uniporter,TEA, tetraethylammonium,VGCC, voltage-gated Ca2+ channel,Apoptosis,NSCLC, non-small cell lung cancer,IP3R (1, 2, 3), IP3 receptor (type 1, type 2, type 3),SOCE, store-operated Ca2+ entry,20-GPPD, 20-O-β-D-glucopyranosyl-20(S)-protopanaxadiol,IP3, inositol 1,4,5-trisphosphate,mAb, monoclonal antibody,PTP, permeability transition pore,TPC2, two-pore channel 2,Cell proliferation,HCX, H+/Ca2+ exchangers,TG, thapsigargin,CTL, cytotoxic T cells,Channel blockers;,ER/SR, endoplasmic/sarcoplasmic reticulum,SERCA, SR/ER Ca2+-ATPase,PMCA, plasma membrane Ca2+-ATPase,NFAT, nuclear factor of activated T cells,CaMKII, calmodulin-dependent protein kinase II,Store-operated Ca2+ entry,Cancer therapy,PKC, protein kinase C,TRP (A, C, M, ML, N, P, V), transient receptor potential (ankyrin, canonical, melastatin, mucolipin, no mechanoreceptor potential C, polycystic, vanilloid),NF-κB, nuclear factor-κB,NCX, Na+/Ca2+ exchanger,Migration,CYP3A4, cytochrome P450 3A4
          TRIM, 1-(2-(trifluoromethyl) phenyl) imidazole, OSCC, oral squamous cell carcinoma cells, SPCA, secretory pathway Ca2+-ATPase, CPZ, capsazepine, CBD, cannabidiol, MLCK, myosin light-chain kinase, RyR, ryanodine receptor, MICU (1, 2, 3), mitochondrial calcium uptake (type 1, type 2, type 3), CBG, cannabigerol, CRAC, Ca2+ release-activated Ca2+ channel, Ca2+ channels, MCUR1, MCU uniporter regulator 1, CaM, calmodulin, ROS, reactive oxygen species, PM, plasma membrane, MCU, mitochondrial Ca2+ uniporter, TEA, tetraethylammonium, VGCC, voltage-gated Ca2+ channel, Apoptosis, NSCLC, non-small cell lung cancer, IP3R (1, 2, 3), IP3 receptor (type 1, type 2, type 3), SOCE, store-operated Ca2+ entry, 20-GPPD, 20-O-β-D-glucopyranosyl-20(S)-protopanaxadiol, IP3, inositol 1,4,5-trisphosphate, mAb, monoclonal antibody, PTP, permeability transition pore, TPC2, two-pore channel 2, Cell proliferation, HCX, H+/Ca2+ exchangers, TG, thapsigargin, CTL, cytotoxic T cells, Channel blockers;, ER/SR, endoplasmic/sarcoplasmic reticulum, SERCA, SR/ER Ca2+-ATPase, PMCA, plasma membrane Ca2+-ATPase, NFAT, nuclear factor of activated T cells, CaMKII, calmodulin-dependent protein kinase II, Store-operated Ca2+ entry, Cancer therapy, PKC, protein kinase C, TRP (A, C, M, ML, N, P, V), transient receptor potential (ankyrin, canonical, melastatin, mucolipin, no mechanoreceptor potential C, polycystic, vanilloid), NF-κB, nuclear factor-κB, NCX, Na+/Ca2+ exchanger, Migration, CYP3A4, cytochrome P450 3A4

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