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Volumn 171, Issue 22, 2014, Pages 5127-5138

Identifying bias in CCR1 antagonists using radiolabelled binding, receptor internalization, β-arrestin translocation and chemotaxis assays

Author keywords

[No Author keywords available]

Indexed keywords

1 [5 CHLORO 2 [2 [4 (4 FLUOROBENZYL) 2 METHYL 1 PIPERAZINYL] 2 OXOETHOXY]PHENYL]UREA; AZD 4818; BETA ARRESTIN; CCX 354; CHEMOKINE RECEPTOR ANTAGONIST; CHEMOKINE RECEPTOR CCR1; CHEMOKINE RECEPTOR CCR1 ANTAGONIST; CP 481715; G PROTEIN COUPLED RECEPTOR; GUANINE NUCLEOTIDE BINDING PROTEIN; MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA; MLN 3897; PS 899877; UNCLASSIFIED DRUG; AZD-4818; CARBANILAMIDE DERIVATIVE; CCR1 PROTEIN, HUMAN; PIPERIDINE DERIVATIVE; QUINOXALINE DERIVATIVE; QUINOXALINE-2-CARBOXYLIC ACID (4-CARBAMOYL-1-(3-FLUOROBENZYL)-2,7-DIHYDROXY-7-METHYLOCTYL)AMIDE; RETINA S ANTIGEN; SPIRO COMPOUND;

EID: 84907183530     PISSN: 00071188     EISSN: 14765381     Source Type: Journal    
DOI: 10.1111/bph.12835     Document Type: Article
Times cited : (9)

References (54)
  • 1
    • 84894823040 scopus 로고    scopus 로고
    • Internalization of the chemokine receptor CCR4 can be evoked by orthosteric and allosteric receptor antagonists
    • Ajram L, Begg M, Slack R, Cryan J, Hall D, Hodgson S et al. (2014). Internalization of the chemokine receptor CCR4 can be evoked by orthosteric and allosteric receptor antagonists. Eur J Pharmacol 729C: 75-85.
    • (2014) Eur J Pharmacol , vol.729 C , pp. 75-85
    • Ajram, L.1    Begg, M.2    Slack, R.3    Cryan, J.4    Hall, D.5    Hodgson, S.6
  • 4
    • 0032946236 scopus 로고    scopus 로고
    • Transduction of intracellular calcium signals through G protein-mediated activation of phospholipase C by recombinant sphingosine 1-phosphate receptors
    • An S, Bleu T, Zheng Y (1999). Transduction of intracellular calcium signals through G protein-mediated activation of phospholipase C by recombinant sphingosine 1-phosphate receptors. Mol Pharmacol 55: 787-794.
    • (1999) Mol Pharmacol , vol.55 , pp. 787-794
    • An, S.1    Bleu, T.2    Zheng, Y.3
  • 5
    • 0036150991 scopus 로고    scopus 로고
    • A chemokine receptor CCR-1 antagonist reduces renal fibrosis after unilateral ureter ligation
    • Anders H, Vielhauer V, Frink M, Linde Y, Cohen C, Blattner S et al. (2002). A chemokine receptor CCR-1 antagonist reduces renal fibrosis after unilateral ureter ligation. J Clin Invest 109: 251-259.
    • (2002) J Clin Invest , vol.109 , pp. 251-259
    • Anders, H.1    Vielhauer, V.2    Frink, M.3    Linde, Y.4    Cohen, C.5    Blattner, S.6
  • 6
    • 80052346775 scopus 로고    scopus 로고
    • Thymoquinone inhibits the CXCL12-induced chemotaxis of multiple myeloma cells and increases their susceptibility to Fas-mediated apoptosis
    • Badr G, Lefevre E, Mohany M (2011). Thymoquinone inhibits the CXCL12-induced chemotaxis of multiple myeloma cells and increases their susceptibility to Fas-mediated apoptosis. PLoS ONE 6: e23741.
    • (2011) PLoS ONE , vol.6 , pp. e23741
    • Badr, G.1    Lefevre, E.2    Mohany, M.3
  • 8
    • 0342322717 scopus 로고    scopus 로고
    • Macrophage inflammatory protein 1-alpha is a potential osteoclast stimulatory factor in multiple myeloma
    • Choi S, Cruz J, Craig F, Chung H, Devlin R, Roodman G et al. (2000). Macrophage inflammatory protein 1-alpha is a potential osteoclast stimulatory factor in multiple myeloma. Blood 96: 671-675.
    • (2000) Blood , vol.96 , pp. 671-675
    • Choi, S.1    Cruz, J.2    Craig, F.3    Chung, H.4    Devlin, R.5    Roodman, G.6
  • 9
    • 0036258990 scopus 로고    scopus 로고
    • G protein-coupled receptor allosterism and complexing
    • Christopoulos A, Kenakin T (2002). G protein-coupled receptor allosterism and complexing. Pharmacol Rev 54: 323-374.
    • (2002) Pharmacol Rev , vol.54 , pp. 323-374
    • Christopoulos, A.1    Kenakin, T.2
  • 11
    • 79955483382 scopus 로고    scopus 로고
    • Pharmacokinetic and pharmacodynamic evaluation of the novel CCR1 antagonist CCX354 in healthy human subjects: Implications for selection of clinical dose
    • Dairaghi D, Zhang P, Wang Y, Seitz L, Johnson D, Miao S et al. (2011). Pharmacokinetic and pharmacodynamic evaluation of the novel CCR1 antagonist CCX354 in healthy human subjects: implications for selection of clinical dose. Clin Pharmacol Ther 89: 726-734.
    • (2011) Clin Pharmacol Ther , vol.89 , pp. 726-734
    • Dairaghi, D.1    Zhang, P.2    Wang, Y.3    Seitz, L.4    Johnson, D.5    Miao, S.6
  • 12
    • 84865171804 scopus 로고    scopus 로고
    • CCR1 blockade reduces tumor burden and osteolysis in vivo in a mouse model of myeloma bone disease
    • Dairaghi D, Oyajobi B, Gupta A, McCluskey B, Miao S, Powers J et al. (2012). CCR1 blockade reduces tumor burden and osteolysis in vivo in a mouse model of myeloma bone disease. Blood 120: 1449-1457.
    • (2012) Blood , vol.120 , pp. 1449-1457
    • Dairaghi, D.1    Oyajobi, B.2    Gupta, A.3    McCluskey, B.4    Miao, S.5    Powers, J.6
  • 15
    • 0032510948 scopus 로고    scopus 로고
    • Antagonists of the receptor-G protein interface block Gi-coupled signal transduction
    • Gilchrist A, Mazzoni M, Dineen B, Dice A, Linden J, Dunwiddie T et al. (1998). Antagonists of the receptor-G protein interface block Gi-coupled signal transduction. J Biol Chem 273: 14912-14919.
    • (1998) J Biol Chem , vol.273 , pp. 14912-14919
    • Gilchrist, A.1    Mazzoni, M.2    Dineen, B.3    Dice, A.4    Linden, J.5    Dunwiddie, T.6
  • 16
    • 84887489607 scopus 로고    scopus 로고
    • The chemokine receptor CCR1 is constitutively active, which leads to G protein-independent, β-arrestin-mediated internalization
    • Gilliland C, Salanga C, Kawamura T, Trejo J, Handel T (2013). The chemokine receptor CCR1 is constitutively active, which leads to G protein-independent, β-arrestin-mediated internalization. J Biol Chem 288: 32194-32210.
    • (2013) J Biol Chem , vol.288 , pp. 32194-32210
    • Gilliland, C.1    Salanga, C.2    Kawamura, T.3    Trejo, J.4    Handel, T.5
  • 17
    • 17144435064 scopus 로고    scopus 로고
    • CP-481 715, a potent and selective CCR1 antagonist with potential therapeutic implications for inflammatory diseases
    • Gladue R, Tylaska L, Brissette W, Lira P, Kath J, Poss C et al. (2003). CP-481 715, a potent and selective CCR1 antagonist with potential therapeutic implications for inflammatory diseases. J Biol Chem 278: 40473-40480.
    • (2003) J Biol Chem , vol.278 , pp. 40473-40480
    • Gladue, R.1    Tylaska, L.2    Brissette, W.3    Lira, P.4    Kath, J.5    Poss, C.6
  • 18
    • 77955631528 scopus 로고    scopus 로고
    • CCR1 antagonists: What have we learned from clinical trials
    • Gladue R, Brown M, Zwillich S (2010). CCR1 antagonists: what have we learned from clinical trials. Curr Top Med Chem 10: 1268-1277.
    • (2010) Curr Top Med Chem , vol.10 , pp. 1268-1277
    • Gladue, R.1    Brown, M.2    Zwillich, S.3
  • 19
    • 84915737888 scopus 로고    scopus 로고
    • Novel combination of compounds to be used in the treatment of airway diseases, especially chronic obstructive pulmonary disease (COPD) and asthma
    • Patent no
    • Hansson J, Eriksson T, Mensonides-Harsema M, Mo J (2008). Novel combination of compounds to be used in the treatment of airway diseases, especially chronic obstructive pulmonary disease (COPD) and asthma. : AstraZeneca. Patent no. WO/2008/103126.
    • (2008) AstraZeneca
    • Hansson, J.1    Eriksson, T.2    Mensonides-Harsema, M.3    Mo, J.4
  • 20
    • 84915737887 scopus 로고    scopus 로고
    • Spiropiperidine compounds, a process of their preparation, pharmaceutical compositions containing them, and their use in the treatment of airway diseases, inflammatory diseases
    • Patent no
    • Hemmerling M, Ivanova S, Mensonides-Harsema M, Schulz H (2009). Spiropiperidine compounds, a process of their preparation, pharmaceutical compositions containing them, and their use in the treatment of airway diseases, inflammatory diseases, COPD or asthma.: AstraZeneca. Patent no. WO/2009/011655.
    • (2009) COPD or Asthma.: AstraZeneca
    • Hemmerling, M.1    Ivanova, S.2    Mensonides-Harsema, M.3    Schulz, H.4
  • 21
    • 14444283367 scopus 로고    scopus 로고
    • Identification and characterization of small molecule functional antagonists of the CCR1 chemokine receptor
    • Hesselgesser J, Ng H, Liang M, Zheng W, May K, Bauman J et al. (1998). Identification and characterization of small molecule functional antagonists of the CCR1 chemokine receptor. J Biol Chem 273: 15687-15692.
    • (1998) J Biol Chem , vol.273 , pp. 15687-15692
    • Hesselgesser, J.1    Ng, H.2    Liang, M.3    Zheng, W.4    May, K.5    Bauman, J.6
  • 22
    • 23844544931 scopus 로고    scopus 로고
    • BX471: A CCR1 antagonist with anti-inflammatory activity in man
    • Horuk R (2005). BX471: a CCR1 antagonist with anti-inflammatory activity in man. Mini Rev Med Chem 5: 791-804.
    • (2005) Mini Rev Med Chem , vol.5 , pp. 791-804
    • Horuk, R.1
  • 23
    • 84891485988 scopus 로고    scopus 로고
    • Structure activity relationships of fused bicyclic and urea derivatives of spirocyclic compounds as potent CCR1 antagonists
    • Hossain N, Mensonides-Harsema M, Cooper M, Eriksson T, Ivanova S, Bergström L (2014). Structure activity relationships of fused bicyclic and urea derivatives of spirocyclic compounds as potent CCR1 antagonists. Bioorg Med Chem Lett 24: 108-112.
    • (2014) Bioorg Med Chem Lett , vol.24 , pp. 108-112
    • Hossain, N.1    Mensonides-Harsema, M.2    Cooper, M.3    Eriksson, T.4    Ivanova, S.5    Bergström, L.6
  • 24
    • 80054927712 scopus 로고    scopus 로고
    • Therapeutic potential of CCR1 antagonists for multiple myeloma
    • Karash A, Gilchrist A (2011). Therapeutic potential of CCR1 antagonists for multiple myeloma. Future Med Chem 3: 1889-1908.
    • (2011) Future Med Chem , vol.3 , pp. 1889-1908
    • Karash, A.1    Gilchrist, A.2
  • 25
    • 0029812311 scopus 로고    scopus 로고
    • The classification of seven transmembrane receptors in recombinant expression systems
    • Kenakin T (1996). The classification of seven transmembrane receptors in recombinant expression systems. Pharmacol Rev 48: 413-463.
    • (1996) Pharmacol Rev , vol.48 , pp. 413-463
    • Kenakin, T.1
  • 26
    • 33751183557 scopus 로고    scopus 로고
    • Determining the potency and molecular mechanism of action of insurmountable antagonists
    • Kenakin T, Jenkinson S, Watson C (2006). Determining the potency and molecular mechanism of action of insurmountable antagonists. J Pharmacol Exp Ther 319: 710-723.
    • (2006) J Pharmacol Exp Ther , vol.319 , pp. 710-723
    • Kenakin, T.1    Jenkinson, S.2    Watson, C.3
  • 27
    • 77955664554 scopus 로고    scopus 로고
    • Tolerability and efficacy of inhaled AZD4818, a CCR1 antagonist, in moderate to severe COPD patients
    • Kerstjens H, Bjermer L, Eriksson L, Dahlström K, Vestbo J (2010). Tolerability and efficacy of inhaled AZD4818, a CCR1 antagonist, in moderate to severe COPD patients. Respir Med 104: 1297-1303.
    • (2010) Respir Med , vol.104 , pp. 1297-1303
    • Kerstjens, H.1    Bjermer, L.2    Eriksson, L.3    Dahlström, K.4    Vestbo, J.5
  • 28
    • 0038386032 scopus 로고    scopus 로고
    • Macrophage inflammatory protein 1-alpha (MIP-1 alpha) triggers migration and signaling cascades mediating survival and proliferation in multiple myeloma (MM) cells
    • Lentzsch S, Gries M, Janz M, Bargou R, Dörken B, Mapara M (2003). Macrophage inflammatory protein 1-alpha (MIP-1 alpha) triggers migration and signaling cascades mediating survival and proliferation in multiple myeloma (MM) cells. Blood 101: 3568-3573.
    • (2003) Blood , vol.101 , pp. 3568-3573
    • Lentzsch, S.1    Gries, M.2    Janz, M.3    Bargou, R.4    Dörken, B.5    Mapara, M.6
  • 30
    • 33846495529 scopus 로고    scopus 로고
    • Molecular characterization of human multiple myeloma cell lines by integrative genomics: Insights into the biology of the disease
    • Lombardi L, Poretti G, Mattioli M, Fabris S, Agnelli L, Bicciato S et al. (2007). Molecular characterization of human multiple myeloma cell lines by integrative genomics: insights into the biology of the disease. Genes Chromosomes Cancer 46: 226-238.
    • (2007) Genes Chromosomes Cancer , vol.46 , pp. 226-238
    • Lombardi, L.1    Poretti, G.2    Mattioli, M.3    Fabris, S.4    Agnelli, L.5    Bicciato, S.6
  • 31
    • 10744221725 scopus 로고    scopus 로고
    • Gene expression profiling of multiple myeloma reveals molecular portraits in relation to the pathogenesis of the disease
    • Magrangeas F, Nasser V, Avet-Loiseau H, Loriod B, Decaux O, Granjeaud S et al. (2003). Gene expression profiling of multiple myeloma reveals molecular portraits in relation to the pathogenesis of the disease. Blood 101: 4998-5006.
    • (2003) Blood , vol.101 , pp. 4998-5006
    • Magrangeas, F.1    Nasser, V.2    Avet-Loiseau, H.3    Loriod, B.4    Decaux, O.5    Granjeaud, S.6
  • 33
    • 33751190044 scopus 로고    scopus 로고
    • Role of CCR1 and CCR5 in homing and growth of multiple myeloma and in the development of osteolytic lesions: A study in the 5TMM model
    • Menu E, De Leenheer E, De Raeve H, Coulton L, Imanishi T, Miyashita K et al. (2006). Role of CCR1 and CCR5 in homing and growth of multiple myeloma and in the development of osteolytic lesions: a study in the 5TMM model. Clin Exp Metastasis 23: 291-300.
    • (2006) Clin Exp Metastasis , vol.23 , pp. 291-300
    • Menu, E.1    De Leenheer, E.2    De Raeve, H.3    Coulton, L.4    Imanishi, T.5    Miyashita, K.6
  • 34
    • 64349119754 scopus 로고    scopus 로고
    • Novel pyrrolidine ureas as C-C chemokine receptor 1 (CCR1) antagonists
    • Merritt J, Liu J, Quadros E, Morris M, Liu R, Zhang R et al. (2009). Novel pyrrolidine ureas as C-C chemokine receptor 1 (CCR1) antagonists. J Med Chem 52: 1295-1301.
    • (2009) J Med Chem , vol.52 , pp. 1295-1301
    • Merritt, J.1    Liu, J.2    Quadros, E.3    Morris, M.4    Liu, R.5    Zhang, R.6
  • 37
    • 0027462365 scopus 로고
    • Molecular cloning, functional expression, and signaling characteristics of a C-C chemokine receptor
    • Neote K, DiGregorio D, Mak J, Horuk R, Schall T (1993). Molecular cloning, functional expression, and signaling characteristics of a C-C chemokine receptor. Cell 72: 415-425.
    • (1993) Cell , vol.72 , pp. 415-425
    • Neote, K.1    Digregorio, D.2    Mak, J.3    Horuk, R.4    Schall, T.5
  • 38
    • 74949096245 scopus 로고    scopus 로고
    • AZD-4818, a chemokine CCR1 antagonist: WO2008103126 and WO2009011653
    • Norman P (2009). AZD-4818, a chemokine CCR1 antagonist: WO2008103126 and WO2009011653. Expert Opin Ther Pat 19: 1629-1633.
    • (2009) Expert Opin Ther Pat , vol.19 , pp. 1629-1633
    • Norman, P.1
  • 39
    • 13844317079 scopus 로고    scopus 로고
    • MIP-1alpha utilizes both CCR1 and CCR5 to induce osteoclast formation and increase adhesion of myeloma cells to marrow stromal cells
    • Oba Y, Lee J, Ehrlich L, Chung H, Jelinek D, Callander N et al. (2005). MIP-1alpha utilizes both CCR1 and CCR5 to induce osteoclast formation and increase adhesion of myeloma cells to marrow stromal cells. Exp Hematol 33: 272-278.
    • (2005) Exp Hematol , vol.33 , pp. 272-278
    • Oba, Y.1    Lee, J.2    Ehrlich, L.3    Chung, H.4    Jelinek, D.5    Callander, N.6
  • 41
    • 67649341169 scopus 로고    scopus 로고
    • Chemokine receptor antagonists: Part 1
    • Pease J, Horuk R (2009). Chemokine receptor antagonists: part 1. Expert Opin Ther Pat 19: 39-58.
    • (2009) Expert Opin Ther Pat , vol.19 , pp. 39-58
    • Pease, J.1    Horuk, R.2
  • 43
    • 84873727207 scopus 로고    scopus 로고
    • 1-(4-Phenylpiperazin-1-yl)-2-(1H-pyrazol-1-yl)ethanones as novel CCR1 antagonists
    • Pennell A, Aggen J, Sen S, Chen W, Xu Y, Sullivan E et al. (2013). 1-(4-Phenylpiperazin-1-yl)-2-(1H-pyrazol-1-yl)ethanones as novel CCR1 antagonists. Bioorg Med Chem Lett 23: 1228-1231.
    • (2013) Bioorg Med Chem Lett , vol.23 , pp. 1228-1231
    • Pennell, A.1    Aggen, J.2    Sen, S.3    Chen, W.4    Xu, Y.5    Sullivan, E.6
  • 45
    • 84890282799 scopus 로고    scopus 로고
    • Biased agonism as a mechanism for differential signaling by chemokine receptors
    • Rajagopal S, Bassoni D, Campbell J, Gerard N, Gerard C, Wehrman T (2013). Biased agonism as a mechanism for differential signaling by chemokine receptors. J Biol Chem 288: 35039-35048.
    • (2013) J Biol Chem , vol.288 , pp. 35039-35048
    • Rajagopal, S.1    Bassoni, D.2    Campbell, J.3    Gerard, N.4    Gerard, C.5    Wehrman, T.6
  • 46
    • 0031875263 scopus 로고    scopus 로고
    • Macrophage scavenger receptor confers an adherent phenotype to cells in culture
    • Robbins A, Horlick R (1998). Macrophage scavenger receptor confers an adherent phenotype to cells in culture. Biotechniques 25: 240-244.
    • (1998) Biotechniques , vol.25 , pp. 240-244
    • Robbins, A.1    Horlick, R.2
  • 47
    • 70450245348 scopus 로고    scopus 로고
    • Increased expression of macrophage inflammatory protein-1alpha on trephine biopsies correlates with extensive bone disease, increased angiogenesis and advanced stage in newly diagnosed patients with multiple myeloma
    • Roussou M, Tasidou A, Dimopoulos M, Kastritis E, Migkou M, Christoulas D et al. (2009). Increased expression of macrophage inflammatory protein-1alpha on trephine biopsies correlates with extensive bone disease, increased angiogenesis and advanced stage in newly diagnosed patients with multiple myeloma. Leukemia 23: 2177-2181.
    • (2009) Leukemia , vol.23 , pp. 2177-2181
    • Roussou, M.1    Tasidou, A.2    Dimopoulos, M.3    Kastritis, E.4    Migkou, M.5    Christoulas, D.6
  • 48
    • 63849093676 scopus 로고    scopus 로고
    • Myeloma bone disease: Recent advances in biology, diagnosis, and treatment
    • Sezer O (2009). Myeloma bone disease: recent advances in biology, diagnosis, and treatment. Oncologist 14: 276-283.
    • (2009) Oncologist , vol.14 , pp. 276-283
    • Sezer, O.1
  • 49
    • 0037147145 scopus 로고    scopus 로고
    • Beta-arrestin2 is critically involved in CXCR4-mediated chemotaxis, and this is mediated by its enhancement of p38 MAPK activation
    • Sun Y, Cheng Z, Ma L, Pei G (2002). Beta-arrestin2 is critically involved in CXCR4-mediated chemotaxis, and this is mediated by its enhancement of p38 MAPK activation. J Biol Chem 277: 49212-49219.
    • (2002) J Biol Chem , vol.277 , pp. 49212-49219
    • Sun, Y.1    Cheng, Z.2    Ma, L.3    Pei, G.4
  • 50
    • 34547619405 scopus 로고    scopus 로고
    • Multiple myeloma plasma cells show different chemokine receptor profiles at sites of disease activity
    • Trentin L, Miorin M, Facco M, Baesso I, Carraro S, Cabrelle A et al. (2007). Multiple myeloma plasma cells show different chemokine receptor profiles at sites of disease activity. Br J Haematol 138: 594-602.
    • (2007) Br J Haematol , vol.138 , pp. 594-602
    • Trentin, L.1    Miorin, M.2    Facco, M.3    Baesso, I.4    Carraro, S.5    Cabrelle, A.6
  • 51
    • 0032479930 scopus 로고    scopus 로고
    • Identification of C-C chemokine receptor 1 (CCR1) as the monocyte hemofiltrate C-C chemokine (HCC)-1 receptor
    • Tsou C, Gladue R, Carroll L, Paradis T, Boyd J, Nelson R et al. (1998). Identification of C-C chemokine receptor 1 (CCR1) as the monocyte hemofiltrate C-C chemokine (HCC)-1 receptor. J Exp Med 188: 603-608.
    • (1998) J Exp Med , vol.188 , pp. 603-608
    • Tsou, C.1    Gladue, R.2    Carroll, L.3    Paradis, T.4    Boyd, J.5    Nelson, R.6
  • 52
    • 33748747498 scopus 로고    scopus 로고
    • Predictions of CCR1 chemokine receptor structure and BX 471 antagonist binding followed by experimental validation
    • Vaidehi N, Schlyer S, Trabanino R, Floriano W, Abrol R, Sharma S et al. (2006). Predictions of CCR1 chemokine receptor structure and BX 471 antagonist binding followed by experimental validation. J Biol Chem 281: 27613-27620.
    • (2006) J Biol Chem , vol.281 , pp. 27613-27620
    • Vaidehi, N.1    Schlyer, S.2    Trabanino, R.3    Floriano, W.4    Abrol, R.5    Sharma, S.6
  • 53
    • 80051761546 scopus 로고    scopus 로고
    • CCR1 as a target for multiple myeloma
    • Vallet S, Anderson K (2011). CCR1 as a target for multiple myeloma. Expert Opin Ther Targets 15: 1037-1047.
    • (2011) Expert Opin Ther Targets , vol.15 , pp. 1037-1047
    • Vallet, S.1    Anderson, K.2
  • 54
    • 36348988548 scopus 로고    scopus 로고
    • MLN-3897, a novel CCR1 inhibitor, impairs osteoclastogenesis and inhibits the interaction of multiple myeloma cells and osteoclasts
    • Vallet S, Raje N, Ishitsuka K, Hideshima T, Podar K, Chhetri S et al. (2007). MLN-3897, a novel CCR1 inhibitor, impairs osteoclastogenesis and inhibits the interaction of multiple myeloma cells and osteoclasts. Blood 110: 3744-3752.
    • (2007) Blood , vol.110 , pp. 3744-3752
    • Vallet, S.1    Raje, N.2    Ishitsuka, K.3    Hideshima, T.4    Podar, K.5    Chhetri, S.6


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