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Volumn 23, Issue 4, 2017, Pages 1025-1035

Identification of CCR2 and CD180 as robust pharmacodynamic tumor and blood biomarkers for clinical use with BRD4/BET inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

6 (4 CHLOROPHENYL) N ETHYL 8 METHOXY 1 METHYL 4H [1,2,4]TRIAZOLO[4,3 A][1,4]BENZODIAZEPINE 4 ACETAMIDE; AZD 5153; BIRABRESIB; BROMODOMAIN INHIBITOR; CD180 ANTIGEN; CHEMOKINE RECEPTOR CCR2; LYMPHOCYTE ANTIGEN; MESSENGER RNA; TUMOR MARKER; UNCLASSIFIED DRUG; AZD5153; BRD4 PROTEIN, HUMAN; CCR2 PROTEIN, HUMAN; CD180 PROTEIN, HUMAN; FUSED HETEROCYCLIC RINGS; LEUKOCYTE ANTIGEN; MYC PROTEIN; MYC PROTEIN, HUMAN; NUCLEAR PROTEIN; PIPERAZINE DERIVATIVE; TRANSCRIPTION FACTOR;

EID: 85012910498     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-16-1658     Document Type: Article
Times cited : (20)

References (30)
  • 1
    • 84912072883 scopus 로고    scopus 로고
    • Development and classes of epigenetic drugs for cancer
    • Dhanak D, Jackson P. Development and classes of epigenetic drugs for cancer. Biochem Biophys Res Commun 2014;455:58-69.
    • (2014) Biochem Biophys Res Commun , vol.455 , pp. 58-69
    • Dhanak, D.1    Jackson, P.2
  • 3
    • 84925625370 scopus 로고    scopus 로고
    • Inhibition of BET bromodomains as a therapeutic strategy for cancer drug discovery
    • Fu L, Tian M, Li X, Li J, Huang J, Ouyang L, et al. Inhibition of BET bromodomains as a therapeutic strategy for cancer drug discovery. Oncotarget 2015;6:5501-16.
    • (2015) Oncotarget , vol.6 , pp. 5501-5516
    • Fu, L.1    Tian, M.2    Li, X.3    Li, J.4    Huang, J.5    Ouyang, L.6
  • 4
    • 84964727676 scopus 로고    scopus 로고
    • Clinical Response of Carcinomas Harboring the BRD4-NUT Oncoprotein to the Targeted Bromodomain Inhibitor OTX015/MK-8628
    • Stathis A, Zucca E, Bekradda M, Gomez-Roca C, Delord J-P, de La Motte Rouge T, et al. Clinical Response of Carcinomas Harboring the BRD4-NUT Oncoprotein to the Targeted Bromodomain Inhibitor OTX015/MK-8628. Cancer Discov 2016;6:492-500.
    • (2016) Cancer Discov , vol.6 , pp. 492-500
    • Stathis, A.1    Zucca, E.2    Bekradda, M.3    Gomez-Roca, C.4    Delord, J.-P.5    De La Motte Rouge, T.6
  • 5
    • 84962523963 scopus 로고    scopus 로고
    • Bromodomain inhibitor OTX015 in patients with acute leukaemia: A dose-escalation, phase 1 study
    • Berthon C, Raffoux E, Thomas X, Vey N, Gomez-Roca C, Yee K, et al. Bromodomain inhibitor OTX015 in patients with acute leukaemia: a dose-escalation, phase 1 study. Lancet Haematol 2016;3:e186-95.
    • (2016) Lancet Haematol , vol.3 , pp. e186-e195
    • Berthon, C.1    Raffoux, E.2    Thomas, X.3    Vey, N.4    Gomez-Roca, C.5    Yee, K.6
  • 6
    • 84962488380 scopus 로고    scopus 로고
    • Bromodomain inhibitor OTX015 in patients with lymphoma or multiple myeloma: A dose-escalation, open-label, pharmacokinetic, phase 1 study
    • Amorim S, Stathis A, Gleeson M, Iyengar S, Magarotto V, Leleu X, et al. Bromodomain inhibitor OTX015 in patients with lymphoma or multiple myeloma: a dose-escalation, open-label, pharmacokinetic, phase 1 study. Lancet Haematol 2016;3:e196-204.
    • (2016) Lancet Haematol , vol.3 , pp. e196-e204
    • Amorim, S.1    Stathis, A.2    Gleeson, M.3    Iyengar, S.4    Magarotto, V.5    Leleu, X.6
  • 10
    • 84986294614 scopus 로고    scopus 로고
    • Triazolopyridazine-based bromodomain and extraterminal inhibitors: The discovery of (3R)-4-[2-[4-[1-(3-methoxy-[1,2,4]triazolo[4,3-b]pyr-idazin-6-yl)-4-piperidyl]phenoxy]ethyl]-1,3-dimethyl-piperazin-2-one (AZD5153)
    • Bradbury RH, Callis R, Carr GR, Chen H, Clark E, Feron L, et al. Triazolopyridazine-based bromodomain and extraterminal inhibitors: the discovery of (3R)-4-[2-[4-[1-(3-methoxy-[1,2,4]triazolo[4,3-b]pyr-idazin-6-yl)-4-piperidyl]phenoxy]ethyl]-1,3-dimethyl-piperazin-2-one (AZD5153). J Med Chem 2016;59:7801-17.
    • (2016) J Med Chem , vol.59 , pp. 7801-7817
    • Bradbury, R.H.1    Callis, R.2    Carr, G.R.3    Chen, H.4    Clark, E.5    Feron, L.6
  • 13
    • 84995428342 scopus 로고    scopus 로고
    • AZD5153: A novel bivalent BET bromodomain inhibitor highly active against hematologic malignancies
    • et al. Aug 29. pii: molcanther.0141.2016. [Epub ahead of print]
    • Rhyasen G, Hattersley M, Yao Y, Dulak A, Wang W, Petteruti P, et al. et al. AZD5153: a novel bivalent BET bromodomain inhibitor highly active against hematologic malignancies. Mol Cancer Ther 2016 Aug 29. pii: molcanther.0141.2016. [Epub ahead of print].
    • (2016) Mol Cancer Ther
    • Rhyasen, G.1    Hattersley, M.2    Yao, Y.3    Dulak, A.4    Wang, W.5    Petteruti, P.6
  • 15
    • 84938249789 scopus 로고    scopus 로고
    • BET inhibitor OTX015 targets BRD2 and BRD4 and decreases c-MYC in acute leukemia cells
    • Coude M-M, Braun T, Berrou J, Dupont M, Bertrand S, Masse A, et al. BET inhibitor OTX015 targets BRD2 and BRD4 and decreases c-MYC in acute leukemia cells. Oncotarget 2015;6:17698-712.
    • (2015) Oncotarget , vol.6 , pp. 17698-17712
    • Coude, M.-M.1    Braun, T.2    Berrou, J.3    Dupont, M.4    Bertrand, S.5    Masse, A.6
  • 16
    • 80055000824 scopus 로고    scopus 로고
    • RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia
    • Zuber J, Shi J, Wang E, Rappaport AR, Herrmann H, Sison EA, et al. RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia. Nature 2011;478:524-8.
    • (2011) Nature , vol.478 , pp. 524-528
    • Zuber, J.1    Shi, J.2    Wang, E.3    Rappaport, A.R.4    Herrmann, H.5    Sison, E.A.6
  • 17
    • 84876222028 scopus 로고    scopus 로고
    • Selective inhibition of tumor oncogenes by disruption of super-enhancers
    • Loven J, Hoke HA, Lin CY, Lau A, Orlando DA, Vakoc CR, et al. Selective inhibition of tumor oncogenes by disruption of super-enhancers. Cell 2013;153:320-34.
    • (2013) Cell , vol.153 , pp. 320-334
    • Loven, J.1    Hoke, H.A.2    Lin, C.Y.3    Lau, A.4    Orlando, D.A.5    Vakoc, C.R.6
  • 18
    • 84943747585 scopus 로고    scopus 로고
    • Disruption of BRD4 at H3K27Ac-enriched enhancer region correlates with decreased c-Myc expression in Merkel cell carcinoma
    • Sengupta D, Kannan A, Kern M, Moreno MA, Vural E, Stack B, et al. Disruption of BRD4 at H3K27Ac-enriched enhancer region correlates with decreased c-Myc expression in Merkel cell carcinoma. Epigenetics 2015;10:460-6.
    • (2015) Epigenetics , vol.10 , pp. 460-466
    • Sengupta, D.1    Kannan, A.2    Kern, M.3    Moreno, M.A.4    Vural, E.5    Stack, B.6
  • 19
    • 84959332179 scopus 로고    scopus 로고
    • HEXIM1 induction is mechanistically involved in mediating anti-AML activity of BET protein bromodomain antagonist
    • Devaraj SGT, Fiskus W, Shah B, Qi J, Sun B, Iyer SP, et al. HEXIM1 induction is mechanistically involved in mediating anti-AML activity of BET protein bromodomain antagonist. Leukemia 2016;30:504-8.
    • (2016) Leukemia , vol.30 , pp. 504-508
    • Devaraj, S.G.T.1    Fiskus, W.2    Shah, B.3    Qi, J.4    Sun, B.5    Iyer, S.P.6
  • 20
    • 84896808244 scopus 로고    scopus 로고
    • Brd4 and HEXIM1: Multiple roles in P-TEFb regulation and cancer
    • Chen R, Yik JHN, Lew QJ, Chao S-H. Brd4 and HEXIM1: multiple roles in P-TEFb regulation and cancer. Biomed Res Int 2014;2014:232870.
    • (2014) Biomed Res Int , vol.2014
    • Chen, R.1    Yik, J.H.N.2    Lew, Q.J.3    Chao, S.-H.4
  • 21
    • 84957837612 scopus 로고    scopus 로고
    • RVX-208, a BET-inhibitor for treating atherosclerotic cardiovascular disease, raises ApoA-I/HDL and represses pathways that contribute to cardiovascular disease
    • Gilham D, Wasiak S, Tsujikawa LM, Halliday C, Norek K, Patel RG, et al. RVX-208, a BET-inhibitor for treating atherosclerotic cardiovascular disease, raises ApoA-I/HDL and represses pathways that contribute to cardiovascular disease. Atherosclerosis 2016;247:48-57.
    • (2016) Atherosclerosis , vol.247 , pp. 48-57
    • Gilham, D.1    Wasiak, S.2    Tsujikawa, L.M.3    Halliday, C.4    Norek, K.5    Patel, R.G.6
  • 22
    • 79952005101 scopus 로고    scopus 로고
    • Efficacy and safety of a novel oral inducer of apolipoprotein a-I synthesis in statin-treated patients with stable coronary artery disease a randomized controlled trial
    • Nicholls SJ, Gordon A, Johansson J, Wolski K, Ballantyne CM, Kastelein JJP, et al. Efficacy and safety of a novel oral inducer of apolipoprotein a-I synthesis in statin-treated patients with stable coronary artery disease a randomized controlled trial. J Am Coll Cardiol 2011;57:1111-9.
    • (2011) J Am Coll Cardiol , vol.57 , pp. 1111-1119
    • Nicholls, S.J.1    Gordon, A.2    Johansson, J.3    Wolski, K.4    Ballantyne, C.M.5    Kastelein, J.J.P.6
  • 24
    • 84921060280 scopus 로고    scopus 로고
    • BET bromodomain inhibition suppresses transcriptional responses to cytokine-Jak-STAT signaling in a gene-specific manner in human monocytes
    • Chan CH, Fang C, Qiao Y, Yarilina A, Prinjha RK, Ivashkiv LB. BET bromodomain inhibition suppresses transcriptional responses to cytokine-Jak-STAT signaling in a gene-specific manner in human monocytes. Eur J Immunol 2015;45:287-97.
    • (2015) Eur J Immunol , vol.45 , pp. 287-297
    • Chan, C.H.1    Fang, C.2    Qiao, Y.3    Yarilina, A.4    Prinjha, R.K.5    Ivashkiv, L.B.6
  • 26
    • 84960110543 scopus 로고    scopus 로고
    • Bromodomain and extra-terminal domain bromodomain inhibition prevents synovial inflammation via blocking IκB kinase-dependent NF-κB activation in rheumatoid fibroblast-like synoviocytes
    • Xiao Y, Liang L, Huang M, Qiu Q, Zeng S, Shi M, et al. Bromodomain and extra-terminal domain bromodomain inhibition prevents synovial inflammation via blocking IκB kinase-dependent NF-κB activation in rheumatoid fibroblast-like synoviocytes. Rheumatology 2016;55:173-84.
    • (2016) Rheumatology , vol.55 , pp. 173-184
    • Xiao, Y.1    Liang, L.2    Huang, M.3    Qiu, Q.4    Zeng, S.5    Shi, M.6
  • 27
    • 84873256270 scopus 로고    scopus 로고
    • BET protein function is required for inflammation: Brd2 genetic disruption and BET inhibitor JQ1 impair mouse macrophage inflammatory responses
    • Belkina AC, Nikolajczyk BS, Denis GV. BET protein function is required for inflammation: Brd2 genetic disruption and BET inhibitor JQ1 impair mouse macrophage inflammatory responses. J Immunol 2013;190:3670-8.
    • (2013) J Immunol , vol.190 , pp. 3670-3678
    • Belkina, A.C.1    Nikolajczyk, B.S.2    Denis, G.V.3
  • 30
    • 85012918232 scopus 로고    scopus 로고
    • The RP105/MD-1 complex: Molecular signaling mechanisms and pathophysiological implications
    • Apr 11. pii: jlb.2VMR1215-582R [Epub ahead of print]
    • Schultz TE, Blumenthal A. The RP105/MD-1 complex: molecular signaling mechanisms and pathophysiological implications. J Leukoc Biol 2016 Apr 11. pii: jlb.2VMR1215-582R [Epub ahead of print].
    • (2016) J Leukoc Biol
    • Schultz, T.E.1    Blumenthal, A.2


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