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Volumn 356, Issue 2, 2015, Pages 656-668

Synergistic antitumor interactions between MK-1775 and panobinostat in preclinical models of pancreatic cancer

Author keywords

CHK1; Drug combination; MK 1775; Pancreatic cancer; Panobinostat

Indexed keywords

2 ALLYL 1 [6 (1 HYDROXY 1 METHYLETHYL) 2 PYRIDINYL] 6 [4 (4 METHYL 1 PIPERAZINYL)ANILINO] 1H PYRAZOLO[3,4 D]PYRIMIDIN 3(2H) ONE; ANTINEOPLASTIC AGENT; CHECKPOINT KINASE 1; HISTONE H2AX; PANOBINOSTAT; RABUSERTIB; CELL CYCLE PROTEIN; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID; INDOLE DERIVATIVE; MESSENGER RNA; NUCLEAR PROTEIN; PROTEIN TYROSINE KINASE; PYRAZOLE DERIVATIVE; PYRIMIDINE DERIVATIVE; SMALL INTERFERING RNA; WEE1 PROTEIN, HUMAN;

EID: 84919494726     PISSN: 03043835     EISSN: 18727980     Source Type: Journal    
DOI: 10.1016/j.canlet.2014.10.015     Document Type: Article
Times cited : (34)

References (49)
  • 2
    • 8244254377 scopus 로고    scopus 로고
    • Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial
    • Burris H.A., Moore M.J., Andersen J., Green M.R., Rothenberg M.L., Modiano M.R., et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J. Clin. Oncol 1997, 15:2403-2413.
    • (1997) J. Clin. Oncol , vol.15 , pp. 2403-2413
    • Burris, H.A.1    Moore, M.J.2    Andersen, J.3    Green, M.R.4    Rothenberg, M.L.5    Modiano, M.R.6
  • 4
    • 0026616796 scopus 로고
    • Inactivation of the p34cdc2-cyclin B complex by the human WEE1 tyrosine kinase
    • Parker L.L., Piwnica-Worms H. Inactivation of the p34cdc2-cyclin B complex by the human WEE1 tyrosine kinase. Science 1992, 257:1955-1957.
    • (1992) Science , vol.257 , pp. 1955-1957
    • Parker, L.L.1    Piwnica-Worms, H.2
  • 5
    • 0029048491 scopus 로고
    • Regulation of the human WEE1Hu CDK tyrosine 15-kinase during the cell cycle
    • Watanabe N., Broome M., Hunter T. Regulation of the human WEE1Hu CDK tyrosine 15-kinase during the cell cycle. EMBO J. 1995, 14:1878-1891.
    • (1995) EMBO J. , vol.14 , pp. 1878-1891
    • Watanabe, N.1    Broome, M.2    Hunter, T.3
  • 6
    • 0030867582 scopus 로고    scopus 로고
    • Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25
    • Sanchez Y., Wong C., Thoma R.S., Richman R., Wu Z., Piwnica-Worms H., et al. Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25. Science 1997, 277:1497-1501.
    • (1997) Science , vol.277 , pp. 1497-1501
    • Sanchez, Y.1    Wong, C.2    Thoma, R.S.3    Richman, R.4    Wu, Z.5    Piwnica-Worms, H.6
  • 7
    • 0030611095 scopus 로고    scopus 로고
    • Mitotic and G2 checkpoint control: regulation of 14-3-3 protein binding by phosphorylation of Cdc25C on serine-216
    • Peng C.Y., Graves P.R., Thoma R.S., Wu Z., Shaw A.S., Piwnica-Worms H. Mitotic and G2 checkpoint control: regulation of 14-3-3 protein binding by phosphorylation of Cdc25C on serine-216. Science 1997, 277:1501-1505.
    • (1997) Science , vol.277 , pp. 1501-1505
    • Peng, C.Y.1    Graves, P.R.2    Thoma, R.S.3    Wu, Z.4    Shaw, A.S.5    Piwnica-Worms, H.6
  • 8
    • 17644432403 scopus 로고    scopus 로고
    • Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint
    • Liu Q., Guntuku S., Cui X.S., Matsuoka S., Cortez D., Tamai K., et al. Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint. Genes Dev 2000, 14:1448-1459.
    • (2000) Genes Dev , vol.14 , pp. 1448-1459
    • Liu, Q.1    Guntuku, S.2    Cui, X.S.3    Matsuoka, S.4    Cortez, D.5    Tamai, K.6
  • 9
    • 0034967556 scopus 로고    scopus 로고
    • ATR-mediated checkpoint pathways regulate phosphorylation and activation of human Chk1
    • Zhao H., Piwnica-Worms H. ATR-mediated checkpoint pathways regulate phosphorylation and activation of human Chk1. Mol. Cell. Biol 2001, 21:4129-4139.
    • (2001) Mol. Cell. Biol , vol.21 , pp. 4129-4139
    • Zhao, H.1    Piwnica-Worms, H.2
  • 10
    • 70949083026 scopus 로고    scopus 로고
    • Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents
    • Hirai H., Iwasawa Y., Okada M., Arai T., Nishibata T., Kobayashi M., et al. Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents. Mol. Cancer Ther 2009, 8:2992-3000.
    • (2009) Mol. Cancer Ther , vol.8 , pp. 2992-3000
    • Hirai, H.1    Iwasawa, Y.2    Okada, M.3    Arai, T.4    Nishibata, T.5    Kobayashi, M.6
  • 11
  • 12
    • 80052491760 scopus 로고    scopus 로고
    • MK-1775, a novel Wee1 kinase inhibitor, radiosensitizes p53-defective human tumor cells
    • Bridges K.A., Hirai H., Buser C.A., Brooks C., Liu H., Buchholz T.A., et al. MK-1775, a novel Wee1 kinase inhibitor, radiosensitizes p53-defective human tumor cells. Clin. Cancer Res 2011, 17:5638-5648.
    • (2011) Clin. Cancer Res , vol.17 , pp. 5638-5648
    • Bridges, K.A.1    Hirai, H.2    Buser, C.A.3    Brooks, C.4    Liu, H.5    Buchholz, T.A.6
  • 13
    • 84897429295 scopus 로고    scopus 로고
    • CHK1 and WEE1 inhibition combine synergistically to enhance therapeutic efficacy in acute myeloid leukemia ex vivo
    • Chaudhuri L., Vincelette N.D., Koh B.D., Naylor R.M., Flatten K.S., Peterson K.L., et al. CHK1 and WEE1 inhibition combine synergistically to enhance therapeutic efficacy in acute myeloid leukemia ex vivo. Haematologica 2014, 99:688-696.
    • (2014) Haematologica , vol.99 , pp. 688-696
    • Chaudhuri, L.1    Vincelette, N.D.2    Koh, B.D.3    Naylor, R.M.4    Flatten, K.S.5    Peterson, K.L.6
  • 14
    • 84882253419 scopus 로고    scopus 로고
    • Preclinical evaluation of the WEE1 inhibitor MK-1775 as single-agent anticancer therapy
    • Guertin A.D., Li J., Liu Y., Hurd M.S., Schuller A.G., Long B., et al. Preclinical evaluation of the WEE1 inhibitor MK-1775 as single-agent anticancer therapy. Mol. Cancer Ther 2013, 12:1442-1452.
    • (2013) Mol. Cancer Ther , vol.12 , pp. 1442-1452
    • Guertin, A.D.1    Li, J.2    Liu, Y.3    Hurd, M.S.4    Schuller, A.G.5    Long, B.6
  • 15
    • 77953711939 scopus 로고    scopus 로고
    • MK-1775, a small molecule Wee1 inhibitor, enhances anti-tumor efficacy of various DNA-damaging agents, including 5-fluorouracil
    • Hirai H., Arai T., Okada M., Nishibata T., Kobayashi M., Sakai N., et al. MK-1775, a small molecule Wee1 inhibitor, enhances anti-tumor efficacy of various DNA-damaging agents, including 5-fluorouracil. Cancer Biol. Ther 2010, 9:514-522.
    • (2010) Cancer Biol. Ther , vol.9 , pp. 514-522
    • Hirai, H.1    Arai, T.2    Okada, M.3    Nishibata, T.4    Kobayashi, M.5    Sakai, N.6
  • 16
    • 84874777985 scopus 로고    scopus 로고
    • Wee1 inhibition by MK-1775 leads to tumor inhibition and enhances efficacy of gemcitabine in human sarcomas
    • Kreahling J.M., Foroutan P., Reed D., Martinez G., Razabdouski T., Bui M.M., et al. Wee1 inhibition by MK-1775 leads to tumor inhibition and enhances efficacy of gemcitabine in human sarcomas. PLoS ONE 2013, 8:e57523.
    • (2013) PLoS ONE , vol.8 , pp. e57523
    • Kreahling, J.M.1    Foroutan, P.2    Reed, D.3    Martinez, G.4    Razabdouski, T.5    Bui, M.M.6
  • 17
    • 79955492036 scopus 로고    scopus 로고
    • MK-1775, a potent Wee1 inhibitor, synergizes with gemcitabine to achieve tumor regressions, selectively in p53-deficient pancreatic cancer xenografts
    • Rajeshkumar N.V., De Oliveira E., Ottenhof N., Watters J., Brooks D., Demuth T., et al. MK-1775, a potent Wee1 inhibitor, synergizes with gemcitabine to achieve tumor regressions, selectively in p53-deficient pancreatic cancer xenografts. Clin. Cancer Res 2011, 17:2799-2806.
    • (2011) Clin. Cancer Res , vol.17 , pp. 2799-2806
    • Rajeshkumar, N.V.1    De Oliveira, E.2    Ottenhof, N.3    Watters, J.4    Brooks, D.5    Demuth, T.6
  • 18
    • 84890471920 scopus 로고    scopus 로고
    • Inhibition of Wee1 sensitizes cancer cells to antimetabolite chemotherapeutics in vitro and in vivo, independent of p53 functionality
    • Van Linden A.A., Baturin D., Ford J.B., Fosmire S.P., Gardner L., Korch C., et al. Inhibition of Wee1 sensitizes cancer cells to antimetabolite chemotherapeutics in vitro and in vivo, independent of p53 functionality. Mol. Cancer Ther 2013, 12:2675-2684.
    • (2013) Mol. Cancer Ther , vol.12 , pp. 2675-2684
    • Van Linden, A.A.1    Baturin, D.2    Ford, J.B.3    Fosmire, S.P.4    Gardner, L.5    Korch, C.6
  • 20
    • 19944432566 scopus 로고    scopus 로고
    • A phase 1 and pharmacodynamic study of depsipeptide (FK228) in chronic lymphocytic leukemia and acute myeloid leukemia
    • Byrd J.C., Marcucci G., Parthun M.R., Xiao J.J., Klisovic R.B., Moran M., et al. A phase 1 and pharmacodynamic study of depsipeptide (FK228) in chronic lymphocytic leukemia and acute myeloid leukemia. Blood 2005, 105:959-967.
    • (2005) Blood , vol.105 , pp. 959-967
    • Byrd, J.C.1    Marcucci, G.2    Parthun, M.R.3    Xiao, J.J.4    Klisovic, R.B.5    Moran, M.6
  • 21
    • 51649110503 scopus 로고    scopus 로고
    • Phase 1 study of the oral isotype specific histone deacetylase inhibitor MGCD0103 in leukemia
    • Garcia-Manero G., Assouline S., Cortes J., Estrov Z., Kantarjian H., Yang H., et al. Phase 1 study of the oral isotype specific histone deacetylase inhibitor MGCD0103 in leukemia. Blood 2008, 112:981-989.
    • (2008) Blood , vol.112 , pp. 981-989
    • Garcia-Manero, G.1    Assouline, S.2    Cortes, J.3    Estrov, Z.4    Kantarjian, H.5    Yang, H.6
  • 22
    • 38949096781 scopus 로고    scopus 로고
    • Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes
    • Garcia-Manero G., Yang H., Bueso-Ramos C., Ferrajoli A., Cortes J., Wierda W.G., et al. Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes. Blood 2008, 111:1060-1066.
    • (2008) Blood , vol.111 , pp. 1060-1066
    • Garcia-Manero, G.1    Yang, H.2    Bueso-Ramos, C.3    Ferrajoli, A.4    Cortes, J.5    Wierda, W.G.6
  • 23
    • 33748063974 scopus 로고    scopus 로고
    • A phase I study of intravenous LBH589, a novel cinnamic hydroxamic acid analogue histone deacetylase inhibitor, in patients with refractory hematologic malignancies
    • Giles F., Fischer T., Cortes J., Garcia-Manero G., Beck J., Ravandi F., et al. A phase I study of intravenous LBH589, a novel cinnamic hydroxamic acid analogue histone deacetylase inhibitor, in patients with refractory hematologic malignancies. Clin. Cancer Res 2006, 12:4628-4635.
    • (2006) Clin. Cancer Res , vol.12 , pp. 4628-4635
    • Giles, F.1    Fischer, T.2    Cortes, J.3    Garcia-Manero, G.4    Beck, J.5    Ravandi, F.6
  • 24
    • 49349104503 scopus 로고    scopus 로고
    • A phase I clinical trial of the histone deacetylase inhibitor belinostat in patients with advanced hematological neoplasia
    • Gimsing P., Hansen M., Knudsen L.M., Knoblauch P., Christensen I.J., Ooi C.E., et al. A phase I clinical trial of the histone deacetylase inhibitor belinostat in patients with advanced hematological neoplasia. Eur. J. Haematol 2008, 81:170-176.
    • (2008) Eur. J. Haematol , vol.81 , pp. 170-176
    • Gimsing, P.1    Hansen, M.2    Knudsen, L.M.3    Knoblauch, P.4    Christensen, I.J.5    Ooi, C.E.6
  • 25
    • 33947581039 scopus 로고    scopus 로고
    • Phase 1 and pharmacologic study of MS-275, a histone deacetylase inhibitor, in adults with refractory and relapsed acute leukemias
    • Gojo I., Jiemjit A., Trepel J.B., Sparreboom A., Figg W.D., Rollins S., et al. Phase 1 and pharmacologic study of MS-275, a histone deacetylase inhibitor, in adults with refractory and relapsed acute leukemias. Blood 2007, 109:2781-2790.
    • (2007) Blood , vol.109 , pp. 2781-2790
    • Gojo, I.1    Jiemjit, A.2    Trepel, J.B.3    Sparreboom, A.4    Figg, W.D.5    Rollins, S.6
  • 26
    • 38949144400 scopus 로고    scopus 로고
    • Tolerability, pharmacodynamics, and pharmacokinetics studies of depsipeptide (romidepsin) in patients with acute myelogenous leukemia or advanced myelodysplastic syndromes
    • Klimek V.M., Fircanis S., Maslak P., Guernah I., Baum M., Wu N., et al. Tolerability, pharmacodynamics, and pharmacokinetics studies of depsipeptide (romidepsin) in patients with acute myelogenous leukemia or advanced myelodysplastic syndromes. Clin. Cancer Res 2008, 14:826-832.
    • (2008) Clin. Cancer Res , vol.14 , pp. 826-832
    • Klimek, V.M.1    Fircanis, S.2    Maslak, P.3    Guernah, I.4    Baum, M.5    Wu, N.6
  • 27
    • 29744454120 scopus 로고    scopus 로고
    • The histone deacetylase (HDAC) inhibitor valproic acid as monotherapy or in combination with all-trans retinoic acid in patients with acute myeloid leukemia
    • Kuendgen A., Schmid M., Schlenk R., Knipp S., Hildebrandt B., Steidl C., et al. The histone deacetylase (HDAC) inhibitor valproic acid as monotherapy or in combination with all-trans retinoic acid in patients with acute myeloid leukemia. Cancer 2006, 106:112-119.
    • (2006) Cancer , vol.106 , pp. 112-119
    • Kuendgen, A.1    Schmid, M.2    Schlenk, R.3    Knipp, S.4    Hildebrandt, B.5    Steidl, C.6
  • 28
    • 84892972702 scopus 로고    scopus 로고
    • Panobinostat enhances cytarabine and daunorubicin sensitivities in AML cells through suppressing the expression of BRCA1, CHK1, and Rad51
    • Xie C., Drenberg C., Edwards H., Caldwell J.T., Chen W., Inaba H., et al. Panobinostat enhances cytarabine and daunorubicin sensitivities in AML cells through suppressing the expression of BRCA1, CHK1, and Rad51. PLoS ONE 2013, 8:e79106.
    • (2013) PLoS ONE , vol.8 , pp. e79106
    • Xie, C.1    Drenberg, C.2    Edwards, H.3    Caldwell, J.T.4    Chen, W.5    Inaba, H.6
  • 29
    • 84884778458 scopus 로고    scopus 로고
    • Panobinostat synergistically enhances the cytotoxic effects of cisplatin, doxorubicin or etoposide on high-risk neuroblastoma cells
    • Wang G., Edwards H., Caldwell J.T., Buck S.A., Qing W.Y., Taub J.W., et al. Panobinostat synergistically enhances the cytotoxic effects of cisplatin, doxorubicin or etoposide on high-risk neuroblastoma cells. PLoS ONE 2013, 8:e76662.
    • (2013) PLoS ONE , vol.8 , pp. e76662
    • Wang, G.1    Edwards, H.2    Caldwell, J.T.3    Buck, S.A.4    Qing, W.Y.5    Taub, J.W.6
  • 30
    • 78349242181 scopus 로고    scopus 로고
    • Mechanisms of synergistic antileukemic interactions between valproic acid and cytarabine in pediatric acute myeloid leukemia
    • Xie C., Edwards H., Xu X., Zhou H., Buck S.A., Stout M.L., et al. Mechanisms of synergistic antileukemic interactions between valproic acid and cytarabine in pediatric acute myeloid leukemia. Clin. Cancer Res 2010, 16:5499-5510.
    • (2010) Clin. Cancer Res , vol.16 , pp. 5499-5510
    • Xie, C.1    Edwards, H.2    Xu, X.3    Zhou, H.4    Buck, S.A.5    Stout, M.L.6
  • 31
    • 84867371231 scopus 로고    scopus 로고
    • Valproic acid synergistically enhances the cytotoxicity of clofarabine in pediatric acute myeloid leukemia cells
    • Xie C., Edwards H., Lograsso S.B., Buck S.A., Matherly L.H., Taub J.W., et al. Valproic acid synergistically enhances the cytotoxicity of clofarabine in pediatric acute myeloid leukemia cells. Pediatr. Blood Cancer 2012, 59:1245-1251.
    • (2012) Pediatr. Blood Cancer , vol.59 , pp. 1245-1251
    • Xie, C.1    Edwards, H.2    Lograsso, S.B.3    Buck, S.A.4    Matherly, L.H.5    Taub, J.W.6
  • 32
    • 84863799519 scopus 로고    scopus 로고
    • Combined inhibition of Chk1 and Wee1: in vitro synergistic effect translates to tumor growth inhibition in vivo
    • Carrassa L., Chila R., Lupi M., Ricci F., Celenza C., Mazzoletti M., et al. Combined inhibition of Chk1 and Wee1: in vitro synergistic effect translates to tumor growth inhibition in vivo. Cell Cycle 2012, 11:2507-2517.
    • (2012) Cell Cycle , vol.11 , pp. 2507-2517
    • Carrassa, L.1    Chila, R.2    Lupi, M.3    Ricci, F.4    Celenza, C.5    Mazzoletti, M.6
  • 34
    • 84868654250 scopus 로고    scopus 로고
    • Unique functions of CHK1 and WEE1 underlie synergistic anti-tumor activity upon pharmacologic inhibition
    • Guertin A.D., Martin M.M., Roberts B., Hurd M., Qu X., Miselis N.R., et al. Unique functions of CHK1 and WEE1 underlie synergistic anti-tumor activity upon pharmacologic inhibition. Cancer Cell Int 2012, 12:45.
    • (2012) Cancer Cell Int , vol.12 , pp. 45
    • Guertin, A.D.1    Martin, M.M.2    Roberts, B.3    Hurd, M.4    Qu, X.5    Miselis, N.R.6
  • 35
    • 84900503589 scopus 로고    scopus 로고
    • Combination of AZD2281 (Olaparib) and GX15-070 (Obatoclax) results in synergistic antitumor activities in preclinical models of pancreatic cancer
    • Chen S., Wang G., Niu X., Zhao J., Tan W., Wang H., et al. Combination of AZD2281 (Olaparib) and GX15-070 (Obatoclax) results in synergistic antitumor activities in preclinical models of pancreatic cancer. Cancer Lett 2014, 348:20-28.
    • (2014) Cancer Lett , vol.348 , pp. 20-28
    • Chen, S.1    Wang, G.2    Niu, X.3    Zhao, J.4    Tan, W.5    Wang, H.6
  • 36
    • 79951864878 scopus 로고    scopus 로고
    • Inhibition of histone deacetylases 1 and 6 enhances cytarabine-induced apoptosis in pediatric acute myeloid leukemia cells
    • Xu X., Xie C., Edwards H., Zhou H., Buck S.A., Ge Y. Inhibition of histone deacetylases 1 and 6 enhances cytarabine-induced apoptosis in pediatric acute myeloid leukemia cells. PLoS ONE 2011, 6:e17138.
    • (2011) PLoS ONE , vol.6 , pp. e17138
    • Xu, X.1    Xie, C.2    Edwards, H.3    Zhou, H.4    Buck, S.A.5    Ge, Y.6
  • 37
    • 32644453700 scopus 로고    scopus 로고
    • Differential gene expression, GATA1 target genes, and the chemotherapy sensitivity of Down syndrome megakaryocytic leukemia
    • Ge Y., Dombkowski A.A., LaFiura K.M., Tatman D., Yedidi R.S., Stout M.L., et al. Differential gene expression, GATA1 target genes, and the chemotherapy sensitivity of Down syndrome megakaryocytic leukemia. Blood 2006, 107:1570-1581.
    • (2006) Blood , vol.107 , pp. 1570-1581
    • Ge, Y.1    Dombkowski, A.A.2    LaFiura, K.M.3    Tatman, D.4    Yedidi, R.S.5    Stout, M.L.6
  • 38
    • 84871273907 scopus 로고    scopus 로고
    • And class II histone deacetylases are potential therapeutic targets for treating pancreatic cancer
    • Wang G., He J., Zhao J., Yun W., Xie C., Taub J.W., et al. and class II histone deacetylases are potential therapeutic targets for treating pancreatic cancer. PLoS ONE 2012, 7:e52095.
    • (2012) PLoS ONE , vol.7 , pp. e52095
    • Wang, G.1    He, J.2    Zhao, J.3    Yun, W.4    Xie, C.5    Taub, J.W.6
  • 39
    • 70350506780 scopus 로고    scopus 로고
    • RUNX1 regulates phosphoinositide 3-kinase/AKT pathway: role in chemotherapy sensitivity in acute megakaryocytic leukemia
    • Edwards H., Xie C., LaFiura K.M., Dombkowski A.A., Buck S.A., Boerner J.L., et al. RUNX1 regulates phosphoinositide 3-kinase/AKT pathway: role in chemotherapy sensitivity in acute megakaryocytic leukemia. Blood 2009, 114:2744-2752.
    • (2009) Blood , vol.114 , pp. 2744-2752
    • Edwards, H.1    Xie, C.2    LaFiura, K.M.3    Dombkowski, A.A.4    Buck, S.A.5    Boerner, J.L.6
  • 40
    • 0020333131 scopus 로고
    • Random-effects models for longitudinal data
    • Laird N.M., Ware J.H. Random-effects models for longitudinal data. Biometrics 1982, 38:963-974.
    • (1982) Biometrics , vol.38 , pp. 963-974
    • Laird, N.M.1    Ware, J.H.2
  • 43
    • 79956224870 scopus 로고    scopus 로고
    • A phase I pharmacological and pharmacodynamic study of MK-1775, a Weel tyrosine kinase inhibitor, in monotherapy and combination with gemcitabine, cisplatin, or carboplatin in patients with advanced solid tumors
    • Leijen S., Schellens J.H., Shapiro G., Pavlick A.C., Tibes R., Demuth T., et al. A phase I pharmacological and pharmacodynamic study of MK-1775, a Weel tyrosine kinase inhibitor, in monotherapy and combination with gemcitabine, cisplatin, or carboplatin in patients with advanced solid tumors. J. Clin. Oncol 2010, 28:3067.
    • (2010) J. Clin. Oncol , vol.28 , pp. 3067
    • Leijen, S.1    Schellens, J.H.2    Shapiro, G.3    Pavlick, A.C.4    Tibes, R.5    Demuth, T.6
  • 44
    • 84872533885 scopus 로고    scopus 로고
    • Combination therapy targeting the Chk1 and Wee1 kinases shows therapeutic efficacy in neuroblastoma
    • Russell M.R., Levin K., Rader J., Belcastro L., Li Y., Martinez D., et al. Combination therapy targeting the Chk1 and Wee1 kinases shows therapeutic efficacy in neuroblastoma. Cancer Res 2013, 73:776-784.
    • (2013) Cancer Res , vol.73 , pp. 776-784
    • Russell, M.R.1    Levin, K.2    Rader, J.3    Belcastro, L.4    Li, Y.5    Martinez, D.6
  • 45
    • 34547864236 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: molecular mechanisms of action
    • Xu W.S., Parmigiani R.B., Marks P.A. Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene 2007, 26:5541-5552.
    • (2007) Oncogene , vol.26 , pp. 5541-5552
    • Xu, W.S.1    Parmigiani, R.B.2    Marks, P.A.3
  • 46
    • 78650791916 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors downregulate checkpoint kinase 1 expression to induce cell death in non-small cell lung cancer cells
    • Brazelle W., Kreahling J.M., Gemmer J., Ma Y., Cress W.D., Haura E., et al. Histone deacetylase inhibitors downregulate checkpoint kinase 1 expression to induce cell death in non-small cell lung cancer cells. PLoS ONE 2010, 5:e14335.
    • (2010) PLoS ONE , vol.5 , pp. e14335
    • Brazelle, W.1    Kreahling, J.M.2    Gemmer, J.3    Ma, Y.4    Cress, W.D.5    Haura, E.6
  • 47
    • 46749139575 scopus 로고    scopus 로고
    • The novel histone deacetylase inhibitor, LBH589, induces expression of DNA damage response genes and apoptosis in Ph- acute lymphoblastic leukemia cells
    • Scuto A., Kirschbaum M., Kowolik C., Kretzner L., Juhasz A., Atadja P., et al. The novel histone deacetylase inhibitor, LBH589, induces expression of DNA damage response genes and apoptosis in Ph- acute lymphoblastic leukemia cells. Blood 2008, 111:5093-5100.
    • (2008) Blood , vol.111 , pp. 5093-5100
    • Scuto, A.1    Kirschbaum, M.2    Kowolik, C.3    Kretzner, L.4    Juhasz, A.5    Atadja, P.6
  • 48
    • 81055149914 scopus 로고    scopus 로고
    • Mechanism of action of proteasome inhibitors and deacetylase inhibitors and the biological basis of synergy in multiple myeloma
    • Hideshima T., Richardson P.G., Anderson K.C. Mechanism of action of proteasome inhibitors and deacetylase inhibitors and the biological basis of synergy in multiple myeloma. Mol. Cancer Ther 2011, 10:2034-2042.
    • (2011) Mol. Cancer Ther , vol.10 , pp. 2034-2042
    • Hideshima, T.1    Richardson, P.G.2    Anderson, K.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.