메뉴 건너뛰기




Volumn 5, Issue 11, 2014, Pages 3836-3848

A virtual screen identified C96 as a novel inhibitor of phosphatidylinositol 3-kinase that displays potent preclinical activity against multiple myeloma in vitro and in vivo

Author keywords

Apoptosis; C96; Multiple myeloma; PI3K AKT signal pathway; Virtual screen

Indexed keywords

AKT1 PROTEIN; AKT3 PROTEIN; C 96; INITIATION FACTOR 4E BINDING PROTEIN 1; MAMMALIAN TARGET OF RAPAMYCIN; MITOGEN ACTIVATED PROTEIN KINASE; PHOSPHATIDYLINOSITOL 3 KINASE; PHOSPHATIDYLINOSITOL 3 KINASE ALPHA; PHOSPHATIDYLINOSITOL 3 KINASE DELTA; PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR; PROTEIN KINASE B; PROTEIN KINASE B BETA; PROTEIN TYROSINE KINASE; SOMATOMEDIN C; SOMATOMEDIN C RECEPTOR; UNCLASSIFIED DRUG; PROTEIN KINASE INHIBITOR;

EID: 84903542968     PISSN: None     EISSN: 19492553     Source Type: Journal    
DOI: 10.18632/oncotarget.1657     Document Type: Article
Times cited : (13)

References (37)
  • 1
    • 42449114035 scopus 로고    scopus 로고
    • Multiple myeloma
    • Kyle RA and Rajkumar SV. Multiple myeloma. Blood. 2008; 111(6):2962-2972.
    • (2008) Blood , vol.111 , Issue.6 , pp. 2962-2972
    • Kyle, R.A.1    Rajkumar, S.V.2
  • 3
    • 84878832465 scopus 로고    scopus 로고
    • Dissecting bortezomib: development, application, adverse effects and future direction
    • Cao B, Li J and Mao X. Dissecting bortezomib: development, application, adverse effects and future direction. Curr Pharm Des. 2013; 19(18):3190-3200.
    • (2013) Curr Pharm Des , vol.19 , Issue.18 , pp. 3190-3200
    • Cao, B.1    Li, J.2    Mao, X.3
  • 5
    • 84888059579 scopus 로고    scopus 로고
    • Cyproheptadine-induced myeloma cell apoptosis is associated with inhibition of the PI3K/AKT signaling
    • Li J, Cao B, Zhou S, Zhu J, Zhang Z, Hou T and Mao X. Cyproheptadine-induced myeloma cell apoptosis is associated with inhibition of the PI3K/AKT signaling. Eur J Haematol. 2013.
    • (2013) Eur J Haematol
    • Li, J.1    Cao, B.2    Zhou, S.3    Zhu, J.4    Zhang, Z.5    Hou, T.6    Mao, X.7
  • 6
    • 79951474743 scopus 로고    scopus 로고
    • A small-molecule inhibitor of D-cyclin transactivation displays preclinical efficacy in myeloma and leukemia via phosphoinositide 3-kinase pathway
    • Mao X, Cao B, Wood TE, Hurren R, Tong J, Wang X, Wang W, Li J, Jin Y and Sun W. A small-molecule inhibitor of D-cyclin transactivation displays preclinical efficacy in myeloma and leukemia via phosphoinositide 3-kinase pathway. Blood. 2011; 117(6):1986-1997.
    • (2011) Blood , vol.117 , Issue.6 , pp. 1986-1997
    • Mao, X.1    Cao, B.2    Wood, T.E.3    Hurren, R.4    Tong, J.5    Wang, X.6    Wang, W.7    Li, J.8    Jin, Y.9    Sun, W.10
  • 7
    • 84857875585 scopus 로고    scopus 로고
    • PI3K signalling in B-and T-lymphocytes: new developments and therapeutic advances
    • So L and Fruman DA. PI3K signalling in B-and T-lymphocytes: new developments and therapeutic advances. Biochem J. 2012; 442(3):465-481.
    • (2012) Biochem J , vol.442 , Issue.3 , pp. 465-481
    • So, L.1    Fruman, D.A.2
  • 11
    • 84868567076 scopus 로고    scopus 로고
    • Role of the microenvironment in mantle cell lymphoma: IL-6 is an important survival factor for the tumor cells
    • Zhang L, Yang J, Qian J, Li H, Romaguera JE, Kwak LW, Wang M and Yi Q. Role of the microenvironment in mantle cell lymphoma: IL-6 is an important survival factor for the tumor cells. Blood. 2012; 120(18):3783-3792.
    • (2012) Blood , vol.120 , Issue.18 , pp. 3783-3792
    • Zhang, L.1    Yang, J.2    Qian, J.3    Li, H.4    Romaguera, J.E.5    Kwak, L.W.6    Wang, M.7    Yi, Q.8
  • 12
    • 59149096169 scopus 로고    scopus 로고
    • Inhibition of class I phosphoinositide 3-kinase activity impairs proliferation and triggers apoptosis in acute promyelocytic leukemia without affecting atra-induced differentiation
    • Billottet C, Banerjee L, Vanhaesebroeck B and Khwaja A. Inhibition of class I phosphoinositide 3-kinase activity impairs proliferation and triggers apoptosis in acute promyelocytic leukemia without affecting atra-induced differentiation. Cancer Res. 2009; 69(3):1027-1036.
    • (2009) Cancer Res , vol.69 , Issue.3 , pp. 1027-1036
    • Billottet, C.1    Banerjee, L.2    Vanhaesebroeck, B.3    Khwaja, A.4
  • 13
    • 79955033762 scopus 로고    scopus 로고
    • Exploring old drugs for the treatment of hematological malignancies
    • Gan F, Cao B, Wu D, Chen Z, Hou T and Mao X. Exploring old drugs for the treatment of hematological malignancies. Curr Med Chem. 2011; 18(10):1509-1514.
    • (2011) Curr Med Chem , vol.18 , Issue.10 , pp. 1509-1514
    • Gan, F.1    Cao, B.2    Wu, D.3    Chen, Z.4    Hou, T.5    Mao, X.6
  • 15
    • 84895426298 scopus 로고    scopus 로고
    • Isotypespecific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
    • Castillo JJ, Iyengar M, Kuritzky B and Bishop KD. Isotypespecific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies. Onco Targets Ther. 2014; 7:333-342.
    • (2014) Onco Targets Ther , vol.7 , pp. 333-342
    • Castillo, J.J.1    Iyengar, M.2    Kuritzky, B.3    Bishop, K.D.4
  • 16
    • 0033581886 scopus 로고    scopus 로고
    • Structural insights into phosphoinositide 3-kinase catalysis and signalling
    • Walker EH, Perisic O, Ried C, Stephens L and Williams RL. Structural insights into phosphoinositide 3-kinase catalysis and signalling. Nature. 1999; 402(6759):313-320.
    • (1999) Nature , vol.402 , Issue.6759 , pp. 313-320
    • Walker, E.H.1    Perisic, O.2    Ried, C.3    Stephens, L.4    Williams, R.L.5
  • 18
    • 68249093818 scopus 로고    scopus 로고
    • Targeting the phosphoinositide 3-kinase pathway in cancer
    • Liu P, Cheng H, Roberts TM and Zhao JJ. Targeting the phosphoinositide 3-kinase pathway in cancer. Nat Rev Drug Discov. 2009; 8(8):627-644.
    • (2009) Nat Rev Drug Discov , vol.8 , Issue.8 , pp. 627-644
    • Liu, P.1    Cheng, H.2    Roberts, T.M.3    Zhao, J.J.4
  • 20
    • 84894266310 scopus 로고    scopus 로고
    • Identification of a promising PI3K inhibitor for the treatment of multiple myeloma through the structural optimization
    • Han K, Xu X, Chen G, Zeng Y, Zhu J, Du X, Zhang Z, Cao B, Liu Z and Mao X. Identification of a promising PI3K inhibitor for the treatment of multiple myeloma through the structural optimization. J Hematol Oncol. 2014; 7(1):9.
    • (2014) J Hematol Oncol , vol.7 , Issue.1 , pp. 9
    • Han, K.1    Xu, X.2    Chen, G.3    Zeng, Y.4    Zhu, J.5    Du, X.6    Zhang, Z.7    Cao, B.8    Liu, Z.9    Mao, X.10
  • 21
    • 38049152900 scopus 로고    scopus 로고
    • PI3 kinase/AKT pathway as a therapeutic target in multiple myeloma
    • Harvey RD and Lonial S. PI3 kinase/AKT pathway as a therapeutic target in multiple myeloma. Future Oncol. 2007; 3(6):639-647.
    • (2007) Future Oncol , vol.3 , Issue.6 , pp. 639-647
    • Harvey, R.D.1    Lonial, S.2
  • 22
    • 84894240917 scopus 로고    scopus 로고
    • The mTOR Signaling Pathway is an Emerging Therapeutic Target in Multiple Myeloma
    • Li J, Zhu J, Cao B and Mao X. The mTOR Signaling Pathway is an Emerging Therapeutic Target in Multiple Myeloma. Curr Pharm Des. 2014; 20:125-35.
    • (2014) Curr Pharm Des , vol.20 , pp. 125-135
    • Li, J.1    Zhu, J.2    Cao, B.3    Mao, X.4
  • 23
    • 84870895081 scopus 로고    scopus 로고
    • Large-scale screening using familial dysautonomia induced pluripotent stem cells identifies compounds that rescue IKBKAP expression
    • Lee G, Ramirez CN, Kim H, Zeltner N, Liu B, Radu C, Bhinder B, Kim YJ, Choi IY and Mukherjee-Clavin B. Large-scale screening using familial dysautonomia induced pluripotent stem cells identifies compounds that rescue IKBKAP expression. Nat Biotechnol. 2012; 30(12): 1244-1248.
    • (2012) Nat Biotechnol , vol.30 , Issue.12 , pp. 1244-1248
    • Lee, G.1    Ramirez, C.N.2    Kim, H.3    Zeltner, N.4    Liu, B.5    Radu, C.6    Bhinder, B.7    Kim, Y.J.8    Choi, I.Y.9    Mukherjee-Clavin, B.10
  • 24
    • 37049009123 scopus 로고    scopus 로고
    • A chemical biology screen identifies glucocorticoids that regulate c-maf expression by increasing its proteasomal degradation through up-regulation of ubiquitin
    • Mao X, Stewart AK, Hurren R, Datti A, Zhu X, Zhu Y, Shi C, Lee K, Tiedemann R and Eberhard Y. A chemical biology screen identifies glucocorticoids that regulate c-maf expression by increasing its proteasomal degradation through up-regulation of ubiquitin. Blood. 2007; 110(12): 4047-4054.
    • (2007) Blood , vol.110 , Issue.12 , pp. 4047-4054
    • Mao, X.1    Stewart, A.K.2    Hurren, R.3    Datti, A.4    Zhu, X.5    Zhu, Y.6    Shi, C.7    Lee, K.8    Tiedemann, R.9    Eberhard, Y.10
  • 27
    • 84863986613 scopus 로고    scopus 로고
    • Discovery of MEK/PI3K dual inhibitor via structure-based virtual screening
    • Park H, Lee S and Hong S. Discovery of MEK/PI3K dual inhibitor via structure-based virtual screening. Bioorg Med Chem Lett. 2012; 22(15):4946-4950.
    • (2012) Bioorg Med Chem Lett , vol.22 , Issue.15 , pp. 4946-4950
    • Park, H.1    Lee, S.2    Hong, S.3
  • 30
    • 84893433556 scopus 로고    scopus 로고
    • Theoretical studies on beta and delta isoformspecific binding mechanisms of phosphoinositide 3-kinase inhibitors
    • Zhu J, Pan P, Li Y, Wang M, Li D, Cao B, Mao X and Hou T. Theoretical studies on beta and delta isoformspecific binding mechanisms of phosphoinositide 3-kinase inhibitors. Mol Biosyst. 2014; 10(3):454-66.
    • (2014) Mol Biosyst , vol.10 , Issue.3 , pp. 454-466
    • Zhu, J.1    Pan, P.2    Li, Y.3    Wang, M.4    Li, D.5    Cao, B.6    Mao, X.7    Hou, T.8
  • 32
    • 84865482902 scopus 로고    scopus 로고
    • Phosphatidylinositol 3-kinase (PI3K) activity bound to insulin-like growth factor-I (IGF-I) receptor, which is continuously sustained by IGF-I stimulation, is required for IGF-I-induced cell proliferation
    • Fukushima T, Nakamura Y, Yamanaka D, Shibano T, Chida K, Minami S, Asano T, Hakuno F and Takahashi S. Phosphatidylinositol 3-kinase (PI3K) activity bound to insulin-like growth factor-I (IGF-I) receptor, which is continuously sustained by IGF-I stimulation, is required for IGF-I-induced cell proliferation. J Biol Chem. 2012; 287(35):29713-29721.
    • (2012) J Biol Chem , vol.287 , Issue.35 , pp. 29713-29721
    • Fukushima, T.1    Nakamura, Y.2    Yamanaka, D.3    Shibano, T.4    Chida, K.5    Minami, S.6    Asano, T.7    Hakuno, F.8    Takahashi, S.9
  • 33
    • 84555178469 scopus 로고    scopus 로고
    • Inhibition of IGF-1R-dependent PI3K activation sensitizes colon cancer cells specifically to DR5-mediated apoptosis but not to rhTRAIL
    • Pennarun B, Kleibeuker JH, Oenema T, Stegehuis JH, de Vries EG and de Jong S. Inhibition of IGF-1R-dependent PI3K activation sensitizes colon cancer cells specifically to DR5-mediated apoptosis but not to rhTRAIL. Cell Oncol (Dordr). 2011; 34(3):245-259.
    • (2011) Cell Oncol (Dordr) , vol.34 , Issue.3 , pp. 245-259
    • Pennarun, B.1    Kleibeuker, J.H.2    Oenema, T.3    Stegehuis, J.H.4    de Vries, E.G.5    de Jong, S.6
  • 34
    • 33644859147 scopus 로고    scopus 로고
    • Inhibition of the phosphatidylinositol-3 kinase/Akt promotes G1 cell cycle arrest and apoptosis in Hodgkin lymphoma
    • Georgakis GV, Li Y, Rassidakis GZ, Medeiros LJ, Mills GB and Younes A. Inhibition of the phosphatidylinositol-3 kinase/Akt promotes G1 cell cycle arrest and apoptosis in Hodgkin lymphoma. Br J Haematol. 2006; 132(4): 503-511.
    • (2006) Br J Haematol , vol.132 , Issue.4 , pp. 503-511
    • Georgakis, G.V.1    Li, Y.2    Rassidakis, G.Z.3    Medeiros, L.J.4    Mills, G.B.5    Younes, A.6
  • 36
    • 84867062548 scopus 로고    scopus 로고
    • A deuterated analog of dasatinib disrupts cell cycle progression and displays antinon-small cell lung cancer activity in vitro and in vivo
    • Ling C, Chen G, Chen G, Zhang Z, Cao B, Han K, Yin J, Chu A, Zhao Y and Mao X. A deuterated analog of dasatinib disrupts cell cycle progression and displays antinon-small cell lung cancer activity in vitro and in vivo. Int J Cancer. 2012; 131(10):2411-2419.
    • (2012) Int J Cancer , vol.131 , Issue.10 , pp. 2411-2419
    • Ling, C.1    Chen, G.2    Chen, G.3    Zhang, Z.4    Cao, B.5    Han, K.6    Yin, J.7    Chu, A.8    Zhao, Y.9    Mao, X.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.