-
1
-
-
84903581591
-
Antibodies to watch in 2014: Mid-year update
-
PMID:24846335
-
Reichert JM. Antibodies to watch in 2014: Mid-year update. mAbs 2014; 6:799-802; PMID:24846335; http://dx.doi.org/10.4161/mabs.29282
-
(2014)
MAbs
, vol.6
, pp. 799-802
-
-
Reichert, J.M.1
-
2
-
-
79957514394
-
HDAC inhibitor SNDX-275 enhances efficacy of trastuzumab in erbB2-overexpressing breast cancer cells and exhibits potential to overcome trastuzumab resistance
-
PMID:21497990
-
Huang X, Wang S, Lee C-K, Yang X, Liu B. HDAC inhibitor SNDX-275 enhances efficacy of trastuzumab in erbB2-overexpressing breast cancer cells and exhibits potential to overcome trastuzumab resistance. Cancer Lett 2011; 307:72-9; PMID:21497990; http://dx.doi.org/10.1016/j.canlet.2011.03.019
-
(2011)
Cancer Lett
, vol.307
, pp. 72-79
-
-
Huang, X.1
Wang, S.2
Lee, C.-K.3
Yang, X.4
Liu, B.5
-
3
-
-
84877987888
-
MEK inhibition increases lapatinib sensitivity via modulation of FOXM1
-
PMID:23531216
-
Gayle SS, Castellino RC, Buss MC, Nahta R. MEK inhibition increases lapatinib sensitivity via modulation of FOXM1. Curr Med Chem 2013; 20:2486-99; PMID:23531216; http://dx.doi.org/10.2174/0929867311320190008
-
(2013)
Curr Med Chem
, vol.20
, pp. 2486-2499
-
-
Gayle, S.S.1
Castellino, R.C.2
Buss, M.C.3
Nahta, R.4
-
4
-
-
78249236544
-
Recombinant human erythropoietin antagonizes trastuzumab treatment of breast cancer cells via Jak2-mediated Src activation and PTEN inactivation
-
PMID:21075308
-
Liang K, Esteva FJ, Albarracin C, Stemke-Hale K, Lu Y, Bianchini G, Yang C-Y, Li Y, Li X, Chen C-T, et al. Recombinant human erythropoietin antagonizes trastuzumab treatment of breast cancer cells via Jak2-mediated Src activation and PTEN inactivation. Cancer Cell 2010; 18:423-35; PMID:21075308; http://dx.doi.org/10.1016/j.ccr.2010.10.025
-
(2010)
Cancer Cell
, vol.18
, pp. 423-435
-
-
Liang, K.1
Esteva, F.J.2
Albarracin, C.3
Stemke-Hale, K.4
Lu, Y.5
Bianchini, G.6
Yang, C.-Y.7
Li, Y.8
Li, X.9
Chen, C.-T.10
-
5
-
-
84897563710
-
Ibrutinib antagonizes rituximab-dependent NK cell-mediated cytotoxicity
-
PMID:24652965
-
Kohrt HE, Sagiv-Barfi I, Rafiq S, Herman SEM, Butchar JP, Cheney C, Zhang X, Buggy JJ, Muthusamy N, Levy R, et al. Ibrutinib antagonizes rituximab-dependent NK cell-mediated cytotoxicity. Blood 2014; 123:1957-60; PMID:24652965; http://dx.doi.org/10.1182/blood-2014-01-547869
-
(2014)
Blood
, vol.123
, pp. 1957-1960
-
-
Kohrt, H.E.1
Sagiv-Barfi, I.2
Rafiq, S.3
Herman, S.E.M.4
Butchar, J.P.5
Cheney, C.6
Zhang, X.7
Buggy, J.J.8
Muthusamy, N.9
Levy, R.10
-
6
-
-
84871765731
-
Targeting B-Cell receptor signaling for anticancer therapy: The Bruton's tyrosine kinase inhibitor ibrutinib induces impressive responses in B-cell malignancies
-
PMID:23045586
-
Wiestner A. Targeting B-Cell receptor signaling for anticancer therapy: the Bruton's tyrosine kinase inhibitor ibrutinib induces impressive responses in B-cell malignancies. J Clin Oncol 2013; 31:128-30; PMID:23045586; http://dx.doi.org/10.1200/JCO.2012.44.4281
-
(2013)
J Clin Oncol
, vol.31
, pp. 128-130
-
-
Wiestner, A.1
-
7
-
-
78751553221
-
CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability
-
PMID:20959606
-
Lannutti BJ, Meadows SA, Herman SEM, Kashishian A, Steiner B, Johnson AJ, Byrd JC, Tyner JW, Loriaux MM, Deininger M, et al. CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability. Blood 2011; 117:591-4; PMID:20959606; http://dx.doi.org/10.1182/blood-2010-03-275305
-
(2011)
Blood
, vol.117
, pp. 591-594
-
-
Lannutti, B.J.1
Meadows, S.A.2
Herman, S.E.M.3
Kashishian, A.4
Steiner, B.5
Johnson, A.J.6
Byrd, J.C.7
Tyner, J.W.8
Loriaux, M.M.9
Deininger, M.10
-
8
-
-
59749099026
-
PI3K inhibitors for cancer treatment: Where do we stand?
-
PMID:19143644
-
Maira S-M, Stauffer F, Schnell C, García-Echeverría C. PI3K inhibitors for cancer treatment: where do we stand? Biochem Soc Trans 2009; 37:265-72; PMID:19143644; http://dx.doi.org/10.1042/BST0370265
-
(2009)
Biochem Soc Trans
, vol.37
, pp. 265-272
-
-
Maira, S.-M.1
Stauffer, F.2
Schnell, C.3
García-Echeverría, C.4
-
9
-
-
77958000904
-
The dual PI3K/mTOR inhibitor, NVP-BEZ235, is efficacious against follicular lymphoma
-
PMID:20703254
-
Bhende PM, Park SI, Lim MS, Dittmer DP, Damania B. The dual PI3K/mTOR inhibitor, NVP-BEZ235, is efficacious against follicular lymphoma. Leukemia 2010; 24:1781-4; PMID:20703254; http://dx.doi.org/10.1038/leu.2010.154
-
(2010)
Leukemia
, vol.24
, pp. 1781-1784
-
-
Bhende, P.M.1
Park, S.I.2
Lim, M.S.3
Dittmer, D.P.4
Damania, B.5
-
10
-
-
33845501828
-
Role of phosphatidylinositol 3′-kinase/AKT pathway in diffuse large B-cell lymphoma survival
-
PMID:16946303
-
Uddin S, Hussain AR, Siraj AK, Manogaran PS, Al-Jomah NA, Moorji A, Atizado V, Al-Dayel F, Belgaumi A, El-Solh H, et al. Role of phosphatidylinositol 3′-kinase/AKT pathway in diffuse large B-cell lymphoma survival. Blood 2006; 108:4178-86; PMID:16946303; http://dx.doi.org/10.1182/blood-2006-04-016907
-
(2006)
Blood
, vol.108
, pp. 4178-4186
-
-
Uddin, S.1
Hussain, A.R.2
Siraj, A.K.3
Manogaran, P.S.4
Al-Jomah, N.A.5
Moorji, A.6
Atizado, V.7
Al-Dayel, F.8
Belgaumi, A.9
El-Solh, H.10
-
11
-
-
78751564397
-
Preclinical studies on the mechanism of action and the anti-lymphoma activity of the novel anti-CD20 antibody GA101
-
PMID:21220500
-
Dalle S, Reslan L, Besseyre de Horts T, Herveau S, Herting F, Plesa A, Friess T, Umana P, Klein C, Dumontet C. Preclinical studies on the mechanism of action and the anti-lymphoma activity of the novel anti-CD20 antibody GA101. Mol Cancer Ther 2011; 10:178-85; PMID:21220500; http://dx.doi.org/10.1158/1535-7163.MCT-10-0385
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 178-185
-
-
Dalle, S.1
Reslan, L.2
De Besseyre Horts, T.3
Herveau, S.4
Herting, F.5
Plesa, A.6
Friess, T.7
Umana, P.8
Klein, C.9
Dumontet, C.10
-
12
-
-
51049109033
-
Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity
-
PMID:18606717
-
Maira S-M, Stauffer F, Brueggen J, Furet P, Schnell C, Fritsch C, Brachmann S, Chène P, De Pover A, Schoemaker K, et al. Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity. Mol Cancer Ther 2008; 7:1851-63; PMID:18606717; http://dx.doi.org/10.1158/1535-7163.MCT-08-0017
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 1851-1863
-
-
Maira, S.-M.1
Stauffer, F.2
Brueggen, J.3
Furet, P.4
Schnell, C.5
Fritsch, C.6
Brachmann, S.7
Chène, P.8
De Pover, A.9
Schoemaker, K.10
-
13
-
-
77649196743
-
Rituximab inhibits B-cell receptor signaling
-
PMID:19965664
-
Kheirallah S, Caron P, Gross E, Quillet-Mary A, Bertrand-Michel J, Fournié J-J, Laurent G, Bezombes C. Rituximab inhibits B-cell receptor signaling. Blood 2010; 115:985-94; PMID:19965664; http://dx.doi.org/10.1182/blood-2009-08-237537
-
(2010)
Blood
, vol.115
, pp. 985-994
-
-
Kheirallah, S.1
Caron, P.2
Gross, E.3
Quillet-Mary, A.4
Bertrand-Michel, J.5
Fournié, J.-J.6
Laurent, G.7
Bezombes, C.8
-
14
-
-
84881225049
-
Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma
-
PMID:23782157
-
Wang ML, Rule S, Martin P, Goy A, Auer R, Kahl BS, Jurczak W, Advani RH, Romaguera JE, Williams ME, et al. Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma. N Engl J Med 2013; 369:507-16; PMID:23782157; http://dx.doi.org/10.1056/NEJMoa1306220
-
(2013)
N Engl J Med
, vol.369
, pp. 507-516
-
-
Wang, M.L.1
Rule, S.2
Martin, P.3
Goy, A.4
Auer, R.5
Kahl, B.S.6
Jurczak, W.7
Advani, R.H.8
Romaguera, J.E.9
Williams, M.E.10
-
15
-
-
84879748062
-
Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia
-
PMID:23782158
-
Byrd JC, Furman RR, Coutre SE, Flinn IW, Burger JA, Blum KA, Grant B, Sharman JP, Coleman M, Wierda WG, et al. Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia. N Engl J Med 2013; 369:32-42; PMID:23782158; http://dx.doi.org/10.1056/NEJMoa1215637
-
(2013)
N Engl J Med
, vol.369
, pp. 32-42
-
-
Byrd, J.C.1
Furman, R.R.2
Coutre, S.E.3
Flinn, I.W.4
Burger, J.A.5
Blum, K.A.6
Grant, B.7
Sharman, J.P.8
Coleman, M.9
Wierda, W.G.10
-
16
-
-
84904252369
-
Ibrutinib versus ofatumumab in previously treated chronic lymphoid leukemia
-
PMID:24881631
-
Byrd JC, Brown JR, O'Brien S, Barrientos JC, Kay NE, Reddy NM, Coutre S, Tam CS, Mulligan SP, Jaeger U, et al. Ibrutinib versus ofatumumab in previously treated chronic lymphoid leukemia. N Engl J Med 2014; 371:213-23; PMID:24881631; http://dx.doi.org/10.1056/NEJMoa1400376
-
(2014)
N Engl J Med
, vol.371
, pp. 213-223
-
-
Byrd, J.C.1
Brown, J.R.2
O'Brien, S.3
Barrientos, J.C.4
Kay, N.E.5
Reddy, N.M.6
Coutre, S.7
Tam, C.S.8
Mulligan, S.P.9
Jaeger, U.10
-
17
-
-
84921033879
-
The HELIOS trial protocol: A Phase III study of ibrutinib in combination with bendamustine and rituximab in relapsed/refractory chronic lymphocytic leukemia
-
PMID:24901734
-
Hallek M, Kay NE, Osterborg A, Chanan-Khan AA, Mahler M, Salman M, Wan Y, Sun S, Zhuang SH, Howes A. The HELIOS trial protocol: a Phase III study of ibrutinib in combination with bendamustine and rituximab in relapsed/refractory chronic lymphocytic leukemia. Future Oncol Lond Engl 2014; 1-9; PMID:24901734; http://dx.doi.org/10.2217/fon.14.119
-
(2014)
Future Oncol Lond Engl
, pp. 1-9
-
-
Hallek, M.1
Kay, N.E.2
Osterborg, A.3
Chanan-Khan, A.A.4
Mahler, M.5
Salman, M.6
Wan, Y.7
Sun, S.8
Zhuang, S.H.9
Howes, A.10
-
18
-
-
84896692766
-
Idelalisib and rituximab in relapsed chronic lymphocytic leukemia
-
PMID:24450857
-
Furman RR, Sharman JP, Coutre SE, Cheson BD, Pagel JM, Hillmen P, Barrientos JC, Zelenetz AD, Kipps TJ, Flinn I, et al. Idelalisib and rituximab in relapsed chronic lymphocytic leukemia. N Engl J Med 2014; 370:997-1007; PMID:24450857; http://dx.doi.org/10.1056/NEJMoa1315226
-
(2014)
N Engl J Med
, vol.370
, pp. 997-1007
-
-
Furman, R.R.1
Sharman, J.P.2
Coutre, S.E.3
Cheson, B.D.4
Pagel, J.M.5
Hillmen, P.6
Barrientos, J.C.7
Zelenetz, A.D.8
Kipps, T.J.9
Flinn, I.10
-
19
-
-
84871806385
-
Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765) has significant activity in patients with relapsed/refractory B-cell malignancies
-
PMID:23045577
-
Advani RH, Buggy JJ, Sharman JP, Smith SM, Boyd TE, Grant B, Kolibaba KS, Furman RR, Rodriguez S, Chang BY, et al. Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765) has significant activity in patients with relapsed/refractory B-cell malignancies. J Clin Oncol 2013; 31:88-94; PMID:23045577; http://dx.doi.org/10.1200/JCO.2012.42.7906
-
(2013)
J Clin Oncol
, vol.31
, pp. 88-94
-
-
Advani, R.H.1
Buggy, J.J.2
Sharman, J.P.3
Smith, S.M.4
Boyd, T.E.5
Grant, B.6
Kolibaba, K.S.7
Furman, R.R.8
Rodriguez, S.9
Chang, B.Y.10
-
20
-
-
79960133279
-
The Bruton tyrosine kinase inhibitor PCI-32765 ameliorates autoimmune arthritis by inhibition of multiple effector cells
-
PMID:21752263
-
Chang BY, Huang MM, Francesco M, Chen J, Sokolove J, Magadala P, Robinson WH, Buggy JJ. The Bruton tyrosine kinase inhibitor PCI-32765 ameliorates autoimmune arthritis by inhibition of multiple effector cells. Arthritis Res Ther 2011; 13:R115; PMID:21752263; http://dx.doi.org/10.1186/ar3400
-
(2011)
Arthritis Res Ther
, vol.13
, pp. R115
-
-
Chang, B.Y.1
Huang, M.M.2
Francesco, M.3
Chen, J.4
Sokolove, J.5
Magadala, P.6
Robinson, W.H.7
Buggy, J.J.8
-
21
-
-
0347447283
-
Neutrophils contribute to the biological antitumor activity of rituximab in a non-Hodgkin's lymphoma severe combined immunodeficiency mouse model
-
PMID:14676108
-
Hernandez-Ilizaliturri FJ, Jupudy V, Ostberg J, Oflazoglu E, Huberman A, Repasky E, Czuczman MS. Neutrophils contribute to the biological antitumor activity of rituximab in a non-Hodgkin's lymphoma severe combined immunodeficiency mouse model. Clin Cancer Res 2003; 9:5866-73; PMID:14676108
-
(2003)
Clin Cancer Res
, vol.9
, pp. 5866-5873
-
-
Hernandez-Ilizaliturri, F.J.1
Jupudy, V.2
Ostberg, J.3
Oflazoglu, E.4
Huberman, A.5
Repasky, E.6
Czuczman, M.S.7
-
22
-
-
45749104147
-
Granulocyte-macrophage colony-stimulating factor potentiates rituximab in patients with relapsed follicular lymphoma: Results of a phase II study
-
PMID:18427151
-
Cartron G, Zhao-Yang L, Baudard M, Kanouni T, Rouillé V, Quittet P, Klein B, Rossi J-F. Granulocyte-macrophage colony-stimulating factor potentiates rituximab in patients with relapsed follicular lymphoma: results of a phase II study. J Clin Oncol 2008; 26:2725-31; PMID:18427151; http://dx.doi.org/10.1200/JCO.2007.13.7729
-
(2008)
J Clin Oncol
, vol.26
, pp. 2725-2731
-
-
Cartron, G.1
Zhao-Yang, L.2
Baudard, M.3
Kanouni, T.4
Rouillé, V.5
Quittet, P.6
Klein, B.7
Rossi, J.-F.8
-
23
-
-
33745070631
-
Antibody-dependent cellular cytotoxicity (ADCC) is mediated by genetically modified antigen-specific human T lymphocytes
-
PMID:16514054
-
Clémenceau B, Congy-Jolivet N, Gallot G, Vivien R, Gaschet J, Thibault G, Vié H. Antibody-dependent cellular cytotoxicity (ADCC) is mediated by genetically modified antigen-specific human T lymphocytes. Blood 2006; 107:4669-77; PMID:16514054; http://dx.doi.org/10.1182/blood-2005-09-3775
-
(2006)
Blood
, vol.107
, pp. 4669-4677
-
-
Clémenceau, B.1
Congy-Jolivet, N.2
Gallot, G.3
Vivien, R.4
Gaschet, J.5
Thibault, G.6
Vié, H.7
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