scholarly article | Q13442814 |
P50 | author | Yukie Takabatake | Q59692005 |
Robert Z Orlowski | Q91428664 | ||
P2093 | author name string | Shuang Chen | |
Steven Grant | |||
Yun Dai | |||
Liang Zhou | |||
Michael W Sanderson | |||
Xin-Yan Pei | |||
Lora B Kramer | |||
Jessica Felthousen | |||
Leena E Youssefian | |||
Wesley W Bodie | |||
P2860 | cites work | Proapoptotic Bak is sequestered by Mcl-1 and Bcl-xL, but not Bcl-2, until displaced by BH3-only proteins | Q24302494 |
ERK1/2-dependent phosphorylation of BimEL promotes its rapid dissociation from Mcl-1 and Bcl-xL | Q24306894 | ||
Seliciclib (CYC202, R-Roscovitine) induces cell death in multiple myeloma cells by inhibition of RNA polymerase II-dependent transcription and down-regulation of Mcl-1 | Q28256819 | ||
Thr 163 phosphorylation causes Mcl-1 stabilization when degradation is independent of the adjacent GSK3-targeted phosphodegron, promoting drug resistance in cancer | Q28484291 | ||
Mitochondrial membrane permeabilization in cell death | Q29547425 | ||
Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors | Q29547463 | ||
Disruption of IkappaB kinase (IKK)-mediated RelA serine 536 phosphorylation sensitizes human multiple myeloma cells to histone deacetylase (HDAC) inhibitors | Q30424831 | ||
Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets, and DNA breakage | Q31160033 | ||
FoxM1 is a general target for proteasome inhibitors | Q33492774 | ||
Cytokinetically quiescent (G0/G1) human multiple myeloma cells are susceptible to simultaneous inhibition of Chk1 and MEK1/2. | Q34017354 | ||
Small molecule modulators of cyclin-dependent kinases for cancer therapy | Q34293568 | ||
Mcl-1: a highly regulated cell death and survival controller | Q34491222 | ||
Disruption of Src function potentiates Chk1-inhibitor-induced apoptosis in human multiple myeloma cells in vitro and in vivo | Q34667764 | ||
Preferential killing of PTEN-null myelomas by PI3K inhibitors through Akt pathway | Q44588841 | ||
Degradation of Mcl-1 by granzyme B: implications for Bim-mediated mitochondrial apoptotic events | Q44795441 | ||
Mcl-1 down-regulation potentiates ABT-737 lethality by cooperatively inducing Bak activation and Bax translocation | Q44926251 | ||
Evidence for a protective role of Mcl-1 in proteasome inhibitor-induced apoptosis. | Q45197519 | ||
IL-6-independent expression of Mcl-1 in human multiple myeloma | Q48010145 | ||
Antisense strategy shows that Mcl-1 rather than Bcl-2 or Bcl-x(L) is an essential survival protein of human myeloma cells. | Q52546411 | ||
The BH3-mimetic GX15-070 synergizes with bortezomib in mantle cell lymphoma by enhancing Noxa-mediated activation of Bak | Q57279398 | ||
Nonionic detergents induce dimerization among members of the Bcl-2 family | Q73343305 | ||
Expression of Mcl-1 in mantle cell lymphoma is associated with high-grade morphology, a high proliferative state, and p53 overexpression | Q78634781 | ||
Management of relapsed and relapsed/refractory multiple myeloma | Q85048468 | ||
Distribution of Bim determines Mcl-1 dependence or codependence with Bcl-xL/Bcl-2 in Mcl-1-expressing myeloma cells | Q35153790 | ||
Role of the tumor microenvironment in mediating de novo resistance to drugs and physiological mediators of cell death | Q35567260 | ||
Mcl-1 regulation and its role in multiple myeloma | Q35910365 | ||
Targeting MEK induces myeloma-cell cytotoxicity and inhibits osteoclastogenesis | Q35989478 | ||
MEK1/2 inhibitors potentiate UCN-01 lethality in human multiple myeloma cells through a Bim-dependent mechanism | Q35990714 | ||
Targeting multiple myeloma cells and their bone marrow microenvironment | Q36009239 | ||
Blockade of the MEK/ERK signalling cascade by AS703026, a novel selective MEK1/2 inhibitor, induces pleiotropic anti-myeloma activity in vitro and in vivo | Q36162685 | ||
CDK inhibitors upregulate BH3-only proteins to sensitize human myeloma cells to BH3 mimetic therapies | Q36170136 | ||
Small molecule obatoclax (GX15-070) antagonizes MCL-1 and overcomes MCL-1-mediated resistance to apoptosis | Q36288687 | ||
Targeting the insulin-like growth factor-1 receptor to overcome bortezomib resistance in preclinical models of multiple myeloma. | Q36333522 | ||
Novel therapeutic strategies targeting growth factor signalling cascades in multiple myeloma | Q36367811 | ||
The role of the bone microenvironment in the pathophysiology and therapeutic management of multiple myeloma: interplay of growth factors, their receptors and stromal interactions | Q36501937 | ||
A major role for Mcl-1 antiapoptotic protein in the IL-6-induced survival of human myeloma cells | Q36675950 | ||
MEK inhibition enhances ABT-737-induced leukemia cell apoptosis via prevention of ERK-activated MCL-1 induction and modulation of MCL-1/BIM complex | Q36706340 | ||
Alternatively spliced glucocorticoid receptor messenger RNAs in glucocorticoid-resistant human multiple myeloma cells. | Q36767790 | ||
Interruption of the Ras/MEK/ERK signaling cascade enhances Chk1 inhibitor-induced DNA damage in vitro and in vivo in human multiple myeloma cells | Q36868759 | ||
Understanding multiple myeloma pathogenesis in the bone marrow to identify new therapeutic targets | Q36889961 | ||
Bim and the pro-survival Bcl-2 proteins: opposites attract, ERK repels | Q36946423 | ||
Tumor cell-specific bioluminescence platform to identify stroma-induced changes to anticancer drug activity. | Q37207049 | ||
Latest advances and current challenges in the treatment of multiple myeloma | Q37986287 | ||
Emerging strategies for targeting cell adhesion in multiple myeloma | Q38041724 | ||
Bone marrow microenvironment in multiple myeloma progression. | Q38055141 | ||
Nucleoside analog ARC targets Mcl-1 to induce apoptosis in leukemia cells | Q38828546 | ||
Molecular mechanisms of acquired proteasome inhibitor resistance | Q39278628 | ||
Mcl-1 Phosphorylation defines ABT-737 resistance that can be overcome by increased NOXA expression in leukemic B cells | Q39360515 | ||
Up-regulation of pro-apoptotic protein Bim and down-regulation of anti-apoptotic protein Mcl-1 cooperatively mediate enhanced tumor cell death induced by the combination of ERK kinase (MEK) inhibitor and microtubule inhibitor | Q39407551 | ||
Activation of ATF4 mediates unwanted Mcl-1 accumulation by proteasome inhibition | Q39435523 | ||
ARC synergizes with ABT-737 to induce apoptosis in human cancer cells | Q39697805 | ||
Noxa up-regulation and Mcl-1 cleavage are associated to apoptosis induction by bortezomib in multiple myeloma | Q40124624 | ||
Cell-cell contact mediated signalling - no fear of contact. | Q40292594 | ||
Apoptosis induced by the kinase inhibitor BAY 43-9006 in human leukemia cells involves down-regulation of Mcl-1 through inhibition of translation | Q40383692 | ||
Mcl-1 is overexpressed in multiple myeloma and associated with relapse and shorter survival. | Q40420617 | ||
VEGF induces Mcl-1 up-regulation and protects multiple myeloma cells against apoptosis | Q40541706 | ||
The HMG-CoA reductase inhibitor simvastatin overcomes cell adhesion-mediated drug resistance in multiple myeloma by geranylgeranylation of Rho protein and activation of Rho kinase | Q40552228 | ||
Extracellular signal-regulated kinases 1/2 are serum-stimulated "Bim(EL) kinases" that bind to the BH3-only protein Bim(EL) causing its phosphorylation and turnover | Q40606380 | ||
Myeloid cell factor-1 is a critical survival factor for multiple myeloma | Q40655990 | ||
Selectively targeting Mcl-1 for the treatment of acute myelogenous leukemia and solid tumors | Q41907705 | ||
Shifting the balance of mitochondrial apoptosis: therapeutic perspectives | Q42474267 | ||
Purported Mcl-1 inhibitor marinopyrrole A fails to show selective cytotoxicity for Mcl-1-dependent cell lines | Q42534915 | ||
Combined treatment with the checkpoint abrogator UCN-01 and MEK1/2 inhibitors potently induces apoptosis in drug-sensitive and -resistant myeloma cells through an IL-6-independent mechanism | Q44182944 | ||
Bone marrow stromal-derived soluble factors and direct cell contact contribute to de novo drug resistance of myeloma cells by distinct mechanisms | Q44452179 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | multiple myeloma | Q467635 |
multiple drug resistance | Q643839 | ||
drug resistance | Q12147416 | ||
P304 | page(s) | e89064 | |
P577 | publication date | 2014-01-01 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Circumvention of Mcl-1-dependent drug resistance by simultaneous Chk1 and MEK1/2 inhibition in human multiple myeloma cells | |
P478 | volume | 9 |
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Q26781203 | Regulation of Bim in Health and Disease |
Q53733720 | Simultaneous targeting of ATM and Mcl-1 increases cisplatin sensitivity of cisplatin-resistant non-small cell lung cancer. |
Q40643079 | Targeting executioner procaspase-3 with the procaspase-activating compound B-PAC-1 induces apoptosis in multiple myeloma cells |
Q92264151 | The Covalent CDK7 Inhibitor THZ1 Potently Induces Apoptosis in Multiple Myeloma Cells In Vitro and In Vivo |
Q37203487 | Treatment of acquired drug resistance in multiple myeloma by combination therapy with XPO1 and topoisomerase II inhibitors |
Q37684621 | XPO1 inhibitor combination therapy with bortezomib or carfilzomib induces nuclear localization of IκBα and overcomes acquired proteasome inhibitor resistance in human multiple myeloma |
Q49238703 | YM155 exerts potent cytotoxic activity against quiescent (G0/G1) multiple myeloma and bortezomib resistant cells via inhibition of survivin and Mcl-1. |