scholarly article | Q13442814 |
P2093 | author name string | Mark Johnson | |
Simon J Cook | |||
Annette S Gillings | |||
Ceri M Wiggins | |||
Kathryn Balmanno | |||
P2860 | cites work | The Hallmarks of Cancer | Q221226 |
Differential targeting of prosurvival Bcl-2 proteins by their BH3-only ligands allows complementary apoptotic function | Q24293924 | ||
Apoptosis initiated when BH3 ligands engage multiple Bcl-2 homologs, not Bax or Bak | Q24296478 | ||
ERK1/2-dependent phosphorylation of BimEL promotes its rapid dissociation from Mcl-1 and Bcl-xL | Q24306894 | ||
RACK1 and CIS mediate the degradation of BimEL in cancer cells | Q24322936 | ||
Bim: a novel member of the Bcl-2 family that promotes apoptosis | Q24532974 | ||
JNK phosphorylation of Bim-related members of the Bcl2 family induces Bax-dependent apoptosis | Q24554008 | ||
The Bcl-2 apoptotic switch in cancer development and therapy | Q24620437 | ||
Glycogen synthase kinase-3 inhibition induces glioma cell death through c-MYC, nuclear factor-kappaB, and glucose regulation | Q24655658 | ||
Novel targeted therapies for Bcr-Abl positive acute leukemias: beyond STI571. | Q27824789 | ||
Mutations of the BRAF gene in human cancer | Q27860760 | ||
Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib | Q27861059 | ||
Intrinsic resistance to the MEK1/2 inhibitor AZD6244 (ARRY-142886) is associated with weak ERK1/2 signalling and/or strong PI3K signalling in colorectal cancer cell lines | Q39819940 | ||
Braf(V600E) cooperates with Pten loss to induce metastatic melanoma | Q39873596 | ||
BH3-only protein Bim more critical than Puma in tyrosine kinase inhibitor-induced apoptosis of human leukemic cells and transduced hematopoietic progenitors carrying oncogenic FLT3. | Q39907753 | ||
Oncogenic B-RafV600E inhibits apoptosis and promotes ERK-dependent inactivation of Bad and Bim. | Q39977634 | ||
Proapoptotic BH3-only BCL-2 family protein BIM connects death signaling from epidermal growth factor receptor inhibition to the mitochondrion | Q40033557 | ||
AZD6244 (ARRY-142886), a potent inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2 kinases: mechanism of action in vivo, pharmacokinetic/pharmacodynamic relationship, and potential for combination in precl | Q40093939 | ||
Apoptosis induction in human melanoma cells by inhibition of MEK is caspase-independent and mediated by the Bcl-2 family members PUMA, Bim, and Mcl-1. | Q40102679 | ||
Imatinib and nilotinib induce apoptosis of chronic myeloid leukemia cells through a Bim-dependant pathway modulated by cytokines | Q40126011 | ||
Apoptosis-based dual molecular targeting by INNO-406, a second-generation Bcr-Abl inhibitor, and ABT-737, an inhibitor of antiapoptotic Bcl-2 proteins, against Bcr-Abl-positive leukemia | Q40131183 | ||
Regulation of osteoclast apoptosis by ubiquitylation of proapoptotic BH3-only Bcl-2 family member Bim. | Q40323778 | ||
Identification of a DEF-type docking domain for extracellular signal-regulated kinases 1/2 that directs phosphorylation and turnover of the BH3-only protein BimEL. | Q40454938 | ||
Roles of Bim in apoptosis of normal and Bcr-Abl-expressing hematopoietic progenitors | Q40540288 | ||
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 | ||
Role of Bim in the survival pathway induced by Raf in epithelial cells | Q40607194 | ||
Phosphorylation of Bim-EL by Erk1/2 on serine 69 promotes its degradation via the proteasome pathway and regulates its proapoptotic function. | Q40626751 | ||
Activation of the ERK1/2 signaling pathway promotes phosphorylation and proteasome-dependent degradation of the BH3-only protein, Bim. | Q40662652 | ||
Activation of ERK1/2 by deltaRaf-1:ER* represses Bim expression independently of the JNK or PI3K pathways | Q40666435 | ||
Colorectal cancer cells with the BRAF(V600E) mutation are addicted to the ERK1/2 pathway for growth factor-independent survival and repression of BIM. | Q41836780 | ||
FOXO transcription factors directly activate bim gene expression and promote apoptosis in sympathetic neurons | Q42918105 | ||
c-Cbl is not required for ERK1/2-dependent degradation of BimEL. | Q43098314 | ||
Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies | Q46595207 | ||
Low-level expression of proapoptotic Bcl-2-interacting mediator in leukemic cells in patients with chronic myeloid leukemia: role of BCR/ABL, characterization of underlying signaling pathways, and reexpression by novel pharmacologic compounds. | Q46757499 | ||
Mutant B-RAF mediates resistance to anoikis via Bad and Bim. | Q46774780 | ||
Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition | Q50335943 | ||
Drivers and passengers | Q59080774 | ||
Proapoptotic Bcl-2 relative Bim required for certain apoptotic responses, leukocyte homeostasis, and to preclude autoimmunity | Q28138855 | ||
Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl‐2 family1 | Q28208950 | ||
Prolonged rapamycin treatment inhibits mTORC2 assembly and Akt/PKB | Q28306356 | ||
betaTrCP- and Rsk1/2-mediated degradation of BimEL inhibits apoptosis | Q28306984 | ||
Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo | Q28368373 | ||
Gefitinib-induced killing of NSCLC cell lines expressing mutant EGFR requires BIM and can be enhanced by BH3 mimetics | Q28469345 | ||
Androgen-dependent apoptosis in male germ cells is regulated through the proto-oncoprotein Cbl | Q28564996 | ||
Dominant-negative c-Jun promotes neuronal survival by reducing BIM expression and inhibiting mitochondrial cytochrome c release | Q28567073 | ||
BIM mediates EGFR tyrosine kinase inhibitor-induced apoptosis in lung cancers with oncogenic EGFR mutations | Q28756824 | ||
The BCL-2 protein family: opposing activities that mediate cell death | Q29547380 | ||
Targeting cancer with small molecule kinase inhibitors | Q29547395 | ||
BRAF mutation predicts sensitivity to MEK inhibition | Q29614281 | ||
FOXOs, cancer and regulation of apoptosis | Q33642512 | ||
Inhibition of the Bcr-Abl tyrosine kinase as a therapeutic strategy for CML. | Q35022505 | ||
Bim and Bad mediate imatinib-induced killing of Bcr/Abl+ leukemic cells, and resistance due to their loss is overcome by a BH3 mimetic. | Q35075545 | ||
MEK1/2 inhibitors sensitize Bcr/Abl+ human leukemia cells to the dual Abl/Src inhibitor BMS-354/825 | Q35804449 | ||
Intrinsic tumour suppression | Q35953133 | ||
MEK1/2 inhibitors potentiate UCN-01 lethality in human multiple myeloma cells through a Bim-dependent mechanism | Q35990714 | ||
Induction of BIM is essential for apoptosis triggered by EGFR kinase inhibitors in mutant EGFR-dependent lung adenocarcinomas | Q36026392 | ||
Promoting apoptosis as a strategy for cancer drug discovery | Q36292878 | ||
ERK promotes tumorigenesis by inhibiting FOXO3a via MDM2-mediated degradation | Q36647913 | ||
Multisite phosphorylation regulates Bim stability and apoptotic activity | Q36756298 | ||
Vorinostat synergistically potentiates MK-0457 lethality in chronic myelogenous leukemia cells sensitive and resistant to imatinib mesylate | Q36787540 | ||
Treatment of B-RAF mutant human tumor cells with a MEK inhibitor requires Bim and is enhanced by a BH3 mimetic | Q36945203 | ||
Bim and the pro-survival Bcl-2 proteins: opposites attract, ERK repels | Q36946423 | ||
The Bcr-Abl tyrosine kinase inhibitor imatinib and promising new agents against Philadelphia chromosome-positive leukemias | Q36967858 | ||
Oncogenic BRAF(V600E) inhibits BIM expression to promote melanoma cell survival | Q37028555 | ||
Oncogene addiction | Q37152445 | ||
Bcl-2 inhibitors: small molecules with a big impact on cancer therapy | Q37275477 | ||
Tumour cell survival signalling by the ERK1/2 pathway | Q37290943 | ||
Unleashing the power of inhibitors of oncogenic kinases through BH3 mimetics | Q37431491 | ||
Bim is a suppressor of Myc-induced mouse B cell leukemia | Q37647369 | ||
Bcl-2-independent Bcr-Abl-mediated resistance to apoptosis: protection is correlated with up regulation of Bcl-xL. | Q38338829 | ||
Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-small-cell lung, breast, colon, and pancreatic cancer | Q38445646 | ||
Downregulation of Bim, a proapoptotic relative of Bcl-2, is a pivotal step in cytokine-initiated survival signaling in murine hematopoietic progenitors | Q39457731 | ||
P433 | issue | 21 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | autophagy | Q288322 |
apoptotic process | Q14599311 | ||
P304 | page(s) | 6050-6062 | |
P577 | publication date | 2009-09-29 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | FEBS Journal | Q1388041 |
P1476 | title | Apoptosis and autophagy: BIM as a mediator of tumour cell death in response to oncogene-targeted therapeutics | |
P478 | volume | 276 |
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Q37317126 | BIM mediates oncogene inactivation-induced apoptosis in multiple transgenic mouse models of acute lymphoblastic leukemia |
Q33642685 | BIMEL is a key effector molecule in oxidative stress-mediated apoptosis in acute myeloid leukemia cells when combined with arsenic trioxide and buthionine sulfoximine |
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Q35353981 | Bim contributes to phenethyl isothiocyanate‐induced apoptosis in breast cancer cells |
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Q36170136 | CDK inhibitors upregulate BH3-only proteins to sensitize human myeloma cells to BH3 mimetic therapies |
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Q39091696 | Dual inhibition of MEK1/2 and EGFR synergistically induces caspase-3-dependent apoptosis in EGFR inhibitor-resistant lung cancer cells via BIM upregulation |
Q38704670 | Efficacy of an HSP90 inhibitor, ganetespib, in preclinical thyroid cancer models |
Q58612606 | Egr-1 is involved in coronary microembolization-induced myocardial injury via Bim/Beclin-1 pathway-mediated autophagy inhibition and apoptosis activation |
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Q42019758 | MEK1/2 inhibition elicits regression of autochthonous lung tumors induced by KRASG12D or BRAFV600E. |
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