review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Frankie Lam | |
Shudong Wang | |||
Christopher Proud | |||
Jinqiang Hou | |||
P2860 | cites work | Hallmarks of Cancer: The Next Generation | Q22252312 |
The Mnks are novel components in the control of TNF alpha biosynthesis and phosphorylate and regulate hnRNP A1 | Q81089022 | ||
Fermentative production of self-toxic fungal secondary metabolites | Q82334465 | ||
High eIF4E, VEGF, and microvessel density in stage I to III breast cancer | Q83190209 | ||
Therapeutic inhibition of MAP kinase interacting kinase blocks eukaryotic initiation factor 4E phosphorylation and suppresses outgrowth of experimental lung metastases | Q83201881 | ||
Negative regulation of protein translation by mitogen-activated protein kinase-interacting kinases 1 and 2 | Q24291466 | ||
The mTOR/PI3K and MAPK pathways converge on eIF4B to control its phosphorylation and activity | Q24293101 | ||
Identification of novel phosphorylation sites required for activation of MAPKAP kinase-2 | Q24312661 | ||
Rak functions as a tumor suppressor by regulating PTEN protein stability and function | Q24312999 | ||
MNK1 and MNK2 regulation in HER2-overexpressing breast cancer lines | Q24320171 | ||
MNK1, a new MAP kinase-activated protein kinase, isolated by a novel expression screening method for identifying protein kinase substrates | Q24322852 | ||
Distinct signaling events downstream of mTOR cooperate to mediate the effects of amino acids and insulin on initiation factor 4E-binding proteins | Q24519078 | ||
Mitogen-activated protein kinases activate the serine/threonine kinases Mnk1 and Mnk2 | Q24532154 | ||
Human eukaryotic translation initiation factor 4G (eIF4G) recruits mnk1 to phosphorylate eIF4E | Q24533512 | ||
The mitogen-activated protein kinase signal-integrating kinase Mnk2 is a eukaryotic initiation factor 4E kinase with high levels of basal activity in mammalian cells | Q24551026 | ||
The selectivity of protein kinase inhibitors: a further update | Q24654622 | ||
Targeting the mTOR signaling network for cancer therapy | Q24658334 | ||
The N and C termini of the splice variants of the human mitogen-activated protein kinase-interacting kinase Mnk2 determine activity and localization | Q24679177 | ||
Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site | Q27638349 | ||
Discovery and characterization of 2-anilino-4- (thiazol-5-yl)pyrimidine transcriptional CDK inhibitors as anticancer agents | Q27665462 | ||
eIF4 initiation factors: effectors of mRNA recruitment to ribosomes and regulators of translation | Q27860920 | ||
Upstream and downstream of mTOR | Q28277365 | ||
Identification and molecular characterization of Mnk1b, a splice variant of human MAP kinase-interacting kinase Mnk1 | Q28280562 | ||
The serine-threonine kinase MNK1 is post-translationally stabilized by PML-RARalpha and regulates differentiation of hematopoietic cells | Q28290732 | ||
The TSC1-2 tumor suppressor controls insulin-PI3K signaling via regulation of IRS proteins | Q28507365 | ||
Loss of MNK function sensitizes fibroblasts to serum-withdrawal induced apoptosis | Q28512029 | ||
Absence of S6K1 protects against age- and diet-induced obesity while enhancing insulin sensitivity | Q29614241 | ||
ERK and p38 MAPK-activated protein kinases: a family of protein kinases with diverse biological functions | Q29615216 | ||
Rational design of inhibitors that bind to inactive kinase conformations | Q29617558 | ||
Molecular mechanisms of translation initiation in eukaryotes | Q29619902 | ||
MNK kinases regulate multiple TLR pathways and innate proinflammatory cytokines in macrophages | Q30445072 | ||
CART classification of human 5' UTR sequences | Q30961644 | ||
Expression of translation initiation factors elF-4E and elF-2alpha and a potential physiologic role of continuous protein synthesis in human platelets | Q32007572 | ||
Phosphorylated eukaryotic translation initiation factor 4 (eIF4E) is elevated in human cancer tissues | Q33584507 | ||
Translational control: the cancer connection | Q33601620 | ||
eIF4E activity is regulated at multiple levels | Q33601634 | ||
eIF4E expression in tumors: its possible role in progression of malignancies | Q33601639 | ||
MNK1 and EIF4E are downstream effectors of MEKs in the regulation of the nuclear export of HDM2 mRNA. | Q40082913 | ||
Characterization of the activity of human MAP kinase-interacting kinase Mnk1b. | Q40115627 | ||
Structural bioinformatics-based design of selective, irreversible kinase inhibitors | Q40307105 | ||
Features in the N and C termini of the MAPK-interacting kinase Mnk1 mediate its nucleocytoplasmic shuttling | Q40638945 | ||
Phosphorylation of eukaryotic initiation factor 4E markedly reduces its affinity for capped mRNA. | Q40766564 | ||
Antisense RNA to eIF4E suppresses oncogenic properties of a head and neck squamous cell carcinoma cell line. | Q40874096 | ||
Reduction of translation initiation factor 4E decreases the malignancy of ras-transformed cloned rat embryo fibroblasts | Q41379829 | ||
Decreasing the level of translation initiation factor 4E with antisense RNA causes reversal of ras-mediated transformation and tumorigenesis of cloned rat embryo fibroblasts. | Q41514552 | ||
Cloning and characterization of KNR4, a yeast gene involved in (1,3)-beta-glucan synthesis | Q41812375 | ||
Expression of the eukaryotic translation initiation factors 4E and 2alpha in non-Hodgkin's lymphomas | Q41822752 | ||
The C-terminal domain of Mnk1a plays a dual role in tightly regulating its activity | Q42457882 | ||
Mitogen-activated protein kinases interacting kinases are autoinhibited by a reprogrammed activation segment | Q42763653 | ||
Upregulation of protein synthesis initiation factor eIF-4E is an early event during colon carcinogenesis | Q42816270 | ||
Phosphorylation of the eukaryotic translation initiation factor eIF4E contributes to its transformation and mRNA transport activities | Q42822974 | ||
Clinical outcome in stage I to III breast carcinoma and eIF4E overexpression | Q48030230 | ||
p53-dependent translational control of senescence and transformation via 4E-BPs. | Q53305156 | ||
Detection of the proto-oncogene eIF4E in surgical margins may predict recurrence in head and neck cancer | Q59263687 | ||
Elevated expression of eIF4E and FGF-2 isoforms during vascularization of breast carcinomas | Q59263692 | ||
The proto-oncogene/translation factor eIF4E: A survey of its expression in breast carcinomas | Q59263746 | ||
Regulated phosphorylation and low abundance of HeLa cell initiation factor eIF-4F suggest a role in translational control. Heat shock effects on eIF-4F | Q69693940 | ||
Overexpression of the proto-oncogene/translation factor 4E in breast-carcinoma cell lines | Q71081176 | ||
Serine 209, not serine 53, is the major site of phosphorylation in initiation factor eIF-4E in serum-treated Chinese hamster ovary cells | Q72036803 | ||
Phosphorylation of eIF-4E on Ser 209 in response to mitogenic and inflammatory stimuli is faithfully detected by specific antibodies | Q73984086 | ||
Expression of eukaryotic translation initiation factors 4E and 2alpha is increased frequently in bronchioloalveolar but not in squamous cell carcinomas of the lung | Q74610149 | ||
[Treatment of non-small cell lung cancer in elderly patients] | Q80467430 | ||
The role of the 5' untranslated region of an mRNA in translation regulation during development | Q33601649 | ||
Expression of eIF4E during head and neck tumorigenesis: possible role in angiogenesis | Q33709452 | ||
mRNAs containing extensive secondary structure in their 5' non-coding region translate efficiently in cells overexpressing initiation factor eIF-4E | Q33938526 | ||
Translational control of malignancy: the mRNA cap-binding protein, eIF-4E, as a central regulator of tumor formation, growth, invasion and metastasis | Q33992131 | ||
Cell cycle checkpoint defects contribute to genomic instability in PTEN deficient cells independent of DNA DSB repair. | Q34017915 | ||
Mnk earmarks eIF4E for cancer therapy | Q34069446 | ||
Combined deficiency for MAP kinase-interacting kinase 1 and 2 (Mnk1 and Mnk2) delays tumor development | Q34069663 | ||
eIF4E phosphorylation promotes tumorigenesis and is associated with prostate cancer progression | Q34069836 | ||
Protein phosphatase 2A negatively regulates eukaryotic initiation factor 4E phosphorylation and eIF4F assembly through direct dephosphorylation of Mnk and eIF4E. | Q34177252 | ||
Survival signalling by Akt and eIF4E in oncogenesis and cancer therapy | Q34306865 | ||
Phosphorylation of eukaryotic translation initiation factor 4E is critical for growth | Q34323752 | ||
Crystal structures of the Mnk2 kinase domain reveal an inhibitory conformation and a zinc binding site | Q34458528 | ||
PI3K and mTOR inhibitors: a new generation of targeted anticancer agents | Q34939865 | ||
Does phosphorylation of the cap-binding protein eIF4E play a role in translation initiation? | Q34992458 | ||
Translational control and metastatic progression: enhanced activity of the mRNA cap-binding protein eIF-4E selectively enhances translation of metastasis-related mRNAs | Q35125475 | ||
Mnk2 and Mnk1 are essential for constitutive and inducible phosphorylation of eukaryotic initiation factor 4E but not for cell growth or development | Q35663786 | ||
Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR inhibitors: rationale and importance to inhibiting these pathways in human health | Q35679353 | ||
Protein kinase inhibitors: insights into drug design from structure. | Q35697409 | ||
eIF-4E expression and its role in malignancies and metastases. | Q35750118 | ||
eIF4E is a central node of an RNA regulon that governs cellular proliferation | Q36119000 | ||
Dissecting eIF4E action in tumorigenesis | Q36209711 | ||
Inhibition of mammalian target of rapamycin induces phosphatidylinositol 3-kinase-dependent and Mnk-mediated eukaryotic translation initiation factor 4E phosphorylation | Q36315668 | ||
Expression of antisense RNA against initiation factor eIF-4E mRNA in HeLa cells results in lengthened cell division times, diminished translation rates, and reduced levels of both eIF-4E and the p220 component of eIF-4F. | Q36741222 | ||
Targeting the PI3K/Akt/mTOR pathway: effective combinations and clinical considerations | Q36742629 | ||
Rapamycin differentially inhibits S6Ks and 4E-BP1 to mediate cell-type-specific repression of mRNA translation | Q36971030 | ||
New modes of translational control in development, behavior, and disease | Q37033136 | ||
Tissue microarray analysis of eIF4E and its downstream effector proteins in human breast cancer | Q37074177 | ||
Cyclin-dependent kinase 9: a key transcriptional regulator and potential drug target in oncology, virology and cardiology. | Q37142722 | ||
eIF4E, the mRNA cap-binding protein: from basic discovery to translational research | Q37149933 | ||
The Mnks: MAP kinase-interacting kinases (MAP kinase signal-integrating kinases). | Q37175518 | ||
Therapeutic resistance resulting from mutations in Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR signaling pathways. | Q37837732 | ||
Roles of the Ras/Raf/MEK/ERK pathway in leukemia therapy. | Q37865381 | ||
Discovery of cercosporamide, a known antifungal natural product, as a selective Pkc1 kinase inhibitor through high-throughput screening | Q39601355 | ||
Dual targeting of AKT and mammalian target of rapamycin: a potential therapeutic approach for malignant peripheral nerve sheath tumor | Q39856372 | ||
P275 | copyright license | Creative Commons Attribution 2.5 Generic | Q18810333 |
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | transport protein | Q2111029 |
ribosomal proteins | Q3408228 | ||
peptide | Q172847 | ||
enzyme | Q8047 | ||
intracellular signaling peptides and proteins | Q67575047 | ||
P304 | page(s) | 118-131 | |
P577 | publication date | 2012-02-01 | |
P1433 | published in | Oncotarget | Q1573155 |
P1476 | title | Targeting Mnks for cancer therapy | |
P478 | volume | 3 |
Q36477529 | 4E-BP restrains eIF4E phosphorylation |
Q38758276 | AMP-activated Protein Kinase Up-regulates Mitogen-activated Protein (MAP) Kinase-interacting Serine/Threonine Kinase 1a-dependent Phosphorylation of Eukaryotic Translation Initiation Factor 4E. |
Q38122226 | Adaptation to chronic mTOR inhibition in cancer and in aging. |
Q36945944 | Adaptations to chronic rapamycin in mice. |
Q27686983 | Advances in targeting signal transduction pathways |
Q38989374 | Approved and Experimental Small-Molecule Oncology Kinase Inhibitor Drugs: A Mid-2016 Overview |
Q35832986 | Chorein addiction in VPS13A overexpressing rhabdomyosarcoma cells |
Q39010703 | Discovery of 5-(2-(phenylamino)pyrimidin-4-yl)thiazol-2(3H)-one derivatives as potent Mnk2 inhibitors: synthesis, SAR analysis and biological evaluation |
Q37180382 | Discovery of a BTK/MNK dual inhibitor for lymphoma and leukemia |
Q38915711 | Dissecting major signaling pathways in prostate cancer development and progression: Mechanisms and novel therapeutic targets |
Q36117958 | Distinct recruitment of human eIF4E isoforms to processing bodies and stress granules |
Q38637354 | Dual abrogation of MNK and mTOR: a novel therapeutic approach for the treatment of aggressive cancers |
Q39038481 | Dynamical insights of Mnk2 kinase activation by phosphorylation to facilitate inhibitor discovery |
Q36556350 | Ectopic NGAL expression can alter sensitivity of breast cancer cells to EGFR, Bcl-2, CaM-K inhibitors and the plant natural product berberine |
Q37099708 | Essential role for the Mnk pathway in the inhibitory effects of type I interferons on myeloproliferative neoplasm (MPN) precursors |
Q41257613 | Expression of eukaryotic initiation factor 4E and 4E binding protein 1 in colorectal carcinogenesis |
Q37660329 | First MNKs degrading agents block phosphorylation of eIF4E, induce apoptosis, inhibit cell growth, migration and invasion in triple negative and Her2-overexpressing breast cancer cell lines |
Q92166398 | First-in-Human, Healthy Volunteers Integrated Protocol of ETC-206, an Oral Mnk 1/2 Kinase Inhibitor Oncology Drug |
Q46713797 | Impact of genetic variations in the MAPK signaling pathway on outcome in metastatic colorectal cancer patients treated with first-line FOLFIRI and bevacizumab: data from FIRE-3 and TRIBE trials |
Q42513156 | Inhibiting ERK/Mnk/eIF4E broadly sensitizes ovarian cancer response to chemotherapy. |
Q37709399 | Inhibiting the MNK-eIF4E-β-catenin axis increases the responsiveness of aggressive breast cancer cells to chemotherapy |
Q37636705 | Inhibition of Mnk enhances apoptotic activity of cytarabine in acute myeloid leukemia cells |
Q36814636 | Inhibition of Mnk kinase activity by cercosporamide and suppressive effects on acute myeloid leukemia precursors |
Q38736366 | Inhibition of Mnk-eIF4E pathway sensitizes the efficacy to chemotherapy in anaplastic thyroid cancer |
Q39778668 | Insights into the Importance of DFD-Motif and Insertion I1 in Stabilizing the DFD-Out Conformation of Mnk2 Kinase |
Q36368266 | Interleukin-10 inhibits lipopolysaccharide-induced tumor necrosis factor-α translation through a SHIP1-dependent pathway |
Q57292823 | MNK1 inhibitor CGP57380 overcomes mTOR inhibitor-induced activation of eIF4E: the mechanism of synergic killing of human T-ALL cells |
Q47649072 | MNK1/2 inhibition limits oncogenicity and metastasis of KIT-mutant melanoma |
Q34545783 | MNKs act as a regulatory switch for eIF4E1 and eIF4E3 driven mRNA translation in DLBCL. |
Q47753117 | Major splice variants and multiple polyadenylation site utilization in mRNAs encoding human translation initiation factors eIF4E1 and eIF4E3 regulate the translational regulators? |
Q34450669 | Mechanical stimulation induces mTOR signaling via an ERK-independent mechanism: implications for a direct activation of mTOR by phosphatidic acid |
Q36635382 | MicroRNA-7 control of β-cell replication |
Q26865459 | Mnk kinase pathway: Cellular functions and biological outcomes |
Q42427245 | New insights into malignant cell survival mechanisms in medulloblastoma |
Q89870181 | Nicotinamide-Ponatinib Analogues as Potent Anti-CML and Anti-AML Compounds |
Q36140862 | Notch signaling sustains the expression of Mcl-1 and the activity of eIF4E to promote cell survival in CLL. |
Q55068343 | Novel C-4 heteroaryl 13-cis-retinamide Mnk/AR degrading agents inhibit cell proliferation and migration and induce apoptosis in human breast and prostate cancer cells and suppress growth of MDA-MB-231 human breast and CWR22Rv1 human prostate tumor x |
Q39114297 | Oncogenic activation of MEK/ERK primes melanoma cells for adaptation to endoplasmic reticulum stress. |
Q94599757 | Osimertinib successfully combats EGFR-negative glioblastoma cells by inhibiting the MAPK pathway |
Q41942808 | Pharmacological targeting of eIF4E in primary CLL lymphocytes |
Q35097767 | Phosphorylated Mnk1 and eIF4E are associated with lymph node metastasis and poor prognosis of nasopharyngeal carcinoma |
Q33620730 | Protein expression of eIF4E and integrin αvβ6 in colon cancer can predict clinical significance, reveal their correlation and imply possible mechanism of interaction |
Q42019006 | Pyrrolopyrimidine Analogues as MKNK Inhibitors |
Q38959287 | Regulatory effects of a Mnk2-eIF4E feedback loop during mTORC1 targeting of human medulloblastoma cells |
Q39139050 | Repression of microRNA-768-3p by MEK/ERK signalling contributes to enhanced mRNA translation in human melanoma |
Q34392470 | Selective anti-cancer agents as anti-aging drugs |
Q54118148 | Signaling pathways involved in the regulation of mRNA translation. |
Q26777735 | Signalling to eIF4E in cancer |
Q38918208 | Simultaneous targeting of androgen receptor (AR) and MAPK-interacting kinases (MNKs) by novel retinamides inhibits growth of human prostate cancer cell lines |
Q55711374 | Small Molecules Targeting the Inactive Form of the Mnk1/2 Kinases. |
Q35567160 | Stat1 stimulates cap-independent mRNA translation to inhibit cell proliferation and promote survival in response to antitumor drugs |
Q38871487 | Sulfoximine substituted quinazolines for pharmaceutical compositions US 20150005278 (A1): a patent evaluation |
Q52340912 | Synergistic effects of inhibiting the MNK-eIF4E and PI3K/AKT/ mTOR pathways on cell migration in MDA-MB-231 cells. |
Q38847261 | TRM6/61 connects PKCα with translational control through tRNAi(Met) stabilization: impact on tumorigenesis. |
Q92524896 | Targeting CDK9 for treatment of colorectal cancer |
Q34365839 | Targeting RNA transcription and translation in ovarian cancer cells with pharmacological inhibitor CDKI-73. |
Q39172901 | Targeting of protein translation as a new treatment paradigm for prostate cancer |
Q38699320 | Targeting translation: eIF4E as an emerging anticancer drug target |
Q38920048 | The MAP kinase-interacting kinases regulate cell migration, vimentin expression and eIF4E/CYFIP1 binding |
Q52684450 | The unfolded protein response: a novel therapeutic target for poor prognostic BRAF mutant colorectal cancer. |
Q36473355 | Therapeutic interventions to disrupt the protein synthetic machinery in melanoma |
Q38791406 | Unveiling new chemical scaffolds as Mnk inhibitors. |
Q36294841 | Up-regulation of translation eukaryotic initiation factor 4E in nucleophosmin 1 haploinsufficient cells results in changes in CCAAT enhancer-binding protein α activity: implications in myelodysplastic syndrome and acute myeloid leukemia. |
Q54988438 | miR-134 increases the antitumor effects of cytarabine by targeting Mnks in acute myeloid leukemia cells. |
Q64107786 | miR-483-5p Targets MKNK1 to Suppress Wilms' Tumor Cell Proliferation and Apoptosis In Vitro and In Vivo |
Q37321076 | peIF4E as an independent prognostic factor and a potential therapeutic target in diffuse infiltrating astrocytomas. |
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