AML1-ETO and C-KIT mutation/overexpression in t(8;21) leukemia: implication in stepwise leukemogenesis and response to Gleevec.
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Receptor tyrosine kinase (c-Kit) inhibitors: a potential therapeutic target in cancer cellsIncomplete radiofrequency ablation enhances invasiveness and metastasis of residual cancer of hepatocellular carcinoma cell HCCLM3 via activating β-catenin signalingHigh levels of the adhesion molecule CD44 on leukemic cells generate acute myeloid leukemia relapse after withdrawal of the initial transforming eventOverexpression and small molecule-triggered downregulation of CIP2A in lung cancerAML1/ETO proteins control POU4F1/BRN3A expression and function in t(8;21) acute myeloid leukemiaOncogenic pathways of AML1-ETO in acute myeloid leukemia: multifaceted manipulation of marrow maturation.Prevalence and prognostic significance of KIT mutations in pediatric patients with core binding factor AML enrolled on serial pediatric cooperative trials for de novo AML.A novel melting curve-based method for detecting c-kit mutations in acute myeloid leukemia.Transcriptional repression of the Neurofibromatosis-1 tumor suppressor by the t(8;21) fusion protein.The AML1-ETO fusion gene and the FLT3 length mutation collaborate in inducing acute leukemia in mice.A human monoclonal antibody targeting the stem cell factor receptor (c-Kit) blocks tumor cell signaling and inhibits tumor growth.Nanoliter multiplex PCR arrays on a SlipChip.Modeling interactions between leukemia-specific chromosomal changes, somatic mutations, and gene expression patterns during progression of core-binding factor leukemiasCTHRC1 is upregulated by promoter demethylation and transforming growth factor-β1 and may be associated with metastasis in human gastric cancer.Down-regulation of microRNAs 222/221 in acute myelogenous leukemia with deranged core-binding factor subunitsRole of the erythropoietin receptor in ETV6/RUNX1-positive acute lymphoblastic leukemia.C-KIT mutation cooperates with full-length AML1-ETO to induce acute myeloid leukemia in miceAcute myeloid leukemia with the 8q22;21q22 translocation: secondary mutational events and alternative t(8;21) transcripts.Suppression of natural killer cells by sorafenib contributes to prometastatic effects in hepatocellular carcinomaMastocytosis: state of the art.Core-binding factor acute myeloid leukemia: Heterogeneity, monitoring, and therapy.Hematopoietic stem-cell transplantation for advanced systemic mastocytosis.In vivo and in vitro effects of heme oxygenase-1 silencing on the survival of acute myelocytic leukemia-M2 cells.Flumatinib, a selective inhibitor of BCR-ABL/PDGFR/KIT, effectively overcomes drug resistance of certain KIT mutants.TRAPPC4-ERK2 interaction activates ERK1/2, modulates its nuclear localization and regulates proliferation and apoptosis of colorectal cancer cellsHigh expression of c-kit mRNA predicts unfavorable outcome in adult patients with t(8;21) acute myeloid leukemia.Neoplasia driven by mutant c-KIT is mediated by intracellular, not plasma membrane, receptor signaling.Oridonin, a diterpenoid extracted from medicinal herbs, targets AML1-ETO fusion protein and shows potent antitumor activity with low adverse effects on t(8;21) leukemia in vitro and in vivo.Roles of STAT3 and ZEB1 proteins in E-cadherin down-regulation and human colorectal cancer epithelial-mesenchymal transitionDistinct classes of c-Kit-activating mutations differ in their ability to promote RUNX1-ETO-associated acute myeloid leukemia.Bortezomib interferes with C-KIT processing and transforms the t(8;21)-generated fusion proteins into tumor-suppressing fragments in leukemia cells.Inhibition of DNA methyltransferase induces G2 cell cycle arrest and apoptosis in human colorectal cancer cells via inhibition of JAK2/STAT3/STAT5 signalling.Acute myeloid leukemia stem cells and CD33-targeted immunotherapyAberrant expression of Treg-associated cytokine IL-35 along with IL-10 and TGF-β in acute myeloid leukemiaRetrospective comparison of fludarabine in combination with intermediate-dose cytarabine versus high-dose cytarabine as consolidation therapies for acute myeloid leukemia.Depletion of RUNX1/ETO in t(8;21) AML cells leads to genome-wide changes in chromatin structure and transcription factor binding.Acute promyelocytic leukemia: a model of molecular target based therapy.Inhibition of JAK1, 2/STAT3 signaling induces apoptosis, cell cycle arrest, and reduces tumor cell invasion in colorectal cancer cells.Skp1 in lung cancer: clinical significance and therapeutic efficacy of its small molecule inhibitorsSignificance of KIT exon 17 mutation depends on mutant level rather than positivity in core-binding factor acute myeloid leukemia
P2860
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P2860
AML1-ETO and C-KIT mutation/overexpression in t(8;21) leukemia: implication in stepwise leukemogenesis and response to Gleevec.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
AML1-ETO and C-KIT mutation/ov ...... nesis and response to Gleevec.
@ast
AML1-ETO and C-KIT mutation/ov ...... nesis and response to Gleevec.
@en
type
label
AML1-ETO and C-KIT mutation/ov ...... nesis and response to Gleevec.
@ast
AML1-ETO and C-KIT mutation/ov ...... nesis and response to Gleevec.
@en
prefLabel
AML1-ETO and C-KIT mutation/ov ...... nesis and response to Gleevec.
@ast
AML1-ETO and C-KIT mutation/ov ...... nesis and response to Gleevec.
@en
P2093
P2860
P50
P356
P1476
AML1-ETO and C-KIT mutation/ov ...... enesis and response to Gleevec
@en
P2093
Guang Yang
Guo-Qiang Chen
Jian-Hua You
Jing-Yi Shi
Sai-Juan Chen
Shu-Min Xiong
P2860
P304
P356
10.1073/PNAS.0408831102
P407
P577
2005-01-13T00:00:00Z