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PIC-1/SUMO-1-modified PML-retinoic acid receptor alpha mediates arsenic trioxide-induced apoptosis in acute promyelocytic leukemia.
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Translocation products in acute myeloid leukemia activate the Wnt signaling pathway in hematopoietic cells.
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Activation of signaling pathways in models of t(6;9)-acute myeloid leukemia.
Annals of Hematology
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Understanding a high-risk acute myeloid leukemia by analyzing the interactome of its major driver mutation.
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2021.
Crizotinib acts as ABL1 inhibitor combining ATP-binding with allosteric inhibition and is active against native BCR/ABL1 and its resistance and compound mutants BCR/ABL1T315I and BCR/ABL1T315I-E255K.
Annals of Hematology
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Mesenchymal soluble factors confer imatinib drug resistance in chronic myelogenous leukemia cells.
Archives of Medical Science
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The t(6;9) associated DEK/CAN fusion protein targets a population of long-term repopulating hematopoietic stem cells for leukemogenic transformation.
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The phosphatase UBASH3B/Sts-1 is a negative regulator of Bcr-Abl kinase activity and leukemogenesis.
Leukemia
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2017.
Ectopic expression of snail and twist in Ph+ leukemia cells upregulates CD44 expression and alters their differentiation potential.
Journal of Cancer
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2016.
Platinum (IV)-fatty acid conjugates overcome inherently and acquired Cisplatin resistant cancer cell lines: an in-vitro study.
BMC Cancer
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BCR: a new target in resistance mediated by BCR/ABL-315I?
Genes & Cancer
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Mian, A. A., Rafiei, A., Haberbosch, I., Zeifman, A., Titov, I., Stroylov, V., Metodieva, A., Stroganov, O., Novikov, F., Brill, B., Chilov, G., Hoelzer, D., Ottmann, O. G. ORCID: https://orcid.org/0000-0001-9559-1330 and Ruthardt, M. ORCID: https://orcid.org/0000-0003-1021-3811
2015.
PF-114, a potent and selective inhibitor of native and mutated BCR/ABL is active against Philadelphia chromosome-positive (Ph+) leukemias harboring the T315I mutation.
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2015.
The functional interplay between the t(9;22)-associated fusion proteins BCR/ABL and ABL/BCR in Philadelphia chromosome-positive Acute Lymphatic Leukemia.
PLOS Genetics
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2015.
Potential use of allosteric inhibitors as strategy to overcome drug resistance in Ph-positive leukemia.
International Journal of Molecular Medicine
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Oancea, Claudia, Rüster, Brigitte, Brill, Boris, Roos, Jessica, Heinssmann, Maria, Bug, Gesine, Mian, Afsar Ali, Guillen, Nathalie Andrea, Kornblau, Steven M., Henschler, Reinhard and Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811
2014.
STAT activation status differentiates leukemogenic from non-leukemogenic stem cells in AML and is suppressed by arsenic in t(6;9)-positive AML.
Genes & Cancer
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2014.
5-lipoxygenase is a candidate target for therapeutic management of stem cell-like cells in acute myeloid leukemia.
Cancer Research
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Differential effects of selective inhibitors targeting the PI3K/AKT/mTOR pathway in acute lymphoblastic leukemia.
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2013.
Oleylamine-carbonyl-valinol inhibits auto-phosphorylation activity of native and T315I mutated Bcr-Abl, and exhibits selectivity towards oncogenic Bcr-Abl in SupB15 ALL cell lines.
Molecular Biology Reports
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Overcoming Bcr-Abl T315I mutation by combination of GNF-2 and ATP competitors in an Abl-independent mechanism.
BMC Cancer
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Allosteric inhibition enhances the efficacy of ABL kinase inhibitors to target unmutated BCR-ABL and BCR-ABL-T315I.
BMC Cancer
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Romanski, Annette, Schwarz, Kerstin, Keller, Maren, Wietbrauk, Sarah, Vogel, Anja, Roos, Jessica, Oancea, Claudia, Brill, Boris, Krämer, Oliver H., Serve, Hubert, Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811 and Bug, Gesine
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Deacetylase inhibitors modulate proliferation and self-renewal properties of leukemic stem and progenitor cells.
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p185(BCR/ABL) has a lower sensitivity than p210(BCR/ABL) to the allosteric inhibitor GNF-2 in Philadelphia chromosome-positive acute lymphatic leukemia.
Haematologica
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Rettinger, Eva, KuçI, Selim, Naumann, Ivonne, Becker, Petra, Kreyenberg, Hermann, Anzaghe, Martina, Willasch, Andre, Koehl, Ulrike, Bug, Gesine, Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811, Klingebiel, Thomas, Fulda, Simone and Bader, Peter
2012.
The cytotoxic potential of interleukin-15-stimulated cytokine-induced killer cells against leukemia cells.
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2011.
Sulindac sulfide reverses aberrant self-renewal of progenitor cells induced by the AML-associated fusion proteins PML/RARα and PLZF/RARα.
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2011.
Oleic acid is the active component in the mushroom Daedalea gibbosa inhibiting Bcr-Abl kinase autophosphorylation activity.
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5-lipoxygenase: underappreciated role of a pro-inflammatory enzyme in tumorigenesis.
Frontiers in Pharmacology
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Bursen, Adelheid, Schwabe, Karen, Rüster, Brigitte, Henschler, Reinhard, Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811, Dingermann, Theo and Marschalek, Rolf
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The AF4·MLL fusion protein is capable of inducing ALL in mice without requirement of MLL·AF4.
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Oligomerization inhibition, combined with allosteric inhibition, abrogates the transformation potential of T315I-positive BCR/ABL.
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Reciprocal t(9;22) ABL/BCR fusion proteins: Leukemogenic potential and effects on B cell commitment.
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The gatekeeper mutation T315I confers resistance against small molecules by increasing or restoring the ABL-kinase activity accompanied by aberrant transphosphorylation of endogenous BCR, even in loss-of-function mutants of BCR/ABL.
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Boehrer, Simone, Chow, Kai U., Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811, Hoelzer, Dieter, Mitrou, Paris S. and Weidmann, Eckhart
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Expression and function of prostate-apoptosis-response-gene-4 in lymphatic cells.
Leukemia & Lymphoma
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Cooperation between constitutively activated c-kit signaling and leukemogenic transcription factors in the determination of the leukemic phenotype in murine hematopoietic stem cells.
International Journal of Oncology
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The effect of the dual Src/Abl kinase inhibitor AZD0530 on Philadelphia positive leukaemia cell lines.
BMC Cancer
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Targeting of the N-terminal coiled coil oligomerization interface by a helix-2 peptide inhibits unmutated and imatinib-resistant BCR/ABL.
International Journal of Cancer
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Effect of histone deacetylase inhibitor valproic acid on progenitor cells of acute myeloid leukemia.
Haematologica
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Arsenic but not all-trans retinoic acid overcomes the aberrant stem cell capacity of PML/RARalpha-positive leukemic stem cells.
Haematologica
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2007.
INNO-406, a novel BCR-ABL/Lyn dual tyrosine kinase inhibitor, suppresses the growth of Ph+ leukemia cells in the central nervous system, and cyclosporine A augments its in vivo activity.
Blood
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Zheng, Xiaomin, Güller, Saskia, Beissert, Tim, Puccetti, Elena and Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811
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BCR and its mutants, the reciprocal t(9;22)-associated ABL/BCR fusion proteins, differentially regulate the cytoskeleton and cell motility.
BMC Cancer
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Prostate-apoptosis-response-gene-4 increases sensitivity to TRAIL-induced apoptosis.
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Clinical trial of valproic acid and all-trans retinoic acid in patients with poor-risk acute myeloid leukemia.
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The integrity of the charged pocket in the BTB/POZ domain is essential for the phenotype induced by the leukemia-associated t(11;17) fusion protein PLZF/RARalpha.
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The aorta-gonad-mesonephros-derived stroma cell line DAS104-4 induces differentiation of leukemic cells.
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Valproic acid stimulates proliferation and self-renewal of hematopoietic stem cells.
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In the erythroleukemic cell line HEL Prostate-apoptosis-response-gene-4 (par-4) fails to down-regulate Bcl-2 and to promote apoptosis.
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Prostate apoptosis response gene-4 (par-4) abrogates the survival function of p185(BCR-ABL) in hematopoietic cells.
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Acute promyelocytic leukemia: PML/RARalpha and the leukemic stem cell.
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Brieger, Angela, Boehrer, Simone, Schaaf, Simone, Nowak, Daniel, Ruthardt, Martin ORCID: https://orcid.org/0000-0003-1021-3811, Kim, Soo-Zin, Atadja, Peter, Hoelzer, Dieter, Mitrou, Paris S, Weidmann, Eckhart and Chow, Kai Uwe
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In bcr-abl-positive myeloid cells resistant to conventional chemotherapeutic agents, expression of Par-4 increases sensitivity to imatinib (STI571) and histone deacetylase-inhibitors.
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Gamma-catenin contributes to leukemogenesis induced by AML-associated translocation products by increasing the self-renewal of very primitive progenitor cells.
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Peroxisome proliferator-activated receptor gamma ligands induce growth inhibition and apoptosis of human B lymphocytic leukemia.
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