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1. Full Text Regulatory effect of resveratrol and prednisolone on MDR1 gene expression in acute lymphoblastic leukemia cell line (CCRF‐CEM): An epigenetic perspective
by Zadi Heydarabad, Milad and Nikasa, Mina and Vatanmakanian, Mousa and Azimi, Ako and Farshdousti Hagh, Majid
Journal of Cellular Biochemistry, ISSN 0730-2312, 06/2018, Volume 119, Issue 6, pp. 4890 - 4896
Chemotherapy is the most common method to treat leukemia as well as other types of human cancers. However, drug resistance has remained as the main challenge... 
prednisolone | MDR1 gene | DNA methylations | acute lymphoblastic leukemia | resveratrol | ACTIVATION | PROTEIN | GLUCOCORTICOIDS | INDEPENDENT APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PREVENTION | PROLIFERATION | MECHANISMS | CANCER | CELL BIOLOGY | RESISTANCE | PROMOTER | Drug resistance in microorganisms | Epigenetic inheritance | Corticosteroids | Genes | Gene expression | Resveratrol | Genetic research | Genetic aspects | Acute lymphocytic leukemia | Methylation | Prednisolone | Cancer | Steroids | Acute lymphatic leukemia | Leukemia | Gene regulation | Multidrug resistance | Lymphatic leukemia | Drug resistance | MDR1 protein | Chemotherapy | Cell death | Regulatory mechanisms (biology) | DNA methylation | P-Glycoprotein | Deoxyribonucleic acid--DNA | Apoptosis
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2. Full Text Interaction between Gallic acid and Asparaginase to potentiate anti-proliferative effect on lymphoblastic leukemia cell line
by Sourani, Zahra and Shirzad, Hedayatollah and Shirzad, Moein and Pourgheysari, Batoul
Biomedicine & Pharmacotherapy, ISSN 0753-3322, 12/2017, Volume 96, pp. 1045 - 1054
Treatment of acute lymphoblastic leukemia (ALL) fails in some cases and the side effects cause mortality in certain patients. Gallic acid (GA), a... 
Asparaginase (ASP) | Gallic acid (GA) | Fas expression | Acute lymphoblastic leukemia | Apoptosis | MEDICINE, RESEARCH & EXPERIMENTAL | INVASION | THERAPY | DIETARY PHENOLICS | PHARMACOLOGY & PHARMACY | PROLIFERATION | CHILDREN | Phenols | Chemotherapy | Drug therapy, Combination | Lymphocytic leukemia | Asparaginase | Cancer
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3. Full Text AKT inhibitor, GSK690693, induces growth inhibition and apoptosis in acute lymphoblastic leukemia cell lines
by Levy, Dana S and Kahana, Jason A and Kumar, Rakesh
Blood, ISSN 0006-4971, 02/2009, Volume 113, Issue 8, pp. 1723 - 1729
The PI3K/AKT signaling is activated in various hematologic malignancies. We evaluated the effect of a novel, pan-AKT kinase inhibitor, GSK690693, on the... 
SURVIVAL | TRANSFORMATION | ACTIVATION | PROTEIN | PATHWAY | PHOSPHORYLATION | ACUTE MYELOID-LEUKEMIA | MUTATIONS | ANTITUMOR-ACTIVITY | HEMATOLOGY | CANCER | Cell Survival - drug effects | B-Lymphocytes - cytology | Apoptosis - drug effects | CD4-Positive T-Lymphocytes - cytology | Humans | Mice, Inbred C57BL | Leukemia, B-Cell - pathology | Drug Resistance, Neoplasm | Cell Division - drug effects | B-Lymphocytes - drug effects | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Lymphoma - drug therapy | Animals | Signal Transduction - drug effects | Oxadiazoles - pharmacology | Cell Line, Tumor | Female | Leukemia, B-Cell - drug therapy | Lymphoma - pathology | Mice | Phosphorylation - drug effects | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | CD4-Positive T-Lymphocytes - drug effects | Proto-Oncogene Proteins c-akt - antagonists & inhibitors
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4. Full Text Hypoxia promotes chemoresistance in acute lymphoblastic leukemia cell lines by modulating death signaling pathways
by Petit, C and Gouel, F and Dubus, I and Heuclin, C and Roget, K and Vannier, J.P
BMC Cancer, ISSN 1471-2407, 09/2016, Volume 16, Issue 1, p. 746
Background: Several studies show that bone marrow (BM) microenvironment and hypoxia condition can promote the survival of leukemic cells and induce resistance... 
ALL | Hypoxia | RPPA | Methotrexate | Prednisolone | Chemoresistance | SURVIVAL | APOPTOSIS | PROTEIN | PREDNISOLONE RESISTANCE | DRUG-RESISTANCE | REVERSAL | IN-VITRO | ONCOLOGY | MULTIDRUG-RESISTANCE | EXPRESSION | ASSOCIATION | Precursor Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Cell Hypoxia - physiology | Cell Survival | Humans | Cell Line, Tumor | Signal Transduction - physiology | Apoptosis - physiology | Drug Resistance, Neoplasm - physiology | Complications and side effects | Prognosis | Genetic aspects | Research | Acute lymphocytic leukemia | Drug therapy | Drug resistance | Risk factors | Life Sciences | Human health and pathology | Pharmacology | Hematology | Pharmaceutical sciences | Cancer
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5. Full Text Vincristine induces procoagulant activity of the human lymphoblastic leukemia cell line Jurkat through the release of extracellular vesicles
by Pluchart, C and Poitevin, G and Colinart-Thomas, M and Guimard, G and Audonnet, S and Terryn, C and Nguyen, P
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, ISSN 0929-5305, 08/2019, Volume 48, Issue 2, pp. 195 - 202
Thromboembolic events are frequent and serious complications of acute lymphoblastic leukaemia treatment. The importance of chemotherapy in the pathogenesis of... 
CARDIAC & CARDIOVASCULAR SYSTEMS | Thrombin generation assay | DOXORUBICIN | Extracellular vesicles | Vincristine | Microparticles | CHILDREN | THROMBIN GENERATION | Acute lymphoblastic leukemia | SURFACE | PERIPHERAL VASCULAR DISEASE | THROMBOEMBOLISM | HEMATOLOGY | Phosphatidylserine | TISSUE FACTOR | Chemotherapy | Anthracyclines | Lymphocytic leukemia | Thrombin | Phospholipids | Thromboembolism | Fluorescence microscopy | Cancer | Flow cytometry | Acute lymphatic leukemia | Leukemia | Tissue factor | Lymphatic leukemia | Thrombosis | Cell surface | Vesicles | Daunorubicin | Annexin V
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6. Full Text Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes
by Tomoyasu, Chihiro and Imamura, Toshihiko and Tomii, Toshihiro and Yano, Mio and Asai, Daisuke and Goto, Hiroaki and Shimada, Akira and Sanada, Masashi and Iwamoto, Shotaro and Takita, Junko and Minegishi, Masayoshi and Inukai, Takeshi and Sugita, Kanji and Hosoi, Hajime
International Journal of Hematology, ISSN 0925-5710, 09/2018, Volume 108, Issue 3, pp. 312 - 318
In this study, we performed genetic analysis of 83 B cell precursor acute lymphoblastic leukemia (B-ALL) cell lines. First, we performed multiplex... 
CDKN2B | BTG1 | IKZF1 | Copy number abnormality | CDKN2A | Acute lymphoblastic leukemia cell line | XENOGRAFT MODELS | PRECURSOR | KINASE | RISK | CHILDRENS ONCOLOGY GROUP | MUTATIONS | FUSIONS | INHIBITOR | HEMATOLOGY | EXPRESSION | Gene Dosage - genetics | Histone-Lysine N-Methyltransferase - genetics | Proto-Oncogene Proteins p21(ras) - genetics | Humans | Janus Kinase 2 - genetics | PAX5 Transcription Factor - genetics | DNA Copy Number Variations - genetics | Ikaros Transcription Factor - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Cyclin-Dependent Kinase Inhibitor p18 - genetics | Cyclin-Dependent Kinase Inhibitor p15 - genetics | Myeloid-Lymphoid Leukemia Protein - genetics | Gene Deletion | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - classification | Cell Line, Tumor | Gene Rearrangement - genetics | Mutation | Neoplasm Proteins - genetics | Genetic research | Medical colleges | Genetic aspects | Acute lymphocytic leukemia | Analysis | Biotechnology | Immunoglobulins | Acute lymphatic leukemia | Copy number | Leukemia | Abnormalities | Tumor cell lines | Lymphatic leukemia | Pax5 protein | Clonal deletion | Lymphocytes B | Janus kinase 2 | Genetic analysis | Heavy chains | Cell lines | Deletion
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7. Full Text A novel method to establish glucocorticoid resistant acute lymphoblastic leukemia cell lines
by Gu, Ling and Zhang, Ge and Zhang, Yanle
Journal of Experimental and Clinical Cancer Research, ISSN 1756-9966, 06/2019, Volume 38, Issue 1, pp. 269 - 12
BackgroundDrug-resistant cell lines, established from drug-sensitive cell lines by drug exposure in vitro, are the most useful cancer models in studies on the... 
Hypoxia | Cell line | Glucocorticoid resistance | Method | Acute lymphoblastic leukemia | IN-VITRO | METABOLISM | ONCOLOGY | BONE-MARROW | AMPK | STRESS | Parenting | Usage | Corticosteroids | Analysis | Acute lymphocytic leukemia | Drug resistance | Methods
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8. Full Text Establishment and characterization of a novel childhood acute lymphoblastic leukemia cell line, HXEX-ALL1, with chromosome 9p and 17p deletions
by Zhu, YP and Yang, R and Gao, J and Zhang, YL and Zhang, G and Gu, L
CANCER CELL INTERNATIONAL, ISSN 1475-2867, 04/2019, Volume 19, Issue 1, p. 113
BackgroundAlthough contemporary chemotherapy has improved the cure rate of childhood acute lymphoblastic leukemia (ALL) to nearly 90%, relapsed/refractory ALL... 
Chromosome 9p deletion | SURVIVAL | Leukemia cell line | Chromosome 17p deletion | ABNORMALITIES | MONOSOMAL KARYOTYPE | CLASSIFICATION | CYTOGENETICS | CHILDREN | RELAPSE | Acute lymphoblastic leukemia | ONCOLOGY | HIGH-RISK | Complex karyotype | PROGNOSTIC-SIGNIFICANCE | Cell culture | Flow cytometry | Pediatrics | Trisomy | Leukemia | Xenotransplantation | Single-nucleotide polymorphism | Culture techniques | Blood | Xenografts | Children | Chromosomes | Medical research | Phenotypes | Acute lymphatic leukemia | Multidrug resistance | Cyclin-dependent kinases | Tumorigenicity | Lymphatic leukemia | Patients | Polymerase chain reaction | Refractory materials | Chemotherapy | Lymphocytes B | Chromosome 9 | Medical prognosis | Cell lines | Cytogenetics | Mice | Lymphomas | Asparaginase | Cancer | Tumors
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9. Full Text Evaluation of the miRNA profiling and effectiveness of the propolis on B-cell acute lymphoblastic leukemia cell line
by Yilmaz, Ugur Cem and Bagca, Bakiye Goker and Karaca, Emin and Durmaz, Asude and Durmaz, Burak and Aykut, Ayca and Kayalar, Husniye and Avci, Cigir Biray and Susluer, Sunde Yilmaz and Gunduz, Cumhur and Cogulu, Ozgur
Biomedicine & Pharmacotherapy, ISSN 0753-3322, 2016, Volume 84, pp. 1266 - 1273
Highlights • Aydın propolis regulates expression levels of both oncogenic and tumor suppressor miRNAs. • Aydın propolis induces apoptotic cell death in ALL... 
Internal Medicine | Medical Education | miRNA | Acute lymphoblastic leukemia | Propolis | Apoptosis | MEDICINE, RESEARCH & EXPERIMENTAL | ACID PHENETHYL ESTER | MICRORNAS | POLYPHENOLIC COMPOUNDS | BETA | GROWTH | PHARMACOLOGY & PHARMACY | EXPRESSION | EXTRACT | Apoptosis - drug effects | Humans | Carcinogenesis - genetics | Gene Expression Regulation, Leukemic - drug effects | MicroRNAs - metabolism | Gene Expression Profiling | Carcinogenesis - pathology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Leukemia, B-Cell - genetics | Cell Line, Tumor | Inhibitory Concentration 50 | Propolis - pharmacology | MicroRNAs - genetics | Epigenetic inheritance | MicroRNA | Cell death | Analysis | Medical genetics | Honeybee | Chemotherapy | Lymphocytic leukemia | Cancer
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10. Full Text C22:0- and C24:0-dihydroceramides Confer Mixed Cytotoxicity in T-Cell Acute Lymphoblastic Leukemia Cell Lines
by Holliday Jr, Michael W and Cox, Stephen B and Kang, Min H and Maurer, Barry J
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, p. e74768
We previously reported that fenretinide (4-HPR) was cytotoxic to acute lymphoblastic leukemia (ALL) cell lines in vitro in association with increased levels of... 
DIHYDROCERAMIDE DESATURASE | CANCER-CELLS | C2-CERAMIDE | MAMMALIAN CERAMIDE SYNTHASES | METABOLISM | MULTIDISCIPLINARY SCIENCES | INVOLVEMENT | N-(4-HYDROXYPHENYL)RETINAMIDE-INDUCED APOPTOSIS | SPHINGOSINE | SPHINGOLIPIDS | FENRETINIDE | Sphingolipids - chemistry | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Fatty Acids - chemistry | Reactive Oxygen Species | Humans | Ceramides - chemistry | Mitochondria - metabolism | Antineoplastic Agents - chemistry | Autophagy | Sphingosine - analogs & derivatives | DNA Fragmentation | Cell Line, Tumor | Culture Media - chemistry | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Sphingosine - chemistry | Ceramides | Acute lymphocytic leukemia | Plant lipids | T cells | Cell death | Fatty acids | Health sciences | Biotechnology | Reactive oxygen species | Toxicity | Leukemia | Cytotoxicity | Lipids | Biochemistry | Lymphocytes T | Desaturase | Fragmentation | Synthesis | Sphinganine | DNA fragmentation | Supplementation | Drug dosages | Deoxyribonucleic acid--DNA | Enzymes | Acute lymphatic leukemia | Ethanol | Caspase | Tumor cell lines | Lymphatic leukemia | Gene expression | Medicine | Testing laboratories | Cell lines | Phagocytosis | Cancer | Apoptosis | Deoxyribonucleic acid | DNA
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11. Full Text Mechanism of Synergy of N-(4-Hydroxyphenyl)Retinamide and ABT-737 in Acute Lymphoblastic Leukemia Cell Lines: Mcl-1 Inactivation
by Kang, Min H and Wan, Zesheng and Kang, Yun Hee and Sposto, Richard and Reynolds, C. Patrick
Journal of the National Cancer Institute, ISSN 0027-8874, 4/2008, Volume 100, Issue 8, pp. 580 - 595
Background ABT-737 is a pan-Bcl-2 inhibitor that has a wide range of single-agent activity against acute lymphoblastic leukemia (ALL) cell lines and... 
BREAST-CANCER | BCL-X-L | LUNG-CANCER | RETINOIC ACID | ONCOLOGY | PHASE-I TRIAL | INDUCED APOPTOSIS | CYTOTOXICITY ASSAY | ACUTE MYELOID-LEUKEMIA | FAMILY PROTEINS | BH3 MIMETIC ABT-737 | Gene Expression Regulation, Enzymologic - drug effects | Phosphorylation | Reactive Oxygen Species - metabolism | Humans | Immunoblotting | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Precursor Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Caspases - metabolism | Biphenyl Compounds - pharmacology | Nitrophenols - pharmacology | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | JNK Mitogen-Activated Protein Kinases - genetics | Mitochondrial Membranes | Cytochromes c - metabolism | Gene Silencing | Fenretinide - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Sulfonamides - pharmacology | Piperazines - pharmacology | Drug Synergism | Proto-Oncogene Proteins c-bcl-2 - drug effects | Cell Line, Tumor | Enzyme Activation | Apoptosis | Antimitotic agents | Dosage and administration | Acute lymphocytic leukemia | Drug therapy | Antineoplastic agents | Proteins | Medical research | Toxicity | Leukemia | Cells | Index Medicus
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12. Full Text Pterostilbene increases Fas expression in T-lymphoblastic leukemia cell lines
by Ramezani, Gelareh and Pourgheysari, Batoul and Shirzad, Hedayatollah and Sourani, Zahra
Research in pharmaceutical sciences, ISSN 1735-5362, 02/2019, Volume 14, Issue 1, pp. 55 - 63
Treatment of acute lymphoblastic leukemia (ALL) has been promising in last decades, but side effects still persist and searching for the least toxic agents... 
Care and treatment | Lymphocytic leukemia | RNA | Tumor necrosis factor | Cancer | Apoptosis | Flowcytometry | Fas | Acute lymphoblastic leukemia | Original | RT-PCR | Pterostilbene
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13. Full Text Targeting FoxM1 transcription factor in T-cell acute lymphoblastic leukemia cell line
by Tüfekçi, Özlem and Yandım, Melis Kartal and Ören, Hale and İrken, Gülersu and Baran, Yusuf
Leukemia Research, ISSN 0145-2126, 2014, Volume 39, Issue 3, pp. 342 - 347
Highlights • FoxM1 mRNA is highly expressed in T-cell acute lymphoblastic leukemia cell line (Jurkat cells). • Targeting FoxM1 by siomycin A and dexamethasone... 
Hematology, Oncology and Palliative Medicine | Jurkat cells | Dexamethasone | FoxM1 | Siomycin A | T-cell acute lymphoblastic leukemia | FORKHEAD BOX M1B | OXIDATIVE STRESS | PHOSPHORYLATION | FACTOR TRIDENT | PROLIFERATION | CANCER | ONCOLOGY | HEMATOLOGY | PROGRESSION | PROGRAM | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - pathology | Antineoplastic Agents, Hormonal - pharmacology | Apoptosis - drug effects | Humans | RNA, Messenger - genetics | Antineoplastic Combined Chemotherapy Protocols | Forkhead Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Peptides - pharmacology | Dexamethasone - pharmacology | Forkhead Transcription Factors - metabolism | Cell Proliferation - drug effects | Forkhead Transcription Factors - antagonists & inhibitors | Gene Expression Regulation, Neoplastic - drug effects | Tumor Cells, Cultured | Cell Cycle - drug effects | Forkhead Box Protein M1 | Real-Time Polymerase Chain Reaction | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Acute lymphocytic leukemia | RNA | T cells
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14. Full Text Effect of Anacardium occidentale leaf extract on human acute lymphoblastic leukaemia cell lines
by Santos, Janaína M and Cury, Nathalia M and Yunes, José A and López, Jorge A and Hernández-Macedo, Maria L
Natural Product Research, ISSN 1478-6419, 06/2019, Volume 33, Issue 11, pp. 1633 - 1636
Anacardium occidentale leaves are used in folk medicine due its therapeutic properties attributed to phenolic compounds. Therefore, this study was undertaken... 
polyphenols | apoptosis | Cashew | leukaemia cells | CHEMISTRY, MEDICINAL | CHEMISTRY, APPLIED | Leaves | Acute lymphatic leukemia | Toxicity | Leukemia | Cell lines | Cell cycle | Phenols | Cytotoxicity | Drug development | Phenolic compounds | Apoptosis | Plant extracts
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