Methotrexate induces oxidative DNA damage and is selectively lethal to tumour cells with defects in the DNA mismatch repair gene MSH2
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The clinical value of aberrant epigenetic changes of DNA damage repair genes in human cancerStem Cell Hierarchy and Clonal Evolution in Acute Lymphoblastic LeukemiaDNA mismatch repair system: repercussions in cellular homeostasis and relationship with agingGenomic scars as biomarkers of homologous recombination deficiency and drug response in breast and ovarian cancersChemoresistance and targeted therapies in ovarian and endometrial cancersMolecular Aspects of Head and Neck Cancer TherapyDrugging the Cancers Addicted to DNA Repair.DNA polymerases as potential therapeutic targets for cancers deficient in the DNA mismatch repair proteins MSH2 or MLH1Drug-Repositioning Screens Identify Triamterene as a Selective Drug for the Treatment of DNA Mismatch Repair Deficient CellsEvolutionarily conserved genetic interactions with budding and fission yeast MutS identify orthologous relationships in mismatch repair-deficient cancer cells.DNA mismatch repair and oxidative DNA damage: implications for cancer biology and treatment.Retinal mitochondrial DNA mismatch repair in the development of diabetic retinopathy, and its continued progression after termination of hyperglycemia.Fusion of the Dhfr/Mtx and IR/MAR gene amplification methods produces a rapid and efficient method for stable recombinant protein production.Cytosine-based nucleoside analogs are selectively lethal to DNA mismatch repair-deficient tumour cells by enhancing levels of intracellular oxidative stress.A phase II clinical trial of 6-mercaptopurine (6MP) and methotrexate in patients with BRCA defective tumours: a study protocol.Emerging tactical strategies for fighting the war on cancer based on the genetic landscapeAn inducible, isogenic cancer cell line system for targeting the state of mismatch repair deficiency.Drug therapy for hereditary cancersVariegated clonality and rapid emergence of new molecular lesions in xenografts of acute lymphoblastic leukemia are associated with drug resistance.Molecular pathways: microsatellite instability in colorectal cancer: prognostic, predictive, and therapeutic implicationsThe role of folate metabolism in orofacial development and clefting.Ectopic expression of human MutS homologue 2 on renal carcinoma cells is induced by oxidative stress with interleukin-18 promotion via p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK) signaling pathways.Rethinking ovarian cancer: recommendations for improving outcomes.Implementation of a Molecular Tumor Board: The Impact on Treatment Decisions for 35 Patients Evaluated at Dartmouth-Hitchcock Medical Center.Genomic instability in human cancer: Molecular insights and opportunities for therapeutic attack and prevention through diet and nutrition.What is wrong with Fanconi anemia cells?Mismatch repair defects and Lynch syndrome: The role of the basic scientist in the battle against cancerDNA mismatch repair and the DNA damage response.Molecular dissection of microsatellite instable colorectal cancerNew perspectives on molecular targeted therapy in ovarian clear cell carcinoma.Hereditary cancer syndromes: utilizing DNA repair deficiency as therapeutic targetThe role of personalized medicine in metastatic colorectal cancer: an evolving landscape.A Novel Chemotherapeutic Agent to Treat Tumors with DNA Mismatch Repair DeficienciesScreening of Pleural Mesotheliomas for DNA-damage Repair Players by Digital Gene Expression Analysis Can Enhance Clinical Management of Patients Receiving Platin-Based Chemotherapy.Methotrexate induces DNA damage and inhibits homologous recombination repair in choriocarcinoma cells.Recently identified and potential targets for colon cancer treatment.Genomic instability in breast and ovarian cancers: translation into clinical predictive biomarkers.The potential of exploiting DNA-repair defects for optimizing lung cancer treatment.Interrelationship between microsatellite instability and microRNA in gastrointestinal cancer.Mapping genetic alterations causing chemoresistance in cancer: identifying the roads by tracking the drivers.
P2860
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P2860
Methotrexate induces oxidative DNA damage and is selectively lethal to tumour cells with defects in the DNA mismatch repair gene MSH2
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年學術文章
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name
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@ast
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@en
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2.
@nl
type
label
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@ast
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@en
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2.
@nl
prefLabel
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@ast
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@en
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2.
@nl
P2093
P2860
P50
P356
P1476
Methotrexate induces oxidative ...... DNA mismatch repair gene MSH2
@en
P2093
Afshan McCarthy
Sarah A Martin
Suzanne Parry
P2860
P304
P356
10.1002/EMMM.200900040
P577
2009-09-01T00:00:00Z