New Topoisomerase I mutations are associated with resistance to camptothecin
about
Pharmacologic resistance in colorectal cancer: a reviewBinding of an Indenoisoquinoline to the topoisomerase-DNA complex induces reduction of linker mobility and strengthening of protein-DNA interactionDecreased camptothecin sensitivity of the stem-cell-like fraction of Caco2 cells correlates with an altered phosphorylation pattern of topoisomerase IRottlerin potentiates camptothecin-induced cytotoxicity in human hormone refractory prostate cancers through increased formation and stabilization of topoisomerase I-DNA cleavage complexes in a PKCδ-independent pathway.Characterization of DNA topoisomerase-1 in Spodoptera exigua for toxicity evaluation of camptothecin and hydoxy-camptothecin.DNA topoisomerase I domain interactions impact enzyme activity and sensitivity to camptothecin.FL118, a novel camptothecin derivative, is insensitive to ABCG2 expression and shows improved efficacy in comparison with irinotecan in colon and lung cancer models with ABCG2-induced resistance.Novel glass slide preparation system for single DNA molecules analysis.Characterization of DNA topoisomerase I in three SN-38 resistant human colon cancer cell lines reveals a new pair of resistance-associated mutationsMolecular mechanism of the camptothecin resistance of Glu710Gly topoisomerase IB mutant analyzed in vitro and in silico.ABCG2 expression in colorectal adenocarcinomas may predict resistance to irinotecan.Sequence selectivity of the cleavage sites induced by topoisomerase I inhibitors: a molecular dynamics study.Topoisomerase I inhibition in colorectal cancer: biomarkers and therapeutic targets.Prediction of novel target genes and pathways involved in irinotecan-resistant colorectal cancer.Topoisomerases: Resistance versus Sensitivity, How Far We Can Go?Resveratrol metabolites inhibit human metastatic colon cancer cells progression and synergize with chemotherapeutic drugs to induce cell death.An overview of quinoline as a privileged scaffold in cancer drug discovery.Distribution bias and biochemical characterization of TOP1MT single nucleotide variants.Camptothecin (CPT) and its derivatives are known to target topoisomerase I (Top1) as their mechanism of action: did we miss something in CPT analogue molecular targets for treating human disease such as cancer?SN38-PEG-PLGA-verapamil nanoparticles inhibit proliferation and downregulate drug transporter ABCG2 gene expression in colorectal cancer cells.Camptothecin exhibits topoisomerase1-independent KMT1A suppression and myogenic differentiation in alveolar rhabdomyosarcoma cells.Liposomal codelivery of an SN38 prodrug and a survivin siRNA for tumor therapyRational development of synergistic combinations of chemotherapy and molecular targeted agents for colorectal cancer treatment
P2860
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P2860
New Topoisomerase I mutations are associated with resistance to camptothecin
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
New Topoisomerase I mutations are associated with resistance to camptothecin
@en
New Topoisomerase I mutations are associated with resistance to camptothecin.
@nl
type
label
New Topoisomerase I mutations are associated with resistance to camptothecin
@en
New Topoisomerase I mutations are associated with resistance to camptothecin.
@nl
prefLabel
New Topoisomerase I mutations are associated with resistance to camptothecin
@en
New Topoisomerase I mutations are associated with resistance to camptothecin.
@nl
P2093
P2860
P50
P356
P1433
P1476
New Topoisomerase I mutations are associated with resistance to camptothecin
@en
P2093
Annick Causse
Arnaud Coquelle
Céline Auzanneau
Céline Gongora
Maguy Del Rio
Nadia Vezzio-Vie
Philippe Pourquier
Sandie Tuduri
Vincent Denis
P2860
P2888
P356
10.1186/1476-4598-10-64
P577
2011-05-27T00:00:00Z
P5875
P6179
1031317520