نتایج جستجو برای: topoisomerase inhibitors

تعداد نتایج: 194843  

Journal: :Molecules 2012
Khac-Minh Thai Quang-Huynh Bui Thanh-Dao Tran Thi-Ngoc-Phuong Huynh

Benzo[c]phenanthridine (BCP) derivatives were identified as topoisomerase I (TOP-I) targeting agents with pronounced antitumor activity. In this study, hologram-QSAR, 2D-QSAR and 3D-QSAR models were developed for BCPs on topoisomerase I inbibitory activity and cytotoxicity against seven tumor cell lines including RPMI8402, CPT-K5, P388, CPT45, KB3-1, KBV-1and KBH5.0. The hologram, 2D, and 3D-QS...

Journal: :Nucleic acids research 2001
C Arnaudeau L Rozier C Cazaux M Defais D Jenssen T Helleday

The RAD51 protein has been shown to participate in homologous recombination by promoting ATP-dependent homologous pairing and strand transfer reactions. In the present study, we have investigated the possible involvement of RAD51 in non-homologous recombination. We demonstrate that overexpression of CgRAD51 enhances the frequency of spontaneous non-homologous recombination in the hprt gene of C...

Journal: :Antimicrobial agents and chemotherapy 1994
C C Dykstra D R McClernon L P Elwell R R Tidwell

Type I and II topoisomerase activities were partially purified from Pneumocystis carinii. The catalytic (strand-passing) activities of both enzymes were selectively inhibited by members of a series of dicationic-substituted bis-benzimidazoles compared with those of topoisomerases of mammalian (calf thymus) origin. The most active inhibitors of the parasite enzymes were also highly effective in ...

Journal: :Cancer research 2006
Lonnie P Swift Ada Rephaeli Abraham Nudelman Don R Phillips Suzanne M Cutts

Doxorubicin (Adriamycin) is one of the most commonly used chemotherapeutic drugs and exhibits a wide spectrum of activity against solid tumors, lymphomas, and leukemias. Doxorubicin is classified as a topoisomerase II poison, although other mechanisms of action have been characterized. Here, we show that doxorubicin-DNA adducts (formed by the coadministration of doxorubicin with non-toxic doses...

2013
Kevin M. Jude Abbey Hartland James M. Berger

Topoisomerases are essential cellular enzymes that maintain the appropriate topological status of DNA and are the targets of several antibiotic and chemotherapeutic agents. High-throughput (HT) analysis is desirable to identify new topoisomerase inhibitors, but standard in vitro assays for DNA topology, such as gel electrophoresis, are time-consuming and are not amenable to HT analysis. We have...

2006
Andrew M. Fry Christine M. Chresta Stella M. Davies M. Claire Walker Adrian L. Harris John A. Hartley John R. W. Masters Ian D. Hickson

Patients with metastatic testis tumors are generally curable using chemotherapy, whereas those with disseminated bladder carcinomas are not. We have compared levels of the nuclear enzyme topoisomerase II in three testis (SuSa, 833K, and GH) and three bladder (RT4, RT112, and HT1376) cancer cell lines which differ in their sensitivity to chemotherapeutic agents. The testis cell lines were more s...

1991
Andrew M. Fry Christine M. Chresta Stella M. Davies M. Claire Walker Adrian L. Harris John A. Hartley John R. W. Masters Ian D. Hickson

Patients with metastatic testis tumors are generally curable using chemotherapy, whereas those with disseminated bladder carcinomas are not. We have compared levels of the nuclear enzyme topoisomerase II in three testis (SuSa, 833K, and GH) and three bladder (RT4, RT112, and HT1376) cancer cell lines which differ in their sensitivity to chemotherapeutic agents. The testis cell lines were more s...

Journal: :Cancer research 1991
A M Fry C M Chresta S M Davies M C Walker A L Harris J A Hartley J R Masters I D Hickson

Patients with metastatic testis tumors are generally curable using chemotherapy, whereas those with disseminated bladder carcinomas are not. We have compared levels of the nuclear enzyme topoisomerase II in three testis (SuSa, 833K, and GH) and three bladder (RT4, RT112, and HT1376) cancer cell lines which differ in their sensitivity to chemotherapeutic agents. The testis cell lines were more s...

Journal: :Cancer research 1989
J M Covey C Jaxel K W Kohn Y Pommier

Camptothecin was recently identified as an inhibitor of mammalian topoisomerase I. Similar to inhibitors of topoisomerase II, camptothecin produces DNA single-strand breaks (SSB) and DNA-protein cross-links (DPC) in mammalian cells. However, their one-to-one association, expected for trapped topoisomerase complexes, has not previously been demonstrated. We have studied camptothecin-induced SSB ...

Journal: :Advances in pharmacology and pharmacy 2022

Lung, prostate, and stomach cancer are the most prevalent cancers among males. Breast, colon, cervical women. The literature also shows that patients suffering from increasing constantly, hence number of different chemotherapy treatments administered is increasing. main objective this review article to summarize effect age on half-life some antineoplastic drugs belonging category Topoisomerase ...

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