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      No Alteration in DNA Topoisomerase I Gene Related to CPT‐11 Resistance in Human Lung Cancer

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          Abstract

          Mutations and reduced expression of DNA topoisomerase I (topo I) gene have been shown to be important in the acquisition of resistance to camptothecin and its analogues in vitro, but their significance has not been verified in vivo. We investigated possible topo I gene mutations and topo I mRNA expression levels in 127 samples obtained from 56 patients with lung tumors, including patients who had developed clinical resistance to topo I inhibitors. No mutations were detected in any of the samples examined and expression levels did not differ significantly between clinically resistant cases and others. However, the topo I mRNA expression level was significantly higher in small cell lung carcinomas than in non‐small cell lung carcinomas (P<0.05). These results suggest that topo I mRNA levels may affect CPT‐11 sensitivity in human lung cancer. However, topo I gene mutations and reduced topo I mRNA expression may not be the main mechanism of clinically acquired resistance to camptothecin analogues in vivo.

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          Most cited references21

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          Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

          A new method of total RNA isolation by a single extraction with an acid guanidinium thiocyanate-phenol-chloroform mixture is described. The method provides a pure preparation of undegraded RNA in high yield and can be completed within 4 h. It is particularly useful for processing large numbers of samples and for isolation of RNA from minute quantities of cells or tissue samples.
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            A general method for isolation of high molecular weight DNA from eukaryotes.

            A new method for isolation of high molecular weight DNA from eukaryotes is presented. This procedure allows preparation of DNA from a variety of tissues such as calf thymus or human placenta and from cells which were more difficult to lyse until now (e.g. Crypthecodinium cuhnii, a dinoflagellate). The DNA obtained in such a way has an average molecular weight of about 200 X 10(6) d and contains very few, if any, single strand breaks.
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              DNA topoisomerase I--targeted chemotherapy of human colon cancer in xenografts.

              Drug development is needed to improve chemotherapy of patients with locally advanced or metastatic colon carcinoma, who otherwise have an unfavorable prognosis. DNA topoisomerase I, a nuclear enzyme important for solving topological problems arising during DNA replication and for other cellular functions, has been identified as a principal target of a plant alkaloid 20(S)-camptothecin. Significantly increased concentrations of this enzyme, compared to that in normal colonic mucosa, were found in advanced stages of human colon adenocarcinoma and in xenografts of colon cancer carried by immunodeficient mice. Several synthetic analogs of camptothecin, selected by tests with the purified enzyme and tissue-culture screens, were evaluated in the xenograft model. Unlike other anticancer drugs tested, 20(RS)-9-amino-camptothecin (9-AC) induced disease-free remissions. The overall drug toxicity was low and allowed for repeated courses of treatment.
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                Author and article information

                Journal
                Jpn J Cancer Res
                Jpn. J. Cancer Res
                10.1111/(ISSN)1349-7006a
                CAS
                Japanese Journal of Cancer Research : Gann
                Blackwell Publishing Ltd (Oxford, UK )
                0910-5050
                1876-4673
                December 1996
                : 87
                : 12 ( doiID: 10.1111/cas.1996.87.issue-12 )
                : 1280-1287
                Affiliations
                [ 1 ]Second Department of Internal Medicine, Hiroshima University, 1‐2‐3 Kasumi, Minami‐ku, Hiroshima 734
                [ 2 ]Department of Integrated Medicine, Hiroshima University School of Medicine, Hiroshima University, 1‐2‐3 Kasumi, Minami‐ku, Hiroshima 734
                [ 3 ]Department of Environment and Mutation Research Institute for Radiation Biology and Medicine, Hiroshima University, 1‐2‐3 Kasumi, Minami‐ku, Hiroshima 734
                Author notes
                [*] [* ]To whom correspondence should be addressed
                Article
                CAE1280
                10.1111/j.1349-7006.1996.tb03144.x
                5921020
                9045964
                3c6b5328-11bc-456c-bf57-50ddb1c32d63
                History
                Page count
                References: 22, Pages: 8
                Categories
                Article
                Custom metadata
                2.0
                December 1996
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.6.9 mode:remove_FC converted:04.11.2015

                topoisomerase i,point mutation,mrna expression,cpt‐11,lung cancer

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