Literature DB >> 427767

Production of sister chromatid exchanges by various cancer chemotherapeutic agents.

A Banerjee, W F Benedict.   

Abstract

Various cancer chemotherapeutic agents have been examined for their ability to produce increases in sister chromatid exchanges. Those agents which had been shown previously to produce oncogenic transformation as well as chromosomal breaks also showed significant increases in sister chromatid exchanges. Those drugs which had not been shown to be oncogenic or clastogenic in cell culture produced no increases in sister chromatid exchanges. In general, concentrations which yielded increases in sister chromatid exchanges were considerably lower than those which had been shown previously to produce oncogenic transformation and chromosomal breakage. This was particularly true for the alkylating agents. Thus, we concur that examining increases in the production of sister chromatid exchanges may be an additional sensitive method for detecting potential mutagenic and/or oncogenic agents in our environment.

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Year:  1979        PMID: 427767

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  9 in total

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3.  Introduction and expression of the bacterial PaeR7 methylase gene in mammalian cells.

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4.  Sister chromatid exchange in lymphocytes from patients with acute lymphoblastic leukemia.

Authors:  M Otter; C G Palmer; R L Baehner
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

Review 5.  Sister chromatid exchange (SCE) and structural chromosome aberration in mutagenicity testing.

Authors:  E Gebhart
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Bleomycin-induced chromosomal aberrations and sister chromatid exchanges in Down lymphocyte cultures.

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Review 8.  Stress, ageing and their influence on functional, cellular and molecular aspects of the immune system.

Authors:  Ana Vitlic; Janet M Lord; Anna C Phillips
Journal:  Age (Dordr)       Date:  2014-02-25

9.  Evidence for somatic gene conversion and deletion in bipolar disorder, Crohn's disease, coronary artery disease, hypertension, rheumatoid arthritis, type-1 diabetes, and type-2 diabetes.

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Journal:  BMC Med       Date:  2011-02-03       Impact factor: 8.775

  9 in total

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