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    Effects of cadmium on metallothionein-I and metallothionein-II mRNA expression in rat ventral, lateral, and dorsal prostatic lobes: quantification by competitive RT-PCR

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    Authors
    Lee, Kai-Fai
    Lau, Kin-Mang
    Ho, Shuk-Mei
    UMass Chan Affiliations
    Department of Surgery, Division of Urology
    Graduate School of Biomedical Sciences
    Document Type
    Journal Article
    Publication Date
    1999-01-12
    Keywords
    Animals; Binding, Competitive; Cadmium; Gene Expression; Kidney; Male; Metallothionein; Prostate; RNA, Messenger; Rats; Reverse Transcriptase Polymerase Chain Reaction; Testis
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    http://dx.doi.org/10.1006/taap.1998.8556
    Abstract
    Highly sensitive, sequence-specific competitive reverse transcriptase-polymerase chain reaction (RT-PCR) protocols were established for the detection and quantification of metallothionein (MT)-I and MT-II messages, in absolute values, in rat tissues. Detection limits for these protocols were in the range of 5 to 10 amol per microgram total RNA. Levels of MT-I and MT-II transcripts in the three major prostatic lobes, kidney, and testis were measured in untreated and cadmium (Cd)-treated rats. The dorsal prostate (DP), lateral prostate (LP), kidney, and testis expressed substantial levels of MT-I and MT-II mRNA while the ventral prostate (VP) had extremely low levels of the transcripts. Cd treatment induced higher levels of MT-I and/or MT-II mRNA expression in all tissues studied with the exception of LP. In the LP, Cd treatment caused reductions of MT-I and MT-II mRNA levels. The Cd-induced levels attained in the VP following Cd exposure were still markedly lower than those found in the kidney, testis, LP, and DP of untreated animals. These findings contradict previous claims that the MT genes in rat VP are unresponsive to Cd activation. The susceptibility of VP to Cd toxicity/carcinogenicity may therefore be explained by low levels of Cd-induced expression rather than lack of induction of MTs.
    Source
    Toxicol Appl Pharmacol. 1999 Jan 1;154(1):20-7. Link to article on publisher's site
    DOI
    10.1006/taap.1998.8556
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/34001
    PubMed ID
    9882588
    Related Resources
    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1006/taap.1998.8556
    Scopus Count
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    Morningside Graduate School of Biomedical Sciences Scholarly Publications

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