Adenocarcinoma of the Kidney. II. Enzyme Histochemistry of Renal Adenocarcinomas Induced in Rats by N-(4′-Fluoro-4-biphenylyl)acetamide

Activities of a broad spectrum of enzymes were studied histochemically in renal adenocarcinomas induced in young male F344 rats by chronic dietary administration of the carcinogen N-(4′-fluoro-4-biphenylyl)acetamide. Enzymes included were: dehydrogenases of glucose-6-phosphate, lactate, succinate, m...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:JNCI : Journal of the National Cancer Institute 1976-10, Vol.57 (4), p.795-808
Hauptverfasser: Heatfield, Barry M., Hinton, David E., Trump, Benjamin F.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 808
container_issue 4
container_start_page 795
container_title JNCI : Journal of the National Cancer Institute
container_volume 57
creator Heatfield, Barry M.
Hinton, David E.
Trump, Benjamin F.
description Activities of a broad spectrum of enzymes were studied histochemically in renal adenocarcinomas induced in young male F344 rats by chronic dietary administration of the carcinogen N-(4′-fluoro-4-biphenylyl)acetamide. Enzymes included were: dehydrogenases of glucose-6-phosphate, lactate, succinate, malate, and a-glycerophosphate; peroxidase (catalase); glucose-6-phosphatase; alkaline and acid phosphatase; Mg2+ ATPase; 5′-nucleotidase; and aminopeptidase. Levels of enzyme activity were estimated visually and scored from 0 (not detectable) to a maximum of 5 (intense). Comparison of estimated activity for each enzyme was made between small neoplastic nodules (stage III tumors) and large adenocarcinomas (stage IV tumors) and between tumors and portions of normal proximal tubules in parenchyma of kidneys from untreated control rats. The results, which revealed nearly identical levels of activity for most enzymes In both stages III and IV tumors, suggested similar metabolic and biologic behavior of these lesions. However, when data for tumors were compared with data for normal proximal tubules, striking differences were observed consistent with: 1) a marked shift of energy metabolism from oxidative to glycolytic production of ATP, with a corresponding reduction in mitochondrial respiration; and 2) simplification of plasma membrane specializations that were possibly associated with a reduction or loss of transport function. These findings were compared with other histochemical, biochemical, and ultrastructural studies of renal adenocarcinomas in rats and man.
doi_str_mv 10.1093/jnci/57.4.795
format Article
fullrecord <record><control><sourceid>istex_pubme</sourceid><recordid>TN_cdi_pubmed_primary_187777</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_HXZ_D2NVMP9B_V</sourcerecordid><originalsourceid>FETCH-LOGICAL-i158t-914cef1939f0242d236a7f33cf27fc6e926dcbd738aa6e99f7ca679cc59944c03</originalsourceid><addsrcrecordid>eNpVkL9OwzAYxC3Ev1IY2Rg8wuDUsZ04HktpaUQpqIIKsUSu7aguiVMlqUSYWHkdHoknIagIiVtOp9-nk-4D4NTHno8F7a2csr2Ae8zjItgBHZ-FGBEfB7uggzHhKIo4OwRHVbXCrQRhB2Dfj3irDvjoa-MKJUtlXZFLWKSwXhp4Y7UzjQfj2IND99bkBo5tVRdqafLWy-bncGaczOD_ggrGTm-U0dA6OJN1BRcNnKJz9vX-iUbZpigLxNDCrpfGNVmTXUhlaplbbY7BXiqzypz8ehc8joYPgzGa3F3Hg_4EWT-IaiR8pkzqCypSTBjRhIaSp5SqlPBUhUaQUKuF5jSSsk0i5UqGXCgVCMGYwrQLzra9680iNzpZlzaXZZNsP9JitMXtTPP6R2X5koSc8iAZPz0nV2Q6v70Xl8mcfgPaXXQn</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Adenocarcinoma of the Kidney. II. Enzyme Histochemistry of Renal Adenocarcinomas Induced in Rats by N-(4′-Fluoro-4-biphenylyl)acetamide</title><source>MEDLINE</source><source>Oxford University Press Journals Digital Archive Legacy</source><creator>Heatfield, Barry M. ; Hinton, David E. ; Trump, Benjamin F.</creator><creatorcontrib>Heatfield, Barry M. ; Hinton, David E. ; Trump, Benjamin F.</creatorcontrib><description>Activities of a broad spectrum of enzymes were studied histochemically in renal adenocarcinomas induced in young male F344 rats by chronic dietary administration of the carcinogen N-(4′-fluoro-4-biphenylyl)acetamide. Enzymes included were: dehydrogenases of glucose-6-phosphate, lactate, succinate, malate, and a-glycerophosphate; peroxidase (catalase); glucose-6-phosphatase; alkaline and acid phosphatase; Mg2+ ATPase; 5′-nucleotidase; and aminopeptidase. Levels of enzyme activity were estimated visually and scored from 0 (not detectable) to a maximum of 5 (intense). Comparison of estimated activity for each enzyme was made between small neoplastic nodules (stage III tumors) and large adenocarcinomas (stage IV tumors) and between tumors and portions of normal proximal tubules in parenchyma of kidneys from untreated control rats. The results, which revealed nearly identical levels of activity for most enzymes In both stages III and IV tumors, suggested similar metabolic and biologic behavior of these lesions. However, when data for tumors were compared with data for normal proximal tubules, striking differences were observed consistent with: 1) a marked shift of energy metabolism from oxidative to glycolytic production of ATP, with a corresponding reduction in mitochondrial respiration; and 2) simplification of plasma membrane specializations that were possibly associated with a reduction or loss of transport function. These findings were compared with other histochemical, biochemical, and ultrastructural studies of renal adenocarcinomas in rats and man.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/57.4.795</identifier><identifier>PMID: 187777</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adenocarcinoma - chemically induced ; Adenocarcinoma - enzymology ; Adenocarcinoma - ultrastructure ; Adenosine Triphosphatases - metabolism ; Alcohol Oxidoreductases - metabolism ; Aminobiphenyl Compounds ; Aminopeptidases - metabolism ; Animals ; Carcinoma - ultrastructure ; Glycolysis ; Kidney Neoplasms - chemically induced ; Kidney Neoplasms - enzymology ; Kidney Neoplasms - ultrastructure ; Male ; Neoplasms, Experimental - chemically induced ; Neoplasms, Experimental - enzymology ; Nucleotidases - metabolism ; Oxidative Phosphorylation ; Oxidoreductases - metabolism ; Phosphoric Monoester Hydrolases - metabolism ; Rats ; Rats, Inbred F344</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1976-10, Vol.57 (4), p.795-808</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/187777$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heatfield, Barry M.</creatorcontrib><creatorcontrib>Hinton, David E.</creatorcontrib><creatorcontrib>Trump, Benjamin F.</creatorcontrib><title>Adenocarcinoma of the Kidney. II. Enzyme Histochemistry of Renal Adenocarcinomas Induced in Rats by N-(4′-Fluoro-4-biphenylyl)acetamide</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>Journal of the National Cancer Institute</addtitle><description>Activities of a broad spectrum of enzymes were studied histochemically in renal adenocarcinomas induced in young male F344 rats by chronic dietary administration of the carcinogen N-(4′-fluoro-4-biphenylyl)acetamide. Enzymes included were: dehydrogenases of glucose-6-phosphate, lactate, succinate, malate, and a-glycerophosphate; peroxidase (catalase); glucose-6-phosphatase; alkaline and acid phosphatase; Mg2+ ATPase; 5′-nucleotidase; and aminopeptidase. Levels of enzyme activity were estimated visually and scored from 0 (not detectable) to a maximum of 5 (intense). Comparison of estimated activity for each enzyme was made between small neoplastic nodules (stage III tumors) and large adenocarcinomas (stage IV tumors) and between tumors and portions of normal proximal tubules in parenchyma of kidneys from untreated control rats. The results, which revealed nearly identical levels of activity for most enzymes In both stages III and IV tumors, suggested similar metabolic and biologic behavior of these lesions. However, when data for tumors were compared with data for normal proximal tubules, striking differences were observed consistent with: 1) a marked shift of energy metabolism from oxidative to glycolytic production of ATP, with a corresponding reduction in mitochondrial respiration; and 2) simplification of plasma membrane specializations that were possibly associated with a reduction or loss of transport function. These findings were compared with other histochemical, biochemical, and ultrastructural studies of renal adenocarcinomas in rats and man.</description><subject>Adenocarcinoma - chemically induced</subject><subject>Adenocarcinoma - enzymology</subject><subject>Adenocarcinoma - ultrastructure</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Alcohol Oxidoreductases - metabolism</subject><subject>Aminobiphenyl Compounds</subject><subject>Aminopeptidases - metabolism</subject><subject>Animals</subject><subject>Carcinoma - ultrastructure</subject><subject>Glycolysis</subject><subject>Kidney Neoplasms - chemically induced</subject><subject>Kidney Neoplasms - enzymology</subject><subject>Kidney Neoplasms - ultrastructure</subject><subject>Male</subject><subject>Neoplasms, Experimental - chemically induced</subject><subject>Neoplasms, Experimental - enzymology</subject><subject>Nucleotidases - metabolism</subject><subject>Oxidative Phosphorylation</subject><subject>Oxidoreductases - metabolism</subject><subject>Phosphoric Monoester Hydrolases - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1976</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkL9OwzAYxC3Ev1IY2Rg8wuDUsZ04HktpaUQpqIIKsUSu7aguiVMlqUSYWHkdHoknIagIiVtOp9-nk-4D4NTHno8F7a2csr2Ae8zjItgBHZ-FGBEfB7uggzHhKIo4OwRHVbXCrQRhB2Dfj3irDvjoa-MKJUtlXZFLWKSwXhp4Y7UzjQfj2IND99bkBo5tVRdqafLWy-bncGaczOD_ggrGTm-U0dA6OJN1BRcNnKJz9vX-iUbZpigLxNDCrpfGNVmTXUhlaplbbY7BXiqzypz8ehc8joYPgzGa3F3Hg_4EWT-IaiR8pkzqCypSTBjRhIaSp5SqlPBUhUaQUKuF5jSSsk0i5UqGXCgVCMGYwrQLzra9680iNzpZlzaXZZNsP9JitMXtTPP6R2X5koSc8iAZPz0nV2Q6v70Xl8mcfgPaXXQn</recordid><startdate>197610</startdate><enddate>197610</enddate><creator>Heatfield, Barry M.</creator><creator>Hinton, David E.</creator><creator>Trump, Benjamin F.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>197610</creationdate><title>Adenocarcinoma of the Kidney. II. Enzyme Histochemistry of Renal Adenocarcinomas Induced in Rats by N-(4′-Fluoro-4-biphenylyl)acetamide</title><author>Heatfield, Barry M. ; Hinton, David E. ; Trump, Benjamin F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i158t-914cef1939f0242d236a7f33cf27fc6e926dcbd738aa6e99f7ca679cc59944c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1976</creationdate><topic>Adenocarcinoma - chemically induced</topic><topic>Adenocarcinoma - enzymology</topic><topic>Adenocarcinoma - ultrastructure</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>Alcohol Oxidoreductases - metabolism</topic><topic>Aminobiphenyl Compounds</topic><topic>Aminopeptidases - metabolism</topic><topic>Animals</topic><topic>Carcinoma - ultrastructure</topic><topic>Glycolysis</topic><topic>Kidney Neoplasms - chemically induced</topic><topic>Kidney Neoplasms - enzymology</topic><topic>Kidney Neoplasms - ultrastructure</topic><topic>Male</topic><topic>Neoplasms, Experimental - chemically induced</topic><topic>Neoplasms, Experimental - enzymology</topic><topic>Nucleotidases - metabolism</topic><topic>Oxidative Phosphorylation</topic><topic>Oxidoreductases - metabolism</topic><topic>Phosphoric Monoester Hydrolases - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heatfield, Barry M.</creatorcontrib><creatorcontrib>Hinton, David E.</creatorcontrib><creatorcontrib>Trump, Benjamin F.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heatfield, Barry M.</au><au>Hinton, David E.</au><au>Trump, Benjamin F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenocarcinoma of the Kidney. II. Enzyme Histochemistry of Renal Adenocarcinomas Induced in Rats by N-(4′-Fluoro-4-biphenylyl)acetamide</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>Journal of the National Cancer Institute</addtitle><date>1976-10</date><risdate>1976</risdate><volume>57</volume><issue>4</issue><spage>795</spage><epage>808</epage><pages>795-808</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>Activities of a broad spectrum of enzymes were studied histochemically in renal adenocarcinomas induced in young male F344 rats by chronic dietary administration of the carcinogen N-(4′-fluoro-4-biphenylyl)acetamide. Enzymes included were: dehydrogenases of glucose-6-phosphate, lactate, succinate, malate, and a-glycerophosphate; peroxidase (catalase); glucose-6-phosphatase; alkaline and acid phosphatase; Mg2+ ATPase; 5′-nucleotidase; and aminopeptidase. Levels of enzyme activity were estimated visually and scored from 0 (not detectable) to a maximum of 5 (intense). Comparison of estimated activity for each enzyme was made between small neoplastic nodules (stage III tumors) and large adenocarcinomas (stage IV tumors) and between tumors and portions of normal proximal tubules in parenchyma of kidneys from untreated control rats. The results, which revealed nearly identical levels of activity for most enzymes In both stages III and IV tumors, suggested similar metabolic and biologic behavior of these lesions. However, when data for tumors were compared with data for normal proximal tubules, striking differences were observed consistent with: 1) a marked shift of energy metabolism from oxidative to glycolytic production of ATP, with a corresponding reduction in mitochondrial respiration; and 2) simplification of plasma membrane specializations that were possibly associated with a reduction or loss of transport function. These findings were compared with other histochemical, biochemical, and ultrastructural studies of renal adenocarcinomas in rats and man.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>187777</pmid><doi>10.1093/jnci/57.4.795</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0027-8874
ispartof JNCI : Journal of the National Cancer Institute, 1976-10, Vol.57 (4), p.795-808
issn 0027-8874
1460-2105
language eng
recordid cdi_pubmed_primary_187777
source MEDLINE; Oxford University Press Journals Digital Archive Legacy
subjects Adenocarcinoma - chemically induced
Adenocarcinoma - enzymology
Adenocarcinoma - ultrastructure
Adenosine Triphosphatases - metabolism
Alcohol Oxidoreductases - metabolism
Aminobiphenyl Compounds
Aminopeptidases - metabolism
Animals
Carcinoma - ultrastructure
Glycolysis
Kidney Neoplasms - chemically induced
Kidney Neoplasms - enzymology
Kidney Neoplasms - ultrastructure
Male
Neoplasms, Experimental - chemically induced
Neoplasms, Experimental - enzymology
Nucleotidases - metabolism
Oxidative Phosphorylation
Oxidoreductases - metabolism
Phosphoric Monoester Hydrolases - metabolism
Rats
Rats, Inbred F344
title Adenocarcinoma of the Kidney. II. Enzyme Histochemistry of Renal Adenocarcinomas Induced in Rats by N-(4′-Fluoro-4-biphenylyl)acetamide
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T16%3A03%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Adenocarcinoma%20of%20the%20Kidney.%20II.%20Enzyme%20Histochemistry%20of%20Renal%20Adenocarcinomas%20Induced%20in%20Rats%20by%20N-(4%E2%80%B2-Fluoro-4-biphenylyl)acetamide&rft.jtitle=JNCI%20:%20Journal%20of%20the%20National%20Cancer%20Institute&rft.au=Heatfield,%20Barry%20M.&rft.date=1976-10&rft.volume=57&rft.issue=4&rft.spage=795&rft.epage=808&rft.pages=795-808&rft.issn=0027-8874&rft.eissn=1460-2105&rft_id=info:doi/10.1093/jnci/57.4.795&rft_dat=%3Cistex_pubme%3Eark_67375_HXZ_D2NVMP9B_V%3C/istex_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/187777&rfr_iscdi=true