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...
Gespeichert in:
Veröffentlicht in: | JNCI : Journal of the National Cancer Institute 1976-10, Vol.57 (4), p.795-808 |
---|---|
Hauptverfasser: | , , |
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 |