Cyclic modulation of enzymes of pyrimidine nucleotide biosynthesis precedes sialoglycoconjugate changes during 2-acetylaminofluorene-induced hepatocarcinogenesis in the rat
Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene- (0.025% in a Farber Basal Carcinogenic diet) induced hepatocarcinogenesis in the rat. Dihydroorotate dehydrogenase, the fourth of six enzymes in...
Saved in:
Published in | Biochimica et biophysica acta Vol. 800; no. 2; pp. 194 - 201 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
30.07.1984
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene- (0.025% in a Farber Basal Carcinogenic diet) induced hepatocarcinogenesis in the rat. Dihydroorotate dehydrogenase, the fourth of six enzymes in de novo pyrimidine biosynthesis, decline in activity while UDP kinase and CTP synthetase showed sequential increases in activity. The alterations in activity appeared to be cyclic, followed by a full or partial return to control values. Three full cycles were monitored. The first cycle preceded nodule formation. The second cycle accompanied nodule formation and preceded sialoglycoconjugate changes reported previously. The third cycle accompanied the early glycoconjugate changes. The cyclic pattern was reproducible in three separate experiments. In each cycle, the order of events was as follows: decrease in dihydroorotate dehydrogenase, sequential increases in UDP kinase, CTP synthetase and CMPsialic acid synthase, and finally increases in the enzyme lactosylceramide: CMPsialic acid sialyltransferase, lipid-soluble sialic acid and total sialic acid. In livers of animals fed 1.87% of the hepatotoxin, 4-acetamidophenol, no biochemical alterations resembling those induced by 2-acetylaminofluorene were obtained, despite acute centrilobular necrosis of the livers. The findings point to a biochemical cascade beginning with administration of carcinogen and continuing through the development of hyperplastic nodules and of frank carcinomas resulting not from hepatotoxicity but as events associated with the hepatocarcinogenic progression. |
---|---|
AbstractList | Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene- (0.025% in a Farber Basal Carcinogenic diet) induced hepatocarcinogenesis in the rat. Dihydroorotate dehydrogenase, the fourth of six enzymes in de novo pyrimidine biosynthesis, declined in activity while UDP kinase and CTP synthetase showed sequential increases in activity. The alterations in activity appeared to be cyclic, followed by a full or partial return to control values. Three full cycles were monitored. The first cycle preceded nodule formation. The second cycle accompanied nodule formation and preceded sialoglycoconjugate changes reported previously. The third cycle accompanied the early glycoconjugate changes. The cyclic pattern was reproducible in three separate experiments. In each cycle, the order of events was as follows: decrease in dihydroorotate dehydrogenase, sequential increases in UDP kinase, CTP synthetase and CMPsialic acid synthase, and finally increases in the enzyme lactosylceramide: CMPsialic acid sialyltransferase, lipid-soluble sialic acid and total sialic acid. In livers of animals fed 1.87% of the hepatotoxin, 4-acetamidophenol, no biochemical alterations resembling those induced by 2-acetylaminofluorene were obtained, despite acute centrilobular necrosis of the livers. The findings point to a biochemical cascade beginning with administration of carcinogen and continuing through the development of hyperplastic nodules and of frank carcinomas resulting not from hepatotoxicity but as events associated with the hepatocarcinogenic progression. Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene- (0.025% in a Farber Basal Carcinogenic diet) induced hepatocarcinogenesis in the rat. Dihydroorotate dehydrogenase, the fourth of six enzymes in de novo pyrimidine biosynthesis, decline in activity while UDP kinase and CTP synthetase showed sequential increases in activity. The alterations in activity appeared to be cyclic, followed by a full or partial return to control values. Three full cycles were monitored. The first cycle preceded nodule formation. The second cycle accompanied nodule formation and preceded sialoglycoconjugate changes reported previously. The third cycle accompanied the early glycoconjugate changes. The cyclic pattern was reproducible in three separate experiments. In each cycle, the order of events was as follows: decrease in dihydroorotate dehydrogenase, sequential increases in UDP kinase, CTP synthetase and CMPsialic acid synthase, and finally increases in the enzyme lactosylceramide: CMPsialic acid sialyltransferase, lipid-soluble sialic acid and total sialic acid. In livers of animals fed 1.87% of the hepatotoxin, 4-acetamidophenol, no biochemical alterations resembling those induced by 2-acetylaminofluorene were obtained, despite acute centrilobular necrosis of the livers. The findings point to a biochemical cascade beginning with administration of carcinogen and continuing through the development of hyperplastic nodules and of frank carcinomas resulting not from hepatotoxicity but as events associated with the hepatocarcinogenic progression. Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene- (0.025% in a Farber Basal Carcinogenic diet) induced hepatocarcinogenesis in the rat. Dihydroorotate dehydrogenase, the fourth of six enzymes in de novo pyrimidine biosynthesis, declined in activity while UDP kinase and CTP synthetase showed sequential increases in activity. The alterations in activity appeared to be cyclic, followed by a full or partial return to control values. Three full cycles were monitored. The first cycle preceded nodule formation. The second cycle accompanied nodule formation and preceded sialoglycoconjugate changes reported previously. The third cycle accompanied the early glycoconjugate changes. The cyclic pattern was reproducible in three separate experiments. In each cycle, the order of events was as follows: decrease in dihydroorotate dehydrogenase, sequential increases in UDP kinase, CTP synthetase and CMPsialic acid synthase, and finally increases in the enzyme lactosylceramide: CMPsialic acid sialyltransferase, lipid-soluble sialic acid and total sialic acid. In livers of animals fed 1.87% of the hepatotoxin, 4-acetamidophenol, no biochemical alterations resembling those induced by 2-acetylaminofluorene were obtained, despite acute centrilobular necrosis of the livers. The findings point to a biochemical cascade beginning with administration of carcinogen and continuing through the development of hyperplastic nodules and of frank carcinomas resulting not from hepatotoxicity but as events associated with the hepatocarcinogenic progression.Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene- (0.025% in a Farber Basal Carcinogenic diet) induced hepatocarcinogenesis in the rat. Dihydroorotate dehydrogenase, the fourth of six enzymes in de novo pyrimidine biosynthesis, declined in activity while UDP kinase and CTP synthetase showed sequential increases in activity. The alterations in activity appeared to be cyclic, followed by a full or partial return to control values. Three full cycles were monitored. The first cycle preceded nodule formation. The second cycle accompanied nodule formation and preceded sialoglycoconjugate changes reported previously. The third cycle accompanied the early glycoconjugate changes. The cyclic pattern was reproducible in three separate experiments. In each cycle, the order of events was as follows: decrease in dihydroorotate dehydrogenase, sequential increases in UDP kinase, CTP synthetase and CMPsialic acid synthase, and finally increases in the enzyme lactosylceramide: CMPsialic acid sialyltransferase, lipid-soluble sialic acid and total sialic acid. In livers of animals fed 1.87% of the hepatotoxin, 4-acetamidophenol, no biochemical alterations resembling those induced by 2-acetylaminofluorene were obtained, despite acute centrilobular necrosis of the livers. The findings point to a biochemical cascade beginning with administration of carcinogen and continuing through the development of hyperplastic nodules and of frank carcinomas resulting not from hepatotoxicity but as events associated with the hepatocarcinogenic progression. |
Author | DeFrees, Shawn A. Heinstein, Peter F. Elliott, William L. James Morré, D. Sawick, David P. Cassady, John M. |
Author_xml | – sequence: 1 givenname: William L. surname: Elliott fullname: Elliott, William L. organization: Department of Medicinal Chemistry and Pharmacognosy, Purdue University, West Lafayette, IN 47907 USA – sequence: 2 givenname: David P. surname: Sawick fullname: Sawick, David P. organization: Department of Medicinal Chemistry and Pharmacognosy, Purdue University, West Lafayette, IN 47907 USA – sequence: 3 givenname: Shawn A. surname: DeFrees fullname: DeFrees, Shawn A. organization: Department of Medicinal Chemistry and Pharmacognosy, Purdue University, West Lafayette, IN 47907 USA – sequence: 4 givenname: Peter F. surname: Heinstein fullname: Heinstein, Peter F. organization: Department of Medicinal Chemistry and Pharmacognosy, Purdue University, West Lafayette, IN 47907 USA – sequence: 5 givenname: John M. surname: Cassady fullname: Cassady, John M. organization: Department of Medicinal Chemistry and Pharmacognosy, Purdue University, West Lafayette, IN 47907 USA – sequence: 6 givenname: D. surname: James Morré fullname: James Morré, D. organization: Department of Medicinal Chemistry and Pharmacognosy, Purdue University, West Lafayette, IN 47907 USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/6331524$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkc2KFDEUhYOMjD2tb6CQleiiNPWTVJULQZrxBwbc6Dqkbm51Z0glZZIaKJ_Jh5z0dOvChWaThHPuufCdK3LhvENCnpfsTclK8ZbVrCmaUvBXXfO6Z0ywQjwim7Jrq6LL3wuy-WN5Qq5ivGX58J5fkktR1yWvmg35tVvBGqCT14tVyXhH_UjR_VwnjMfnvAYzGW0cUreARZ-MRjoYH1eXDhhNpHNAQJ3t0Sjr93YFD97dLnuVkMJBuX3W9BKM29OqUIBptWoyzo928QEdFsbpJUfQA84qeVABsrrPyjHeOJoX0aDSU_J4VDbis_O9Jd8_Xn_bfS5uvn76svtwU0DN21QI4GOnh1YLGLQSjFet5rxv-dh3I-t7qETVVTCUzTCIkgvAGgeVFRhHoXqst-TlKXcO_seCMcnJREBrlUO_RNmVGWnVNNn44mxchgm1nDMrFVZ5xpv1dycdgo8x4CjBpAfKKShjZcnksUp57Ekee5JdIx-qzBFb0vw1_Dv-P2PvT2OYCd0ZDDKCQZfxmtxTktqbfwfcAxfiu6E |
CitedBy_id | crossref_primary_10_1016_0006_2952_88_90060_3 crossref_primary_10_1039_c3cp52692e crossref_primary_10_1016_0024_3205_88_90390_6 crossref_primary_10_1016_S0021_9258_19_50416_1 crossref_primary_10_1016_0006_2952_92_90289_U crossref_primary_10_1021_jp065034t crossref_primary_10_1039_C5CP02016F crossref_primary_10_1016_0006_2952_90_90657_7 crossref_primary_10_1021_jp512860r |
Cites_doi | 10.1016/0065-2571(80)90005-9 10.1093/jnci/60.6.1313 10.1016/0005-2760(84)90314-X 10.1016/0014-5793(70)80523-3 10.1159/000224817 10.1016/S0021-9258(19)52451-6 10.1016/S0304-3835(79)80018-X 10.1093/jnci/60.6.1329 10.1016/0065-2571(74)90023-5 10.1126/science.185697 10.1016/0041-008X(71)90328-0 10.1002/jss.400090203 10.1038/271071a0 10.1016/S0021-9258(18)63103-5 10.1016/0065-2571(78)90064-X 10.1038/253567a0 10.1126/science.182.4115.935 |
ContentType | Journal Article |
Copyright | 1984 |
Copyright_xml | – notice: 1984 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1016/0304-4165(84)90060-6 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry Biology |
EISSN | 1872-8006 |
EndPage | 201 |
ExternalDocumentID | 6331524 10_1016_0304_4165_84_90060_6 0304416584900606 |
Genre | Journal Article |
GroupedDBID | --- --K --M .~1 0R~ 1B1 1RT 1~. 1~5 23N 3O- 4.4 457 4G. 53G 5GY 5RE 5VS 7-5 71M 8P~ 9JM AACTN AAEDT AAEDW AAIAV AAIKJ AAKOC AALRI AAOAW AAQFI AAQXK AAXUO ABEFU ABFNM ABGSF ABMAC ABUDA ABXDB ABYKQ ACDAQ ACIUM ACRLP ADBBV ADEZE ADMUD ADUVX AEBSH AEHWI AEKER AFKWA AFTJW AFXIZ AGHFR AGRDE AGUBO AGYEJ AHHHB AIEXJ AIKHN AITUG AJBFU AJOXV ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ ASPBG AVWKF AXJTR AZFZN BKOJK BLXMC CS3 DOVZS EBS EFJIC EFLBG EJD EO8 EO9 EP2 EP3 FDB FEDTE FGOYB FIRID FNPLU FYGXN G-2 G-Q GBLVA HLW HVGLF HZ~ IHE J1W KOM LX3 M41 MO0 N9A O-L O9- OAUVE OHT OZT P-8 P-9 PC. Q38 R2- ROL RPZ SBG SCC SDF SDG SDP SES SEW SPCBC SSU SSZ T5K UQL WH7 WUQ XJT XPP ~G- AAHBH AATTM AAXKI AAYWO AAYXX ABWVN ACRPL ACVFH ADCNI ADNMO AEIPS AEUPX AFJKZ AFPUW AGCQF AGQPQ AGRNS AIGII AIIUN AKBMS AKRWK AKYEP ANKPU APXCP BNPGV CITATION SSH -~X .55 .GJ ABJNI AFFNX AI. CGR CUY CVF ECM EIF F5P H~9 MVM NPM PKN TWZ VH1 X7M Y6R YYP ZGI ~KM 7X8 |
ID | FETCH-LOGICAL-c357t-6c5f8db7d6cbda60527d55975f98f099c26282cb14bb6156ce3ebaf09cff6a9e3 |
ISSN | 0304-4165 0006-3002 |
IngestDate | Fri Jul 11 03:14:14 EDT 2025 Wed Feb 19 02:36:30 EST 2025 Tue Jul 01 03:49:07 EDT 2025 Thu Apr 24 22:55:27 EDT 2025 Fri Feb 23 02:36:17 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | Sialoglycoconjugate change Pyrimidine nucleotide synthesis Carcinogenesis (Rat liver) Acetylaminofluorene |
Language | English |
License | https://www.elsevier.com/tdm/userlicense/1.0 |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c357t-6c5f8db7d6cbda60527d55975f98f099c26282cb14bb6156ce3ebaf09cff6a9e3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PMID | 6331524 |
PQID | 81165244 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | proquest_miscellaneous_81165244 pubmed_primary_6331524 crossref_citationtrail_10_1016_0304_4165_84_90060_6 crossref_primary_10_1016_0304_4165_84_90060_6 elsevier_sciencedirect_doi_10_1016_0304_4165_84_90060_6 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 1900 |
PublicationDate | 1984-07-30 |
PublicationDateYYYYMMDD | 1984-07-30 |
PublicationDate_xml | – month: 07 year: 1984 text: 1984-07-30 day: 30 |
PublicationDecade | 1980 |
PublicationPlace | Netherlands |
PublicationPlace_xml | – name: Netherlands |
PublicationTitle | Biochimica et biophysica acta |
PublicationTitleAlternate | Biochim Biophys Acta |
PublicationYear | 1984 |
Publisher | Elsevier B.V |
Publisher_xml | – name: Elsevier B.V |
References | Goldenthal (BIB28) 1971 Williams, Morris, Weber (BIB18) 1975; 253 Otal-Brun, Webb (BIB13) 1979; 6 Weber, Olah, Lui, Kizaki, Tzeng, Takeda (BIB15) 1980; 18 Cheema, Yogeeswaran, Morris, Murray (BIB6) 1970; 11 Fishman, Brady (BIB1) 1976; 194 Weber, Shiotani, Kizaki, Tzeng, Williams, Gladstone (BIB16) 1978; 16 Mitchell, Jollow, Potter, Davis, Gillett, Brodie (BIB25) 1973; 187 Merritt, Morré, Keenan (BIB9) 1978; 60 Epstein, Ito, Merkow, Farber (BIB20) 1967; 27 Keenan, Morré (BIB7) 1973; 182 Lowry, Rosebrough, Farr, Randall (BIB23) 1951; 193 Siddiqui, Hakomori (BIB8) 1970; 30 Sweeney, Hoffman (BIB17) 1973; 33 Higgins, Anderson (BIB21) 1931; 12 Richardson, Baker, Morré, Keenan (BIB4) 1975; 417 Kizaki, Williams, Morris, Weber (BIB12) 1980; 40 Williams, Davis (BIB27) 1977; 18 Keppler (BIB29) 1977; 37 Williams, Kizaki, Weber, Morris (BIB19) 1978; 271 Hakomori (BIB2) 1975; 417 Veselý, Ĉihák (BIB30) 1973; 28 Creek, Walter, Evers, Yeo, Elliott, Heinstein, Morré, Morré (BIB10) 1984; 793 Thorgeisson, Felton, Nebert (BIB26) 1975; 11 Savage, Weinfeld (BIB22) 1970; 245 Merritt, Richardson, Keenan, Morré (BIB5) 1978; 60 Ahmed, Baker (BIB11) 1980; 40 Finco, Duncan, Schall, Prasse (BIB24) 1975; 166 Morré, Kloppel, Merritt, Keenan (BIB3) 1978; 9 Sweeney, Parton, Hoffman (BIB14) 1974; 12 Weber (10.1016/0304-4165(84)90060-6_BIB15) 1980; 18 Hakomori (10.1016/0304-4165(84)90060-6_BIB2) 1975; 417 Sweeney (10.1016/0304-4165(84)90060-6_BIB14) 1974; 12 Higgins (10.1016/0304-4165(84)90060-6_BIB21) 1931; 12 Richardson (10.1016/0304-4165(84)90060-6_BIB4) 1975; 417 Keenan (10.1016/0304-4165(84)90060-6_BIB7) 1973; 182 Weber (10.1016/0304-4165(84)90060-6_BIB16) 1978; 16 Williams (10.1016/0304-4165(84)90060-6_BIB18) 1975; 253 Lowry (10.1016/0304-4165(84)90060-6_BIB23) 1951; 193 Veselý (10.1016/0304-4165(84)90060-6_BIB30) 1973; 28 Siddiqui (10.1016/0304-4165(84)90060-6_BIB8) 1970; 30 Cheema (10.1016/0304-4165(84)90060-6_BIB6) 1970; 11 Kizaki (10.1016/0304-4165(84)90060-6_BIB12) 1980; 40 Finco (10.1016/0304-4165(84)90060-6_BIB24) 1975; 166 Keppler (10.1016/0304-4165(84)90060-6_BIB29) 1977; 37 Williams (10.1016/0304-4165(84)90060-6_BIB27) 1977; 18 Fishman (10.1016/0304-4165(84)90060-6_BIB1) 1976; 194 Sweeney (10.1016/0304-4165(84)90060-6_BIB17) 1973; 33 Ahmed (10.1016/0304-4165(84)90060-6_BIB11) 1980; 40 Merritt (10.1016/0304-4165(84)90060-6_BIB9) 1978; 60 Williams (10.1016/0304-4165(84)90060-6_BIB19) 1978; 271 Thorgeisson (10.1016/0304-4165(84)90060-6_BIB26) 1975; 11 Otal-Brun (10.1016/0304-4165(84)90060-6_BIB13) 1979; 6 Creek (10.1016/0304-4165(84)90060-6_BIB10) 1984; 793 Mitchell (10.1016/0304-4165(84)90060-6_BIB25) 1973; 187 Merritt (10.1016/0304-4165(84)90060-6_BIB5) 1978; 60 Morré (10.1016/0304-4165(84)90060-6_BIB3) 1978; 9 Epstein (10.1016/0304-4165(84)90060-6_BIB20) 1967; 27 Savage (10.1016/0304-4165(84)90060-6_BIB22) 1970; 245 Goldenthal (10.1016/0304-4165(84)90060-6_BIB28) 1971 |
References_xml | – volume: 16 start-page: 3 year: 1978 end-page: 19 ident: BIB16 publication-title: Adv. Enzyme Reg. – volume: 12 start-page: 186 year: 1931 end-page: 202 ident: BIB21 publication-title: Arch. Pathol. – volume: 166 start-page: 469 year: 1975 end-page: 476 ident: BIB24 publication-title: J. Am. Vet. Med. Assoc. – volume: 9 start-page: 157 year: 1978 end-page: 177 ident: BIB3 publication-title: J. Supramol. Struct. – volume: 11 start-page: 181 year: 1970 end-page: 184 ident: BIB6 publication-title: FEBS Lett. – volume: 28 start-page: 204 year: 1973 end-page: 226 ident: BIB30 publication-title: Oncology – volume: 793 start-page: 133 year: 1984 end-page: 140 ident: BIB10 publication-title: Biochim. Biophys. Acta – volume: 182 start-page: 935 year: 1973 end-page: 937 ident: BIB7 publication-title: Science – volume: 60 start-page: 1313 year: 1978 end-page: 1327 ident: BIB5 publication-title: J. Natl. Can. Inst. – volume: 40 start-page: 3559 year: 1980 end-page: 3563 ident: BIB11 publication-title: Cancer Res. – volume: 6 start-page: 39 year: 1979 end-page: 44 ident: BIB13 publication-title: Cancer Lett. – volume: 18 start-page: 3 year: 1980 end-page: 26 ident: BIB15 publication-title: Adv. Enzyme Reg. – volume: 30 start-page: 2930 year: 1970 end-page: 2936 ident: BIB8 publication-title: Cancer Res. – volume: 40 start-page: 3921 year: 1980 end-page: 3927 ident: BIB12 publication-title: Cancer Res. – volume: 245 start-page: 2529 year: 1970 end-page: 2534 ident: BIB22 publication-title: J. Biol. Chem. – volume: 27 start-page: 1702 year: 1967 end-page: 1711 ident: BIB20 publication-title: Cancer Res. – volume: 18 start-page: 27 year: 1977 end-page: 40 ident: BIB27 publication-title: Proc. Eur. Soc. Toxicol. – volume: 271 start-page: 71 year: 1978 end-page: 72 ident: BIB19 publication-title: Nature – volume: 60 start-page: 1329 year: 1978 end-page: 1337 ident: BIB9 publication-title: J. Natl. Can. Inst. – volume: 12 start-page: 385 year: 1974 end-page: 396 ident: BIB14 publication-title: Adv. Enzyme Reg. – volume: 253 start-page: 567 year: 1975 end-page: 569 ident: BIB18 publication-title: Nature – volume: 37 start-page: 911 year: 1977 end-page: 917 ident: BIB29 publication-title: Cancer Res. – volume: 11 start-page: 159 year: 1975 end-page: 165 ident: BIB26 publication-title: Mol. Pharmacol. – volume: 33 start-page: 394 year: 1973 end-page: 396 ident: BIB17 publication-title: Cancer Res. – volume: 193 start-page: 265 year: 1951 end-page: 275 ident: BIB23 publication-title: J. Biol. Chem. – volume: 417 start-page: 55 year: 1975 end-page: 89 ident: BIB2 publication-title: Biochim. Biophys. Acta – volume: 187 start-page: 185 year: 1973 end-page: 194 ident: BIB25 publication-title: J. Pharmacol. Exp. Therap. – volume: 417 start-page: 175 year: 1975 end-page: 186 ident: BIB4 publication-title: Biochim. Biophys. Acta – volume: 194 start-page: 906 year: 1976 end-page: 915 ident: BIB1 publication-title: Science – start-page: 185 year: 1971 end-page: 207 ident: BIB28 publication-title: Tox. Appl. Pharmacol. – volume: 18 start-page: 3 year: 1980 ident: 10.1016/0304-4165(84)90060-6_BIB15 publication-title: Adv. Enzyme Reg. doi: 10.1016/0065-2571(80)90005-9 – volume: 60 start-page: 1313 year: 1978 ident: 10.1016/0304-4165(84)90060-6_BIB5 publication-title: J. Natl. Can. Inst. doi: 10.1093/jnci/60.6.1313 – volume: 417 start-page: 55 year: 1975 ident: 10.1016/0304-4165(84)90060-6_BIB2 publication-title: Biochim. Biophys. Acta – volume: 40 start-page: 3559 year: 1980 ident: 10.1016/0304-4165(84)90060-6_BIB11 publication-title: Cancer Res. – volume: 166 start-page: 469 year: 1975 ident: 10.1016/0304-4165(84)90060-6_BIB24 publication-title: J. Am. Vet. Med. Assoc. – volume: 187 start-page: 185 year: 1973 ident: 10.1016/0304-4165(84)90060-6_BIB25 publication-title: J. Pharmacol. Exp. Therap. – volume: 793 start-page: 133 year: 1984 ident: 10.1016/0304-4165(84)90060-6_BIB10 publication-title: Biochim. Biophys. Acta doi: 10.1016/0005-2760(84)90314-X – volume: 33 start-page: 394 year: 1973 ident: 10.1016/0304-4165(84)90060-6_BIB17 publication-title: Cancer Res. – volume: 11 start-page: 181 year: 1970 ident: 10.1016/0304-4165(84)90060-6_BIB6 publication-title: FEBS Lett. doi: 10.1016/0014-5793(70)80523-3 – volume: 18 start-page: 27 year: 1977 ident: 10.1016/0304-4165(84)90060-6_BIB27 – volume: 12 start-page: 186 year: 1931 ident: 10.1016/0304-4165(84)90060-6_BIB21 publication-title: Arch. Pathol. – volume: 37 start-page: 911 year: 1977 ident: 10.1016/0304-4165(84)90060-6_BIB29 publication-title: Cancer Res. – volume: 28 start-page: 204 year: 1973 ident: 10.1016/0304-4165(84)90060-6_BIB30 publication-title: Oncology doi: 10.1159/000224817 – volume: 417 start-page: 175 year: 1975 ident: 10.1016/0304-4165(84)90060-6_BIB4 publication-title: Biochim. Biophys. Acta – volume: 193 start-page: 265 year: 1951 ident: 10.1016/0304-4165(84)90060-6_BIB23 publication-title: J. Biol. Chem. doi: 10.1016/S0021-9258(19)52451-6 – volume: 6 start-page: 39 year: 1979 ident: 10.1016/0304-4165(84)90060-6_BIB13 publication-title: Cancer Lett. doi: 10.1016/S0304-3835(79)80018-X – volume: 60 start-page: 1329 year: 1978 ident: 10.1016/0304-4165(84)90060-6_BIB9 publication-title: J. Natl. Can. Inst. doi: 10.1093/jnci/60.6.1329 – volume: 12 start-page: 385 year: 1974 ident: 10.1016/0304-4165(84)90060-6_BIB14 publication-title: Adv. Enzyme Reg. doi: 10.1016/0065-2571(74)90023-5 – volume: 194 start-page: 906 year: 1976 ident: 10.1016/0304-4165(84)90060-6_BIB1 publication-title: Science doi: 10.1126/science.185697 – start-page: 185 year: 1971 ident: 10.1016/0304-4165(84)90060-6_BIB28 publication-title: Tox. Appl. Pharmacol. doi: 10.1016/0041-008X(71)90328-0 – volume: 9 start-page: 157 year: 1978 ident: 10.1016/0304-4165(84)90060-6_BIB3 publication-title: J. Supramol. Struct. doi: 10.1002/jss.400090203 – volume: 271 start-page: 71 year: 1978 ident: 10.1016/0304-4165(84)90060-6_BIB19 publication-title: Nature doi: 10.1038/271071a0 – volume: 27 start-page: 1702 year: 1967 ident: 10.1016/0304-4165(84)90060-6_BIB20 publication-title: Cancer Res. – volume: 245 start-page: 2529 year: 1970 ident: 10.1016/0304-4165(84)90060-6_BIB22 publication-title: J. Biol. Chem. doi: 10.1016/S0021-9258(18)63103-5 – volume: 16 start-page: 3 year: 1978 ident: 10.1016/0304-4165(84)90060-6_BIB16 publication-title: Adv. Enzyme Reg. doi: 10.1016/0065-2571(78)90064-X – volume: 30 start-page: 2930 year: 1970 ident: 10.1016/0304-4165(84)90060-6_BIB8 publication-title: Cancer Res. – volume: 253 start-page: 567 year: 1975 ident: 10.1016/0304-4165(84)90060-6_BIB18 publication-title: Nature doi: 10.1038/253567a0 – volume: 40 start-page: 3921 year: 1980 ident: 10.1016/0304-4165(84)90060-6_BIB12 publication-title: Cancer Res. – volume: 11 start-page: 159 year: 1975 ident: 10.1016/0304-4165(84)90060-6_BIB26 publication-title: Mol. Pharmacol. – volume: 182 start-page: 935 year: 1973 ident: 10.1016/0304-4165(84)90060-6_BIB7 publication-title: Science doi: 10.1126/science.182.4115.935 |
SSID | ssj0000595 ssj0025309 |
Score | 1.3298786 |
Snippet | Three enzymatic activities associated with pyrimidine nucleotide biosynthesis were monitored at weekly or bi-weekly intervals during 2-acetylaminofluorene-... |
SourceID | proquest pubmed crossref elsevier |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 194 |
SubjectTerms | 2-Acetylaminofluorene Acetaminophen - toxicity Acetylaminofluorene Animals Carbon-Nitrogen Ligases Carcinogenesis (Rat liver) Dihydroorotate Oxidase - metabolism Ligases - metabolism Liver Neoplasms, Experimental - chemically induced Liver Neoplasms, Experimental - enzymology Liver Regeneration Male Nucleoside-Diphosphate Kinase - metabolism Pyrimidine nucleotide synthesis Pyrimidine Nucleotides - biosynthesis Rats Rats, Inbred F344 Sialoglycoconjugate change Starvation - metabolism |
Title | Cyclic modulation of enzymes of pyrimidine nucleotide biosynthesis precedes sialoglycoconjugate changes during 2-acetylaminofluorene-induced hepatocarcinogenesis in the rat |
URI | https://dx.doi.org/10.1016/0304-4165(84)90060-6 https://www.ncbi.nlm.nih.gov/pubmed/6331524 https://www.proquest.com/docview/81165244 |
Volume | 800 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF6FVgguCAoV4bkHkECWgx_rzfoYBaqIAkKoFb1Z9npNjVI7SuyD-5v4iRyYya7tAGlLuViW116vNJ9nvhnPzhDyInSkzMaxtJMgEzYL4VMMZeDYacATP2ApH3u4G_njJz47Zu9PgpPB4OdG1lJdJSN5vnVfyf9IFa6BXHGX7DUk200KF-Ac5AtHkDAc_0nG00ZijeqzMjVNuJD6qeK8OdOlZBcNNu1KkUgWWLe4rPJUWUlerpoCiB_WIlmAxlMp3L7KMYwzb0BBlsX3GqNrZlfwqt3L6NmxVFUDGMqLMpvXJZbDtMGprzGJ4BQMWwWWcSlh9Buq0HzVZlECzH77e5yX8jTHQgWWqnA9Or4SY2WPeNSWwrZWdYJRop719_klJkxkfRh1IaK4bQq_TtO3Pncjb9XBUmltiI3iC2vSDc1UDvTY9PtcpypbB6M-EOKGgq0jrM6GvvQdZgO_DDaVu3CcDRR7G6ra1c2VjdX3dEjlL4OiYxvd1MD6BXuJJtzh4Hb3RrRNHPjDtnYZj20yHc4U4UyRYNF6lojfILseODmgpXcnh1--HvZMIlh3Dere3m79dPmb7torwV6b1VxErS5yndYU6uguuWN8HzrRQL5HBqrYIzd1N9Rmj9yats0H75MfGtq0hzYtM2qgjac9tGkPbboJbdpCm26BNjXQphra9FJo023QpnlB4UUUoP2AHB-8O5rObNNYxJZ-MK5sLkExpck45TJJY3DovXGKnnWQhSIDl0l63BOeTFyWJMD4uVS-SmIYkVnG41D5-2SnKAv1kFDuyjALYxYI6TAmpBAumMHYd2B-N3W9IfFbmUTSVN3H5i_z6DJEDIndPbXQVWeuuH_cijsyzFkz4ghwfMWTz1t0RCBi_FsYF6qsV5HAwlxA_odkX4OmWwn3fWD97NE1F_mY3O4_2ydkp1rW6ikw-ip5ZoD_C7wN-h0 |
linkProvider | Library Specific Holdings |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Cyclic+modulation+of+enzymes+of+pyrimidine+nucleotide+biosynthesis+precedes+sialoglycoconjugate+changes+during+2-acetylaminofluorene-induced+hepatocarcinogenesis+in+the+rat&rft.jtitle=Biochimica+et+biophysica+acta.+General+subjects&rft.au=Elliott%2C+William+L.&rft.au=Sawick%2C+David+P.&rft.au=DeFrees%2C+Shawn+A.&rft.au=Heinstein%2C+Peter+F.&rft.date=1984-07-30&rft.issn=0304-4165&rft.volume=800&rft.issue=2&rft.spage=194&rft.epage=201&rft_id=info:doi/10.1016%2F0304-4165%2884%2990060-6&rft.externalDBID=n%2Fa&rft.externalDocID=10_1016_0304_4165_84_90060_6 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0304-4165&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0304-4165&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0304-4165&client=summon |