Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0019204 (hepatocellular carcinoma)
 71,386 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Nuclear mono- and poly(ADP-ribosyl) protein conjugates formed in living hepatoma AH 7974 cells in response to treatment with the alkylating agent dimethyl sulfate have been studied. They were isolated from the perchloric acid precipitate of freshly prepared nuclei in a relatively pure form and with an overall yield of more than 80%, utilizing aminophenylboronic acid-agarose chromatography. Exposure of the cells to 400 microM dimethyl sulfate led to a transient rise of ADP-ribosylated proteins. After 20 min, the level of endogenous poly(ADP-ribosyl) residues increased by a factor of 21, amounting to a final value of 772 +/- 57 pmol/mg of DNA while the mono(ADP-ribosyl) residues were raised to even higher concentrations (1864 pmol/mg of DNA), corresponding to a 12-fold stimulation as compared to untreated cells. As a result of dimethyl sulfate treatment, the amount of acceptor protein being modified by (ADP-ribose)n was elevated 15-fold, reaching a final proportion of 2.3 +/- 0.4% of total nuclear protein. The increase in (ADP-ribosyl)n-modified proteins was suppressed by benzamide, a potent inhibitor of poly(ADP-ribose) synthetase. More than half of the nuclear mono- and poly(ADP-ribosyl) residues were linked to histone H2B. The modifying residues could be removed from the major acceptor by treatment with 0.1 M NaOH, but not with neutral hydroxylamine. Minor amounts of other histones, especially of histone H4, were possibly also ADP-ribosylated under the stimulating effect of dimethyl sulfate. In addition, several nonhistone proteins with apparent molecular masses of 100-116 and 170 kDa were found to carry substantial amounts of mono- and poly(ADP-ribose).
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PMID:ADP-ribosylation of nuclear proteins in vivo. Identification of histone H2B as a major acceptor for mono- and poly(ADP-ribose) in dimethyl sulfate-treated hepatoma AH 7974 cells. 672 73

Dimethylnitrosamine given after partial hepatectomy reduces the synthesis of DNA, histone, and, to a lesser extent, of nonhistone proteins, the inhibition being general rather than for specific nuclear proteins. The extent of inhibition of macromolecular synthesis is greatest when the carcinogen is given a few hours after the operation. As a higher incidence of hepatocellular carcinoma is induced when dimethylnitrosamine is injected later, during the wave of DNA replication, it appears that inhibition of nuclear protein synthesis is not a relevant factor in carcinogenesis, unless it relates to loss of a specific non-histone protein present in small amounts. Analysis of sequentially extracted groups of non-histone proteins by 2D electrophoresis did not reveal any changes produced by treatment with dimethylnitrosamine. Animals fed a diet containing diethylnitrosamine showed an increased incorporation of amino acid into histone. Electrophoretic analysis of non-histone proteins revealed two reproducible effects of feeding the carcinogenic diet: relative to the bulk of nuclear non-histone protein, there was a reduction in the amount of a slightly basic 65000 mol. wt. polypeptide, and an increase in the level of a high molecular weight protein that was almost undetectable in material from normal rats. As these changes were not induced by partial hepatectomy of normal animals, it is possible that they are related to malignancy rather than to the associated increase in cell replication.
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PMID:The behaviour of nuclear proteins during nitrosamine-induced carcinogenesis. 688 31

Immunological tests and 2-dimensional gel electrophoresis revealed differences between the nuclear proteins from normal and malignant liver cells. Immunization of rabbits with a nuclear nonhistone protein fraction isolated from normal mouse liver resulted in antisera that in immunofluorescence gave nuclear staining in sections of normal liver, but did not stain nuclei of a transplantable mouse hepatoma. Antisera prepared against a nuclear protein fraction from the hepatoma allowed immunofluorescent staining of hepatoma nuclei but did not stain nuclei from normal liver. Nuclei in liver regeneration after injury caused by administration of carbon tetrachloride stained with antiserum against normal nuclei but not with antisera against hepatoma nuclei. Neither antiserum stained nuclei in fetal liver cells. The presence of differing sets of nuclear proteins in the normal and malignant liver cells was indicated by 2-dimensional gel electrophoresis. Approximately 300 polypeptides were resolved by this technique. Most of these were quantitatively different in the normal and hepatoma nonhistone protein preparations. Several qualitative differences also seemed to be present. Nonhistone proteins from regenerating liver shared some polypeptides with hepatoma that were absent in normal liver. Nuclear proteins characteristic of malignant tissues may provide clues toward the understanding of gene regulation in malignant cells, and some of them could become useful tumor markers.
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PMID:Differences in the nuclear proteins of normal and malignant liver cells. 702 32

RNA polymerase II was purified from Morris hepatoma 3924A by a series of ion-exchange and affinity column chromatographic fractionations, followed by sucrose gradient centrifugation in the presence of 0.3 M KC1. Purified RNA polymerase II had a specific activity of greater than 400 nmol of UMP incorporated (30 min)-1 (mg of protein)-1 by using double-stranded DNA as template. The purified enzyme contained five polypeptides (Mr 214 000, 140 000, 33 000, 25 000, and 21 000) that were present in molar quantities and two additional polypeptides (Mr 19 000 and 18 000) that had a combined molar ratio of 1.0. The cyclic AMP independent nuclear protein kinase NII, also purified from hepatoma 3924A, was able to phosphorylate RNA polymerase II polypeptides of Mr 214 000, 140 000, and 21 000. Phosphorylation of the polymerase was accompanied by enhanced transcription of double-stranded DNA, heat-denatured DNA, and poly[d-(A-T)]. The elevation in RNA polymerase activity was dependent upon the presence of hydrolyzable ATP and resulted from an increased number of RNA molecules synthesized in vitro. The average length of RNA chains was not affected by the kinase. Under similar conditions, protein kinase NII also stimulated homologous RNA polymerase I. In contrast to the phosphorylation of polymerase II, modification of polymerase I resulted in an increase in the average size, but not number, of RNA chains synthesized. The specificity of the NII kinase-catalyzed reaction was demonstrated by the inability of another homologous protein kinase, NI, to phosphorylate or activate RNA polymerase II.
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PMID:Phosphorylation of deoxyribonucleic acid dependent RNA polymerase II by nuclear protein kinase NII: mechanism of enhanced ribonucleic acid synthesis. 711 96

In this study we have further characterized the response of liver-derived cells to glucocorticoid treatment using the rat hepatoma, Fu5-5. Using two-dimensional electrophoresis we have examined changes in the synthetic rates of cytosol proteins following glucocorticoid administration by using [35S]methionine. We have also demonstrated changes in the incorporation of 32P by several cytosol proteins after hormone treatment. One of these changes occurs within 1 h of hormone treatment. We were unable to detect any changes in the nuclear protein content of Fu5-5 cells after glucocorticoid treatment. We then compared the glucocorticoid-regulated changes in cytosol protein synthesis in Fu5-5 cells with those of the H35 rat hepatoma, monolayer cultures of rat hepatocytes and the response of rat liver in vivo. This examination revealed that although nearly all of the eighteen hormonally responsive proteins appeared to be present in all of the cells types, only three were responsive to glucocorticoid in more than one system. Moreover, the response patterns were often reversed in different cell types, the same protein being induced in one cell type and repressed in another.
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PMID:An electrophoretic characterization of the glucocorticoid response of the Fu5-5 rat hepatoma cell line. 712 96

A comparative study of the nuclear matrix proteins of rat liver and Zajdela hepatoma cells was performed. The polyacrylamide SDS electrophoretic profile of the hepatoma nuclear matrix proteins differed from those of the liver by the presence of high molecular weight (over 135 KD) bands. Four nuclear matrix fractions were isolated by a subsequent treatment of the preparation with an aqueous solution of EDTA and 0,025 N sodium hydroxide. The bulk of the nuclear matrix proteins of both liver and hepatoma were alkali-soluble. The percentage of the alkali-insoluble residue and of the water-soluble fraction in the Zajdela hepatoma nuclear matrix was 3.5 and 1.7 times that of the liver, respectively. In the course of 60 min incubation of the liver mince or Zajdela hepatoma cells with 14C-Chlorella protein hydrolyzate in vitro the nuclear matrix proteins incorporated by 10-20% more label than did the total nuclear protein, the specific activity of the alkali-insoluble residue being twice higher that of the whole nuclear matrix protein. After 15 min of incubation the label was rather evenly spread along the gel, containing labelled protein bands separated according to their molecular weight. However, after 30 min and especially 60 min of incubation the label markedly prevailed in the high molecular weight proteins.
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PMID:[Fractionation and biosynthesis of rat liver and Zajdela hepatoma nuclear matrix proteins]. 723 94

A cyclic-nucleotide independent heparin-sensitive nuclear protein kinase (NII) from the Morris hepatoma 3924A has been purified by a combination of ion exchange and affinity chromatographic procedures and velocity gradient centrifugation. The purified kinase had a molecular weight of 140,000 as determined by gel filtration. Two polypeptides (Mr = 42,000 and 25,600) were present in the purified preparation in approximately equimolar concentrations. The protein kinase employed Mg2+ and Co2+ as divalent ion and preferred the nonhistone proteins, casein or phosvitin, as protein acceptors. In the presence of Mg2+, it utilized both ATP and GTP as substrates and transferred the terminal nucleotide phosphate to serine and threonine residues of the protein acceptor. Phosphorylation of casein was stimulated by polyamines, particularly spermine. This polyamine preferentially enhanced phosphate transfer to threonine. The enzyme was inhibited by several compounds including heparin, the o-n-octyloxime of rifamycin (AF/013), 3'-dATP, o-phenanthroline, polynucleotides, and ADP. Of these inhibitors, heparin was the most potent and completely abolished kinase activity at a concentration of 0.1 micrograms/ml. The kinase could be autophosphorylated by incubation with Mg2+ and [gamma-32P]ATP; under these conditions phosphorylation was confined to the polypeptide of Mr = 24,600 and was completely inhibited by heparin. Based on the unique properties of NII protein kinase (ability to use GTP, stimulation by spermine, sensitivity to heparin), a selective assay was developed which could measure NII activity in the presence of other nuclear kinases. Under the optimal assay conditions, the nuclear extract of hepatoma 3924A was found to contain at least five times more NII kinase activity than that of normal adult liver. Analysis of extensively purified preparations from the two sources confirmed these results. After purification 11 times more NII protein kinase activity was obtained from hepatoma 3924A than from liver. Although hepatoma and liver protein kinases exhibited many common properties, they displayed distinct nucleotide saturation kinetics. The apparent Km for ATP was 10 microM for hepatoma protein kinase and 24 microM for the liver enzyme.
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PMID:A heparin-sensitive nuclear protein kinase. Purification, properties, and increased activity in rat hepatoma relative to liver. 725 4

We have recently purified a cyclic nucleotide-independent, heparin-sensitive nuclear protein kinase (NII) from Morris hepatoma 3924A and demonstrated an apparent relationship of this kinase to the two subunits (Mr = 42,000 and 24,600) of RNA polymerase I. When homogeneous protein kinase NII was recombined with purified homologous RNA polymerase I containing limiting quantities of endogenous kinase, RNA synthesis was stimulated as much as 5-fold during a 90-min incubation. The enhanced RNA synthesis was due to an increase in the average RNA chain length; protein kinase did not alter the number of RNA molecules synthesized by the polymerase. Phosphorylation of RNA polymerase occurred at serine and threonine moieties. Unlike the NII kinase, purified homologous NI kinase did not phosphorylate RNA polymerase I and, as a result, did not alter transcription. These data indicate that 1) RNA polymerase I is activated by protein kinase NII, 2) endogenous protein kinase NII remaining with highly purified RNA polymerase I does not fully phosphorylate RNA polymerase I in vitro, and 3) protein kinase NII is capable of regulating RNA polymerase I activity by preventing premature termination of RNA chains.
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PMID:Activation of purified hepatoma RNA polymerase I by homologous protein kinase NII. 728 32

A nuclear protein kinase, designated NII, was purified essentially to homogeneity from the Morris hepatoma 3924A. In the presence of excess Mg2+, phosphorylation of casein by the kinase was stimulated by spermine (1-5 mM) and was inhibited completely by 0.1 microgram/ml heparin. The apparent Km for casein was reduced in the presence of spermine. Spermine preferentially augmented phosphorylation of threonine residues. The kinase was also associated with highly purified RNA polymerase I and appears to correspond to two polypeptides (Mr 42,000 and 24,600) of the polymerase. RNA polymerase I polypeptides of Mr 120,000 (S2), Mr 65,000 (S3) and Mr 24,600 (S5) were phosphorylated by the endogenous kinase. Spermine enhanced phosphorylation of the RNA polymerase I subunits as much as 20-fold. Phosphorylation activated RNA polymerase I; the phosphorylated enzyme synthesized longer product with no apparent effect on the number of RNA chains initiated.
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PMID:Spermine-mediated phosphorylation of RNA polymerase I and its effect on transcription. 733 1

Two-dimensional polyacrylamide gel electrophoresis patterns of 32P-labeled nuclear proteins in Novikoff hepatoma and regenerating liver relatively small number of the many nuclear protein spots were phosphorylated. The major phosphoprotein spots differed in size and shape from the stained protein spots. Seven phosphoproteins, 125/5.8, 125/7.2, 100/5.9, 85/5.9, 56/5.1, and 50/5.1 (mol. wt. x 10-(3)/pI in the Novikoff hepatoma nuclei were not found in the 18-h regenerating liver nuclei. One nuclear phosphoprotein, 54/6.5, was found in the liver but not in the hepatoma. The four major phosphoproteins, 45/5.3-6.0, 40/5.3-6.0, 35/5.3-6.0, and 25/5.8-6.8 containing about 60% of the total 32Pi of the nuclear proteins, were found in both types of cells. These proteins were of unusual density and shape. Some proteins, such as 125/5.8 and 85/5.9, were enriched in 0.01 M tris extract of the tumor, and proteins 125/7.2 and 56/6.1 were enriched in 0.35 M NaCl extract of the tumor.
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PMID:Two-dimensional gel electrophoresis of nuclear phosphoproteins of Novikoff hepatoma and regenerating liver. 743 33


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