Oncogene Expression in Liver Regeneration and Hepatocarcinogenesis
1983; Lippincott Williams & Wilkins; Volume: 3; Issue: 6 Linguagem: Inglês
10.1002/hep.1840030621
ISSN1527-3350
AutoresNelson Fausto, Peter R. Shank,
Tópico(s)Plant tissue culture and regeneration
ResumoHepatologyVolume 3, Issue 6 p. 1016-1023 Special ArticlesFree Access Oncogene Expression in Liver Regeneration and Hepatocarcinogenesis Nelson Fausto, Corresponding Author Nelson Fausto Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912Nelson Fausto, M.D., Department of Pathology, Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912.===Search for more papers by this authorPeter R. Shank, Peter R. Shank Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912Search for more papers by this author Nelson Fausto, Corresponding Author Nelson Fausto Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912Nelson Fausto, M.D., Department of Pathology, Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912.===Search for more papers by this authorPeter R. Shank, Peter R. Shank Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912Search for more papers by this author First published: 1983 https://doi.org/10.1002/hep.1840030621Citations: 93AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat References 1 Bishop JM. Cellular oncogenes and retroviruses. Ann Rev Biochem 1983; 52: 301– 354. 2 Bishop JM, Varmus H. Functions and origins of retroviral transforming genes. In: RA Weis, N Teich, H Varmus, et al. eds. RNA tumor viruses. New York: Cold Spring Harbor Laboratory, 1982: 999– 1108. 3 Bister K, Duesberg PH. Genetic structure and transforming genes of avian retroviruses. In: G Klein, ed. Advances in viral oncology. New York: Raven Press, 1982: 3– 42. 4 Cooper GM. Cellular transforming genes. Science 1982; 218: 801– 806. 5 Stehelin D, Varmus HE, Bishop JM, et al. DNA related to the transforming gene(s) of avian sarcoma viruses is present in normal avian DNA. Nature 1976; 260: 170– 173. 6 Bishop JM, Courtneidge SA, Levinson AD, et al. Origin and function of avian retrovirus transforming genes. Cold Spr. Har. Symp. on Quant Biol. 1979; XLIV: 919– 930. 7 Kloetzer WS, Maxwell SA, Arlinghaus RB. PSSgag-mos encoded by tsllO Moloney murine sarcoma virus has an associated protein kinase activity. Proc Natl Acad Sci USA 1983; 80: 412– 416. 8 Scolnick EM. Transformation by rat derived oncogenic retroviruses. Micro Biol Rev 1981; 45: 1– 8. 9 Kenj S, Goldfarb M, Perucho M, et al. Isolation and preliminary characterization of the transforming gene of a human neuroblastoma cell line. Proc Natl Acad Sci USA 1983; 80: 383– 387. 10 Abrams HD, Rohrschneider LR, Eisenman RN. Nuclear location of the putative transforming protein of avian myleocytomatosis virus. Cell 1982; 29: 427– 439. 11 Donner P, Bunte T, Greiser-Wilke I, et al. Decreased DNA binding ability of the purified transformation-specific proteins from deletion mutants of the acute avian leukemia virus MC29. Proc Natl Acad Sci USA 1983; 80: 2861– 2865. 12 Papkoff J, Nigg EA, Hunter T. The transforming protein Moloney murine sarcoma virus is a soluble cytoplasmic protein. Cell 1983; 33: 161– 172. 13 Oskarsson M, McClements WL, Blair DG, et al. Properties of a normal mouse cell DNA sequence (sarc) homologous to the src sequence of Moloney sarcoma virus. Science 1980; 207: 1222– 1224. 14 DeFeo D, Gonda MA, Yound YA, et al. Analysis of two divergent rat genomic clones homologous to the transforming gene of Harvey murine sarcoma virus. Proc Natl Acad Sci USA 1981; 178: 3328– 3332. 15 Hayward WA, Neel BG, Astrin SM. Activation of a cellular one gene by promoter insertion in ALV-induced lymphoid leukosis. Nature 1981; 290: 475– 480. 16 Goubin G, Goldman DS, Luce J, et al. Molecular cloning and nucleotide sequence of a transforming gene detected by transfec-tion of chicken B-cell lymphoma DNA. Nature 1983; 302: 114– 119. 17 Tabin CJ, Bradley SM, Bargmann CI, et al. Mechanism of activation of a human oncogene. Nature 1982; 300: 143– 149. 18 Reddy EP, Reynolds RK, Santos E, et al. A point mutation is responsible for the acquisition of transforming properties by the T24 human bladder carcinoma oncogene. Nature 1982; 300: 149– 152. 19 Taparowsky E, Suard Y, Fasano O, et al. Activation of the T24 bladder carcinoma transforming gene is linked to a single amino acid change. Nature 1982: 300: 762– 765. 20 Feinberg AP, Vogelstein B, Droller MJ, et al. Mutation affecting the 12th amino acid of c-Ha-nw oncogene product occurs infrequently in human cancer. Science 1983; 220: 1175– 1177. 21 Chang EH, Furth ME, Scolnick EM, et al. Tumorigenic transformation of mamallian cells induced by a normal human gene homologous to the oncogene of Harvey murine sarcoma virus. Nature 1982; 297: 479– 483. 22 Lane M-A, Sainteen A, Cooper GM. Stage-specific transforming genes of human and mouse B-and T-lymphocyte neoplasm. Cell 1982; 28: 873– 880. 23 Gonda TJ, Sheiness DK, Bishop JM. Transcripts from the cellular homologs of retroviral oncogenes: distribuaraong chicken tissues. Molec Cell Biol 1982; 2: 617– 624. 24 Westin EH, Gallo RC, Arya SK, et al. Differential expression of the amv gene in human hemotopoietic cells. Proc Natl Acad Sci USA 1982; 79: 2194– 2198. 25 Cotton PC, Brugge JS. Neural tissues express high levels of the cellularsrc gene product pp60src. Molec Cell Biol 1983; 3: 1157– 1162. 26 Muller R, Slamon DJ, Adamson ED, et al. Transcription of e-ocn genes c-rasKl and c-fms during mouse development. Molec Cell Biol 1983; 3: 1062– 1069. 27 Muller R, Slamon DJ, Tremblay JM, et al. Differential expression of cellular oncogenes during pre- and postnatal developmental of the mouse. Nature 1982; 299: 640– 644. 28 Doolittle RF, Hunkapiller MW, Hood L, et al. Simian sarcoma virus one gene -sis is derived from the gene (or genes) encoding a platelet-derived growth factor. Science 1983; 221: 275– 277. 29 Bucher NLR, Malt RA. Regeneration of liver and kidney. Boston: Little, Brown and Co., 1971. 30 Grisham JW. Morphologic study of deoxyribonucleic acid synthesis and cell proliferation in regenerating rat liver: autoradiography with thymidine-H3. Cancer Res 1962; 22: 842– 849. 31 Lewan L, Yngner T, Engelbrecht C. The biochemistry of the regenerating liver. Int J Biochem 1974; 8: 477– 487. 32 Ord MG, Stocken LA. Nuclear-protein changes in the cell cycle: interphase studies with regenerating rat liver. Biochem Soc Trans 1980; 8: 759– 766. 33 Cajone F, Bernelli-Zazzera A. Protein synthesis in regenerating liver. Int J Biochem 1980; 12: 537– 544. 34 Fausto N. Messenger RNA in regenerating liver: implications for the understanding of regulated growth. Molec Cell Biochem (in press). 35 Church RB, McCarthy BJ. Ribonucleic acid synthesis in regenerating and embryonic liver. I. Synthesis of new species of RNA during regeneration of mouse liver after partial hepatectomy. J Molec Biol 1967; 23: 459– 475. 36 Tedeschi MV, Colbert DA, Fausto N. Transcription of the non-repetitive genome in liver hypertrophy and the homology between nuclear RNA of normal and 12h-regenerating liver. Biochim Bio-phys Acta 1978: 521: 641– 649. 37 Scholia CA, Tedeschi MV, Fausto N. Gene expression and the diversity of polysomal messenger RNA sequences in regenerating liver. J Biol Chem 1980; 255: 2855– 2860. 38 Fausto N, Schultz-Ellison G, Atryzek V, et al. Distribution and specificity of sequences in polyadenylated nuclear RNA of normal, regenerating and neoplastic liver. J Biol Chem 1982; 257: 2200– 2206. 39 Wilkes PR, Birnie GD, Paul J. Changes in nuclear and polysomal polyadenylated RNA sequences during rat liver regeneration. Nucleic Acids Res 1979; 6: 2193– 2208. 40 Krieg L, Alonso A, Volm M. Kinetic complexity of nuclear poly(A)-containing RNA in normal and regenerating rat liver. Eur J Biochem 1979; 96: 77– 85. 41 Grady LJ, Campbell WP, North AB. Sequence diversity of nuclear and polysomal polyadenylated and non-polyadenylated RNA in normal and regenerating rat liver. Eur J Biochem 1981; 115: 241– 245. 42 Petropoulos C, Andrews G, Tamaoki T, et al. α-Fetoprotein and albumin mRNA levels in liver regeneration and carcinogenesis. J Biol Chem 1983; 258: 4901– 4906. 43 Sala-Trepat JM, Dever J, Sargent TD, et al. Changes in expression of albumin and a-fetoprotein genes during rat liver development and neoplasia. Biochemistry 1979; 18: 2167– 2178. 44 Princen HMG, Selten GCM, Selton-Versteegen AME, et al. Distribution of mRNAs of fibrinogen polypeptides and albumin in free and membrane-bound polyribosomes and induction of α-fetoprotein mRNA synthesis during liver regeneration after partial hepatectomy. Biochim Biophys Acta 1982; 699: 121– 130. 45 Tamaoki T, Fausto N. Expression of the alpha-fetoprotein gene during development, regeneration and carcinogenesis. In: C Stein, J Stein, eds. Recombinant DNA approaches to studying control of cell proliferation. New York: Academic Press (in press). 46 Goyette M, Petropoulos CJ, Shank PR, et al. Expression of a cellular oncogene during liver regeneration. Science 1983; 219: 510– 512. 47 Fausto N, Goyette M, Petropoulos CJ, et al. Oncogene expression during liver regeneration. J Cell Biol 1982; 95: 476A. 48 Goyette M, Petropoulos CJ, Shank PR, et al. Oncogene expression during liver carcinogenesis (submitted for publication). 49 Bucher NLR, McGowan JA. Regeneration: regulatory mechanisms. In: R Wright, KGMM Alberti, S Karran, et al., eds. Liver and biliary disease. Philadelphia: W. B. Saunders Co., 1979: 210– 227. 50 Leffert HL, Koch KS, Moran T, et al. Hormonal control of rat liver regeneration. Gastroenterology 1979; 76: 1470– 1482. 51 St. Hilaire RJ, Jones AL. Epidermal growth factor: its biologic and metabolic effects with emphasis on the hepatocyte. Hepatology 1982; 2: 601– 613. 52 Earp HS, O'Keefe EJO. Epidermal growth factor receptor number decreases during rat liver regeneration. J. Clin Invest 1981; 67: 1580– 1583. 53 Hynes R. Phosphorylation of vinculin by pp60arc: what might it mean? Cell 1982; 28: 437– 438. 54 Riibsamen H, Saltenberger K, Friis R, et al. Cytosolyc malic dehydrogenase activity is associated with a putative substrate for the transforming gene product of Rous sarcoma virus. Proc Natl Acad Sci USA 1982; 79: 228– 232. 55 Erikson E, Shealy DJ, Erikson RL. Evidence that viral transforming gene products and epidermal growth factor stimulate phosphorylation of the same cellular protein with similar specificity. J Biol Chem 1981; 256: 11381– 11384. 56 Soderquist AM, Carpenter G. Developments in the mechanism of growth factor action: activation of protein kinase by epidermal growth factor. Fed Proc 1983; 42: 2615– 2620. 57 Cooper JA, Reiss NA, Schwartz RJ, et al. Three glycolytic enzymes are phosphorylated at tyrosine in cells transformed by Rous sarcoma virus. Nature 1983; 302: 218– 223. 58 Geiger B, Dutton AH, Tokuyasu KT, et al. Immunoelectron microscope studies of membrane-microfilament interactions: distributions of a-actinin, tropomyosin and vinculin in intestinal epithelial brush border and chicken gizzard smooth muscle cells. J Cell Biol 1981; 91: 614– 628. 59 Rubin RA, O'Keefe EJ, Earp HS. Alteration of epidermal growth factor-dependent phosphorylation during rat liver regeneration. J Biol Chem 1982; 79: 776– 7780. 60 Meyer DJ, Yancy SB, Revel JP. Intercellular communication in normal and regenerating rat liver: a quantitative analysis. J Cell Biol 1981; 91: 505– 523. 61 Traub O, Druge PH, Willecke K. Degradation and resynthesis of gap junction protein in plasma membranes of regenerating liver after partial hepatectomy or cholestasis. J Biol Chem 1983; 80: 755– 759. 62 Sell S, Ruoslahti E. Expression of fibronectin and laminin in the rat liver after partial hepatectomy, during carcinogenesis, and in transplantable hepatocellular carcinomas. J Natl Cancer Inst 1982; 69: 1105– 1114. 63 Strain AJ, McGowan J, Bucher NLR. Stimulation of DNA synthesis in primary cultures of adult rat hepatocytes by rat platelet-associated substance(s). In Vitro 1982; 18: 108– 116. 64 Roberts AB, Frolik CA, Anzano MA, et al. Transforming growth factors from neoplastic and nonneoplastic tissues. Fed Proc 1983; 42: 2621– 2526. 65 Shinozuka H, Lombardi B, Sell S, et al. Early histological and functional alterations of ethionine liver carcinogenesis in rats fed a choline-deficient diet. Cancer Res 1978; 38: 1092– 1098. 66 Yaswen P, Hayner NT, Fausto N. Isolation of oval cells by centrifugal elutriation and comparison with other cell types purified from normal and preneoplastic liver. Cancer Res 1983 (in press). 67 Hayner NT, Braun L, Yaswen P, et al. Isozyme profiles of oval cells, parenchymal cells and biliary cells isolated by centrifugal elutriation from normal and preneoplastic liver. Cancer Res 1983 (in press). 68 Kauffmann WK, Kaufman DG, Rice JM, et al. Possible inhibition of rat hepatocyte proliferation by hydrocortisone and its effect on cell cycle-dependent hepatocarcinogenesis by N-methyl-N-nitro-sourea. Cancer Res 1981; 41: 4653– 4660. 69 Columbano A, Rajalakshmi S, Sarma DSR. Requirement of cell proliferation for the initiation of liver carcinogenesis as assayed by three different procedures. Cancer Res 1981; 41: 2079– 2083. 70 Vincent RN, Mukherjee BB, Mobry PM, et al. Changes in transcription of endogenous type-C virus genome during mouse liver regeneration. J Gen Virol 1976; 33: 411– 419. 71 Yunis JJ. The chromosomal basis of human neoplasia. Science 1983; 221: 227– 236. 72 Schwab M, Alitalo K, Varmus H, et al. A cellular oncogene (c-Ki-ras) is amplified, overexpressed, and located within karyotypic abnormalities in mouse adrenocortical tumor cells. Nature 1983; 303: 497– 501. 73 McGowan J, Atryzek V, Fausto N. Effects of protein-deprivation on the regeneration of rat liver after partial hepatectomy. Biochem J 1979; 180: 25– 35. 74 Short J, Armstrong NB, Zemel R, et al. I. A role for amino acids in the induction of deoxyribonucleic acid synthesis in liver. Biochem Biophys Res Comm 1973; 50: 430– 437. 75 Atryzek V, Fausto N. Accumulation of polyadenylated mRNA during liver regeneration. Biochemistry 1979; 18: 1281– 1287. Citing Literature Volume3, Issue61983Pages 1016-1023 ReferencesRelatedInformation
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