Skip to main content
Log in

Apoptosis of human BEL-7402 hepatocellular carcinoma cells released by antisense H-ras DNA-in vitro and in vivo studies

  • Original Paper
  • Experimental Oncology
  • Published:
Journal of Cancer Research and Clinical Oncology Aims and scope Submit manuscript

Abstract

Recent findings suggest that over-expression of activated H-ras inhibited apoptotic cell death by blocking the activity of apoptotic endonuclease(s). This study was designed using antisense H-ras oligodeoxynucleotides (ODN) to evaluate whether alterations of H-ras expression in BEL-7402 human hepatocellular carcinoma cells could influence the induction of apoptosis in vitro and in vivo. We found that, in vitro, continuous suppression of H-ras expression could decrease the proliferation of BEL-7402 cells and inhibit H-ras-induced entry into S phase. In situ end labeling showed that a large number of cells underwent apoptotic cell death after treatment with antisense H-ras ODN (P<0.01), and gel electrophoresis of DNA extracted from these cells demonstrated a typical DNA ladder, characteristic of apoptosis. In vivo study indicated that pretreatment with antisense H-ras significantly retarded tumor growth in comparison with the untreated controls or tumors treated with non-specific ODN (P<0.01,P<0.01). In situ end-labeling revealed that pronounced apoptotic nuclei were also present in the tissue treated with antisense H-ras ODN (P<0.01). Immunocyto-histochemical study showed that expression of p21H-ras was significantly decreased after treatment with antisense H-ras. These results indicate that suppression of H-ras over-expression by antisense ODN could effectively inhibit tumor growth and revive the apoptotic pathway by releasing the activity of apoptotic endonuclease(s). The data also suggest the need for further studies to elucidate molecular events involved in antisense H-ras-released apoptosis and evaluate its therapeutic implications.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

ODN :

oligodeoxynucleotides

HCC :

hepatocellular carcinoma

PBS :

phosphate-buffered saline

References

  • Ansari B, Coates PJ, Greenstein BD, Hall PA (1993) In situ endlabelling detects DNA strand breaks in apoptosis and other physiological and pathological states. J Pathol 170:1–8

    PubMed  Google Scholar 

  • Arends MJ, McGregor AH, Toft NJ, Brown EJH, Wyllie AH (1993) Susceptibility to apoptosis is differentially regulated by c-myc and Ha-ras oncogenes and is associated with endonuclease availability. Br J Cancer 68:1127–1133

    PubMed  Google Scholar 

  • Arends MJ, McGregor AH, Wyllie AH (1994) Apoptosis is inversely related to necrosis and determines net growth in tumors bearing constitutively expressedmyc, ras, andHPV oncogenes. Am J Pathol 144:1045–1057

    PubMed  Google Scholar 

  • Barbacid M (1987)ras genes. Annu Rev Biochem 56:779–927

    PubMed  Google Scholar 

  • Bernards A (1995) Neurofibromatosis type 1 and Ras-mediated signalling: filling in the gaps. Biochim biophys Acta 1242:43–59

    PubMed  Google Scholar 

  • Bissonnette RP, Echeverri F, Mahboubi A, Green DR (1992) Apoptotic cell death induced by c-myc is inhibited bybcl-2. Nature 359:552–554

    PubMed  Google Scholar 

  • Bos JL (1988) Theras gene family and human carcinogenesis. Mutat Res 195:255–271

    PubMed  Google Scholar 

  • Bos JL (1989)ras oncogenes in human cancer: a review. Cancer Res 49:4682–4689

    PubMed  Google Scholar 

  • Bos JL (1995) P21Ras: an oncoprotein functioning in growth factor-induced signal transduction. Eur J Cancer 31A:1051–1054

    Google Scholar 

  • Burt RK, Garfield S, John K, Thorgeirsson SS (1988) Transformation of rat liver epithelial cells with v-Ha-ras or v-raf causes expression of MDR-1, glutathione-S-transferase-P and increased resistance to cytotoxic chemicals. Carcinogenesis 9:2329–2332

    PubMed  Google Scholar 

  • Calabretta B, Skorski T, Szczylik C, Zon G (1993) Prospects for gene-directed therapy with antisense oligodeoxynucleotides. Cancer Treat Rev 19:169–179

    PubMed  Google Scholar 

  • Carson DN, Riboro JM (1993) Apoptosis and disease. Lancet 341:1251–1254

    PubMed  Google Scholar 

  • Carter G, Lemoine NR (1993) Antisense technology for cancer therapy: does it make sense? Br J Cancer 67:869–876

    PubMed  Google Scholar 

  • Charlotte F, Lermine A, Martin N, Geleyn Y, Nollet M, Gaulard P, Zafrani ES (1994) Immunohistochemical detection ofbcl-2 protein in normal and pathological human liver. Am J Pathol 144:460–465

    PubMed  Google Scholar 

  • Chen CH, Zhang J, Ling CC (1994) Transfected c-myc and c-Ha-ras modulate radiation-induced apoptosis in rat embryo cells. Radiat Res 139:307–315

    PubMed  Google Scholar 

  • Chen FH, Xia QJ, Li YX (1991) RNA-RNA in situ hybridization for study of expression of c-myc and H-ras-1 genes in human primary liver cell carcinoma. Tumor (Shanghai) 11:193–194

    Google Scholar 

  • Cheng RM, Chu TH, Yeh HJ, et al. (1979) Establishment of three human hepatocellular carcinoma cell lines cultured in vitro and their characteristics. China Sci 12:1225–1233

    Google Scholar 

  • Chin KV, Ueda K, Pastan I, Gottesman MM (1992) Modulation of activity of the promotor of the humanMDR1 gene byras and p53. Science 255:459–462

    PubMed  Google Scholar 

  • Clarke AR, Purdie CA, Harrison DJ, Bird CC, Hooper ML, Wyllie AH (1993) Thymocyte apoptosis induced by p53-dependent and independent pathways. Nature 362:849–852

    PubMed  Google Scholar 

  • Cohen JJ (1993) Apoptosis. Immunol Today 14:126–130

    PubMed  Google Scholar 

  • Collins MKL, Revas AL (1993) The control of apoptosis in mammalian cells. Trends Biol Sci 18:307–309

    Google Scholar 

  • Compton MM (1992) A biochemical hallmark of apoptosis: internucleosomal degradation of the genome. Cancer Metastasis Rev 11:105–119

    PubMed  Google Scholar 

  • Crook AT (1993) Progress toward oligonuleotide therapeutics pharmacodynamic properties. FASEB J 7:533–539

    PubMed  Google Scholar 

  • Eastman A (1995) Survival factors, intracellular signal transduction, and the activation of endonucleases in apoptosis. Semin Cancer Biol 6:45–53

    PubMed  Google Scholar 

  • Evan GI, Wyllie AH, Gilbert CS, Littlewood TD, Land H, Brooks M, Waters CM, Penn LZ, Hancock DC (1992) Induction of apoptosis in fibroblasts by c-myc protein. Cell 69:119–128

    PubMed  Google Scholar 

  • Fanidi A, Harrington EA, Aevan GI (1992) Cooperative interaction between c-myc andbcl-2 proto-oncogenes. Nature 359:554–556

    PubMed  Google Scholar 

  • Fernandez A, Fosdick LJ, Marin MC, Diaz C, McDonnell TJ, Ananthaswamy HN, McConkey DJ (1995) Differential regulation of endogenous endonuclease activation in isolated murine fibroblast nuclei by ras and bcl-2. Oncogene 10: 769–774

    PubMed  Google Scholar 

  • Fernandez-Sarabia MJ, Bishoff JR (1994)bcl-2 associated with theras-related protein R-ras p23. Nature 366:274–275

    Google Scholar 

  • Frisch SM, Francis H (1994) Disruption of epithelial cell-matrix interaction induces apoptosis. J Cell Biol 124:619–626

    PubMed  Google Scholar 

  • Gray GD, Hernandez OM, Hebel D, Root M, Pow-Sang JM, Wickstrom E (1993) Antisense DNA inhibition of tumor growth induced by c-Ha-ras oncogene in nude mice. Cancer Res 53:577–580

    PubMed  Google Scholar 

  • Greig RG, Koestler TP, Trainer DL, Corwin SP, Miles L, Kline T, Sweet R, Yokoyama S, Poste G (1985) Tumorigenic and metastatic properties of normal andras-transfected NIH 3T3 cells. Proc Natl Acad Sci USA 82:3698–3701

    PubMed  Google Scholar 

  • Gulbins E, Bissonnette R, Mahboubi A, Martin S, Nishioka W, Brunner T, Baier G, Baier-Bitterlich G, Byrd C, Lang F (1995) Fas-induced apoptosis is mediated via a ceramide-initiates Ras signaling pathway. Immunity 2:341–351

    PubMed  Google Scholar 

  • Harrington EA, Fanidi A, Evan GI (1994) Oncogenes and cell death. Curr Opin Genet Dev 4:120–129

    PubMed  Google Scholar 

  • Helene C (1991) Rational design of sequence-specific oncogene inhibitors based on antisense and antigene oligonucleotides. Eur J Cancer 27:1460–1471

    Google Scholar 

  • Hockenbery DM, Oltvai ZN, Yin XM, Milliamanb CL, Korsmeyer SJ (1993) Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell 75:241–251

    PubMed  Google Scholar 

  • Hofmann M, Rudy W, Gunthert U, Zimmer SG, Zawadzki V, Zoller M, Lichtner RB, Herrlich P, Ponta H (1993) A link betweenras and metastatic behavior of tumor cells:ras induces CD44 promoter activity and leads to low-level expression of metastasis-specific variants of CD44 in CREF cells. Cancer Res 53:1516–1521

    PubMed  Google Scholar 

  • Hu QJ, Klippel A, Muslin AJ, Fantl WJ, Williams LT (1995) Rasdependent induction of cellular responses by constitutively active phosphatidylinositol-3 kinase. Science 268:100–102

    PubMed  Google Scholar 

  • Huschtscha LI, Jeitner TM, Andersson CE, Bartier WA, Tattersall MHN (1994) Identification of apoptotic and necrotic human leukemic cells by flow cytometry. Exp Cell Res 212:161–165

    PubMed  Google Scholar 

  • Jacks T, Fazeli A, Schmitt EM, Bronson RT, Goodell MA, Weinberg RA (1992) Effects of an Rb mutation in the mouse. Nature 259:295–300

    Google Scholar 

  • Kerbel RS, Kobayashi H, Graham CH (1994) Intrinsic or acquired drug resistance and metastasis: are they linked phenotypes? J Cell Biochem 56:37–47

    PubMed  Google Scholar 

  • Kerr JFR, Wyllie AH, Currie AR (1972) Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br J Cancer 26:239–245

    PubMed  Google Scholar 

  • Khosravi-Far R, Der CJ (1994) The Ras signal transduction pathway. Cancer Metastasis Rev 13:67–89

    PubMed  Google Scholar 

  • Laio Y, Tang ZY, Liu KD (1994) Protooncogenes and apoptosis. Chin J Cancer Biother 1:70–74

    Google Scholar 

  • Lee EY, Chang CY, Hu N, Wang YCJ, Lai CC, Herrup K, Lee WH (1992) Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis. Nature 259:288–294

    Google Scholar 

  • Lin HJ, Eviner V, Prendergast GC, White E (1995) Activated H-ras rescues E1A-induced apoptosis and cooperate with E1A to overcome p53-dependent growth arrest. Mol Cell Biol 15:4536–4544

    PubMed  Google Scholar 

  • Lowe SW, Ruley HE, Jacks T, Housman DE (1993) p53-dependent apoptosis modulates the cytotoxicity of anti-cancer agents. Cell 74:957–967

    PubMed  Google Scholar 

  • Malcomson RD, Oren M, Wyllie AH, Harrison DJ (1995) P53-independent death and p53-induced protection against apoptosis in fibroblasts treated with chemotherapeutic drugs. Br J Cancer 72:952–957

    PubMed  Google Scholar 

  • Marshall MS (1995) Ras target proteins in eukaryotic cells. FASEB J 9:1311–1318

    PubMed  Google Scholar 

  • Martin SJ, Green DR (1995) Apoptosis and cancer: the failure of controls on cell death and cell survival. Crit Rev Oncol Hematol 18:137–153

    PubMed  Google Scholar 

  • McConkey DJ, Fernandez A, Trent J, Ananthaswamy HN (1995) Oncogene regulation of endonuclease activation in apoptosis. Cancer Lett 94:9–16

    PubMed  Google Scholar 

  • Metelev V, Agrawal S (1992) Ion-exchange high-performance liquid chromatography analysis of oligodeoxyribonucleotide phosphorothioates. Anal Biochem 200:342–346

    PubMed  Google Scholar 

  • Milligan JF, Matteucci MD, Martin JC (1993) Current concepts in antisense drug design. J Med Chem 36:1923–1937

    PubMed  Google Scholar 

  • Mirabelli CK, Crooke ST (1993) Antisense oligonucleotides in the context of modern molecular drug discovery and development. In: Antisense research and applications. Crooke ST, Bernard L (eds) CRC, Boca Raton, Fla, pp 7–35

    Google Scholar 

  • Mitsuhashi BY, Filmus BJ, Shirasawa S, Sasazuki T, Kerbel RS (1995) Mutantras oncogenes upregulate VEGF/VPF expression: implications for induction and inhibition of tumour angiogenesis. Cancer Res 55:4575–4580

    PubMed  Google Scholar 

  • Moore J, Boswell S, Hoffman R, Burgess G, Hromas R (1993) Mutation H-ras over-expression inhibits a random apoptotic nuclease in myeloid leukemia cells. Leuk Res 17:703–709

    PubMed  Google Scholar 

  • Nicoletti I, Migliorati G, Pagliacci MC, Grignani F, Riccardi C (1991) A rapid and simple method for measuring thymocyte apoptosis by propidium iodide staining and flow cytometry. J Immunol Methods 139:271–279

    PubMed  Google Scholar 

  • Nooter K, Boersma AWM, Oostrum RG, Burger H, Jochemsen A, Stoter G (1995) Constitutive expression of the c-H-ras oncogene inhibit doxorubicin-induced apoptosis and promotes cell survival in a rhabdomyosarcoma cell line. Br J Cancer 71:556–561

    PubMed  Google Scholar 

  • Oberhammer FA, Pavelka M, Shama S, Tiefenbacher R, Purchio AF, Bursch W, Schulte-Hermann R (1992) Induction of apoptosis in cultured hepatocytes and in regressing liver by transforming growth factor β1. Proc Natl Acad Sci USA 89:5408–5412

    PubMed  Google Scholar 

  • Oren M (1992) The involvement of oncogenes and tumor suppressor genes in the control of apoptosis. Cancer Metastasis Rev 11:141–148

    PubMed  Google Scholar 

  • Packham G, Cleveland JL (1995) C-myc and apoptosis. Biochim Biophys Acta 1242:11–28

    PubMed  Google Scholar 

  • Patel T, Gores GJ (1995) Apoptosis and hepatobiliary disease. Hepatology 21:1725–1741

    PubMed  Google Scholar 

  • Reddy EP (1983) Nucleotide sequence analysis of the T24 human bladder carcinoma oncogene. Science 220:1061–1063

    PubMed  Google Scholar 

  • Reed JC (1994) Bcl-2 and the regulation of programmed cell death. J Cell Biol 124:1–6

    PubMed  Google Scholar 

  • Rose JK, Gallione CJ (1981) Nucleotide sequences of the mRNAs encoding the vesicular stomatosis G and M proteins determined from cDNA clones containing the complete coding regions. J Virol 39:519–528

    PubMed  Google Scholar 

  • Sakai N, Ogiso Y, Fujita H, Watari H, Koike T, Kuzumaki N (1994) Induction of apoptosis by a dominant negative H-ras mutant (116Y) in K562 cells. Exp Cell Res 215:131–136

    PubMed  Google Scholar 

  • Scanlon KJ, Ohta Y, Ishida H, Kijima H, Ohkawa T, Kaminski A, Tsai J, Horng G, Kashani-Sabet MK (1995) Oligonucleotidemediated modulation of mammalian gene expression. FASEB J 9:1288–1296

    PubMed  Google Scholar 

  • Schwartz LM, Osborne BA (1993) Programmed cell death, apoptosis and killer genes. Immunol Today 14:582–590

    PubMed  Google Scholar 

  • Shack S, Chen LC, Miller AC, Danes R, Amid D (1995) Increased susceptibility ofras-transformed cells to phenylacetate is associated with inhibition of p21 ras isoprenylation and phenotypic reversion. Int J Cancer 63:124–129

    PubMed  Google Scholar 

  • Shaw P, Bovey R, Tardy S, Sahli R, Sordt B, Costa J (1992) Induction of apoptosis by wild-type p53 in a colon tumor-derived cell line. Proc Natl Acad Sci USA 89:4495–4499

    PubMed  Google Scholar 

  • Spaargaren M, Martin GA, McCorcomick F, Fernandez-Sarabia MJ, Bischoff JR (1994) Theras-related protein R-ras interacts directly with Raf-1 in a GTP-dependent manner. Biochem J 300:303–307

    PubMed  Google Scholar 

  • Spaargaren M, Bischoff JR, McCormick F (1995) Signal transduction by Ras-like GTPases: a potential target for anticancer drugs. Gene Expr 4:345–356

    PubMed  Google Scholar 

  • Stein CA, Cheng YC (1993) Antisense olignucleotides as therapeutic agents-is the bullet really magical? Science 261:1004–1012

    PubMed  Google Scholar 

  • Steller H (1995) Mechanisms and genes of cellular suicide. Science 267:1445–1449

    PubMed  Google Scholar 

  • Stewart BW (1994) Mechanisms of apoptosis: integration of genetic, biochemical, and cellular indicators. J Natl Cancer Inst 17:1286–1296

    Google Scholar 

  • Tabor E (1994) Tumor suppressor genes, growth factor genes, and oncogenes in hepatitis B virus-associated hepatocellular carcinoma. J Med Virol 42:357–365

    PubMed  Google Scholar 

  • Tang ZY (1996) Small hepatocellular carcinoma: past, present and future. Chin Med J 109:21–24

    PubMed  Google Scholar 

  • Thompson CB (1995) Apoptosis in pathogenesis and treatment of disease. Science 267:1456–1462

    PubMed  Google Scholar 

  • Wagner RW (1994) Gene inhibition using antisense oligodeoxynucleotides. Nature 372:333–335

    PubMed  Google Scholar 

  • Wickstrom EL, Bacon TA, Gonzalez A, Freeman DL, Lyman GH, Wicksrom E (1988) Human promyelocytic leukemia HL-60 cell proliferation and c-myc protein expression are inhibited by antisense pentadecadeoxynucleotide targeted against c-myc mRNA. Proc Natl Acad Sci USA 85:1028–1032

    PubMed  Google Scholar 

  • Williams GT, Smith CA (1993) Molecular regulation of apoptosis: genetic controls on cell death. Cell 74:777–779

    PubMed  Google Scholar 

  • Wong Y, Lin ZY (1996) Preliminary study on the relationship between the H-ras oncogene and the metastasis or invasion of hepatocellular carcinoma. In: Tang ZY, Ye SL (eds) Recent progress in liver cancer and hepatitis. Beijing International Academic Publishers, Beijing, p 80

    Google Scholar 

  • Wood AC, Waters CM, Garner A, Hickman JA (1994) Changes in c-myc expression and kinetics of dexamethasone-induced programmed cell death (apoptosis) in human lymphoid leukaemia cells. Br J Cancer 69:663–669

    PubMed  Google Scholar 

  • Wyllie AH (1992) Apoptosis and regulation of cell numbers in normal and neoplastic tissues: an overview. Cancer Metastasis Rev 11:95–103

    PubMed  Google Scholar 

  • Wyllie AH, Rose KA, Morris RG, Steel CM, Foster E, Spandidos DA (1987) Rodent fibroblast tumors expressing humanmyc andras genes: growth, metastasis and endogenous oncogene expression. Br J Cancer 56:251–259

    PubMed  Google Scholar 

  • Zon G, Geiser TG (1991) Phosphorothioate oligonucleotides: chemistry, purification, analysis, scale-up and future direction. Anticancer Drug Des 6:539–568

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Liao, Y., Tang, ZY., Liu, KD. et al. Apoptosis of human BEL-7402 hepatocellular carcinoma cells released by antisense H-ras DNA-in vitro and in vivo studies. J Cancer Res Clin Oncol 123, 25–33 (1997). https://doi.org/10.1007/BF01212611

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01212611

Key words

Navigation