DOI QR코드

DOI QR Code

Suppression of Human Prostate Cancer Cell Growth by β-Lapachone via Down-regulation of pRB Phosphorylation and Induction of Cdk Inhibitor p21WAF1/CIP1

  • Choi, Yung-Hyun (Department of Biochemistry, College of Oriental Medicine, Dong-Eui University and Research Center for Oriental Medicine) ;
  • Kang, Ho-Sung (Department of Molecular Biology, College of Natural Sciences, Pusan National University) ;
  • Yoo, Mi-Ae (Department of Molecular Biology, College of Natural Sciences, Pusan National University)
  • Published : 2003.03.31

Abstract

The product of a tree (Tabebuia avellanedae) from South America, $\beta$-lapachone, is known to exhibit various pharmacological properties, the mechanisms of which are poorly understood. The aim of the present study was to further elucidate the possible mechanisms by which $\beta$-lapachone exerts its anti-proliferative action in cultured human prostate cancer cells. We observed that the proliferation-inhibitory effect of $\beta$-lapachone was due to the induction of apoptosis, which was confirmed by observing the morphological changes and cleavage of the poly(ADP-ribose) polymerase protein. A DNA flow cytometric analysis also revealed that $\beta$-lapachone arrested the cell cycle progression at the G1 phase. The effects were associated with the down-regulation of the phosphorylation of the retinoblastoma protein (pRB) as well as the enhanced binding of pRB and the transcription factor E2F-1. Also, $\beta$-lapachone suppressed the cyclindependent kinases (Cdks) and cyclin E-associated kinase activity without changing their expressions. Furthermore, this compound induced the levels of the Cdk inhibitor $p21^{WAF1/CIP1}$ expression in a p53-independent manner, and the p21 proteins that were induced by $\beta$-lapachone were associated with Cdk2. $\beta$-lapachone also activated the reporter construct of a p21 promoter. Overall, our results demonstrate a combined mechanism that involves the inhibition of pRB phosphorylation and induction of p21 as targets for $\beta$-lapachone. This may explain some of its anticancer effects.

Keywords

References

  1. Boorstein, R. J. and Pardee, A. B. (1984) $\beta$-Iapachone greatly enhances MMS lethality to human fibroblasts. Biochem. Biophys. Res. Commun. 118, 828-834. https://doi.org/10.1016/0006-291X(84)91469-4
  2. Boothman, D. A., Trask, D. K. and Pardee, A. B. (1989) Inhibition of potentially lethal DNA damage repair in human tumor cells by $\beta$-lapachone, an activator of topoisomerase I. Cancer Res. 49, 605-612.
  3. Choi, Y. H., Lee, S. J., Nguyen, P., Jang, J. S., Lee, J., Wu, M. L., Takano, E., Maki, M., Henkart, P. A. and Trepel, J. B. (1997) Regulation of cyclin D1 by cal pain protease. J. BioI. Chem. 272, 28479-28484. https://doi.org/10.1074/jbc.272.45.28479
  4. Choi, Y. H., Lee, W. H., Park, K. Y. and Zhang, L. (2000) p53- independent induction of p21 (WAF1/CIP1), reduction of cyclin B1 and G2/M arrest by the isoflavone genistein in human prostate carcinoma cells. Jpn. J. Cancer. Res. 91, 164-173. https://doi.org/10.1111/j.1349-7006.2000.tb00928.x
  5. Cruz, F. S., Docampo, R. and Boveris, A. (1978) Generation of superoxide anions and hydrogen peroxide from $\beta$-Iapachone in bacteria. Antimicrob. Agents Chemother. 14, 630-633. https://doi.org/10.1128/AAC.14.4.630
  6. Datto, M. B., Yu, Y. and Wang, X. F. (1995) Functional analysis of the transfonning growth factor $\beta$ responsive elements in the WAF/Cip1/p21 promoter. J. Biol. Chem. 270, 28623-28628. https://doi.org/10.1074/jbc.270.48.28623
  7. DeGregori, J., Leone, G., Ohtani, K., Miron, A. and Nevins, J. R. (1995) E2F-I accumulation bypasses a G1 arrest resulting from the inhibition of G1 cyclin-dependent kinase activity. Genes Dev. 9, 2873-2887. https://doi.org/10.1101/gad.9.23.2873
  8. Docampo, R., Cruz, F. S., Boveris, A., Muniz, R. P. and Esquivel, D. M. (1979) $\beta$-Lapachone enhancement of lipid peroxidation and superoxide anion and hydrogen peroxide fonnation by sarcoma 180 ascites tumor cells. Biochem. Pharmacol. 28, 723-728. https://doi.org/10.1016/0006-2952(79)90348-4
  9. EI-Deiry, W. S., Tokino, T., Velculesco, V. E., Levy, D. B., Parsons, R., Trent, J. M., Lin, D., Mercer, E. W., Kinzler. K. W. and Vogelstain, B. (1993) WAFI, a potential mediator of p53 suppression. Cell 75, 817-825. https://doi.org/10.1016/0092-8674(93)90500-P
  10. Evans, V. G. (1993) Multiple pathways to apoptosis. Cell BioI. Int. 17, 461-476. https://doi.org/10.1006/cbir.1993.1087
  11. Frydman, B., Marton, L. J., Sun, J. S., Neder, K., Witiak, D. T., Liu, A. A., Wang, H. M., Mao, Y., Wu, H. Y., Sanders, M. M. and Liu, L. F. (1997) Induction of DNA topoisomerase II- mediated DNA cleavage by $\beta$-lapachone and related naphthoquinones. Cancer Res. 57, 620-627.
  12. Goijman, S. G. and Stoppani, A. O. (1985) Effects of $\beta$lapachone, a peroxide-generating quinone, on macromolecule synthesis and degradation in Trypanosoma cruzi. Arch. Biochem. Biophys. 240, 273-280. https://doi.org/10.1016/0003-9861(85)90033-5
  13. Guiraud, P., Steiman, R., Campos-Takaki, G. M., Seigle-Murandi, F. and Simeon de Buochberg, M. (1994) Comparison of antibacterial and antifungal activities of lapachol and $\beta$-lapachone. Planta Med. 60, 373-374. https://doi.org/10.1055/s-2006-959504
  14. Kim, M.-J., Jung, J., Choi, E. C., Park, H.-Y. and Lee, K. (2001) Identification of the interaction between rat translationally controlled tumor protein/IgE-dependent histamine releasing factor and myosin light chain. J. Biochem. Mol. BioI. 34, 526-530.
  15. Koff, A., Giordano, A., Desai, D., Yamashita, K., Harper, J. W., Elledge. S., Nishimoto, T., Morgan, D. O., Franza, B. R. and Roberts, J. M. (1992) Formation and activation of a cyclin E- cdk2 complex during the G1 phase of the human cell cycle. Science 272. 1689-1694.
  16. Kozlowski, J. M., Isaiah, J. F., Campbell, D., Xu, Z. L., Kaighn, M. E. and Hart, I. R. (1984) Metastatic behavior of human tumor cell lines grown in the nude mouse. Cancer Res. 44, 3522-3529.
  17. Li, C. J., Averboukh, L. and Pardee, A. B. (1993) $\beta$-Lapachone, a novel DNA topoisomerase I inhibitor with a mode of action different from camptothecin. J. Biol. Chem. 268, 22463-22468.
  18. Li, C. J., Wang, C. and Pardee, A. B. (1995) Induction of apoptosis by $\beta$-lapachone in human prostate cancer cells. Cancer Res. 55, 3712-3715.
  19. Li, Y, Li, C. J., Yu, D. and Pardee A.B. (2000) Potent induction of apoptosis by beta-Iapachone in human multiple myeloma cell lines and patient cells. Mol. Med. 6, 1008- 1015.
  20. Loo, D. T. and Rillema, J. R. (1998) Measurement of cell death. Methods Cell BioI. 57, 251-264. https://doi.org/10.1016/S0091-679X(08)61583-6
  21. Lopes, J. N., Cruz. F. S., Docampo, R, Vasconcellos, M. E., Sampaio, M. C., Pinto, A. V. and Gilbert, B. (1978) In vitro and in vivo evaluation of the toxicity of 1,4-naphthoquinone and 1,2-naphthoquinone derivatives against Trypanosoma cruzi. Ann. Trop. Med. Parasitol. 72, 523-531.
  22. Manna, S. K., Gad, Y. P., MUkhopadhyay, A. and Aggarwal, B. B. (1999) Suppression of tumor necrosis factor-activated nuclear transcription factor-$\kappa$B, activator protein-1, c-Jun N-terminal kinase, and apoptosis by $\beta$-lapachone. Biochem. Pharmacol. 57, 763-774. https://doi.org/10.1016/S0006-2952(98)00354-2
  23. Matsushime, H., Ewen, M. E., Strom, D. K., Kato, J. Y., Hanks, S. K, Roussel, M. F. and Sherr, C. J. (1992) Identification and properties of an atypical catalytic subunit (p34PSK-J3/cdk4) for mammalian D type G1 cyclins. Cell 71, 323-334. https://doi.org/10.1016/0092-8674(92)90360-O
  24. Pardee, A. B., Li, Y. Z. and Li, C. J. (2002) Cancer therapy with beta-Iapachone. Curr. Cancer Drug Targets 2, 227-242. https://doi.org/10.2174/1568009023333854
  25. Planchon, S. M., Wuerzberger, S., Frydman, B., Witiak, D. T., Hutson, P., Church, D. R., Wilding, G. and Boothman, D. A. (1995) $\beta$-lapachone-mediated apoptosis in human promyelocytic leukemia (HL-60) and human prostate cancer cells: a p53-independent response. Cancer Res. 55, 3706-3711.
  26. Rubin, S. J., Hallahan, D. E., Ashman, C. R., Brachman, D. G., Beckett, M. A, Virudachalam, S., Yandell, D. W. and Weichselbaum, R. R. (1991) Two prostate carcinoma cell lines demonstrate abnormalities in tumor suppressor genes. J. Surg. Oncol. 46, 31-36. https://doi.org/10.1021/jm00374a010
  27. Schaffner-Sabba, K., Schmidt-Ruppin, K. H., Wehrli, W., Schuerch, A. R. and Wasley, J. W. (1984) $\beta$-Lapachone: synthesis of derivatives and activities in tumor models. J. Med. Chem. 27, 990-994. https://doi.org/10.1021/jm00374a010
  28. Scovassi, A. I., Denegri, M., Donzelli, M., Rossi, L., Bernardi, R., Mandarino, A, Frouin, I. and Negri, C. (1998) Poly(ADP- ribose) synthesis in cells undergoing apoptosis: an attempt to face death before PARP degradation. Eur. J. Histochem. 42, 251-258.
  29. Shim, M. J., Kim, H. J., Yang, S. J., Lee, I. S., Choi. H. I. and Kim, T. (2002) Arsenic trioxide induces apoptosis in chronic myelogenous leukemia K562 cells: possible involvement of p38 MAP kinase. J. Biochem. Mol. Biol. 35, 377-383. https://doi.org/10.5483/BMBRep.2002.35.4.377
  30. Sidle, A., Palaty, C., Dirks, P., Wiggan, O., Kiess, M., Gill, R. M., Wong, A. K. and Hamel, P. A. (1996) Activity of the retinoblastoma family proteins, pRB, p107, and p130, during cellular proliferation and differentiation. Crit. Rev. Biochem. Mol. BioI. 31, 237-271. https://doi.org/10.3109/10409239609106585
  31. Vanni, A, Fiore, M., De Salvia, R., Cundari, E., Ricordy, R., Ceccarelli, R. and Degrassi, F. (1998) DNA damage and cytotoxicity induced by $\beta$-lapachone: relation to poly(ADP-ribose) polymerase inhibition. Mutat. Res. 401, 55-63. https://doi.org/10.1016/S0027-5107(97)00273-X
  32. Vogt, A., Sun, J., Qian, Y., Hamilton, A. D. and Sebti, S. M.(1997) The geranylgeranyltransferase-I inhibitor GGTI-298 arrests human tumor cells in G0/G1 and induces p21(WAF1/CIPI/SDII) in a p53-independent manner. J. Biol. Chem. 272, 27224-27229. https://doi.org/10.1074/jbc.272.43.27224
  33. Waldman, T., Kinzler, K. W. and Vogelstain, B. (1995) p21 is necessary for the p53-mediated G1 arrest in human cancer cells. Cancer Res. 55, 5187-5190.
  34. Weinberg, R. A. (1995) The retinoblastoma protein and cell cycle control. Cell 81, 323-330. https://doi.org/10.1016/0092-8674(95)90385-2
  35. Xiong, Y., Hannon, G., Zhang, H., Casso, D., Kobayashi, R. and Beach, D. (1993) p21 is a universal inhibitor of cyclin kinases. Nature 366, 701-704. https://doi.org/10.1038/366701a0
  36. Zeng, Y. X. and E1-Deiry, W. S. (1996) Regulation of $p21^{WAFI/CIPI}$ expression by p53-independent pathways. Oncogene 12, 1557- 1564.

Cited by

  1. New tricks for old drugs: the anticarcinogenic potential of DNA repair inhibitors vol.37, pp.5-7, 2006, https://doi.org/10.1007/s10735-006-9043-8
  2. IFNγ-mediated inhibition of cell proliferation through increased PKCδ-induced overexpression of EC-SOD vol.45, pp.11, 2012, https://doi.org/10.5483/BMBRep.2012.45.11.003
  3. Molluscicidal activities of six species of Bignoniaceae from north–eastern Brazil, as measured againstBiomphalaria glabrataunder laboratory conditions vol.101, pp.4, 2007, https://doi.org/10.1179/136485907X176427
  4. Induction of Egr-1 Is Associated with Anti-Metastatic and Anti-Invasive Ability of β-Lapachone in Human Hepatocarcinoma Cells vol.71, pp.9, 2007, https://doi.org/10.1271/bbb.70103
  5. Furanonaphthoquinones from Tabebuia avellanedae induce cell cycle arrest and apoptosis in the human non-small cell lung cancer cell line A549 vol.11, 2015, https://doi.org/10.1016/j.phytol.2014.09.013
  6. β-lapachone-Induced Apoptosis of Human Gastric Carcinoma AGS Cells Is Caspase-Dependent and Regulated by the PI3K/Akt Pathway vol.22, pp.3, 2014, https://doi.org/10.4062/biomolther.2014.026
  7. Anti-inflammatory effects of β-lapachone in lipopolysaccharide-stimulated BV2 microglia vol.7, pp.4, 2007, https://doi.org/10.1016/j.intimp.2006.12.006
  8. Petrotetrayndiol A induces cell cycle arrest and apoptosis in SK-MEL-2 human melanoma cells through cytochrome c-mediated activation of caspases vol.232, pp.2, 2006, https://doi.org/10.1016/j.canlet.2005.02.030
  9. (β-lapachone Regulates Tight Junction Proteins, Claudin-3 and -4, in Human Hepatocarcinoma Cells. vol.17, pp.9, 2007, https://doi.org/10.5352/JLS.2007.17.9.1298
  10. Apoptosis-related Markers for Predicting Progression of Prostate Cancer vol.70, pp.1, 2007, https://doi.org/10.1016/S1726-4901(09)70292-8
  11. Natural products: An evolving role in future drug discovery vol.46, pp.10, 2011, https://doi.org/10.1016/j.ejmech.2011.07.057
  12. Wood colour in Lapacho (Tabebuia serratifolia): chemical composition and industrial implications vol.47, pp.4, 2013, https://doi.org/10.1007/s00226-013-0534-y
  13. Beta-Lapachone Suppresses Non-small Cell Lung Cancer Proliferation through the Regulation of Specificity Protein 1 vol.38, pp.9, 2015, https://doi.org/10.1248/bpb.b15-00159
  14. The Chemical Biology of Naphthoquinones and Its Environmental Implications vol.52, pp.1, 2012, https://doi.org/10.1146/annurev-pharmtox-010611-134517
  15. In vitrometabolism ofβ-lapachone (ARQ 501) in mammalian hepatocytes and cultured human cells vol.23, pp.1, 2009, https://doi.org/10.1002/rcm.3835
  16. β-Lapachone-Induced Apoptosis is Associated with Inhibition of Cyclooxygenase-2 Activity in Human Lung Cancer A549 Cells vol.21, pp.10, 2011, https://doi.org/10.5352/JLS.2011.21.10.1494
  17. -Lapachone, a Quinone Isolated from Tabebuia avellanedae, Induces Apoptosis in HepG2 Hepatoma Cell Line Through Induction of Bax and Activation of Caspase vol.9, pp.2, 2006, https://doi.org/10.1089/jmf.2006.9.161