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HSP90 Inhibition Suppresses PGE2 Production via Modulating COX-2 and 15-PGDH Expression in HT-29 Colorectal Cancer Cells

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Abstract

The existence of multiple-interactive roles between several signaling pathways in tumorigenesis shows the significance of pharmacological factors like heat shock protein 90 (HSP90) inhibitors which control several signaling pathways simultaneously. HSP90 as a molecular chaperone supports the active conformational structure and function of several oncogenic signal proteins, termed “client” proteins, some of them act as a link between cancer and inflammation. Prostaglandin E2 (PGE2) is one of the major mediators of inflammation in colorectal cancer development and progress. However, the relationship between chaperone activity of HSP90 and PGE2 levels remains unclear. We evaluated the inhibitory effects of 17-demethoxy-17-allylamino geldanamycin (1 7-AAG), an HSP90 inhibitor, on PGE2 levels in HT-29 colorectal cancer cells. For the first time, we showed inhibitory effects of 17-AAG, on PGE2 levels in HT-29 colorectal cancer cells. 17-AAG inhibited PMA-induced cyclooxygenase-2 (COX-2) mRNA expression and protein level. We showed 15-hydroxyprostaglandin dehydrogenase (15-PGDH) expression induced by 17-AAG treatment at both mRNA and protein levels. In conclusion, we found that inhibitory effects of 17-AAG on PGE2 levels in HT-29 colorectal cancer cells were mediated through modulating COX-2 and 15-PGDH expression.

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References

  1. Ricchi, P., R. Zarrilli, A. Di Palma, and A.M. Acquaviva. 2003. Nonsteroidal anti-inflammatory drugs in colorectal cancer: from prevention to therapy. British Journal of Cancer 88: 803–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Tuynman, J.B., M.P. Peppelenbosch, and D.J. Richel. 2004. COX-2 inhibition as a tool to treat and prevent colorectal cancer. Critical Reviews in Oncology/Hematology 52: 81–101.

    Article  CAS  PubMed  Google Scholar 

  3. Goetz, M.P., D.O. Toft, M.M. Ames, and C. Erlichman. 2003. The HSP90 chaperone complex as a novel target for cancer therapy. Annals of Oncology 14: 1169–76.

    Article  CAS  PubMed  Google Scholar 

  4. Khanna, M., F. Wang, I. Jo, W.E. Knabe, S.M. Wilson, L. Li, K. Bum-Erdene, J. Li, G. W Sledge, R. Khanna, and S.O. Meroueh. 2011. Targeting multiple conformations leads to small molecule inhibitors of the uPAR.uPA protein-protein interaction that block cancer cell invasion. ACS Chemical Biology 6: 1232–43.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Li, Y., T. Zhang, S.J. Schwartz, and D. Sun. 2009. New developments in HSP90 inhibitors as anti-cancer therapeutics: mechanisms, clinical perspective and more potential. Drug Resistance Updates 12: 17–27.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Bai, L., S. Xu, W. Chen, Z. Li, X. Wang, H. Tang, and Y. Ling. 2011. Blocking NF-kappaB and Akt by HSP90 inhibition sensitizes Smac mimetic compound 3-induced extrinsic apoptosis pathway and results in synergistic cancer cell death. Apoptosis 16: 45–54.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Wang, X., W. Ju, J. Renouard, J. Aden, S.A. Belinsky, and Y. Lin. 2006. 17-allylamino-17-demethoxygeldanamycin synergistically potentiates tumor necrosis factor-induced lung cancer cell death by blocking the nuclear factor-kappaB pathway. Cancer Research 66: 1089–95.

    Article  CAS  PubMed  Google Scholar 

  8. Lilja, A., C.E. Weeden, K. McArthur, T. Nguyen, A. Donald, Z.X. Wong, L. Dousha, S. Bozinovski, R. Vlahos, C.J. Burns, M.L. Asselin-Labat, et al. 2015. HSP90 inhibition suppresses lipopolysaccharide-induced lung inflammation in vivo. PLoS One 10, e0114975.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Sevin M, Girodon F, Garrido C, and de Thonel A. HSP90 and HSP70: Implication in inflammation processes and therapeutic approaches for myeloproliferative neoplasms. 2015. Mediators Inflamm: 970242. doi: 10.1155/2015/970242.

  10. Hance, M.W., K.D. Nolan, and J.S. Isaacs. 2014. The double-edged sword: conserved functions of extracellular HSP90 in wound healing and cancer. Cancers (Basel) 6: 1065–97.

    Article  CAS  Google Scholar 

  11. Chen, W., Z. Li, L. Bai, and Y. Lin. 2011. NF-kappa B in lung cancer, a carcinogenesis mediator and a prevention and therapy target. Frontiers in Bioscience (Landmark Edition) 16: 1172–85.

    Article  CAS  Google Scholar 

  12. Wang, D., and R.N. DuBois. 2014. PPAR delta and PGE signaling pathways communicate and connect inflammation to colorectal cancer. Inflamm Cell Signal 1, 10.14800/ics.338.

    PubMed Central  Google Scholar 

  13. Na, H.K., J.M. Park, H.G. Lee, H.N. Lee, S.J. Myung, and Y.J. Surh. 2011. 15-Hydroxyprostaglandin dehydrogenase as a novel molecular target for cancer chemoprevention and therapy. Biochemical Pharmacology 82: 1352–60.

    Article  CAS  PubMed  Google Scholar 

  14. Nakanishi, M., and D.W. Rosenberg. 2013. Multifaceted roles of PGE2 in inflammation and cancer. Seminars in Immunopathology 35: 123–37.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Castro-Sanchez, L., N. Agra, C. LlorenteIzquierdo, O. Motino, M. Casado, L. Bosca, and P. Martín-Sanz. 2013. Regulation of 15-hydroxyprostaglandin dehydrogenase expression in hepatocellular carcinoma. The International Journal of Biochemistry & Cell Biology 45: 2501–11.

    Article  CAS  Google Scholar 

  16. Ataee, R., S. Ajdary, M. Rezayat, M.A. Shokrgozar, S. Shahriari, and M.R. Zarrindast. 2010. Study of 5HT3 and HT4 receptor expression in HT-29 cell line and human colon adenocarcinoma tissues. Archives of Iranian Medicine 13: 120–5.

    CAS  PubMed  Google Scholar 

  17. Ruijter, J.M., C. Ramakers, W.M. Hoogaars, Y. Karlen, O. Bakker, M.J. van den Hoff, and A.F. Moorman. 2009. Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data. Nucleic Acids Research 37, e45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Xian, Y.F., Y.C. Li, S.P. Ip, Z.X. Lin, X.P. Lai, and Z.R. Su. 2011. Anti-inflammatory effect of patchouli alcohol isolated from Pogostemonis Herba in LPS-stimulated RAW264.7 macrophages. ExpTher Med 2: 545–50.

    CAS  Google Scholar 

  19. Choi, Y.E., C. Battelli, J. Watson, J. Liu, J. Curtis, A.N. Morse, U.A. Matulonis, D. Chowdhury, and P.A. Konstantinopoulos. 2014. Sublethal concentrations of 17-AAG suppress homologous recombination DNA repair and enhance sensitivity to carboplatin and olaparib in HR proficient ovarian cancer cells. Oncotarget 5: 2678–87.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Kacimi, R., and M.A. Yenari. 2015. Pharmacologic heat shock protein 70 induction confers cytoprotection against inflammation in gliovascular cells. Glia 63: 1200–12.

    Article  PubMed  Google Scholar 

  21. Kaltschmidt, B., R.A. Linker, J. Deng, and C. Kaltschmidt. 2002. Cyclooxygenase-2 is a neuronal target gene of NF-kappaB. BMC Molecular Biology 3: 16.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Zarghi, A., and S. Arfaei. 2011. Selective COX-2 inhibitors: a review of their structure-activity relationships. Iran Journal of Pharmacy Research 10: 655–83.

    CAS  Google Scholar 

  23. Holla, V.R., J.R. Mann, Q. Shi, and R.N. DuBois. 2006. Prostaglandin E2 regulates the nuclear receptor NR4A2 in colorectal cancer. The Journal of Biological Chemistry 281: 2676–82.

    Article  CAS  PubMed  Google Scholar 

  24. Haggar, F.A., and R.P. Boushey. 2009. Colorectal cancer epidemiology: incidence, mortality, survival, and risk factors. Clinical Colon & Rectal Surgery 22: 191–7.

    Article  Google Scholar 

  25. Weinstein, I.B., and A.K. Joe. 2006. Mechanisms of disease: oncogene addiction—a rationale for molecular targeting in cancer therapy. Nature Clinical Practice. Oncology 3: 448–57.

    Article  CAS  PubMed  Google Scholar 

  26. Kang, S., A. Min, S.A. Im, S.H. Song, S.G. Kim, H.A. Kim, H.J. Kim, D.Y. Oh, H.S. Jong, T.Y. Kim, and Y.J. Bang. 2015. TGF-beta suppresses COX-2 expression by tristetraprolin-mediated RNA destabilization in A549 human lung cancer cells. Cancer Research and Treatment 47: 101–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Lee, K.H., A.H. Jang, and C.G. Yoo. 2015. 17-Allylamino-17-demethoxygeldanamycin and the enhancement of PS-341-induced lung cancer cell death by blocking the NF-kappaB and PI3K/Akt pathways. American Journal of Respiratory Cell and Molecular Biology 53: 412–21.

    Article  CAS  PubMed  Google Scholar 

  28. Reti, A., G. Barna, E. Pap, V. Adleff, V. LK, A. Jeney, J. Kralovánszky, and B. Budai. 2009. Enhancement of 5-fluorouracil efficacy on high COX-2 expressing HCA-7 cells by low dose indomethacin and NS-398 but not on low COX-2 expressing HT-29 cells. Pathology Oncology Research 15: 335–44.

    Article  CAS  PubMed  Google Scholar 

  29. Kaidi, A., D. Qualtrough, A.C. Williams, and C. Paraskeva. 2006. Direct transcriptional up-regulation of cyclooxygenase-2 by hypoxia-inducible factor (HIF)-1 promotes colorectal tumor cell survival and enhances HIF-1 transcriptional activity during hypoxia. Cancer Research 66: 6683–91.

    Article  CAS  PubMed  Google Scholar 

  30. Csiki, I., K. Yanagisawa, N. Haruki, S. Nadaf, J.D. Morrow, D.H. Johnson, and D.P. Carbone. 2006. Thioredoxin-1 modulates transcription of cyclooxygenase-2 via hypoxia-inducible factor-1 alpha in non-small cell lung cancer. Cancer Research 66: 143–50.

    Article  CAS  PubMed  Google Scholar 

  31. Lu, D., C. Han, and T. Wu. 2014. 15-PGDH inhibits hepatocellular carcinoma growth through 15-keto-PGE2/PPAR gamma-mediated activation of p21WAF1/Cip1. Oncogene 33: 1101–12.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Chi, X., B.M. Freeman, M. Tong, Y. Zhao, and H.H. Tai. 2009. 15-Hydroxyprostaglandin dehydrogenase (15-PGDH) is up-regulated by flurbiprofen and other non-steroidal anti-inflammatory drugs in human colon cancer HT29 cells. Archives of Biochemistry and Biophysics 487: 139–45.

    Article  CAS  PubMed  Google Scholar 

  33. Wakimoto, N., I. Wolf, D. Yin, J. O’Kelly, T. Akagi, L. Abramovitz, K.L. Black, H.H. Tai, and H.P. Koeffler. 2008. Nonsteroidal anti-inflammatory drugs suppress glioma via 15-hydroxyprostaglandin dehydrogenase. Cancer Research 68: 6978–86.

    Article  CAS  PubMed  Google Scholar 

  34. Casciani, V., E. Marinoni, A.D. Bocking, M. Moscarini, R. Di Iorio, and J.R. Challis. 2008. Opposite effect of phorbol ester PMA on PTGS2 and PGDH mRNA expression in human choriontrophoblast cells. Reproductive Sciences 15: 40–50.

    Article  CAS  PubMed  Google Scholar 

  35. Tong, M., Y. Ding, and H.H. Tai. 2006. Reciprocal regulation of cyclooxygenase-2 and 15-hydroxyprostaglandin dehydrogenase expression in A549 human lung adenocarcinoma cells. Carcinogenesis 27: 2170–9.

    Article  CAS  PubMed  Google Scholar 

  36. Jang, T.J., K.H. Jeon, and K.H. Jung. 2009. Cyclooxygenase-2 expression is related to the epithelial-to-mesenchymal transition in human colon cancers. Yonsei Medical Journal 31: 818–24.

    Article  Google Scholar 

  37. Chandramouli, A., M.E. Mercado-Pimentel, A. Hutchinson, A. Gibadulinova, E.R. Olson, S. Dickinson, R. Shañas, J. Davenport, J. Owens, A.K. Bhattacharyya, J.W. Regan, et al. 2010. The induction of S100p expression by the prostaglandin E(2) (PGE(2))/EP4 receptor signaling pathway in colon cancer cells. Cancer Biology & Therapy 10: 1056–66.

    Article  CAS  Google Scholar 

  38. Dufour, M., S. Faes, A. Dormond-Meuwly, N. Demartines, and O. Dormond. 2014. PGE2-induced colon cancer growth is mediated by mTORC1. Biochemical and Biophysical Research Communications 451: 587–91.

    Article  CAS  PubMed  Google Scholar 

  39. Altorki, N.K., K. Subbaramaiah, and A.J. Dannenberg. 2003. Cyclooxygenase-2: a target for the prevention and treatment of cancers of the upper digestive tract. Progress in Experimental Tumor Research 37: 107–23.

    Article  CAS  PubMed  Google Scholar 

  40. Solomon, S.D., J.J. McMurray, M.A. Pfeffer, J. Wittes, R. Fowler, P. Finn, W.F. Anderson, A. Zauber, E. Hawk, and M. Bertagnolli. 2005. Cardiovascular risk associated with celecoxib in a clinical trial for colorectal adenoma prevention. New England Journal of Medicine 352: 1071–80.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

The authors thank the Deputy of Research Affairs of Kerman University of Medical Sciences for funding this project.

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Correspondence to M. Saravani.

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Mohammadi, A., Yaghoobi, M., Gholamhoseinian Najar, A. et al. HSP90 Inhibition Suppresses PGE2 Production via Modulating COX-2 and 15-PGDH Expression in HT-29 Colorectal Cancer Cells. Inflammation 39, 1116–1123 (2016). https://doi.org/10.1007/s10753-016-0343-1

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