Skip to main content

Advertisement

Log in

EphA2 Up-regulation induced by deoxycholic acid in human colon carcinoma cells, an involvement of extracellular signal-regulated kinase and p53-independence

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

Abstract

Purpose

The EphA2 receptor protein tyrosine kinase gene has been shown to be over-expressed or functionally altered in a number of human tumors, including colon cancer, but little is known about the regulation of this new oncoprotein. In order to explore the mechanism of EphA2 up-regulation in cancer cells, we examined the change of expression of EphA2 gene induced by deoxycholic acid (DCA) and elucidated its possible pathways in human colon cancer cells.

Methods

Western blot and RT-PCR were used to assess the protein expression and messenger RNA in several colon cancer cell lines, which harbor various p53 status. The inhibition study to interfere the MAPK pathway was performed by using various chemicals and by transfecting dominant negative mutant plasmids.

Results

Up-regulation of EphA2 induced by DCA was observed in a dose- and time-dependent fashion both in mRNA and protein levels. This regulation is constant regardless of p53 status including wild, mutant or knocked out in the colon cell lines used. This induction was in part blocked by either erk1/2 inhibitors or dominant negative mutants erk1/2 plasmids.

Conclusions

These results suggest that DCA induced up-regulation of EphA2 in colon cancer cells is due to activation of erk1/2 cascade, and is p53-independent. Taken together with the roles of EphA2 and DCA in tumorigenesis, which have been independently reported, our observation will provide a new mechanistic basis of DCA commitment in carcinogenesis.

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.

Fig. 1A–C
Fig. 2
Fig. 3A,B
Fig. 4A,B
Fig. 5

Similar content being viewed by others

References

  • Adachi M, Fukuda M, Nishida E (1999) Two co-existing mechanisms for nuclear import of MAP kinase: passive diffusion of a monomer and active transport of a dimer. Embo J 18:5347−5358

    Article  CAS  PubMed  Google Scholar 

  • Bunz F, Dutriaux A, Lengauer C, Waldman T, Zhou S, Brown JP, Sedivy JM, Kinzler KW, Vogelstein B (1998) Requirement for p53 and p21 to sustain G2 arrest after DNA damage. Science 282:1497−1501

    Article  CAS  PubMed  Google Scholar 

  • Cheng N, Brantley DM, Chen J (2002) The ephrins and Eph receptors in angiogenesis. Cytokine Growth Factor Rev 13:75−85

    Article  CAS  PubMed  Google Scholar 

  • Crowley-Weber CL, Payne CM, Gleason-Guzman M, Watts GS, Futscher B, Waltmire CN, Crowley C, Dvorakova K, Bernstein C, Craven M, Garewal H, Bernstein H (2002) Development and molecular characterization of HCT-116 cell lines resistant to the tumor promoter and multiple stress-inducer, deoxycholate. Carcinogenesis 23:2063−2080

    Article  CAS  PubMed  Google Scholar 

  • Debruyne PR, Bruyneel EA, Li X, Zimber A, Gespach C, Mareel MM (2001) The role of bile acids in carcinogenesis. Mutat Res 480/481:359−369

  • Dobashi Y, Sugimura H, Sakamoto A, Mernyei M, Mori M, Oyama T, Machinami R (1994) Stepwise participation of p53 gene mutation during dedifferentiation of human thyroid carcinomas Diagn. Mol Pathol 3:9−14

    CAS  Google Scholar 

  • Dohn M, Jiang J, Chen X (2001) Receptor tyrosine kinase EphA2 is regulated by p53-family proteins and induces apoptosis. Oncogene 20:6503−6515

    Article  CAS  PubMed  Google Scholar 

  • Holder N, Klein R (1999) Eph receptors and ephrins: effectors of morphogenesis. Development 126:2033−2044

    CAS  PubMed  Google Scholar 

  • Lechner S, Muller-Ladner U, Schlottmann K, Jung B, McClelland M, Ruschoff J, Welsh J, Scholmerich J, Kullmann F (2002) Bile acids mimic oxidative stress induced upregulation of thioredoxin reductase in colon cancer cell lines. Carcinogenesis 23:1281−1288

    Article  CAS  PubMed  Google Scholar 

  • Li Z, Wang Y, Song J, Kataoka H, Yoshii S, Gao C, Zhou J, Ota S, Tanaka M, Sugimura H (2002) Genomic structure of the human beta-PIX gene and its alteration in gastric cancer. Cancer Lett 177:203−208

    Article  CAS  PubMed  Google Scholar 

  • Liu W, Ahmad SA, Jung YD, Reinmuth N, Fan F, Bucana CD, Ellis LM (2002) Coexpression of ephrin-Bs and their receptors in colon carcinoma. Cancer 94:934–939

    Article  CAS  PubMed  Google Scholar 

  • Martinez JD, Stratagoules ED, LaRue JM, Powell AA, Gause PR, Craven MT, Payne CM, Powell MB, Gerner EW, Earnest DL (1998) Different bile acids exhibit distinct biological effects: the tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation. Nutr Cancer 31:111–118

    CAS  PubMed  Google Scholar 

  • Qiao D, Stratagouleas ED, Martinez JD (2001a) Activation and role of mitogen-activated protein kinases in deoxycholic acid-induced apoptosis. Carcinogenesis 22:35–41

    Article  CAS  PubMed  Google Scholar 

  • Qiao L, Studer E, Leach K, McKinstry R, Gupta S, Decker R, Kukreja R, Valerie K, Nagarkatti P, El Deiry W, Molkentin J, Schmidt-Ullrich R, Fisher PB, Grant S, Hylemon PB, Dent P (2001b) Deoxycholic acid (DCA) causes ligand-independent activation of epidermal growth factor receptor (EGFR) and FAS receptor in primary hepatocytes: inhibition of EGFR/mitogen-activated protein kinase- signaling module enhances DCA-induced apoptosis. Mol Biol Cell 12:2629–2645

    CAS  PubMed  Google Scholar 

  • Robbins DJ, Zhen E, Owaki H, Vanderbilt CA, Ebert D, Geppert TD, Cobb MH (1993) Regulation and properties of extracellular signal-regulated protein kinases 1 and 2 in vitro. J Biol Chem 268:5097–5106

    CAS  PubMed  Google Scholar 

  • Robinson MJ, Harkins PC, Zhang J, Baer R, Haycock JW, Cobb MH, Goldsmith EJ (1996) Mutation of position 52 in ERK2 creates a nonproductive binding mode for adenosine 5′-triphosphate. Biochemistry 35:5641–5646

    Article  CAS  PubMed  Google Scholar 

  • Stephenson SA, Slomka S, Douglas EL, Hewett PJ, Hardingham JE (2001) Receptor protein tyrosine kinase EphB4 is up-regulated in colon cancer. BMC Mol Biol 2:15

    Article  CAS  PubMed  Google Scholar 

  • Walker-Daniels J, Riese DJ 2nd , Kinch MS (2002) c-Cbl-dependent EphA2 protein degradation is induced by ligand binding. Mol Cancer Res 1:79–87

    CAS  PubMed  Google Scholar 

  • Walker-Daniels J, Hess AR, Hendrix MJ, Kinch MS (2003) Differential regulation of EphA2 in normal and malignant cells. Am J Pathol 162:1037–1042

    CAS  PubMed  Google Scholar 

  • Wang Y, Ota S, Kataoka H, Kanamori M, Li Z, Band H, Tanaka M, Sugimura H (2002) Negative regulation of EphA2 receptor by Cbl. Biochem Biophys Res Commun 296:214–220

    Article  CAS  PubMed  Google Scholar 

  • Yoon JH, Higuchi H, Werneburg NW, Kaufmann SH, Gores GJ (2002) Bile acids induce cyclooxygenase-2 expression via the epidermal growth factor receptor in a human cholangiocarcinoma cell line. Gastroenterology 122:985–993

    CAS  PubMed  Google Scholar 

  • Zelinski DP, Zantek ND, Stewart JC, Irizarry AR, Kinch MS (2001) EphA2 overexpression causes tumorigenesis of mammary epithelial cells. Cancer Res 61:2301–2306

    CAS  PubMed  Google Scholar 

  • Zelinski DP, Zantek ND, Walker-Daniels J, Peters MA, Taparowsky EJ, Kinch MS (2002) Estrogen and Myc negatively regulate expression of the EphA2 tyrosine kinase. J Cell Biochem 85:714–720

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We would like to thank Vogelstein B. for kindly providing HCT116 p53−/− and p53+/+ cell lines, Cobb M.H., Nishida E., and Matsuda M. for kindly providing MAPK plasmids, and Wang Y.J. for technical assistance. This work was supported by grants-in-aid from the Ministry of Education, Culture, Science, Sports, and Technology of Japan (to H.S.), and the Ministry of Health, Labour, and Welfare of Japan (H.S. and M.T.), and the Smoking Research Foundation (to H.S).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Haruhiko Sugimura.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, Z., Tanaka, M., Kataoka, H. et al. EphA2 Up-regulation induced by deoxycholic acid in human colon carcinoma cells, an involvement of extracellular signal-regulated kinase and p53-independence. J Cancer Res Clin Oncol 129, 703–708 (2003). https://doi.org/10.1007/s00432-003-0493-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00432-003-0493-z

Keywords

Navigation