Skip to main content
Log in

Expression of Src and FAK in Hepatocellular Carcinoma and the Effect of Src Inhibitors on Hepatocellular Carcinoma In Vitro

  • Original Article
  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

The expressions of c-Src and focal adhesion kinase (FAK) were studied in 65 Chinese patients with hepatocellular carcinoma (HCC) by immunohistochemistry using rabbit monoclonal antibodies. Expressions of total Src, an active form of Src, and FAK were found in 44/65 (67.7%), 36/45 (55.4%), and 33/56 (58.9%) HCC cases, respectively. There was a good correlation between the expression of total Src, active form of Src, and FAK in these HCC cases (P < 0.001). Expression of Src was not correlated to any clinical parameters, cancer cell phenotypic markers, and pathologic features apart from a positive correlation with alpha-fetoprotein (P < 0.01). The expression of FAK was correlated with earlier onset and the expression of Ki-67 but not proliferating cell nuclear antigen (PCNA) in these HCC cases. Four liver-cancer-derived cell lines (three derived from HCC and one from hepatoblastoma) were then tested with inhibitors against Src. A small molecule, KX2-391, designed to target the substrate binding pocket of Src, was found to have more broad-spectrum activity and better potency than Dasatinib, an adenosine triphosphate (ATP)-competitive inhibitor in vitro. Our data indicates that Src and FAK expression are both elevated and active in Chinese patients with HCC and that Src may play a key role in supporting HCC progression. Src antagonism with specific inhibitors may be an attractive treatment paradigm for patients with HCC.

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

Access this article

Subscribe and save

Springer+
from $39.99 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

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

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Rous P. Transmission of a malignant new growth by means of a cell-free filtrate. JAMA. 1983;250:1445–1449. doi:10.1001/jama.250.11.1445.

    Article  PubMed  CAS  Google Scholar 

  2. Stehelin D, Varmus HE, Bishop JM, Vogt PK. DNA related to the transforming gene(s) of avian sarcoma viruses is present in normal avian DNA. Nature. 1976;260:170–173. doi:10.1038/260170a0.

    Article  PubMed  CAS  Google Scholar 

  3. Czernilofsky AP, Levinson AD, Varmus HE, Bishop JM, Tischer E, Goodman HM. Nucleotide sequence of an avian sarcoma virus oncogene (src) and proposed amino acid sequence for gene product. Nature. 1980;287:198–203. doi:10.1038/287198a0.

    Article  PubMed  CAS  Google Scholar 

  4. Martin GS. The hunting of src. Natl Rev. 2001;2:467–473. doi:10.1038/35073094.

    Article  CAS  Google Scholar 

  5. Alper Ö, Bowden ET. Novel insights in c-Src. Curr Pharm Des. 2005;11:1119–1130. doi:10.2174/1381612053507576.

    Article  PubMed  CAS  Google Scholar 

  6. Frame MC. Newest findings on the oldest oncogene; how activated src does it. J Cell Sci. 2004;117:989–998. doi:10.1242/jcs.01111.

    Article  PubMed  CAS  Google Scholar 

  7. Summy JM, Gallick GE. Src family kinases in tumor progression and metastasis. Cancer Metastasis Rev. 2003;22:337–358. doi:10.1023/A:1023772912750.

    Article  PubMed  CAS  Google Scholar 

  8. Russello SV, Shore SK. Src in human carcinogenesis. Front Biosci. 2004;9:139–144.

    PubMed  CAS  Google Scholar 

  9. Weis S, Cui J, Barnes L, Cheresh D. Endothelial barrier disruption by VEGF-mediated src activity potentiates tumor cell extravasation and metastasis. J Cell Biol. 2004;167:223–229. doi:10.1083/jcb.200408130.

    Article  PubMed  CAS  Google Scholar 

  10. McLean GW, Carragher NO, Avizienyte E, Evans J, Brunton VG, Frame MC. The role of focal-adhesion kinase in cancer—a new therapeutic opportunity. Nat Rev Cancer. 2005;5:505–515. doi:10.1038/nrc1647.

    Article  PubMed  CAS  Google Scholar 

  11. Hanks SK, Polte TR. Signaling through focal adhesion kinase. Bioessays. 1997;19:137–145. doi:10.1002/bies.950190208.

    Article  PubMed  CAS  Google Scholar 

  12. Parsons JT. Focal adhesion kinase: the first 10 years. J Cell Sci. 2003;116:1409–1416. doi:10.1242/jcs.00373.

    Article  PubMed  CAS  Google Scholar 

  13. Han NM, Fleming RY, Curley SA, Gallick GE. Overexpression of focal adhesion kinase in human colorectal carcinoma liver metastases: independence from c-src or c-yes activation. Ann Surg Oncol. 1997;4:264–268. doi:10.1007/BF02306620.

    Article  PubMed  CAS  Google Scholar 

  14. Golubovskaya VM, Gross S, Kaur AS, et al. Simultaneous inhibition of focal adhesion kinase and src enhances detachment and apoptosis in colon cancer cell lines. Mol Cancer Res. 2003;1:755–764.

    PubMed  CAS  Google Scholar 

  15. WHO. Global cancer rates could increase by 50% to 15 million by 2020. http://www.who.int.mediacentre/news/releases/2003/pr27/en/print.html. Accessed 14 April 2008.

  16. El-Serag HB, Mason AC. Rising incidence of hepatocellular carcinoma in the United States. N Engl J Med. 1999;340:745–750. doi:10.1056/NEJM199903113401001.

    Article  PubMed  CAS  Google Scholar 

  17. Wu PC, Fang JWS, Lau VKT, Lai CL, Lo CK, Lau JYN. Classification of hepatocellular carcinoma according to hepatocellular and biliary differentiation markers. Am J Pathol. 1996;149:1167–1175.

    PubMed  CAS  Google Scholar 

  18. Kawakatsu H, Sakai T, Takagaki Y, et al. A new monoclonal antibody which selectively recognizes the active form of src tyrosine kinase. J Biol Chem. 1996;271:5680–5685. doi:10.1074/jbc.271.10.5680.

    Article  PubMed  CAS  Google Scholar 

  19. Okada M, Howell BW, Broome MA, Cooper JA. Deletion of the SH3 domain of src interferes with regulation by the phosphorylated carboxyl-terminal tyrosine. J Biol Chem. 1993;268:18070–18075.

    PubMed  CAS  Google Scholar 

  20. Tremblay L, Hauck W, Aprikian AG, Begin LR, Chapdelaine A, Chevalier A. Focal adhesion kinase (pp125FAK) expression, activation and association with paxillin and p50CSK in human metastatic prostate carcinoma. Int J Cancer. 1996;68:164–171. doi:10.1002/(SICI)1097-0215(19961009)68:2<169::AID-IJC4>3.0.CO;2-W.

  21. Bristol-Myers Squibb Company. Sprycel® package insert, Princeton, NJ. 2006. http://packageinserts.bms.com/pi/pi_sprycel.pdf. Accessed 15 April 2008.

  22. Hangauer Jr D. US Patent on KXO1: compositions for treating cell proliferation disorders. Patent No. 7,300,931 B2. 27 Nov 2007.

  23. Wu PC, Lau VKT, Fang JWS, Lai VC, Lai CL, Lau JYN. Imbalance between cell proliferation and cellular DNA fragmentation in hepatocellular carcinoma. Liver. 1999;19:444–451. doi:10.1111/j.1478-3231.1999.tb00076.x.

    Article  PubMed  CAS  Google Scholar 

  24. Masaki T, Okada M, Shiratori Y, et al. pp60c-src activation in hepatocellular carcinoma of humans and LEC rats. Hepatology. 1998;27:1257–1264. doi:10.1002/hep.510270511.

    Article  PubMed  CAS  Google Scholar 

  25. Ito Y, Kawakatsu H, Takeda T, et al. Activation of c-src gene product in hepatocellular carcinoma is highly correlated with the indices of early stage phenotype. J Hepatol. 2001;35:68–73. doi:10.1016/S0168-8278(01)00077-0.

    Article  PubMed  CAS  Google Scholar 

  26. Itoh S, Maeda T, Shimada M, et al. Role of expression of focal adhesion kinase in progression of hepatocellular carcinoma. Clin Cancer Res. 2004;10:2812–2817. doi:10.1158/1078-0432.CCR-1046-03.

    Article  PubMed  CAS  Google Scholar 

  27. Fujii T, Koshikawa K, Nomoto S, et al. Focal adhesion kinase is overexpressed in hepatocellular carcinoma and can serve as an independent prognostic factor. J Hepatol. 2004;41:104–111. doi:10.1016/j.jhep.2004.03.029.

    Article  PubMed  CAS  Google Scholar 

  28. Mitra SK, Schlaepfer DD. Integrin-regulated FAK-Src signaling in normal and cancer cells. Curr Opin Cell Biol. 2006;18:516–523. doi:10.1016/j.ceb.2006.08.011.

    Article  PubMed  CAS  Google Scholar 

  29. Owens LV, Xu L, Craven RJ, et al. Overexpression of the focal adhesion kinase (p125FAK) in invasive human tumors. Cancer Res. 1995;55:2752–2755.

    PubMed  CAS  Google Scholar 

  30. Park SS, Eom YW, Kim EH, et al. Involvement of c-Src kinase in the regulation of TGR-beta1-induced apoptosis. Oncogene. 2004;23(37):6272–6281. doi:10.1038/sj.onc.1207856.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We would like to thank Professor PC Wu, Dr. Vicky CH Lai, and Professor CL Lai for the supply of clinical materials; Mrs. Patti Tran and Dr. Michael Selsted for the use of their laboratory facilities; and Dr. Lyn Dyster, Dr. Allen Barnett, Dr. Johnson YN Lau, and Dr. Sum-Ping Lee for their critical reading of the manuscript and support of the project.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jane W. S. Fang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lau, G.M., Lau, G.M., Yu, GL. et al. Expression of Src and FAK in Hepatocellular Carcinoma and the Effect of Src Inhibitors on Hepatocellular Carcinoma In Vitro. Dig Dis Sci 54, 1465–1474 (2009). https://doi.org/10.1007/s10620-008-0519-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue date:

  • DOI: https://doi.org/10.1007/s10620-008-0519-0

Keywords