Skip to main content

Advertisement

Log in

Significant alterations in the expression pattern of kallikrein-related peptidase genes KLK4, KLK5 and KLK14 after treatment of breast cancer cells with the chemotherapeutic agents epirubicin, docetaxel and methotrexate

  • Research Article
  • Published:
Tumor Biology

Abstract

Given that 1.3 million new cases of breast cancer are universally registered among women and approximately 36 % of the patients die annually, the revelation of new predictive markers for treatment efficiency is of vital importance. Recently, our group has depicted that KLK4, KLK5, and KLK14 are differentially expressed in breast carcinoma. The objective of this study was to determine and investigate the expression pattern of the KLK4, KLK5, and KLK14 genes in breast cancer cells after treatment with established chemotherapeutic agents. We evaluated these genes’ expression after treatment of the BT-20 cells with epirubicin, docetaxel and methotrexate, determining their cytotoxic effect by MTT and trypan blue assays. The relative quantification of genes’ mRNA levels was performed by using the SYBR Green® chemistry, and the HPRT1 served as an endogenous control gene. The drugs triggered apoptosis in treated cells and induced deregulations in the expression of the above KLKs. The most significant alterations were a 12-fold and tenfold increase of KLK5 in docetaxel and methotrexate-treated cells, respectively, while the KLK4 levels decreased by ten-fold in epirubicin, five-fold in docetaxel and twenty-fold in methotrexate treated-cells, compared to the untreated ones. In the case of KLK14 levels, a twofold increase in epirubicin and threefold decrease in methotrexate-treated cells were observed. Present significant alterations in the expression pattern of KLK4, KLK5, and KLK14 could comprise an initial stage for predicting chemotherapy response in breast cancer and should be further investigated as predictive markers in the future.

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. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61:69–90.

    Article  PubMed  Google Scholar 

  2. Kaufmann M, von Minckwitz G, Bear HD, Buzdar A, McGale P, Bonnefoi H, Colleoni M, Denkert C, Eiermann W, Jackesz R, Makris A, Miller W, Pierga JY, Semiglazov V, Schneeweiss A, Souchon R, Stearns V, Untch M, Loibl S. Recommendations from an international expert panel on the use of neoadjuvant (primary) systemic treatment of operable breast cancer: New perspectives 2006. Ann Oncol. 2007;18:1927–34.

    Article  PubMed  CAS  Google Scholar 

  3. Lari SA, Kuerer HM. Biological markers in dcis and risk of breast recurrence: a systematic review. J Cancer. 2011;2:232–61.

    Article  PubMed  Google Scholar 

  4. Potti A, Dressman HK, Bild A, Riedel RF, Chan G, Sayer R, Cragun J, Cottrill H, Kelley MJ, Petersen R, Harpole D, Marks J, Berchuck A, Ginsburg GS, Febbo P, Lancaster J, Nevins JR. Genomic signatures to guide the use of chemotherapeutics. Nat Med. 2006;12:1294–300.

    Article  PubMed  CAS  Google Scholar 

  5. Thomadaki H, Scorilas A. Molecular profile of breast versus ovarian cancer cells in response to treatment with the anticancer drugs cisplatin, carboplatin, doxorubicin, etoposide and taxol. Biol Chem. 2008;389:1427–34.

    Article  PubMed  CAS  Google Scholar 

  6. Yousef GM, Chang A, Scorilas A, Diamandis EP. Genomic organization of the human kallikrein gene family on chromosome 19q13.3-q13.4. Biochem Biophys Res Commun. 2000;276:125–33.

    Article  PubMed  CAS  Google Scholar 

  7. Paliouras M, Borgono C, Diamandis EP. Human tissue kallikreins: the cancer biomarker family. Cancer Lett. 2007;249:61–79.

    Article  PubMed  CAS  Google Scholar 

  8. Lundwall A, Brattsand M. Kallikrein-related peptidases. Cell Mol Life Sci. 2008;65:2019–38.

    Article  PubMed  CAS  Google Scholar 

  9. Sotiropoulou G, Pampalakis G, Diamandis EP. Functional roles of human kallikrein-related peptidases. J Biol Chem. 2009;284:32989–94.

    Article  PubMed  CAS  Google Scholar 

  10. Borgono CA, Michael IP, Diamandis EP. Human tissue kallikreins: physiologic roles and applications in cancer. Mol Cancer Res. 2004;2:257–80.

    PubMed  CAS  Google Scholar 

  11. Obiezu CV, Diamandis EP. Human tissue kallikrein gene family: applications in cancer. Cancer Lett. 2005;224:1–22.

    Article  PubMed  CAS  Google Scholar 

  12. Emami N, Diamandis EP. Utility of kallikrein-related peptidases (KLKs) as cancer biomarkers. Clin Chem. 2008;54:1600–7.

    Article  PubMed  CAS  Google Scholar 

  13. Schmitt M, Magdolen V. Using kallikrein-related peptidases (KLK) as novel cancer biomarkers. Thromb Haemost. 2009;101:222–4.

    PubMed  CAS  Google Scholar 

  14. Kontos CK, Scorilas A. Kallikrein-related peptidases (KLKs): a gene family of novel cancer biomarkers. Clin Chem Lab Med. 2012. doi:10.1515/cclm-2012-0247.

  15. Papachristopoulou G, Avgeris M, Scorilas A. Expression analysis and study of KLK4 in benign and malignant breast tumours. Thromb Haemost. 2009;101:381–7.

    PubMed  CAS  Google Scholar 

  16. Avgeris M, Papachristopoulou G, Polychronis A, Scorilas A. Down-regulation of kallikrein-related peptidase 5 (KLK5) expression in breast cancer patients: a biomarker for the differential diagnosis of breast lesions. Clin Proteomics. 2011;8:5.

    Article  PubMed  CAS  Google Scholar 

  17. Papachristopoulou G, Avgeris M, Charlaftis A, Scorilas A. Quantitative expression analysis and study of the novel human kallikrein-related peptidase 14 gene (KLK14) in malignant and benign breast tissues. Thromb Haemost. 2011;105:131–7.

    Article  PubMed  CAS  Google Scholar 

  18. Magklara A, Brown TJ, Diamandis EP. Characterization of androgen receptor and nuclear receptor co-regulator expression in human breast cancer cell lines exhibiting differential regulation of kallikreins 2 and 3. Int J Cancer J Int Du Cancer. 2002;100:507–14.

    Article  CAS  Google Scholar 

  19. Hernandez-Vargas H, Palacios J, Moreno-Bueno G. Telling cells how to die: docetaxel therapy in cancer cell lines. Cell Cycle. 2007;6:780–3.

    Article  PubMed  CAS  Google Scholar 

  20. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65:55–63.

    Article  PubMed  CAS  Google Scholar 

  21. Jain PT, Pento JT, Graves DC. Cell-growth quantitation methods for the evaluation of antiestrogens in human breast cancer cells in culture. J Pharmacol Toxicol Methods. 1992;27:203–7.

    Article  PubMed  CAS  Google Scholar 

  22. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(−delta delta c(t)) method. Methods. 2001;25:402–8.

    Article  PubMed  CAS  Google Scholar 

  23. Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative C(t) method. Nat Protoc. 2008;3:1101–8.

    Article  PubMed  CAS  Google Scholar 

  24. Morales S, Lorenzo A, Ramos M, Ballesteros P, Mendez M, Almanza C, Castellanos J, Moreno-Nogueira JA, Casal J, Lizon J, Oltra A, Frau A, Machengs I, Galan A, Belon J, Llorca C. Docetaxel plus epirubicin is a highly active, well-tolerated, first-line chemotherapy for metastatic breast cancer: results of a large, multicentre phase ii study. Cancer Chemother Pharmacol. 2004;53:75–81.

    PubMed  CAS  Google Scholar 

  25. Hainsworth JD, Yardley DA, Spigel DR, Meluch AA, Rinaldi D, Schnell FM, Greco FA. Docetaxel and epirubicin as first-line treatment for patients with metastatic breast cancer: A Minnie Pearl Cancer Research Network Phase II Trial. Cancer Invest. 2006;24:469–73.

    Article  PubMed  CAS  Google Scholar 

  26. Bonadonna G, Valagussa P, Moliterni A, Zambetti M, Brambilla C. Adjuvant cyclophosphamide, methotrexate, and fluorouracil in node-positive breast cancer: the results of 20 years of follow-up. N Engl J Med. 1995;332:901–6.

    Article  PubMed  CAS  Google Scholar 

  27. Emami N, Diamandis EP. New insights into the functional mechanisms and clinical applications of the kallikrein-related peptidase family. Mol Oncol. 2007;1:269–87.

    Article  PubMed  Google Scholar 

  28. Mavridis K, Scorilas A. Prognostic value and biological role of the kallikrein-related peptidases in human malignancies. Future Oncol. 2010;6:269–85.

    Article  PubMed  CAS  Google Scholar 

  29. Borgono CA, Diamandis EP. The emerging roles of human tissue kallikreins in cancer. Nat Rev Cancer. 2004;4:876–90.

    Article  PubMed  CAS  Google Scholar 

  30. Floros KV, Thomadaki H, Katsaros N, Talieri M, Scorilas A. mRNA expression analysis of a variety of apoptosis-related genes, including the novel gene of the bcl2-family, bcl2l12, in hl-60 leukemia cells after treatment with carboplatin and doxorubicin. Biol Chem. 2004;385:1099–103.

    Article  PubMed  CAS  Google Scholar 

  31. Thomadaki H, Scorilas A. Breast cancer cells response to the antineoplastic agents cisplatin, carboplatin, and doxorubicin at the mrna expression levels of distinct apoptosis-related genes, including the new member, bcl2l12. Ann N Y Acad Sci. 2007;1095:35–44.

    Article  PubMed  CAS  Google Scholar 

  32. Thomadaki H, Mavridis K, Talieri M, Scorilas A. Treatment of pc3 prostate cancer cells with mitoxantrone, etoposide, doxorubicin and carboplatin induces distinct alterations in the expression of kallikreins 5 and 11. Thromb Haemost. 2009;101:373–80.

    PubMed  CAS  Google Scholar 

  33. Mavridis K, Talieri M, Scorilas A. KLK5 gene expression is severely upregulated in androgen-independent prostate cancer cells after treatment with the chemotherapeutic agents docetaxel and mitoxantrone. Biol Chem. 2010;391:467–74.

    Article  PubMed  CAS  Google Scholar 

  34. Talieri M, Devetzi M, Scorilas A, Prezas P, Ardavanis A, Apostolaki A, Karameris A. Evaluation of kallikrein-related peptidase 5 expression and its significance for breast cancer patients: association with kallikrein-related peptidase 7 expression. Anticancer Res. 2011;31:3093–100.

    PubMed  CAS  Google Scholar 

  35. Yousef GM, Scorilas A, Kyriakopoulou LG, Rendl L, Diamandis M, Ponzone R, Biglia N, Giai M, Roagna R, Sismondi P, Diamandis EP. Human kallikrein gene 5 (KLK5) expression by quantitative PCR: an independent indicator of poor prognosis in breast cancer. Clin Chem. 2002;48:1241–50.

    PubMed  CAS  Google Scholar 

  36. Yousef GM, White NM, Kurlender L, Michael I, Memari N, Robb JD, Katsaros D, Stephan C, Jung K, Diamandis EP. The kallikrein gene 5 splice variant 2 is a new biomarker for breast and ovarian cancer. Tumour Biol: J Int Soc Oncodevelopmental Biol Med. 2004;25:221–7.

    Article  CAS  Google Scholar 

  37. Tsume Y, Amidon GL. The feasibility of enzyme targeted activation for amino acid/dipeptide monoester prodrugs of floxuridine; cathepsin d as a potential targeted enzyme. Molecules. 2012;17:3672–89.

    Article  PubMed  CAS  Google Scholar 

  38. Tsume Y, Hilfinger JM, Amidon GL. Enhanced cancer cell growth inhibition by dipeptide prodrugs of floxuridine: increased transporter affinity and metabolic stability. Mol Pharm. 2008;5:717–27.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by a research grant from Empirikion Foundation, Athens, Greece as well as by the Hellenic Society of Medical Oncology.

Conflicts of interest

None

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Andreas Scorilas.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Papachristopoulou, G., Talieri, M. & Scorilas, A. Significant alterations in the expression pattern of kallikrein-related peptidase genes KLK4, KLK5 and KLK14 after treatment of breast cancer cells with the chemotherapeutic agents epirubicin, docetaxel and methotrexate. Tumor Biol. 34, 369–378 (2013). https://doi.org/10.1007/s13277-012-0558-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13277-012-0558-1

Keywords

Navigation