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The Influence of Methylated Septin 9 Gene on RNA and Protein Level in Colorectal Cancer

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Pathology & Oncology Research

Abstract

Colorectal cancer is one of the leading death causes in the world. Specificity and sensitivity of the present screening methods are unsuitable and their compliance is too low. Nowadays the most effective method is the colonoscopy, because it gives not only macroscopic diagnosis but therapeutic possibility as well, however the compliance of the patients is very low. Hence development of new diagnostic methods is needed. Altered expression of septin 9 was found in several tumor types including colorectal cancer. The aim of this study was to detect the methylation related mRNA and protein expression changes of septin 9 in colorectal adenoma-dysplasia-carcinoma sequence and to analyze its reversibility by demethylation treatment. Septin 9 protein expression showed significant difference between normal and colorectal cancer (CRC) samples (p < 0,001). According to biopsy microarray results, septin 9 mRNA expression decreased in the progression of colon neoplastic disease (p < 0,001). In laser microdissected epithelial cells, septin 9 significantly underexpressed in CRC compared to healthy controls (p < 0,001). The expression of septin9_v1 region was higher in the healthy samples, while septin9_v2, v4, v4*, v5 overexpression were detected in cancer epithelial cells compared to normal. The septin 9 mRNA and protein levels of HT29 cells increased after demethylation treatment. The increasing methylation of septin 9 gene during colorectal adenoma-dysplasia-carcinoma sequence progression is reflected in the decreasing mRNA and protein expression, especially in the epithelium. These changes can be reversed by demethylation agents converting this screening marker gene into therapeutic target.

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References

  1. Boyle P, Ferlay J (2005) Cancer incidence and mortality in Europe, 2004. Ann Oncol 16:481–488

    Article  PubMed  CAS  Google Scholar 

  2. Jemal A, Murray T, Ward E et al (2005) Cancer statistics, 2005. CA Cancer J Clin 55:10–30

    Article  PubMed  Google Scholar 

  3. Ebert MP, Model F, Mooney S et al (2006) Aristaless-like homeobox-4 gene methylation is a potential marker for colorectal adenocarcinomas. Gastroenterology 131:1418–1430

    Article  PubMed  CAS  Google Scholar 

  4. Lofton-Day C, Model F, Devos T et al (2008) DNA methylation biomarkers for blood-based colorectal cancer screening. Clin Chem 54:414–423

    Article  PubMed  CAS  Google Scholar 

  5. Grützmann R, Molnar B, Pilarsky C et al (2008) Sensitive detection of colorectal cancer in peripheral blood by septin 9 DNA methylation assay. PLoS ONE 3:e3759

    Article  PubMed  Google Scholar 

  6. Devos T, Tetzner R, Model F et al (2009) Circulating methylated SEPT9 DNA in plasma is a biomarker for colorectal cancer. Clin Chem 55:1337–1346

    Article  PubMed  CAS  Google Scholar 

  7. Scott M, Hyland PL, McGregor G et al (2005) Multimodality expression profiling shows SEPT9 to be overexpressed in a wide range of human tumours. Oncogene 24:4588–4700

    Article  Google Scholar 

  8. Galamb O, Györffy B, Sipos F (2008) Inflammation, adenoma and cancer: objective classification of colon biopsy specimens with gene expression signature. Dis Markers 25:1–16

    PubMed  CAS  Google Scholar 

  9. Hall PA, Russell SE (2004) The pathobiology of the septin gene family. J Pathol 204:489–505

    Article  PubMed  CAS  Google Scholar 

  10. Russell SE, McIlhatton MA, Burrows JF (2000) Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors. Cancer Res 60:4729–4734

    PubMed  CAS  Google Scholar 

  11. Kalikin LM, Sims HL, Petty EM (2000) Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors. Genomics 63:165–172

    Article  PubMed  CAS  Google Scholar 

  12. Burrows JF, Chanduloy S, McIlhatton MA et al (2003) Altered expression of the septin gene, SEPT9, in ovarian neoplasia. J Pathol 201:581–588

    Article  PubMed  CAS  Google Scholar 

  13. Montagna C, Lyu MS, Hunter K et al (2003) The Septin 9 (MSF) gene is amplified and overexpressed in mouse mammary gland adenocarcinomas and human breast cancer cell lines. Cancer Res 63:2179–2187

    PubMed  CAS  Google Scholar 

  14. Tatsumi K, Taki T, Taniwaki M et al (2001) The CDCREL1 gene fused to MLL in de novo acute myeloid leukemia with t(11;22)(q23;q11.2) and its frequent expression in myeloid leukemia cell lines. Genes Chromosom Cancer 30:230–235

    Article  PubMed  CAS  Google Scholar 

  15. Kim HJ, Ki CS, Park Q et al (2003) MLL/SEPTIN6 chimeric transcript from invins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature. Genes Chromosom Cancer 38:8–12

    Article  PubMed  CAS  Google Scholar 

  16. Kojima K, Sakai I, Hasegawa A et al (2004) FLJ10849, a septin family gene, fuses MLL in a novel leukemia cell line CNLBC1 derived from chronic neutrophilic leukemia in transformation with t(4;11)(q21;q23). Leukemia 18:998–1005

    Article  PubMed  CAS  Google Scholar 

  17. Tanaka M, Tanaka T, Matsuzaki S et al (2003) Rapid and quantitative detection of human septin family Bradeion as a practical diagnostic method of colorectal and urologic cancers. Med Sci Monit 9:61–68

    Google Scholar 

  18. Kim DS, Hubbard SL, Peraud A et al (2004) Analysis of mammalian septin expression in human malignant brain tumors. Neoplasia 6:168–178

    Article  PubMed  CAS  Google Scholar 

  19. Model F, Osborn N, Ahlquist D et al (2007) Identification and validation of colorectal neoplasia-specific methylation markers for accurate classification of disease. Mol Cancer Res 5:153–163

    Article  PubMed  CAS  Google Scholar 

  20. Tóth K, Galamb O, Spisák S et al (2009) Free circulating DNA based colorectal cancer screening from peripheral blood: the possibility of the methylated septin 9 gene marker. Orv Hetil 150:969–977

    Article  PubMed  Google Scholar 

  21. Scott M, McCluggage WG, Hillan KJ et al (2006) Altered patterns of transcription of the septin 9 gene, SEPT9, in ovarian tumorigenesis. Int J Cancer 118:1325–1329

    Article  PubMed  CAS  Google Scholar 

  22. Montagna C, Lyu MS, Hunter K (2003) The Septin 9 (MSF) gene is amplified and overexpressed in mouse mammary gland adenocarcinomas and human breast cancer cell lines. Cancer Res 63:2179–2187

    PubMed  CAS  Google Scholar 

  23. Gonzalez ME, Peterson EA, Privette LM (2007) High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes. Cancer Res 67:8554–8564

    Article  PubMed  CAS  Google Scholar 

  24. Liu ZJ, Wang G, Cai Y (2009) Androgen receptor CpG island methylation status in human leukemia cancer cells. Cancer Investig 27:156–162

    Article  CAS  Google Scholar 

  25. Yap OW, Bhat G, Liu L et al (2009) Epigenetic modifications of the Estrogen receptor beta gene in epithelial ovarian cancer cells. Anticancer Res 29:139–144

    PubMed  CAS  Google Scholar 

  26. Deng G, Kakar S, Okudiara K et al (2009) Unique methylation pattern of oncostatin m receptor gene in cancers of colorectum and other digestive organs. Clin Cancer Res 15:1519–1526

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Kinga Tóth.

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Tóth, K., Galamb, O., Spisák, S. et al. The Influence of Methylated Septin 9 Gene on RNA and Protein Level in Colorectal Cancer. Pathol. Oncol. Res. 17, 503–509 (2011). https://doi.org/10.1007/s12253-010-9338-7

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  • DOI: https://doi.org/10.1007/s12253-010-9338-7

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