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Lack of Relationships between FGF19 Staining Pattern, Lymph Node Metastasis and Locally Invasive Characteristics of the Tumor in Colorectal Cancers

  • Unal, Hakan Umit (Gastroenterology Department, Baskent University Faculty of Medicine) ;
  • Demiralay, Ebru (Pathology Department, Baskent University Faculty of Medicine) ;
  • Tepeoglu, Merih (Pathology Department, Baskent University Faculty of Medicine) ;
  • Fidan, Cihan (Family Medicine, Baskent University Faculty of Medicine) ;
  • Kilickap, Saadettin (Preventive Oncology, Hacettepe University Cancer Institute)
  • Published : 2013.05.30

Abstract

Introduction: Colorectal cancers are in the top of the cancer-related causes of death in the world and lymph node metastasis is accepted as the primary prognostic factor. In this study, correlations of FGF19 staining pattern with local invasion and lymph node metastasis in a series of colorectal cancers were investigated. Methods: This studyincluded 81 colorectal cancer patients who underwent surgery in our hospital with no evidence of preoperative radiological distant metastasis. Routine pathological examination of the resection material was performed in order to identify vascular, perineural and serosal infiltration, regional lymph node metastasis and the degree of differentiation. Tumor tissue samples were stained with an immunohistochemistry method for FGF 19 evaluation and the staining pattern was statistically compared with the above mentioned characteristics of the tumors. Results: The patient population consisted of 47 females and 34 males with a median age of 70 years. In 40 patients regional lymph nodes were positive and 51%, 32% and 38% had serosal, perineural and vascular invasion. While 64 cases were moderately-differentiated, 11 cases were well-differentiated and 6 poorlydifferentiated, there was no association with FGF 19 staining, including intensity. Conclusion: No evidence of significant statistically correlation was found between FGF 19 staining pattern and serosal, perineural, vascular invasion, lymph node involvement and degree of differentiation.

Keywords

References

  1. Ainsworth PD, Johnson MA (2010). The prognostic significance of the metastatic lymph node ratio in Dukes stage C colorectal cancer in a district general hospital. Colorectal Dis, 12, 1219-22. https://doi.org/10.1111/j.1463-1318.2009.02026.x
  2. Compton C, Fenoglio-Preiser CM, Pettigrew N, Fielding LP (2000). American joint committee on cancer prognostic factors consensus conference: colorectal working group. Cancer, 88, 1739-57. https://doi.org/10.1002/(SICI)1097-0142(20000401)88:7<1739::AID-CNCR30>3.0.CO;2-T
  3. Desnoyers LR, Pai R, Ferrando RE, et al (2008). Targeting FGF19 inhibits tumor growth in colon cancer xenograft and FGF19 transgenic hepatocellular carcinoma models. Oncogene, 27, 85-97. https://doi.org/10.1038/sj.onc.1210623
  4. Engstrom W, Granerus M (2006). Effects of fibroblast growth factors 19 and 20 on cell multiplication and locomotion in a human embryonal carcinoma cell line (Tera-2) in vitro. Anticancer Res, 26, 3307-10.
  5. Feng S, Dakhova O, Creighton CJ, Ittmann M (2013). Endocrine Fibroblast Growth Factor FGF19 Promotes Prostate Cancer Progression. Cancer Res, 73, 2551-62. https://doi.org/10.1158/0008-5472.CAN-12-4108
  6. French DM, Lin BC, Wang M, et al (2012). Targeting FGFR4 inhibits hepatocellular carcinoma in preclinical mouse models. PLoS One, 7, 36713. https://doi.org/10.1371/journal.pone.0036713
  7. Gout S, Huot J (2008). Role of cancer microenvironment in metastasis: focus on colon cancer. Cancer Microenviron. 1, 69-83. https://doi.org/10.1007/s12307-008-0007-2
  8. Hyeon J, Ahn S, Lee JJ, Song DH, Park CK (2013). Expression of Fibroblast Growth Factor 19 Is Associated with Recurrence and Poor Prognosis of Hepatocellular Carcinoma. Dig Dis Sci, [Epub ahead of print].
  9. Jemal A, Bray F, Center MM, et al (2011). Global cancer statistics. CA Cancer J Clin, 61, 69-90. https://doi.org/10.3322/caac.20107
  10. Johnson PM, Porter GA, Ricciardi R, Baxter NN (2006). Increasing negative lymph node count is independently associated with improved long-term survival in stage IIIB and IIIC colon cancer. J Clin Oncol, 24, 3570-5. https://doi.org/10.1200/JCO.2006.06.8866
  11. Karamitopoulou E, Zlobec I, Patsouris E, Peros G, Lugli A (2011). Loss of E-cadherin independently predicts the lymph node status in colorectal cancer. Pathology, 43, 133-7. https://doi.org/10.1097/PAT.0b013e3283425b7f
  12. Katoh M (2006). Cross-talk of WNT and FGF signaling pathways at GSK3beta to regulate beta-catenin and SNAIL signaling cascades. Cancer Biol Ther, 5, 1059-64. https://doi.org/10.4161/cbt.5.9.3151
  13. Lin BC, Desnoyers LR (2012). FGF19 and cancer. Adv Exp Med Biol, 728, 183-94. https://doi.org/10.1007/978-1-4614-0887-1_12
  14. Miyake A, Nakayama Y, Konishi M, Itoh N (2005). Fgf19 regulated by Hh signaling is required for zebrafish forebrain development. Dev Biol, 288, 259-75. https://doi.org/10.1016/j.ydbio.2005.09.042
  15. Nicholes K, Guillet S, Tomlinson E, et al (2002). A mouse model of hepatocellular carcinoma: ectopic expression of fibroblast growth factor 19 in skeletal muscle of transgenic mice. Am J Pathol, 160, 2295-307. https://doi.org/10.1016/S0002-9440(10)61177-7
  16. Ornitz DM (2005). FGF signaling in the developing endochondral skeleton. Cytokine Growth Factor Rev, 16, 205-13. https://doi.org/10.1016/j.cytogfr.2005.02.003
  17. Pai R, Dunlap D, Qing J, et al (2008). Inhibition of fibroblast growth factor 19 reduces tumor growth by modulating betacatenin signaling. Cancer Res, 68, 5086-95. https://doi.org/10.1158/0008-5472.CAN-07-2325
  18. Quirke P, Williams GT, Ectors N, et al (2007). The future of the TNM staging system in colorectal cancer: time for a debate? Lancet Oncol, 8, 651-7. https://doi.org/10.1016/S1470-2045(07)70205-X
  19. Rosenberg R, Friederichs J, Schuster T, et al (2008). Prognosis of patients with colorectal cancer is associated with lymph node ratio: a single-center analysis of 3,026 patients over a 25-year time period. Ann Surg, 248, 968-78. https://doi.org/10.1097/SLA.0b013e318190eddc
  20. Royston D, Jackson DG (2009). Mechanisms of lymphatic metastasis in human colorectal adenocarcinoma. J Pathol, 217, 608-19. https://doi.org/10.1002/path.2517
  21. Siffroi-Fernandez S, Felder-Schmittbuhl MP, Khanna H, Swaroop A, Hicks D (2008). FGF19 exhibits neuroprotective effects on adult mammalian photoreceptors in vitro. Invest Ophthalmol Vis Sci, 49, 1696-704. https://doi.org/10.1167/iovs.07-1272
  22. Wang J, Hassett JM, Dayton MT, Kulaylat MN (2008). Lymph node ratio: role in the staging of node-positive colon cancer. Ann Surg Oncol, 15, 1600-8. https://doi.org/10.1245/s10434-007-9716-x
  23. Wu X, Ge H, Lemon B, et al (2010). FGF19-induced hepatocyte proliferation is mediated through FGFR4 activation. J Biol Chem, 285, 5165-70. https://doi.org/10.1074/jbc.M109.068783
  24. Xie MH, Holcomb I, Deuel B, et al (1999). FGF-19, a novel fibroblast growth factor with unique specificity for FGFR4. Cytokine, 11, 729-35. https://doi.org/10.1006/cyto.1999.0485

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