Abstract
Background/Aims
Early detection of polyp is important for the prevention of colorectal cancer (CRC). There have been few studies to investigate the relationship between colorectal adenoma and family history of CRC (FHCRC) in Korea. The aim of this study was to identify the relationship between colorectal adenoma and FHCRC.
Methods
Between March 2009 and September 2010, 225 patients with adenomatous polyps were included. Their medical records with clinical history and size, numbers, histology of polyps were reviewed. Immunohistochemical staining using Bcl-2, Bax, p-AKT, NF-κB, and β-catenin antibodies were performed. We compared the histology of adenoma and expression of immunohistochemical staining according to the existence of FHCRC.
Results
The incidence of colorectal adenoma increased in case of FHCRC (p=0.029). In patients with FHCRC, the mean age of patients was 49 years old and younger than patients without FHCRC. In addition in patients with FHCRC, the incidence of advanced adenoma was significantly higher than in patients without FHCRC (p=0.001). The expression of Bax was significantly lower in patients with FHCRC than without FHCRC (p=0.046).
Conclusions
There was a tendency for polyp to develop in their younger ages and to be more advanced adenomas in patients with FHCRC. The low expression of Bax, tumor suppressor gene, might be associated with the development of polyps in patient with FHCRC. Therefore, patients with FHCRC may be better to start screening colonoscopy earlier than patient without FHCRC.
References
1. Cancer facts and figures 2010 in the Republic of Korea. [Internet]. 2010. cited 2012.4.21. Goyang (Korea): National Cancer Center;Available from: www.cancer.go.kr/cms/data/edudata/__icsFiles/afieldfile/2010/07/21/cancer_fact_figures_2010_english.pdf.
2. Jackman RJ, Mayo CW. The adenoma-carcinoma sequence in cancer of the colon. Surg Gynecol Obstet. 1951. 93:327–330.
3. Bond JH. Practice Parameters Committee of the American College of Gastroenterology. Polyp guideline: diagnosis, treatment, and surveillance for patients with colorectal polyps. Am J Gastroenterol. 2000. 95:3053–3063.
4. Karin M. NF-kappaB and cancer: mechanisms and targets. Mol Carcinog. 2006. 45:355–361.
5. Moon KM, Park YJ, Kim HS, et al. Correlation of beta-catenin and p53 protein expression with clinico-pathologic characteristics of colorectal Cancer. J Korean Soc Coloproctol. 2002. 18:311–316.
6. Behrens J, Jerchow BA, Würtele M, et al. Functional interaction of an axin homolog, conductin, with beta-catenin, APC, and GSK3beta. Science. 1998. 280:596–599.
7. Yu LL, Yu HG, Yu JP, Luo HS, Xu XM, Li JH. Nuclear factor-kappaB p65 (RelA) transcription factor is constitutively activated in human colorectal carcinoma tissue. World J Gastroenterol. 2004. 10:3255–3260.
8. Sinicrope FA, Ruan SB, Cleary KR, Stephens LC, Lee JJ, Levin B. Bcl-2 and p53 oncoprotein expression during colorectal tumorigenesis. Cancer Res. 1995. 55:237–241.
9. Kim TM, Kim JS, Han SW, et al. Clinical predictors of recurrent venous thromboembolism: a single institute experience in Korea. Thromb Res. 2009. 123:436–443.
10. Lee SJ, Jin SM, Lee SH, et al. Expression of Bcl-2, Bax and p27 in patients with papillary thyroid cancer with or without lymph node metastasis. Korean J Otorhinolaryngol-Head Neck Surg. 2010. 53:153–158.
11. Kim TJ, Lee JW, Song SY, et al. Increased expression of p - AKT is associated with radiation resistance in cervical cancer. Br J Cancer. 2006. 94:1678–1682.
12. Lee SD. Immunohistochemical analysis of nuclear factor, p38, and cyclin D1 proteins in premalignant lesions and carcinomas of the colorectal mucosa. Korean J Gastroenterol. 2008. 52:359–367.
13. Zali MR, Moaven O, Aghdaee HA. Clinicopathological significance of E-cadherin, β-catenin and p53 expression in gastric adenocarinoma. J Res Med Sci. 2009. 14:239–247.
14. Fuchs CS, Giovannucci EL, Colditz GA, Hunter DJ, Speizer FE, Willett WC. A prospective study of family history and the risk of colorectal cancer. N Engl J Med. 1994. 331:1669–1674.
15. Wilschut JA, Habbema JD, Ramsey SD, Boer R, Looman CW, van Ballegooijen M. Increased risk of adenomas in individuals with a family history of colorectal cancer: results of a meta-analysis. Cancer Causes Control. 2010. 21:2287–2293.
16. Wark PA, Wu K, van't Veer P, Fuchs CF, Giovannucci EL. Family history of colorectal cancer: a determinant of advanced adenoma stage or adenoma multiplicity? Int J Cancer. 2009. 125:413–420.
17. Neklason DW, Thorpe BL, Ferrandez A, et al. Colonic adenoma risk in familial colorectal cancer--a study of six extended kindreds. Am J Gastroenterol. 2008. 103:2577–2584.
18. Atkin WS, Saunders BP. British Society for Gastroenterology. Association of Coloproctology for Great Britain and Ireland. Surveillance guidelines after removal of colorectal adenomatous polyps. Gut. 2002. 51:Suppl 5. V6–V9.
19. Nam JH, Yang CH. Clinical characteristics and risk factors of colon polyps in gyeongju and pohang area. Korean J Gastroenterol. 2008. 52:142–149.
20. Strum WB. Impact of a family history of colorectal cancer on the prevalence of advanced adenomas of the rectosigmoid colon at flexible sigmoidoscopy in 3147 asymptomatic patients. Dig Dis Sci. 2006. 51:2048–2052.
21. Song HJ, Jung SA, Kim HS, et al. The characteristics of colorectal adenoma with colonoscopic polypectomy in population under 50 years old: the KASID prospective multicenter study. Intest Res. 2005. 3:18–26.
22. American Cancer Society. Colorectal cancer facts and figures 2011-2013. 2011. Atlanta: American Cancer Society.
23. Park IJ, Kim HC, Yoon YS, Yu CS, Jang SJ, Kim JC. Clinicopathological characteristics of colorectal cancer with family history: an evaluation of family history as a predictive factor for microsatellite instability. J Korean Med Sci. 2007. 22:Suppl. S91–S97.
24. Ricciardiello L, Goel A, Mantovani V, et al. Frequent loss of hMLH1 by promoter hypermethylation leads to microsatellite instability in adenomatous polyps of patients with a single first-degree member affected by colon cancer. Cancer Res. 2003. 63:787–792.
25. Resnick MB, Routhier J, Konkin T, Sabo E, Pricolo VE. Epidermal growth factor receptor, c-MET, beta-catenin, and p53 expression as prognostic indicators in stage II colon cancer: a tissue microarray study. Clin Cancer Res. 2004. 10:3069–3075.
26. Aranha MM, Borralho PM, Ravasco P, et al. NF-kappaB and apoptosis in colorectal tumourigenesis. Eur J Clin Invest. 2007. 37:416–424.
27. Miyashita T, Krajewski S, Krajewska M, et al. Tumor suppressor p53 is a regulator of bcl-2 and bax gene expression in vitro and in vivo. Oncogene. 1994. 9:1799–1805.
28. Krajewska M, Moss SF, Krajewski S, Song K, Holt PR, Reed JC. Elevated expression of Bcl-X and reduced Bak in primary colorectal adenocarcinomas. Cancer Res. 1996. 56:2422–2427.
29. Hao CY, Moore DH, Wong P, Bennington JL, Lee NM, Chen LC. Alteration of gene expression in macroscopically normal colonic mucosa from individuals with a family history of sporadic colon cancer. Clin Cancer Res. 2005. 11:1400–1407.
30. Sun M, Wang G, Paciga JE, et al. AKT1/PKBalpha kinase is frequently elevated in human cancers and its constitutive activation is required for oncogenic transformation in NIH3T3 cells. Am J Pathol. 2001. 159:431–437.