Significance of B-catenin Immunohistochemical Expression in Colorectal Carcinoma

Authors

  • Zilan Aziz Abdulrahman Department of Histopathology, Rizgary Teaching Hospital, Erbil.
  • Ava Tahir Ismael Department of Clinical Analysis, College of Pharmacy, Hawler Medical University, Erbil.
  • Jalal Ali Jalal Department of Pathology, College of Medicine, Hawler Medical University, Erbil
  • Wahda Muhammed Taib Alnuaimy Department of Pathology, College of Medicine, University of Mosul.

DOI:

https://doi.org/10.56056/amj.2018.42

Keywords:

B-catenin, Colorectal cancer, Immunohistochemistry

Abstract

Background and objectives: Colorectal cancer is the third leading cause of cancer death worldwide and B- catenin has a role in the development of colorectal cancer. The objective of this study was to investigate the B-catenin expression of colorectal carcinoma and assess its correlation with some clinicopathological parameters in Erbil, Kurdistan of Iraq.

Methods: Retrospective study of 100 patients with colorectal cancer collected between January 2015 and January 2017. Clinicopathological parameters were investigated in relation to nuclear and cytoplasmic B-catenin expression.

Results: In 100 specimens of colorectal carcinomas was found to be nuclear (21.6%) and cytoplasm (66.1%). B-catenin was expressed more frequently in patients? 50 years (67.9%), and more commonly in females (60.7%). Left side colon was more frequently affected (85.7%) than the right side (14.3%) with a signifi- cant correlation. Well to moderately differentiated tumors showed higher intensity (89.3%) than poorly differentiated cases (10.7%). Non-mucinous tumors (92.9%) stained more intensely than mucinous tumor (7.1%). 52% of tumor cells were grade I, 37% grade II and 11% grade III. The result of association for B-catenin combined nuclear and cyto- plasmic with intensity of nuclear staining was highly significant. Higher staining intensity is observed in patients with positive nodal status (60.7%) and stage III-IV (60.7%) than those of stage I-II (39.3%).

Conlision: B-catenin was studied in 100 specimens of colorectal cancers, with nuclear staining observed in (21.6%) and cytoplasmic reactivity in (66.1%). Significance was found between intensity of immunoexpression and cellular localization of B-catenin, as well as with clinical parameters of increasing age, female gender, and left sided colonic tumors on another hand

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References

Siegel R, Miller K, Fedewa S, Ahnen D, Meester R, Barzi A, et al. Colorectal Cancer Statistics, 2017. CA CANCER J CLIN. 2017;67:177- 193.

Othman RT, Abdulljabar R, Saeed A, Kittani SS, Sulaiman HM, Mo- hammed SA, et al Cancer incidence rates in the Kurdistan region/Iraq from 2007-2009. Asian Pac J Cancer Prev. 2011.;12(5):12614.

Adil H. Al-Humadi Epidemiology of Colon & Rectal Cancer in Iraq. World Journal of Colorectal Surgery. Berkely Electronic Press. 2008; 1(1).

Weisburger JH: Causes, relevant mechanisms, and prevention of large bowel cancer. Seminar in Oncol.1991; 18:316-36.

Al-Sohaily S, Biankin A, Leong R, Kohonen-Corish M, Warusavi¬tarne J.. Molecular pathways in colorectal cancer. J Gastroenterol Hepatol. 2012;27(9):1423–31.

White BD, Chien AJ, Dawson DW Dysregulation of Wnt/be- ta-catenin signaling in gastrointestinal cancers.Gastroenter- ol.2012;142(2):219–32.

Wodarz A, Nusse R. Mechanisms of Wnt signaling in development. Annu Rev Cell Dev Biol. 1998;14:59-88.

Norwood MG, Bailey N, Nanji M, Gillies RS, Nicholson A, Ubhi S, et al. Cytoplasmic beta-catenin accumulation is a good prognostic mark- er in upper and lower gastrointestinal adenocarcinomas. Histopathol.(2010);57(1):101–11.

Wangefjord S, Brandstedt J, Lindquist KE, Nodin B, Jirstrom K, Eb¬er- hard J.. Associations of beta-catenin alterations and MSI screen¬ing status with expression of key cell cycle regulating proteins and survival from colorectal cancer. Diagn Pathol. (2013);8:10.

Stanczak A, Stec R, Bodnar L, Olszewski W, Cichowicz M, Kozlow’s ki W, et al. Prognostic significance of Wnt-1, beta-catenin and E-cad- herin expression in advanced colorectal carcinoma. Pathol Oncol Res. (2011);17(4):955–63.

Martensson A, Oberg A, Jung A, Cederquist K, Stenling R, Palmqvist R.. Beta-catenin expression in relation to genetic instability and progno- sis in colorectal cancer. Oncol Rep (2007);17(2):447–52.

Russo A, Bazan V, Iacopetta B, Kerr D, Soussi T, and Gebbia N. The TP53 Colorectal Cancer International Collaborative Study on Prognos- tic and Predictive Significance of p53 Mutation: Influence of Tumor Site, Type of Mutation, and Adjuvant Treatment. J Clin Oncol (2005); 23(3):7518-28.

Hamilton SR, Vogelstein B, Kudo S, Riboli E, Nakamura S, Hainaut P et al. Tumors of the colon and rectum. In: S.R. Hamilton and L. A. Aalto- nen (eds.), World Health Organization Classification of Tumors. Pathol- ogy and Genetics of Tumors of the Digestive System. Lyon, France: IARC Press. (2000); pp. 103-43

Compton CC. Colorectal Carcinoma: Diagnostic, Prognostic, and Molecular Features. Mod Pathol; 2003;16(4):376-88.

Jeremy R Jass, Kelli G Biden, Margaret C Cummings, Lisa A Simms, Michael Walsh, Estelle Schoch, et al. Characterization of a subtype of colorectal cancer combining features of the suppressor and mild muta- tor pathways. J Clin Pathol; 1999; 52:455-60.

Salim T, Sjolander A, and Sand-Dejmek1 J. Nuclear expression of Glycogen synthase kinase-3b and lack of membranous b-catenin is correlated with poor survival in colon cancer. Int J Cancer:2013; 133, 807-15.

Mojarad E; Kashfi S; Mirtalebi H; Almasi S; Charles V; Farahani R, et al. Prognostic Significance of Nuclear B-Catenin Expression in Patients with Colorectal Cancer from Iran. Iran Red Crescent Med J;2015; 17(7): e22324. DOI: 10.5812/ircmj.22324v2.

Aldrubi1 I, Abdul-Majeed B, and Mukhlis F. Effect of JCV on Expres- sion of B -Catenin in Colorectal Carcinoma, Int J Curr Microbiol App Sci.2015;4(12): 215-28.

Qasim Z. CO-expression of (VEGF A, VEGF C, COX2 and EGFR) bio- markers in human colorectal cancer and their association with lymph node metastasis and angiogenesis. A Thesis Submitted to College of Medicine-Al-NahrainUniversity.2010.

A.Majid, T, Shakir W and Mahmmod S. Colorectal Carcinoma Presentation and Management.Colorectal Carcin Iraqi Postgrad Medic J.2009; 8.

Hamilton SR, Bosman FT, Bofetta P. Carcinoma of the Colon and Rectum. In: WHO Classification of tumors of the digestive system. WHO Classification of tumors of the digestive system. 2010;134-46..

Hana D, Al-Attraqhchi A and Khattab Y. Molecular and Immunohisto- chemical Detection of JC Polyomavirus in Human Colorectal Cancer in Sample of Iraqi Patients. Intern J Scien EngineRes. 2015; 6934.

Wong S C C, Lo E S F, Chan A K C, Lee K C, Hsiao L. Nuclear B cat- enin as a potential prognostic and diagnostic marker in a patient with colorectal cancer from Hong Kong. Jclin Mol Pathol;2003; 56:347-52.

Iwamoto M, Ahnen DJ, Franklin WA, Maltzman TH. Expression be- ta-catenin and full-length APC protein in normal and neoplastic colonic tissues. Carcinogen.2000; 21:1935–40.

Hong SK, Gul YA, Ithnin H, Talib A, Seow HF. Expression of beta-cat- enin, COX-2, and iNOS in colorectal cancer: relevance of COX- 2 and iNOS inhibitors for treatment in Malaysia. Asian J Surg. 2004;27(1):10- 7.

Kobayashi M, Honma1 T, Matsuda1 Y, Suzuki1 Y, Narisawa1 R, Ajio- kaet Y al. Nuclear translocation of beta-catenin in colorectal cancer. Brit J Can. 2000;82(10), 1689-93 © 2000 Cancer Research Campaign DOI: 10.1054/ box.1999.1112, available online at http://www.ideali- brary.com on

Aust DE, Terdiman JP, Willenbucher RF, Chew K, Ferrell L, Florendo C, et al. Altered distribution of beta-catenin, and its binding proteins E-cadherin and APC, in ulcerative colitis-related colorectal cancers. Mod Pathol. 2001; 14(1):29-39.

Wong NA, Pignatelli M. Beta-catenin–a linchpin in colorectal car- cinogenesis Am J Pathol 2002.;160:389-401.

Yachida S, Mudali S, Martin SA, Montgomery EA, Iacobuzio- Dona- hue CA. Beta-Catenin Nuclear Labeling is a Common Feature of Sessile Serrated Adenomas and Correlates with Early Neoplastic Progression Following BRAF Activation. Am J Surg Pathol. 2009;33(12):1823-32.

Wong S, Fong L, Lee K. The prognostic and diagnostic significance of b-Catenin nuclear immunostaining in colorectal cancer. Clin Cancer Res. 2004;10:1401-8.

Kawasaki T, Noshoy K, Ohnishi M, Suemoto Y, Kirknerz GJ, Dehari R, et al. Correlation of B-catenin localization with cyclooxygenase-2 expression and CpG island methylator phenotype (CIMP) in colorectal cancer. Neoplasia. 2007;9(7):569-77.

Moon WS, Park HS, Lee H, Pai R, Tarnawski AS, Kim KR, et al. Co-ex- pression of COX-2, C-met, and beta-catenin in cells forming the inva- sive front of gallbladder cancer. Cancer Res Treat. 2005;37(3):171-6.

Kim S, Im D, Kim S, Ryu J, Hwang S, Seong J, et al. B-Catenin regulates expression of cyclooxygenase-2 in particular chondrocytes. Biochem Biophys Res Commun. 2002;296:221-6.

Toth L, Andras C, Molnar C, Tanyi M, Csiki Z, Molnar P. et al. In¬ves- tigation of beta-catenin and E-cadherin expression in Dukes B2 stage colorectal cancer with tissue microarray method. Is it a marker of meta- static potential in rectal cancer? Pathol Oncol Res. 2012;18(2):429-37.

Lugli A, Zlobec I, Minoo P, Baker K, Tornillo L, Terracciano L, et al. Prognostic significance of the Wnt signaling pathway molecules APC, beta-catenin, and E-cadherin in colorectal cancer: a tissue microar- ray-based analysis. Histopathol. 2007;50(4):453-64.

Kitagawa T, Matsumoto K, Nagafuchi A, Tsukita S, Suzuki H. Co-ex- pression of E-cadherin and alpha-catenin molecules in colorectal can- cer. Surg Today.1999;29(6):511-8.

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Published

2023-03-15

How to Cite

Abdulrahman , Z. A. ., Ismael , A. T. ., Jalal, J. A. ., & Taib Alnuaimy , W. M. (2023). Significance of B-catenin Immunohistochemical Expression in Colorectal Carcinoma. AMJ (Advanced Medical Journal) , 4(1), 48-53. https://doi.org/10.56056/amj.2018.42

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