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. 2012 Sep;24(3):190-5.
doi: 10.1007/s11670-012-0190-z.

Clinicopathological Significance of Mucin 2 Immuno-histochemical Expression in Colorectal Cancer: A Meta-Analysis

Affiliations

Clinicopathological Significance of Mucin 2 Immuno-histochemical Expression in Colorectal Cancer: A Meta-Analysis

Li Li et al. Chin J Cancer Res. 2012 Sep.

Abstract

Objective: To evaluate the association between mucin 2 (MUC2) expression and clinicopathological characters of colorectal cancer.

Methods: A literature search was performed on December 31, 2010 according to defined selection criteria. We evaluated the correlation between MUC2 (detected by immunohistochemistry) and clinicopathological characters of colorectal cancer. According to the tumor histological type, differentiation, location and TNM staging of colorectal carcinoma, we divided the clinicopathological characteristics into different subgroups. Fixed and random effects models were applied for estimation of the summarized risk ratios (RRs) and 95% confidence intervals (CIs) in different subgroups. Finally, forest plots and funnel plots were created to allow for visual comparison of the results or the effect of publication bias.

Results: According with the inclusive criteria, fourteen studies (n=1,558) were eligible for the meta-analysis. We observed a trend towards a correlation of MUC2 higher positivity in mucinous than non-mucinous carcinoma (RR, 2.10; 95% CI, 1.30-3.40; P=0.002) and less positivity in distal than proximal colon (RR, 0.74; 95% CI, 0.64-0.85; P=0.000). There was no statistically significance for the association between MUC2 expression and differentiation or TNM staging of colorectal cancer, but MUC2 overexpression tended to be associated with the presence of T stage tumor (RR, 1.17; P=0.052).

Conclusion: MUC2 overexpression was associated with the mucinous and proximal colorectal cancer.

Keywords: Colorectal cancer; Immunohistochemistry; MUC2; Meta-analysis.

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Conflict of interest statement

Disclosure of Potential Conflicts of Interest: No potential conflicts of interest were disclosed.

Figures

Figure 1
Figure 1
Study-specific RRs with 95% CIs of MUC2 positivity and funnel plots. A, C: Mucinous vs. non-mucinous carcinoma; B, D: Distal vs. proximal subgroup. s indicates standard error.
Figure 2
Figure 2
Study-specific RRs with 95% CIs of MUC2 positivity (A) and funnel plots (B) in T3 & T4 vs. T1 & T2 subgroup. s indicates standard error.

References

    1. Byrd JC, Bresalier RS. Mucins and mucin binding proteins in colorectal cancer. Cancer Metastasis Rev 2004; 23:77-99 - PubMed
    1. Velcich A, Yang W, Heyer J, et al. Colorectal cancer in mice genetically deficient in the mucin MUC2. Science 2002; 295: 1726-9 - PubMed
    1. Aksoy N, Corfield AP, Sheehan JK. Preliminary study pointing out a significant alteration in the biochemical composition of MUC2 in colorectal mucinous carcinoma. Clin Biochem 2000; 33:167-73 - PubMed
    1. Taylor CR. Standardization in immunohistochemistry: the role of antigen retrieval in molecular morphology. Biotech Histochem 2006; 81: 3-12 - PubMed
    1. Gurevich LE, Kazantseva IA, Korsakova NA, et al. Expression of type 1 and type 2 mucins in colonic epithelial tumors. Arkh Patol 2007; 69:12-6 - PubMed