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Association of Helicobacter pylori with colorectal cancer development
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Abstract
Background: Helicobacter pylori (H. pylori) may be associated with colorectal cancer. However, the underlying mechanisms are still unclear. Objectives: Explore the serostatus of H. pylori cytotoxicity-associated gene A product (CagA) in patients with colorectal carcinoma, and assess the association of H. pylori with colorectal cancer via c-Myc and MUC-2 proteins at tumor tissues. Methods: H. pylori CagA IgG antibodies were screened using enzyme-linked immunosorbent assay (ELISA) in 30 patients with colorectal carcinoma and 30 cancer-free control subjects. Paraffin-embedded blocks were examined for the expression of c-Myc and MUC-2 protein by immunohistochemistry. Results: H. pylori CagA seropositivity increased significantly among colorectal cancer patients (p <0.05). The expression of c-Myc and MUC-2 in colorectal carcinoma patients was over-expressed (80%), and downexpressed (63%) in resection margins (p <0.05). c-Myc over-expression and MUC-2 down-expression were associated with CagA-positive rather than CagA-negative H. pylori patients. In 16 CagA seropositive vs. 14 CagA seronegative patients, the expression rate was 97.3% vs. 64.2% and 33.3% vs. 78.5% for cMyc and MUC-2, respectively. CagA IgG level was significantly higher in positive than in negative c-Myc patients (p= 0.036), and in negative than in positive MUC-2 patients (p= 0.044). c-Myc and MUC-2 were positively and inversely correlated with CagA IgG level (p <0.05). Conclusions: CagA-seropositive H. pylori is most probably associated with colorectal cancer development. Part of the underlying mechanism for such association might be via alterations in expression of MUC-2, which depletes the mucous protective layer in the colo-rectum, and c-Myc, which stimulates the growth of cancerous cells.
Walter de Gruyter GmbH
Title: Association of Helicobacter pylori with colorectal cancer development
Description:
Abstract
Background: Helicobacter pylori (H.
pylori) may be associated with colorectal cancer.
However, the underlying mechanisms are still unclear.
Objectives: Explore the serostatus of H.
pylori cytotoxicity-associated gene A product (CagA) in patients with colorectal carcinoma, and assess the association of H.
pylori with colorectal cancer via c-Myc and MUC-2 proteins at tumor tissues.
Methods: H.
pylori CagA IgG antibodies were screened using enzyme-linked immunosorbent assay (ELISA) in 30 patients with colorectal carcinoma and 30 cancer-free control subjects.
Paraffin-embedded blocks were examined for the expression of c-Myc and MUC-2 protein by immunohistochemistry.
Results: H.
pylori CagA seropositivity increased significantly among colorectal cancer patients (p <0.
05).
The expression of c-Myc and MUC-2 in colorectal carcinoma patients was over-expressed (80%), and downexpressed (63%) in resection margins (p <0.
05).
c-Myc over-expression and MUC-2 down-expression were associated with CagA-positive rather than CagA-negative H.
pylori patients.
In 16 CagA seropositive vs.
14 CagA seronegative patients, the expression rate was 97.
3% vs.
64.
2% and 33.
3% vs.
78.
5% for cMyc and MUC-2, respectively.
CagA IgG level was significantly higher in positive than in negative c-Myc patients (p= 0.
036), and in negative than in positive MUC-2 patients (p= 0.
044).
c-Myc and MUC-2 were positively and inversely correlated with CagA IgG level (p <0.
05).
Conclusions: CagA-seropositive H.
pylori is most probably associated with colorectal cancer development.
Part of the underlying mechanism for such association might be via alterations in expression of MUC-2, which depletes the mucous protective layer in the colo-rectum, and c-Myc, which stimulates the growth of cancerous cells.
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