Rectal cancer is a common malignancywith a less than 5-year postoperative survival rate. Although it often metastasizes via the lymph and blood, the detailed mechanism of this process remains unclear. This study investigated the relationship between vascular endothelial growth factor-C (VEGF-C) expression and lymphangiogenesis, as well as its relation to lymphatic metastasis of rectal cancer. To address this question, VEGF-C expression in rectal cancer and normal tissue adjacent to tumor was assessed by immunohistochemistry. The lymphatic endothelial cell-specific marker D2-40 was used to label lymphatic endothelial cells and the lymphatic vessel density (LVD) was subsequently quantified. As expected, the expression of VEGF-C in rectal cancer (75%) was significantly higher than in normal adjacent tissue (25%), and this level correlated with differentiation, Dukes stage, and lymph node metastasis, though not with sex or age. The LVD was higher in VEGF-C positive rectal cancer than in VEGF-C negative rectal cancer, and was also higher in lymphatic metastases than in non-lymphatic metastases. These results indicate that expression of VEGF-C may impact the prognosis of rectal cancer via its effect on the formation of new lymphatic vessels. This represents a significant advance in the study of the genesis and development of rectal cancer, and may have value in clinical care.
Keywords: Rectal cancer; and lymphatic metastasis; lymphangiogenesis; lymphatic vessel density; vascular endothelial growth factor-C.
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