Abstract

To investigate the level of expression of proto-oncogene Wip1 and its physiological significance in colorectal cancer. Immunohistochemistry, semi-quantitative RT-PCR, and Western blotting were used to analyze Wip1 mRNA and protein expression in 120 cases of colorectal cancer and normal tissues to study relationships with clinical symptoms and disease prognosis. The level of Wip1 protein expression was found to be significantly higher in colorectal cancer tissues (85% (102/120)) than in normal tissues (30% (36/120)) (P < 0.05). The relative amount of Wip1 protein in colorectal cancer tissue was also found to be significantly higher (P < 0.05) than in normal tissues (1.060±0.02 and 0.640±0.023, respectively). Semi-quantitative RT-PCR showed average Wip1 mRNA expression levels to be 1.113 ±0.018 and 0.658±0.036 for colorectal cancer tissue and adjacent normal tissue (P < 0.05). The level of Wip1 protein expression was not correlated with age, gender, or tumor site, but appeared linked with lymph node metastasis, Dukes stage, histological grade, and liver metastasis. Individuals with high and low levels of Wip1 expression showed statistically significant differences in the five-year overall survival and recurrence-free survival rates (P < 0.05). Wip1 mRNA and protein are highly expressed in colorectal cancers and may be associated with colorectal cancer development and progression.

Highlights

  • Over the past 30 years, the incidence and mortality of colorectal cancer have increased significantly

  • We used immunohistochemistry, Western blot analysis, and semi-quantitative RT-PCR to study Wip1 expression in colorectal cancer tissues and normal tissues to explore the role of Wip1 in the development of colorectal cancer

  • Wip1 staining ranged from light yellow to brown

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Summary

Introduction

Over the past 30 years, the incidence and mortality of colorectal cancer have increased significantly. We used immunohistochemistry, Western blot analysis, and semi-quantitative RT-PCR to study Wip expression in colorectal cancer tissues and normal tissues to explore the role of Wip in the development of colorectal cancer

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