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Objective: To evaluate the relationship between the expressions of cyclin D1 and p27kip1 in the canceration course of the stomach. Methods: The immunohistochemical staining technique (SP method) was used to detect the expressions of cyclin D1, p27kip1 in chronic superficial gastritis (CSG), chronic atrophic gastritis (CAG), intestinal metaplasia (IM), dysplasia (DYS), gastric carcinoma (GCA) biopsy specimens. Results: The positive cyclin D1 expression rates increased with the progressing from CAG→IM→DYS→GCA respectively, and those in IM, DYS and GCA were different from those in CSG, P < 0.05, while DYS group was indifferent from GCA group, P > 0. 05. The positive p27kip1 expression rates decreased with the mucosa progressing from CAG→IM→DYS→GCA. There was a negative correlation between the expression cyclin D1 and p27kip1 (γ = -0.53, P = 0.000). Conclusion: Expression rates of cyclin D1 in the canceration course of the stomach mucosa trend were increased and those of p27kip1 were decreased; the abnormal expressions of them were found in the early term of the canceration course of the stomach mucosa, and the inverse expression suggests there may be a negative feedback regulatory loop between cyclin D1 and p27kip1.
Methods: The immunohistochemical staining technique (SP method) was used to detect the expressions of cyclin D1, p27kip1 in chronic superficial gastritis (CSG) Results: The positive cyclin D1 expression rates increased with the progressing from CAG → IM → DYS → GCA respectively, and those in IM, DYS and GCA were different from those in CSG, P <0.05 while while DYS group was indifferent from GCA group, P> 0.05. The positive p27kip1 expression rates decreased with the mucosa progressing from CAG → IM → DYS → GCA. There was a negative correlation between the expression of cyclin D1 and p27kip1 (γ = -0.53, P = 0.000). Conclusion: Expression rates of cyclin D1 in the canceration course of the stomach mucosa trend were increased and those of p27ki p1 were decreased; the abnormal expressions of them were found in the early term of the canceration course of the stomach mucosa, and the inverse expression suggests there may be a negative feedback regulatory loop between cyclin D1 and p27kip1.