机构地区:[1]福建省漳州卫生职业学院,福建省漳州市363000 [2]福建省漳州市医院病理科,福建省漳州市363000
出 处:《世界华人消化杂志》2008年第32期3631-3636,共6页World Chinese Journal of Digestology
基 金:福建省漳州市科技局资助项目; No. Z07020~~
摘 要:目的:探讨三叶因子3(trefoil factor 3,TFF3)和CD147在不同胃黏膜病变中的表达与间质微血管(microvessel density,MVD)值的关系.方法:利用组织芯片技术制作302例的组织芯片,同时采用S-P免疫组化方法检测TFF3、CD147和CD34表达.结果:萎缩性胃炎、不典型增生和胃癌各组TFF3表达均高于浅表性胃炎和正常组(48.3%,51.9%,41.7%vs13.3%;48.3%,51.9%,41.7%vs3.6%,均P<0.01);胃癌CD147表达和MVD高于正常胃黏膜、浅表性胃炎、萎缩性胃炎和不典型增生(78.9%vs14.3%,43.3%,51.2%,59.3%;31.86±9.92vs26.10±6.82,24.74±5.49,20.77±6.87,14.95±6.28,均P<0.05),浅表性胃炎CD147表达和MVD与正常胃黏膜之间差异显著(43.3%vs14.3%;20.77±6.87vs14.95±6.28,均P<0.05).TFF3、CD147表达和MVD与胃癌淋巴结转移和TNM分期有关(P<0.05),TFF3表达与胃癌组织学类型有关(P<0.05),CD147表达与胃癌分化程度和胃癌浸润深度有关(P<0.01),MVD与胃癌浸润深度有关(P<0.05).TFF3、CD147阳性表达的MVD高于阴性的(35.47±9.41vs29.27±9.50;33.33±9.62vs26.40±9.17,P<0.01).TFF3和CD147表达与MVD呈显著正相关(r=0.323,r=0.279).TFF3(+)/CD147(+)者在深度浸润(T3-4)、临床分期TNMⅢ-Ⅳ、淋巴结转移的比率和MVD最高,且明显高于TFF3(-)/CD147(-)者(P<0.05).结论:TFF3、CD147和CD34在胃黏膜癌变和癌变后的恶性演进过程中起重要作用,可作为胃癌的早期诊断和预测胃癌发生转移的重要指标.AIM: To investigate expression of trefoil factor 3 (TFF3) and CD147 in gastric mucosa, and their correlation with microvessel density (MVD) in carcinogenesis of gastric mucosa. METHODS: Three hundred and two sample tissues were prepared using tissue microarray. At the same time, S-P immunohistochemical methods were applied to detect expression of TFF3, CD147 and CD34. RESULTS: TFF3 expression was significantly higher in atrophic gastritis, atypical hyperplasia and gastric cancinoma than in normal controls or in superficial gastritis (48.3%, 51.9%, 41.7% vs 13.3%; 48.3%, 51.9%, 41.7% vs 3.6%, all P 〈 0.01). CD147 expression and MVD were higher in gastric cancinoma than in normal controls, superficial gastritis, atrophic gastritis or in atypical hyperplasia (78.9% vs 14.3%, 43.3%, 51.2%, 59.3%; 31.86 ± 9.92 vs 26.10 ± 6.82, 24.74 ± 5.49, 20.77 ± 6.87, 14.95 ± 6.28, all P 〈 0.05). There was significant difference in CD147 expression and MVD between superficial gastritis and normal controls (43.3% vs 14.3%; 20.77 ± 6.87 vs 14.95 ± 6.28, all P 〈 0.05). TFF3 and CD147 expression and MVD were correlated with lymph node metastasis and TNM staging (all P 〈 0.05). TFF3 expression was correlated with histological type (P 〈 0.05), CD147 expression was correlated with tumor differentiation (P 〈 0.01). CD147 expression and MVD were correlated to depth of invasion (P 〈 0.05). MVD with positive expressions of TFF3, survivin and CD147 was higher than that with negative expression (35.47 ± 9.41 vs 29.27 ± 9.50; 33.33 ± 9.62 vs 26.40 ± 9.17, all P 〈 0.01). The expression of TFF and CD147 and MVD were positively correlated(r = 0.323, r = 0.279). Rate of the deeper tumor invasion (T3-4), TNM categories (TNMⅢ-Ⅳ), lymph node metastasis and MVD reached the highest in TFF3(+)/CD147(+) and were markedly higher in TFF3(+)/CD147(+) than TFF3(-)/CD147(-) (P 〈 0.05). CONCLUSION: TFF3, CD147 and CD34 may play impo
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