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机构地区:[1]山东大学附属省立医院小儿外科,济南250021
出 处:《中华小儿外科杂志》2011年第10期764-768,共5页Chinese Journal of Pediatric Surgery
摘 要:目的 研究小儿预后良好型(FH)肾母细胞瘤(Wilms肿瘤)组织中p53和-1α(HIF-1α)表达水平及其与肿瘤侵袭性的关系.方法 采用免疫组化S-P法检测57例原发Wilms肿瘤组织、21例侵袭灶和10例正常肾脏组织中p53和HIF-1α的表达.结果 p53/HIF-1α在78例Wilms肿瘤组织和10例正常肾脏组织中的阳性表达分别为29.5%(23/78)/39.7%(31/78)和0%/0%,其差异有统计学意义(x2=3.992,P<0.05;x2=6.136,P<0.05).p53蛋白的表达差异在各临床分期间有统计学意义(x2=13.152,P<0.05);侵袭组原发灶和非侵袭组的原发灶中p53蛋白阳性率分别为33.3%(7/21)和8.3%(3/36),两组比较其差别有统计学意义(x2=5.730,P<0.05);而HIF-1α在各临床病理因素中的表达差异均无统计学意义(P>0.05).p53/HIF-1α蛋白在21例原发灶及其对应的侵袭灶中的表达差异均有统计学意义(Z=-2.093,P<0.05; Z=-2.723,P<0.01).在78例Wilms肿瘤组织中p53和HIF-1α蛋白表达具有正相关性(x2=36.210,P<0.001,r=0.681).结论 p53和HIF-1α与Wlims肿瘤的侵袭性相关,这为进一步了解Wilms肿瘤浸润、转移的机制及靶向治疗提供新的思路.Objective To investigate the p53 and HIF-1 α expressions in favorable-histology type of Wilms tumor.Methods The expressions of p53 and HIF-1α were detected in 57 primary Wilms tumors,21 invasive lesions,and 10 normal renal tissues by S-P immunohistochemistry.Results Positive staining of p53 was 29.5% (23/78) in tumors while no positive staining could be found in normal tissues (x2 =3.992,P〈0.05).The positive staining of HIF-1α was 39.7% (31/78) while no positive staining could be found in normal tissues(x2 =6.136,P〈0.05).The expression of p53 in different clinic stages had statistical difference (x2 =13.152,P〈0.05).Positive rate of p53 expression in the primary tumor tissues of invasive group and non-invasive group was 33.3 % (7/21) and 8.3 % (3/36),respectively (x2 =5.730,P〈0.05).There was no significant difference between HIF expression and clinopathological factors (P〉0.05).Significant statistical difference was detected for p53 and HIF-1αexpressions in 21 primary Wilms tumors and matched invasive lesions (Z =- 2.093,P〈0.05/Z =-2.723,P〈0.01).The expressions of p53 and HIF-1α in 78 Wilms tumor tissues were positively correlated (x2 =36.210,P〈0.001,r=0.681 ).Conclusions p53 and HIF-1α expressions are correlated with the invasiveness of Wilms tumor.This provides us a new sight into the mechanism of the infiltration and metastases and therapeutic target of the Wilms tumor.
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