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β-連環(huán)蛋白表達(dá)與膀胱癌臨床病理及預(yù)后關(guān)系的Meta分析

發(fā)布時(shí)間:2018-06-12 01:22

  本文選題:β-連環(huán)蛋白 + 膀胱癌 ; 參考:《蘭州大學(xué)》2017年碩士論文


【摘要】:目的:分析β-連環(huán)蛋白(β-catenin)在膀胱癌中異常表達(dá)情況,系統(tǒng)評(píng)價(jià)其異常表達(dá)與膀胱癌患者之間的臨床、病理學(xué)特征或疾病預(yù)后的相關(guān)性,探討β-catenin是否能夠成為治療膀胱癌的有效藥理學(xué)靶點(diǎn)。方法:對(duì)“主題詞+自由詞”在中國(guó)CNKI文獻(xiàn)總庫(kù)6.0版本(1996年~2016年9月12日)、維普科技類(lèi)期刊庫(kù)6.5 (1989年~2016年9月12日)、中文生物醫(yī)學(xué)類(lèi)電子庫(kù)(CBM) (1978年~2016年9月12日)、萬(wàn)方數(shù)據(jù)(會(huì)議、期刊、論文等)平臺(tái)(1988年~2016年9月12日)、CDSR (Cochrane系統(tǒng)評(píng)價(jià)電子庫(kù))(2016年1期)、EMBase (1974年~2016年9月12日)、PubMed/Medline (1975年~2016年9月12日)及谷歌學(xué)術(shù)網(wǎng)頁(yè)行網(wǎng)上查找,并翻閱期刊出版物行手工搜找,截止到2016年09月12日。遵照MOOSE (2000版)規(guī)范完成系統(tǒng)評(píng)價(jià)流程,對(duì)所納入各個(gè)CCS (病例-對(duì)照研究)的一般信息行定性總結(jié)、分析,用Revman manager (5.3版本)工具行數(shù)據(jù)定量分析。用OR值、HR值、95% CI值等來(lái)評(píng)估結(jié)果,用Chi2檢驗(yàn)、其P值來(lái)異質(zhì)性結(jié)果,用Z檢驗(yàn)、其P值評(píng)估偏倚。結(jié)果:最終歸入13個(gè)研究記錄,內(nèi)容為CCS記錄,包括了 862例膀胱癌患者,76例正常膀胱粘膜人群,含8篇英文文獻(xiàn),5篇中文文獻(xiàn)。Meta分析結(jié)果如下述:(1)膀胱癌組中的β-catenin表達(dá)水平高于正常膀胱粘膜組(95%CI =(7.61-50.48) ; OR= 19.60; P 0.00001),差異有統(tǒng)計(jì)學(xué)意義。(2)肌層浸潤(rùn)性膀胱癌組中的β-catenin表達(dá)水平高于淺表性膀胱癌組(95%CI =(3.68-7.30);OR = 5.18; P 0.00001),差異有統(tǒng)計(jì)學(xué)意義。(3)高級(jí)別胱癌組中的β-catenin表達(dá)水平高于低級(jí)別膀胱癌組(95%CI= (2.89-5.71); OR = 4.06; P 0.00001),差異有統(tǒng)計(jì)學(xué)意義。(4) β-catenin表達(dá)與性別無(wú)顯著相關(guān)(95%CI = (0.57, 1.96);OR = 1.06; P = 0.85),差異沒(méi)有統(tǒng)計(jì)學(xué)意義。(5) β-catenin表達(dá)水平與腫瘤數(shù)目(多/單發(fā))無(wú)顯著性相關(guān)(95%CI= (0.36,1.88) ; OR = 0.82; P = 0.63),差異沒(méi)有統(tǒng)計(jì)學(xué)意義。(6) β-catenin表達(dá)水平和膀胱癌無(wú)進(jìn)展生存期(PFS)相關(guān)(95%CI= (1.22,6.14) ; HR = 2.74; P = 0.01),差異有統(tǒng)計(jì)學(xué)意義。結(jié)論:本論文Meta分析結(jié)果闡明,膀胱癌組β-連環(huán)蛋白表達(dá)水平高于正常膀胱粘膜組,即β-連環(huán)蛋白的高表達(dá)可能與膀胱癌發(fā)生有關(guān)。伴隨著β-連環(huán)蛋白表達(dá)水平升高,膀胱癌有一個(gè)更高TNM分期和病理級(jí)別,PFS越短,但與其膀胱癌腫瘤數(shù)目、性別則無(wú)顯著性相關(guān)。以上分析提示β-連環(huán)蛋白有可能預(yù)測(cè)出存在的初期癌變,或成為膀胱癌診斷的生物標(biāo)志物。
[Abstract]:Objective: to analyze the abnormal expression of 尾 -catenin in bladder cancer, and to evaluate systematically the relationship between the abnormal expression and the clinical, pathological features or prognosis of bladder cancer. To investigate whether 尾-catenin can be an effective pharmacological target in the treatment of bladder cancer. Methods: the "subject word free words" in the Chinese CNKI literature library 6.0 version (1996 ~ 12 September 2016), Weip Science and Technology Journal Library 6.5 (1989 ~ 2016 12 September, Chinese Biomedical Electronic Library CBM) (1978 ~ 12 September 2016) Universal data Journals, papers, etc.) platform (1988-12 September 2016 / CDSR / Cochrane systematic Review Electronic Library (2016-1) / EMBase (1974-Sept. 12, 2016) and Google academic Web site search, and manual search of journal publications, As of September 12, 2016. According to the MOOSE / 2000 version), the system evaluation process was completed. The general information of each CCS (case-control study) was qualitatively summarized and analyzed, and the quantitative analysis of the data was carried out with the Revman manager version 5.3. The results were evaluated with OR value and HR value of 95% CI, with Chi2 test, P value as heterogeneity result, and with Z test with P value to evaluate bias. Results: the CCS records were included in 13 study records, including 862 bladder cancer patients and 76 normal bladder mucosa patients. The expression of 尾 -catenin in bladder cancer group was higher than that in normal bladder mucosa group (7.61-50.48); OR = 19.60; P 0.00001, the difference was statistically significant. The expression level of 尾 -catenin in the high grade cystadenocarcinoma group was higher than that in the low grade bladder cancer group (2.89-5.71; OR = 4.06; P 0.00001, P 0.00001). The expression level of 尾 -catenin in the high grade cystadenocarcinoma group was higher than that in the lower grade bladder cancer group (2.89-5.71; OR = 4.06; P 0.00001, the difference was statistically significant) 尾 -catenin expression and 尾 -catenin expression in the high grade cystadenocarcinoma group were higher than those in the lower grade bladder cancer group. There was no significant correlation between sex (95 CI = 0.57, 1.96 or = 1.06; P = 0.85, P = 0.85). There was no significant correlation between 尾 -catenin expression level and the number of tumors (multiple / single). There was no significant correlation between 95 CI = 0.36% 1.88); OR = 0.82; P = 0.63N, there was no significant difference between 尾 -catenin expression and tumor number (multiple / single); OR = 0.82; P = 0.63N, there was no significant difference in 尾 -catenin expression. The level of PFS was significantly correlated with PFS), HR = 2.74 and P = 0.01, respectively. Conclusion: the results of Meta-analysis indicate that the expression of 尾 -catenin in bladder cancer is higher than that in normal bladder mucosa, that is, the high expression of 尾 -catenin may be related to the occurrence of bladder cancer. With the increase of 尾 -catenin expression, the higher TNM stage and pathological grade of bladder cancer were, the shorter the PFS was, but there was no significant correlation between the number of bladder cancer tumors and the sex. These results suggest that 尾-catenin may be a biomarker for the diagnosis of bladder cancer.
【學(xué)位授予單位】:蘭州大學(xué)
【學(xué)位級(jí)別】:碩士
【學(xué)位授予年份】:2017
【分類(lèi)號(hào)】:R737.14

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