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Action and mechanism of Fas and Fas ligand in immune escape of gallbladder carcinoma

机译:Fas和Fas配体在胆囊癌免疫逃逸中的作用和机制

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摘要

AIM: To study the role of Fas and Fas ligand (FasL) in biological behaviors of gallbladder carcinoma, and their correlated action and mechanism in tumor escape.METHODS: Streptavidin-biotin-peroxidase immunohisto-chemistry technique was used to study the expression of Fas and FasL protein in 26 gallbladder carcinoma tissues, 18 gallbladder adenoma tissues, 3 gallbladder dysplasia tissues and 20 chronic cholecystitis tissues. Apoptosis of the infiltrating lymphocytes in these tissues was studied by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labeling (TUNEL) method. Expression of both proteins and apoptosis of the tumor infiltrating lymphocytes in cancer tissues of primary foci was compared with clinicopathological features of gallbladder carcinoma.RESULTS: The positive rates of Fas were not significantly different among carcinoma, adenoma, dysplasia and chronic cholecystitis. The positive rate of FasL in carcinoma was significantly higher than that in chronic cholecystitis (χ2 = 4.89, P<0.05). The apoptotic index (AI) in carcinoma was significantly higher than that in adenoma (t’ = 4.19, P<0.01) and chronic cholecystitis (t’ = 8.06, P<0.01). The AI was significantly lower in well-differentiated carcinoma and Nevin I-III carcinoma than that in poorly-differentiated carcinoma (t’ = 2.63, P<0.05) and Nevin IV-V carcinoma (t’ = 3.33, P<0.01). The confidence interval (CI) of infiltrating lymphocytes in adenoma, chronic cholecystitis, well-differentiated carcinoma and Nevin I-III carcinoma was very significantly lower than that in carcinoma (t’ = 6.99, P<0.01), adenoma (t’ = 3.66, P<0.01), poorly-differentiated carcinoma (t’ = 5.31, P<0.01) and Nevin IV-V carcinoma (t’ = 3.76, P<0.01), respectively. The CI of apoptosis of infiltrating lymphocytes in well-differentiated carcinoma was significantly lower than that in poorly-differentiated carcinoma (t = 2.52, P<0.05), and was not significantly lower in Nevin I-III carcinoma than in Nevin IV-V carcinoma (t = 1.42, P>0.05). Apoptosis of infiltrating lymphocytes was not discovered in adenoma and chronic cholecystitis.CONCLUSION: FasL expressed in gallbladder carcinoma cells permits tumor cells to escape from immune surveillance of organism by inducing apoptosis in infiltrating lymphocytes of carcinoma tissues. Up-regulation of FasL expression plays an important role in invasive depth, histological classification and metastasis of gallbladder carcinoma.
机译:目的:研究Fas和FasL配体(FasL)在胆囊癌生物学行为中的作用及其在肿瘤逃逸中的相关作用和机制。方法:链霉亲和素-生物素-过氧化物酶免疫组织化学技术研究Fas和胆囊癌的表达。 FasL和FasL蛋白在26个胆囊癌组织,18个胆囊腺瘤组织,3个胆囊发育不良组织和20个慢性胆囊炎组织中。通过末端脱氧核苷酸转移酶(TdT)介导的dUTP缺口末端标记(TUNEL)方法研究了这些组织中浸润淋巴细胞的凋亡。比较原发灶癌组织中蛋白质的表达和肿瘤浸润淋巴细胞的凋亡与胆囊癌的临床病理特征。结果:癌,腺瘤,异型增生和慢性胆囊炎的Fas阳性率无明显差异。癌中FasL的阳性率明显高于慢性胆囊炎(χ 2 = 4.89,P <0.05)。癌的凋亡指数(AI)显着高于腺瘤(t'= 4.19,P <0.01)和慢性胆囊炎(t'= 8.06,P <0.01)。高分化癌和Nevin I-III癌的AI明显低于低分化癌(t'= 2.63,P <0.05)和Nevin IV-V癌(t'= 3.33,P <0.01)。腺瘤,慢性胆囊炎,高分化癌和Nevin I-III癌中浸润淋巴细胞的置信区间(CI)显着低于癌(t'= 6.99,P <0.01),腺瘤(t'= 3.66) ,P <0.01),低分化癌(t'= 5.31,P <0.01)和内文IV-V癌(t'= 3.76, P <0.01)。高分化癌中浸润淋巴细胞凋亡的CI显着低于弱分化癌( t = 2.52, P <0.05),但不显着与Nevin IV-V癌相比,Nevin I-III癌的发病率要低( t = 1.42, P

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