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首页> 外文期刊>American Journal of Dermatopathology >Expression of tumor necrosis factor-related apoptosis-inducing ligand death receptors DR4 and DR5 in human nonmelanoma skin cancer
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Expression of tumor necrosis factor-related apoptosis-inducing ligand death receptors DR4 and DR5 in human nonmelanoma skin cancer

机译:肿瘤坏死因子相关的凋亡诱导配体死亡受体DR4和DR5在人非黑素瘤皮肤癌中的表达

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Death receptors 4 and 5 (DR4 and DR5) are cell surface receptors that when activated by their ligand tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) triggers apoptosis in most cancer cells but not in normal cells. Currently, it remains unclear whether DR4 and DR5 are involved in immune surveillance against nonmelanoma skin cancer (NMSC) progression. The aim of this study was to investigate the expression of DR4 and DR5 in NMSC and relate the results to the established clinicopathologic prognostic factors. This study was conducted on about 80 skin specimens from patients with NMSC (40 basal cell carcinoma and 40 squamous cell carcinoma) and diagnosed and confirmed by biopsy. Immunohistochemical analysis for DR4 and DR5 was carried out on formalin-fixed paraffin-embedded sections of skin tissues using avidin-biotin peroxidase method. Significant expression of both DR4 and DR5 was observed in NMSC cases. There was statistically significant association between DR4 and DR5 expression in squamous cell carcinoma and each of tumor site and lymph node metastasis. There was statistically significant association between DR4 expression in basal cell carcinoma and histopathologic subtypes (high expression in nodular type) and between DR5 expression and tumor site (high expression in sun-exposed area). In conclusion, expression of TRAIL receptors that mediate extrinsic apoptotic pathway in NMSC may be suggestive of a reassessment of the suitability of TRAIL-based strategy in future NMSC therapies.
机译:死亡受体4和5(DR4和DR5)是细胞表面受体,当被其配体激活时,肿瘤坏死因子相关的凋亡诱导配体(TRAIL)在大多数癌细胞中触发凋亡,而在正常细胞中则不会。目前,尚不清楚DR4和DR5是否参与针对非黑素瘤皮肤癌(NMSC)进展的免疫监视。这项研究的目的是调查DR4和DR5在NMSC中的表达并将结果与​​已建立的临床病理预后因素相关联。这项研究是对大约80例来自NMSC患者的皮肤样本(40例基底细胞癌和40例鳞状细胞癌)进行的,并通过活检进行了诊断和确认。使用抗生物素蛋白-生物素过氧化物酶法在福尔马林固定石蜡包埋的皮肤组织切片上进行DR4和DR5的免疫组织化学分析。在NMSC病例中观察到DR4和DR5均显着表达。鳞状细胞癌中DR4和DR5表达与肿瘤部位和淋巴结转移均存在统计学意义的相关性。基底细胞癌中DR4表达与组织病理学亚型(结节型高表达)之间,DR5表达与肿瘤部位(日晒区域高表达)之间存在统计学上的显着关联。总之,介导外源性凋亡途径的TRAIL受体在NMSC中的表达可能暗示了对基于TRAIL的策略在未来NMSC治疗中的适用性的重新评估。

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