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首页> 外文期刊>Annals of diagnostic pathology >Immunohistochemical detection of X-linked inhibitor of apoptosis in head and neck squamous cell carcinoma.
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Immunohistochemical detection of X-linked inhibitor of apoptosis in head and neck squamous cell carcinoma.

机译:免疫组化检测头颈鳞状细胞癌X连锁凋亡抑制剂。

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摘要

The X-linked inhibitor of apoptosis (XIAP) is the most potent member of the IAP group of structurally related caspase inhibitors. Experimental and clinical evidence implicates XIAP in resistance to cancer therapy and in clinical aggressiveness of certain tumors. We examined the expression of XIAP in head and neck squamous cell carcinoma (SCC). Four-micrometer sections from 59 routinely processed specimens of head and neck SCC were subjected to citrate-based antigen retrieval, followed by incubation with monoclonal anti-XIAP antibody (BD Biosciences, San Jose, Calif) and EnVision Plus reagents (Dako, Carpinteria, Calif). Granular cytoplasmic staining was considered positive; the extent and intensity of staining were recorded. Normal squamous epithelium was either nonstaining (n=22), displayed generally weak basal staining (n=9), or moderate basal staining (n=1). Squamous dysplasia or carcinoma in situ was either nonstaining (10 of 18 cases) or displayed generally weak staining (8 of 18 cases). Varying degrees of XIAP positivity were found in 41 (69.5%) of 59 carcinomas. Most of the nonstaining and weakly staining carcinomas were well or moderately differentiated. In contrast, intense and extensive staining was most frequently found in poorly differentiated carcinomas. In keratinized tumor nests, staining was strongest peripherally and became diminished in central keratinized zones. New parameters of tumor aggressiveness are needed for more effective triaging of patients to appropriately aggressive therapies. The present findings suggest that the potent apoptotic inhibitor XIAP may be such a biomarker in head and neck SCCs, of resistance to apoptosis-inducing therapies, and, possibly, of responsiveness to a new class of XIAP-suppressive drugs presently in clinical trials for other malignancies or in preclinical development.
机译:X连锁凋亡抑制剂(XIAP)是IAP组中与结构相关的半胱天冬酶抑制剂的最有效成员。实验和临床证据表明XIAP对癌症治疗具有抵抗力,并且对某些肿瘤的临床侵袭性具有影响。我们检查了XIAP在头颈部鳞状细胞癌(SCC)中的表达。对来自59个常规处理过的头颈SCC标本的四微米切片进行柠檬酸盐基抗原提取,然后与单克隆抗XIAP抗体(BD Biosciences,San Jose,CA)和EnVision Plus试剂(Dako,Carpinteria,牛)。颗粒细胞质染色被认为是阳性;记录染色的程度和强度。正常鳞状上皮要么不染色(n = 22),要么表现出较弱的基础染色(n = 9),要么表现为中度基础染色(n = 1)。鳞状异型增生或原位癌要么不染色(18例中的10例),要么表现出一般较弱的染色(18例中的8例)。 XIAP阳性的程度在59例癌症中的41例(69.5%)中被发现。大多数不染色和弱染色的癌均已分化良好或中等。相反,在低分化的癌中最常发现强烈和广泛的染色。在角质化的肿瘤巢中,外周染色最强,在中央角质化区变淡。需要将肿瘤侵袭性的新参数用于将患者更有效地分类为适当侵袭性治疗。本研究结果表明,有效的凋亡抑制剂XIAP可能是头颈SCC中的这种生物标志物,对诱导凋亡的疗法具有抗性,并且可能对目前在其他临床试验中对新型XIAP抑制药物的应答性恶性肿瘤或临床前发展。

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