非淋巴性恶性肿瘤的实验室研究

CLIVE A. MEANWELL, GEORGE BLACKLEDGE
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引用次数: 0

摘要

与恶性转化相关的基因表达异常引起许多表型变化,包括癌细胞产生的物质在数量或质量上与正常细胞的产物不同。这些“癌症标志物”或肿瘤相关抗原可作为非淋巴样肿瘤的筛查、诊断、分期、组织病理学评估和监测治疗的客观参数。已经开发出针对甲胎蛋白、癌胚抗原、人绒毛膜促性腺激素和其他一些癌症标志物的特异性和敏感性试验。已建立的试验依赖于放射免疫测定或酶联免疫测定中的多克隆异源抗血清。在这种情况下,单克隆抗体的理论优势尚未得到认识。然而,在实体肿瘤的组织病理学评估中,单克隆抗体确实比广泛吸收的多克隆抗血清显示出实际优势,这些试剂的进一步发展是值得期待的。宿主-肿瘤免疫相互作用的研究表明,未来对非淋巴样肿瘤的常规检查可能包括对自身反应性的评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Laboratory Investigation of Non-lymphoid Malignancy

Abnormalities of genetic expression associated with malignant transformation cause a number of phenotypic changes including the production of substances by cancer cells which differ quantitatively or qualitatively from the products of normal cells. These ‘cancer markers’ or tumour associated antigens may be used as objective parameters in screening, diagnosis, staging, histopathological evaluation and monitoring treatment of non-lymphoid neoplasia. Specific and sensitive tests for alphafetoprotein, carcinoembryonic antigen, human chorionic gonadotropin and a number of other cancer markers have been developed. Established tests rely upon polyclonal heterologous antisera in radioimmunoassay or enzyme-linked immunoassay. Theoretical advantages of monoclonal antibodies in this setting have yet to be realized. Monoclonal antibodies do however show practical advantages over extensively absorbed polyclonal antisera in the histopathological evaluation of solid tumours and further progress with these reagents is expected. Studies of host-tumour immunological interactions suggest that future routine investigations of non-lymphoid neoplasia may include assessments of autochthonous reactivity.

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