Stewart M F, Crosby S R, Gibson S, Twentyman P R, White A
University of Manchester, Department of Clinical Biochemistry, Hope Hospital, Salford, UK.
Br J Cancer. 1989 Jul;60(1):20-4. doi: 10.1038/bjc.1989.212.
A panel of 18 well characterised human small cell lung cancer (SCLC) cell lines was assessed for the production of adrenocorticotrophin (ACTH) and its precursor peptides, pro-opiomelanocortin (POMC) and pro-ACTH. These precursor peptides were measured directly using a novel two-site immunoradiometric assay (IRMA) based on monoclonal antibodies, in conjunction with a similar IRMA for ACTH 1-39. Significant concentrations of ACTH precursors were secreted by 10 of the 18 cell lines (56%). The low levels of ACTH immunoreactivity detected in seven cell lines could be accounted for by the known cross-reactivity of precursors in the ACTH IRMA. This suggests there is little, if any, processing of ACTH precursors to ACTH. Cell pellet extracts contained undetectable or low levels of ACTH precursors and ACTH, indicating that these peptides are not stored intracellularly. During the growth of the SCLC cells in vitro ACTH precursors accumulated progressively in the culture medium. Thus the combination of a direct assay for the ACTH precursors and the panel of SCLC cell lines provides a valuable in vitro model for the expression of POMC in human tumours.
对一组18种特征明确的人小细胞肺癌(SCLC)细胞系进行了促肾上腺皮质激素(ACTH)及其前体肽、阿黑皮素原(POMC)和前ACTH生成情况的评估。这些前体肽采用基于单克隆抗体的新型双位点免疫放射分析(IRMA)直接检测,并结合用于ACTH 1-39的类似IRMA。18个细胞系中有10个(56%)分泌了显著浓度的ACTH前体。在7个细胞系中检测到的低水平ACTH免疫反应性可由ACTH IRMA中前体已知的交叉反应来解释。这表明ACTH前体几乎没有(如果有的话)加工成ACTH。细胞沉淀提取物中ACTH前体和ACTH含量不可检测或很低,表明这些肽不是储存在细胞内。在SCLC细胞体外生长过程中,ACTH前体在培养基中逐渐积累。因此,ACTH前体的直接检测方法与SCLC细胞系组合为POMC在人类肿瘤中的表达提供了一个有价值的体外模型。