Laborda J, Sausville E A, Hoffman T, Notario V
Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892.
J Biol Chem. 1993 Feb 25;268(6):3817-20.
Gastrin releasing peptide is mitogenic for mouse Swiss 3T3 fibroblasts and certain human small cell lung carcinoma (SCLC) cells but not for mouse Balb/c 3T3 fibroblasts. To identify new molecules associated with the gastrin releasing peptide-responsive phenotype, clones isolated from a differential cDNA library between Swiss and Balb/c 3T3 fibroblasts were used to screen for their expression in human SCLC cell lines. Using this approach, we have isolated and characterized human and mouse cDNA clones encoding a novel protein. This protein is a putative transmembrane protein belonging to the epidermal growth factor-like superfamily. In vitro transcription and translation studies detect a 42-kDa protein, in agreement with the size predicted from the translated cDNA sequence. This protein (termed Delta-like or dlk) is highly homologous to invertebrate homeotic proteins, including Delta, and Notch, the products of neurogenic loci involved in normal neural differentiation in Drosophila. dlk is expressed in tumors with neuroendocrine features, such as neuroblastoma, pheochromocytoma, and a subset of SCLC cell lines. However, its expression in normal tissues is restricted to the adrenal gland and placenta. These data suggest that dlk may be involved in neuroendocrine differentiation and, because of its cellular location and restricted expression in normal tissues, it may be a potential therapeutic target in neuroendocrine tumors, particularly SCLC.
胃泌素释放肽对小鼠瑞士3T3成纤维细胞和某些人小细胞肺癌(SCLC)细胞有促有丝分裂作用,但对小鼠Balb/c 3T3成纤维细胞无此作用。为了鉴定与胃泌素释放肽反应表型相关的新分子,从瑞士3T3和Balb/c 3T3成纤维细胞之间的差异cDNA文库中分离出的克隆用于筛选它们在人SCLC细胞系中的表达。利用这种方法,我们分离并鉴定了编码一种新蛋白质的人和小鼠cDNA克隆。这种蛋白质是一种推定的跨膜蛋白,属于表皮生长因子样超家族。体外转录和翻译研究检测到一种42 kDa的蛋白质,与从翻译的cDNA序列预测的大小一致。这种蛋白质(称为Delta样或dlk)与无脊椎动物同源异型蛋白高度同源,包括Delta和Notch,它们是果蝇正常神经分化中涉及的神经源位点的产物。dlk在具有神经内分泌特征的肿瘤中表达,如神经母细胞瘤、嗜铬细胞瘤和一部分SCLC细胞系。然而,它在正常组织中的表达仅限于肾上腺和胎盘。这些数据表明dlk可能参与神经内分泌分化,并且由于其细胞定位和在正常组织中的限制性表达,它可能是神经内分泌肿瘤,特别是SCLC中的潜在治疗靶点。