Woll P J, Rozengurt E
Imperial Cancer Research Fund, Lincoln's Inn Fields, London, UK.
Br J Cancer. 1988 Jun;57(6):579-86. doi: 10.1038/bjc.1988.132.
Bombesins are potent growth factors for murine Swiss 3T3 cells. Using these cells in chemically defined conditions we have been able to characterise the bombesin receptor and the early signals preceding DNA synthesis. We describe two substance P analogues [DArg1, DPro2, DTrp7,9, Leu11] substance P and [DArg1, DPhe5, DTrp7,9, Leu11] substance P which competitively block the binding of bombesins to their receptor and all the events leading to mitogenesis. Bombesins are secreted by human small cell lung cancers (SCLC) and may act as autocrine growth factors for these tumours, so the development of peptide bombesin antagonists could have therapeutic implications. We demonstrate that the antagonists can reversibly inhibit the growth of SCLC in vitro, with relatively little effect on other lung tumours.
蛙皮素是小鼠瑞士3T3细胞的强效生长因子。在化学成分明确的条件下使用这些细胞,我们得以对蛙皮素受体以及DNA合成之前的早期信号进行表征。我们描述了两种P物质类似物,即[D精氨酸1,D脯氨酸2,D色氨酸7,9,亮氨酸11]P物质和[D精氨酸1,D苯丙氨酸5,D色氨酸7,9,亮氨酸11]P物质,它们能竞争性地阻断蛙皮素与其受体的结合以及所有导致有丝分裂的事件。蛙皮素由人小细胞肺癌(SCLC)分泌,可能作为这些肿瘤的自分泌生长因子,因此肽类蛙皮素拮抗剂的开发可能具有治疗意义。我们证明,这些拮抗剂能在体外可逆地抑制SCLC的生长,而对其他肺部肿瘤的影响相对较小。