O'Byrne K J, Halmos G, Pinski J, Groot K, Szepeshazi K, Schally A V, Carney D N
ICRF Clinical Oncology Unit, Churchill Hospital, Headington, Oxford, U.K.
Eur J Cancer. 1994;30A(11):1682-7. doi: 10.1016/0959-8049(94)00351-5.
Experimental evidence suggests that somatostatin analogues may have a role to play in the management of lung tumours. We evaluated membrane preparations of nine small cell lung cancer (SCLC) cell lines and of tumour samples from 3 patients with non-small cell lung cancer (NSCLC), 1 patient with an atypical carcinoid and another with a bronchial carcinoid for the presence of specific binding sites for RC-160, a potent growth inhibitory octapeptide analogue of somatostatin. Specific binding was noted on six of nine SCLC lines. Radio-receptor assay on the cell line NCI H 69 showed evidence of two specific binding sites for RC-160, one with high affinity and the other with low affinity. Binding sites were also found on all five tumour samples. Scatchard analysis indicated the presence of a single class of receptors with high affinity in each case. Histological assessment of the resected specimens before binding assay showed them to be comprised of tumour cells and necrotic tissue, stroma and/or inflammatory cells. Therefore, the specific binding of RC-160 may be to tissues other than the tumour cells. In 3 patients, from whom the tumour samples were obtained, radiolabelled somatostatin analogue scintigraphy using [111In] pentetreotide was performed prior to surgery. In all cases, the radiolabel localised the disease. This study demonstrates the presence of specific binding sites for RC-160 in SCLC. Furthermore, the detection of specific binding in vitro and in vivo in NSCLC and intrapulmonary carcinoids demonstrates that these tumours contain cells which express specific binding sites for somatostatin. These results suggest that RC-160 may have a role to play as a therapeutic agent in lung cancer.
实验证据表明,生长抑素类似物可能在肺癌治疗中发挥作用。我们评估了9个小细胞肺癌(SCLC)细胞系以及3例非小细胞肺癌(NSCLC)患者、1例非典型类癌患者和1例支气管类癌患者的肿瘤样本的膜制剂,以检测生长抑素强效生长抑制八肽类似物RC - 160的特异性结合位点。在9个SCLC细胞系中的6个上发现了特异性结合。对NCI H 69细胞系进行的放射受体分析显示存在RC - 160的两个特异性结合位点,一个具有高亲和力,另一个具有低亲和力。在所有5个肿瘤样本中也发现了结合位点。Scatchard分析表明在每种情况下均存在一类具有高亲和力的受体。在结合测定之前对切除标本进行的组织学评估显示它们由肿瘤细胞、坏死组织、基质和/或炎性细胞组成。因此,RC - 160的特异性结合可能是针对肿瘤细胞以外的组织。在获取肿瘤样本的3例患者中,术前使用[111In]喷曲肽进行了放射性标记生长抑素类似物闪烁扫描。在所有病例中,放射性标记均定位了病变。本研究证明了SCLC中存在RC - 160的特异性结合位点。此外,在NSCLC和肺内类癌中体外和体内特异性结合的检测表明,这些肿瘤含有表达生长抑素特异性结合位点的细胞。这些结果表明,RC - 160可能作为一种治疗剂在肺癌中发挥作用。