Gembitsky D S, De Angelis P M, Reichelt K L, Elgjo K
Department of Biomedical Sciences, Creighton University School of Medicine, Omaha, Nebraska 68178-0405, USA.
Cell Prolif. 2000 Apr;33(2):91-9. doi: 10.1046/j.1365-2184.2000.00166.x.
The melanocyte-inhibiting tripeptide (MTP) pyroGlu-Phe-GlyNH2 is present in tissue cultures of non-transformed melanocytes and melanoma cells and influences melanocyte growth in vitro. The objective of the present study was to investigate a possible effect of MTP on the in vivo growth of B16A2, a monoclonal experimental melanoma. The B16A2 clone was established by the limited dilution technique. It has a reduced DNA content and displays slower growth both in vivo and in vitro compared to the parent cell line (B16). B16A2 cells were injected subcutaneously into hairless mice at four sites (300 000 cells in 0.25 ml buffer/site). MTP was given by i.p. injection 3 times a week at two concentrations (1 pmol and 1 nmol/animal). The control animals received the equal volume of solvent. The animals were sacrificed 1 and 2 weeks after tumour transplantation, and all tumours were weighed. One week after transplantation, the animals who received 1 pmol MTP had fewer tumours and a reduced tumour load. Two weeks after the transplantation, the differences between control and treated animals were no longer observed. The results indicate that MTP temporarily delays in vivo tumour growth.
抑制黑素细胞的三肽(MTP)焦谷氨酸-苯丙氨酸-甘氨酰胺存在于未转化的黑素细胞和黑色素瘤细胞的组织培养物中,并在体外影响黑素细胞的生长。本研究的目的是调查MTP对单克隆实验性黑色素瘤B16A2体内生长的可能影响。B16A2克隆通过有限稀释技术建立。与亲本细胞系(B16)相比,它的DNA含量降低,在体内和体外的生长都较慢。将B16A2细胞在四个部位皮下注射到无毛小鼠体内(每个部位0.25 ml缓冲液中含300 000个细胞)。MTP通过腹腔注射,每周3次,采用两种浓度(1 pmol和1 nmol/动物)。对照动物接受等量的溶剂。在肿瘤移植后1周和2周处死动物,并对所有肿瘤称重。移植后1周,接受1 pmol MTP的动物肿瘤较少且肿瘤负荷降低。移植后2周,未观察到对照动物和处理动物之间的差异。结果表明,MTP可暂时延缓体内肿瘤生长。