Geldof A A, De Kleijn M A, Rao B R, Newling D W
Department of Urology, Academisch Ziekenhuis Vrije Universiteit, Amsterdam, The Netherlands.
J Cancer Res Clin Oncol. 1997;123(2):107-12. doi: 10.1007/BF01269888.
The prevalence of nerve growth factor (NGF) production in different human prostatic tumor cell lines (DU145, PC-3, LNCaP-FGC) was investigated using a specific enzyme-linked immunosorbent assay (ELISA) and compared to that of different human and rat prostatic tissue samples. In addition, the biological effects of NGF beta addition to the human prostatic cancer cell cultures were investigated. The ELISA technique showed the DU145 cell line to secrete measurable levels of NGF in the culture medium. When neurite-outgrowth determination in a pheochromocytoma cell line was used as a bioassay, the NGF synthesized by DU145 cells was confirmed to exhibit functional biological activity. No effect of exogenously added NGF could be established on tumor cell proliferation, on the basis of either colorimetric tetrazolium-based staining assay or bromodeoxyuridine incorporation. Also the expression of prostate specific acid phosphatase was not influenced by NGF addition. However, the in vitro invasive capacity (Matrigel) of DU145 cells was significantly increased by inclusion of 50 ng or 100 ng NGF beta/ml culture medium. In view of the clinically well-known perineural invasion of prostate cancer cells, the possible involvement of NGF as a (paracrine) factor in prostatic cancer metastatic behavior should be investigated further.
使用特异性酶联免疫吸附测定(ELISA)研究了不同人前列腺肿瘤细胞系(DU145、PC-3、LNCaP-FGC)中神经生长因子(NGF)的产生情况,并与不同人和大鼠前列腺组织样本进行了比较。此外,还研究了向人前列腺癌细胞培养物中添加NGFβ的生物学效应。ELISA技术显示DU145细胞系在培养基中分泌可测量水平的NGF。当将嗜铬细胞瘤细胞系中的神经突生长测定用作生物测定时,证实DU145细胞合成的NGF具有功能性生物学活性。基于比色四唑染色测定或溴脱氧尿苷掺入法,未发现外源性添加的NGF对肿瘤细胞增殖有影响。此外,添加NGF也不影响前列腺特异性酸性磷酸酶的表达。然而,通过在培养基中加入50 ng或100 ng NGFβ/ml,DU145细胞的体外侵袭能力(基质胶)显著增加。鉴于临床上众所周知的前列腺癌细胞神经周围浸润,应进一步研究NGF作为(旁分泌)因子在前列腺癌转移行为中的可能作用。