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半胱氨酸蛋白酶抑制剂可在体外降低恶性黑色素瘤细胞的侵袭能力。

Cysteine proteinase inhibitors reduce malignant melanoma cell invasion in vitro.

作者信息

Bjørnland K, Buø L, Kjønniksen I, Larsen M, Fodstad O, Johansen H T, Aasen A O

机构信息

Institute for Surgical Research, Rikshospitalet, Oslo, Norway.

出版信息

Anticancer Res. 1996 Jul-Aug;16(4A):1627-31.

PMID:8712680
Abstract

Proteolytic enzymes are believed to be necessary for tumor cell invasion. We have studied the effects of the cysteine proteinase inhibitor E-64 and the serine and cysteine proteinase inhibitor leupeptin, on the ability of human malignant melanoma cells (LOX) to pass through an artificial basement membrane. Transwell chambers containing filters coated with the reconstituted basement membrane, Matrigel, were used. Nontoxic concentrations of the proteinase inhibitors reduced the invasion of LOX cells through Matrigel. E-64 (250 mumol/l) by 27% and leupepetin (250 micrograms/ml) by 46%. The proteinase inhibitors did not alter the growth rate of the tumor cells, their motility through uncoated filters, or their attachment to the Matrigel coated wells. Our results indicate that cysteine proteinases are involved in the degradation of basement membranes and thus contribute to the invasion of malignant melanoma cells.

摘要

蛋白水解酶被认为是肿瘤细胞侵袭所必需的。我们研究了半胱氨酸蛋白酶抑制剂E-64以及丝氨酸和半胱氨酸蛋白酶抑制剂亮抑酶肽对人恶性黑色素瘤细胞(LOX)穿过人工基底膜能力的影响。使用了装有包被有重组基底膜基质胶的滤膜的Transwell小室。蛋白酶抑制剂的无毒浓度降低了LOX细胞通过基质胶的侵袭能力。E-64(250μmol/L)降低了27%,亮抑酶肽(250μg/ml)降低了46%。蛋白酶抑制剂并未改变肿瘤细胞的生长速率、它们通过未包被滤膜的运动能力或它们对包被有基质胶的孔的附着能力。我们的结果表明,半胱氨酸蛋白酶参与基底膜的降解,从而促进恶性黑色素瘤细胞的侵袭。

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