Antimetastatic effect of PSK, a protein-bound polysaccharide, against the B16-BL6 mouse melanoma.

Invasion & metastasis Pub Date : 1996-01-01
K Matsunaga, M Ohhara, Y Oguchi, H Iijima, H Kobayashi
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Abstract

We examined the effect of PSK, a protein-bound polysaccharide, upon in vivo metastasis and in vitro invasion of the B16-BL6 mouse melanoma cells. (1) PSK suppressed in vivo artificial and spontaneous lung metastases of B16-BL6 in C57BL/6 mice. (2) PSK in a dose-dependent fashion suppressed in vitro invasion and chemotaxis of the tumor cells using filters coated with a reconstituted basement membrane. (3) PSK had little effect on DNA synthesis in tumor cells in vitro, but suppressed tumor cell adhesion to, degradation of, and haptotaxis to components of the basement membrane. (4) PSK suppressed the binding of tumor cells to components of the basement membrane. These findings suggest that PSK may suppress metastasis through inhibition of tumor cell invasion and that this effect is the result of interactions between PSK and components of the basement membrane.

蛋白结合多糖PSK对B16-BL6小鼠黑色素瘤的抗转移作用。
我们研究了PSK(一种蛋白结合多糖)对B16-BL6小鼠黑色素瘤细胞体内转移和体外侵袭的影响。(1) PSK抑制C57BL/6小鼠体内B16-BL6的人工和自发肺转移。(2) PSK以剂量依赖的方式抑制肿瘤细胞的体外侵袭和趋化性,使用包覆重组基膜的过滤器。(3) PSK对肿瘤细胞DNA合成影响不大,但抑制肿瘤细胞对基底膜成分的粘附、降解和趋近性。(4) PSK抑制肿瘤细胞与基底膜组分的结合。这些发现表明PSK可能通过抑制肿瘤细胞侵袭来抑制转移,这种作用是PSK与基底膜成分相互作用的结果。
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