Inhibition of lung colonization of mouse colon 26 adenocarcinoma by recombinant mouse interferon beta through a modification of platelet function.

Abstract:

:Recombinant murine interferon beta (MuIFN-beta) given i.v. efficiently inhibited both pulmonary arrest and formation of lung colonies of NL-17, a highly metastatic variant of mouse colon adenocarcinoma 26. NL-17 was rather resistant to MuIFN-beta in vitro and was highly resistant to natural killer cells of mice even though they were treated in vivo with MuIFN-beta. Platelets isolated from MuIFN-beta-treated mice showed reduced aggregating activity induced by NL-17. Since lung colonization by NL-17 is influenced by platelet aggregation, the inhibition of colonization by MuIFN-beta could be partly mediated through modification of platelet function in vivo. The effect of MuIFN-beta on platelet function and its subsequent inhibition of lung colony formation give new insights into the action of recombinant MuIFN-beta.

journal_name

Clin Exp Metastasis

authors

Tsuruo T,Saito H,Watanabe M,Sugimoto Y,Yamori T,Oh-Hara T

doi

10.1007/BF00117793

subject

Has Abstract

pub_date

1990-03-01 00:00:00

pages

203-13

issue

2

eissn

0262-0898

issn

1573-7276

journal_volume

8

pub_type

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