Both types of treatment increased the frequency of subcutaneous takes but cell pretreatment with L M D alone increased resulting tumour volumes. The effects of L M D were not reflected in any alteration of the viability index in dye exclusion test or in the aggregability of the tumour cells.The attachment of tumour cells onto the vascular endothelium is an indispensable step in the formation of blood-borne metastases. On the assumption that low molecular weight dextran (LMD) might hinder this attachment by its flowpromoting and anticoagulant properties, the effect of L M D has previously been tested on intravenously induced metastases in some experimental systems. In rats LMD increased the number of gross metastases from Walker 256 carcinoma cells (Fisher and Fisher, 1966;Garvie and Matheson, 1966). Promoting as well as inhibiting effects of LMD on experimental metastases were found with syngeneic rat tumours, while L M D reduced the number of pulmonary takes from a mouse tumour (Rudenstam, 1967). In rabbits given V2 carcinoma cells intravenously L M D either did not alter metastasis formation (Wood et al., 1967) or increased it (Fisher and Fisher, 1968).The evaluation of these conflicting results is hampered, apart from differences in experimental design, by the consistent use of tumours giving rise to metastases only in the lungs and/or liver. The absence of manifest metastases in other organs may give a false picture of changes induced in the tumour cell distribution (Hagmar and Boeryd, 1969). The use of rats, in which dextran may provoke an " anaphylactoid reaction " (Kato and Gozsy, 1960), and in most cases allogeneic tumour-host systems, also renders the interpretation of results difficult.The aim of the present investigation was to test the effect of L M D on intravenously-induced metastases in a syngeneic tumour-host system, where metastases can be recorded in other organs besides lungs and liver. The study includes a comparison between L M D pretreatment of animals and L M D preincubation of tumour cells. This experimental design serves to test if L M D