Antiproliferative effect of vitamin A on xenotransplanted CaMa-15 cells.
In vitro and in vivo investigations have shown that nontoxic treatment with vitamin A (retinol) has an inhibitory effect on the growth of malignant cells. The tumorigenic CaMa -15 cell line responds to both retinol and retinoic acid under both anchorage-dependent and anchorage-independent conditions, reducing growth or colony formation by at least 50%. To date, there have been few studies on the effects of vitamin A on xenotransplanted neoplastic cells. Twenty-five adult female nude rats (rnu/rnu) were inoculated in the inguinal fat pad with 10(6) CaMa -15 cells, a tumorigenic epithelial cell line. The rats were divided into three groups: ten high dose (3 mg retinol/day i.p.); five low dose (30 micrograms retinol/day i.p.); and ten controls (corn oil i.p.). All animals were housed in specific-pathogen-free conditions and permitted access to sterile laboratory chow (5.4 micrograms retinol/g chow) and water ad libitum. Rats were sacrificed at 21 days after inoculation. Onset of tumor development occurred between Days 9 and 13 in all groups. Tumors grew progressively and were reduced in mean diameter by 26% (p = less than 0.05) with high-dose retinol and 44% (p = less than 0.02) by low-dose treatment. No clinical signs of vitamin A toxicity were apparent. Necropsy and radiological examination revealed no evidence of toxic effects or metastases. These results indicate that vitamin A can reduce the growth of xenotransplanted tumorigenic cells at nontoxic levels in T-cell-deficient hosts. The nude rat offers a potential model to study the inhibitory effects of retinoids on xenotransplanted cancers.[1]References
- Antiproliferative effect of vitamin A on xenotransplanted CaMa-15 cells. Wetherall, N.T., Mitchell, W.M., Halter, S.A. Cancer Res. (1984) [Pubmed]
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