Swainsonine protects both murine and human haematopoietic systems from chemotherapeutic toxicity

The haematopoietic system is sensitive to cytotoxic damage and is often the site of dose-limiting toxicity. We previously reported that swainsonine, a n inhibitor of protein glycosylation, reduced the bone marrow toxicity resu lting from a single dose of anticancer drugs in otherwise healthy mice. How ever, more important questions are (1) can swainsonine protect tumour-beari ng mice without interfering with the anti-tumour effects of the drugs, and (2) can swainsonine stimulate haematopoietic activity of human, as well as murine, bone marrow. We demonstrate here that swainsonine protects C57BL/6 mice bearing melanoma-derived tumours from cyclophosphamide-induced toxicit y without interfering with the drug's ability to inhibit tumour growth. Sim ilar results were obtained in vivo with 3'-azido-3'-deoxythymidine (AZT), a myelosuppressive agent often used in therapy for acquired immune deficienc y syndrome. Swainsonine increased both total bone marrow cellularity and th e number of circulating white blood cells in mice treated with doses of AZT that typically lead to severe myelosuppression. Swainsonine also increased the number of erythroid and myeloid colony forming cells (CFCs) in short-t erm cultures of murine bone marrow, restoring the number of progenitor cell s to the control level in the presence of ATT doses that reduced CFCs by 80 %. With respect to the sensitivity of human haematopoietic cells to swainso nine, we show that swainsonine protected human myeloid progenitor cells fro m AZT toxicity in vitro. These results suggest that swainsonine may be usef ul as an adjuvant in several types of human chemotherapy.