Key result
High-dose cyclophosphamide linked to altered expression of ~300 genes, down-regulating immune activation and rejection pathways.
Why the study?
Treatment-related morbidity and mortality limit hematopoietic stem cell transplantation, and the effects of cyclophosphamide on gene expression during conditioning are not well understood.
Does cyclophosphamide alter the gene expression profile in patients undergoing conditioning prior to stem cell transplantation?
Observational (n=11)
No
Does cyclophosphamide alter the gene expression profile in patients undergoing conditioning prior to stem cell transplantation?
Cyclophosphamide treatment prior to stem cell transplantation significantly alters the expression of genes related to immune activation and graft rejection, providing insight into its mechanism of action.
Gene expression profile during cyclophosphamide conditioning in 11 HSCT patients is now described; hypothesis-generating for toxicity mechanisms and requires validation.
BACKGROUND: Hematopoietic stem cell transplantation is a curative treatment for several haematological malignancies. However, treatment related morbidity and mortality still is a limiting factor. Cyclophosphamide is widely used in condition regimens either in combination with other chemotherapy or with total body irradiation. METHODS: We present the gene expression profile during cyclophosphamide treatment in 11 patients conditioned with cyclophosphamide for 2 days followed by total body irradiation prior to hematopoietic stem cell transplantation. 299 genes were identified as specific for cyclophosphamide treatment and were arranged into 4 clusters highly down-regulated genes, highly up-regulated genes, early up-regulated but later normalized genes and moderately up-regulated genes. RESULTS: Cyclophosphamide treatment down-regulated expression of several genes mapped to immune/autoimmune activation and graft rejection including CD3, CD28, CTLA4, MHC II, PRF1, GZMB and IL-2R, and up-regulated immune-related receptor genes, e.g. IL1R2, IL18R1, and FLT3. Moreover, a high and significant expression of ANGPTL1 and c-JUN genes was observed independent of cyclophosphamide treatment. CONCLUSION: This is the first investigation to provide significant information about alterations in gene expression following cyclophosphamide treatment that may increase our understanding of the cyclophosphamide mechanism of action and hence, in part, avoid its toxicity. Furthermore, ANGPTL1 remained highly expressed throughout the treatment and, in contrast to several other alkylating agents, cyclophosphamide did not influence c-JUN expression.
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El‐Serafi et al. (2014) conducted an observational in Haematological malignancies (n=11). Cyclophosphamide vs. Pre-treatment baseline was evaluated on Differentially expressed genes specific for cyclophosphamide treatment. High-dose cyclophosphamide conditioning prior to stem cell transplantation significantly altered the expression of 299 genes, notably down-regulating immune activation and graft rejection pathways.
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