Key result
Ginsenoside Rg3 combined with cyclophosphamide significantly inhibited growth and angiogenesis of ovarian cancer and improved survival time in mice compared to control.
Why the study?
Does the combination of ginsenoside Rg3 and cyclophosphamide inhibit growth and angiogenesis in a mouse model of human ovarian cancer?
Population
28 female athymic mice transplanted with human ovarian cancer cells (SKOV-3)
Comparison
Ginsenoside Rg3 combined with cyclophosphamide… vs Control group, Ginsenoside Rg3 alone, and CTX…
Design
Preclinical, Divided randomly into 4 groups
Authors
Loading...
Does not support clinical use in ovarian cancer; leaves open translation of murine anti-tumor effects to human trials.
Does the combination of ginsenoside Rg3 and cyclophosphamide inhibit growth and angiogenesis in a mouse model of human ovarian cancer?
In a preclinical model of ovarian cancer, the combination of ginsenoside Rg3 and cyclophosphamide synergistically inhibited tumor growth and angiogenesis while improving survival.
Xu et al. (2007) studied Ovarian cancer (n=28). Ginsenoside Rg3 combined with cyclophosphamide (CTX) vs. Control, ginsenoside Rg3 alone, or CTX alone was evaluated on Tumour growth, angiogenesis, and survival time. Ginsenoside Rg3 combined with cyclophosphamide significantly inhibited growth and angiogenesis of ovarian cancer and improved survival time in mice compared to control.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: