Abstract

Inhibitory effects of Maclura amboinenesis Bl, one plant used traditionally for the treatment of cancers, on metastatic potential of highly metastatic B16F10 melanoma cells were investigated in vitro. Cell proliferation was assessed using the MTT colorimetric assay. Details of metastatic capabilities including invasion, migration and adhesion of B16F10 melanoma cells were examined by Boyden Chamber invasion and migration, scratch motility and cell attachment assays, respectively. The results demonstrated that n-hexane and chloroform extracts exhibited potent anti-proliferative effects (p<0.01), whereas the methanol and aqueous extracts had less pronounced effects after 24 h exposure. Bioactivity-guided chromatographic fractionation of both active n-hexane and chloroform extracts led to the isolation of two main prenylated xanthones and characterization as macluraxanthone and gerontoxanthone-I, respectively, their structures being identified by comparison with the spectral data. Interestingly, both exhibited potent effective effects. At non-toxic effective doses, n-hexane and chloroform extracts (10 and 30 μg/ml) as well as macluraxanthone and gerontoxanthone-I (3 and 10 μM) significantly inhibited B16F10 cell invasion, to a greater extent than 10 μM doxorubicin, while reducing migration of cancer cells without cellular cytotoxicity. Moreover, exposure of B16F10 melanoma cells to high concentrations of chloroform (30 μg/ml) and geratoxanthone-I (20 μM) for 24 h resulted in delayed adhesion and retarded colonization. As insights into mechanisms of action, typical morphological changes of apoptotic cells e.g. membrane blebbing, chromatin condensation, nuclear fragmentation, apoptotic bodies and loss of adhesion as well as cell cycle arrest in the G1 phase with increase of sub-G1 cell proportions, detected by Hoechst 33342 staining and flow cytometry were observed, suggesting DNA damage and subsequent apoptotic cell death. Taken together, our findings indicate for the first time that active n-hexane and chloroform extracts as well as macluraxanthone and gerontoxanthone-I isolated from Maclura amboinensis Bl. roots affect multistep of cancer metastasis processes including proliferation, adhesion, invasion and migration, possibly through induction of apoptosis of highly metastatic B16F10 melanoma cells. Based on these data, M. amboinensis Bl. represents a potential candidate novel chemopreventive and/or chemotherapeutic agent. Additionally, they also support its ethno-medicinal usage for cancer prevention and/or chemotherapy.

Highlights

  • Cancer metastasis is the most important cause of cancer death in patients

  • Our findings indicate for the first time that active n-hexane and chloroform extracts as well as macluraxanthone and gerontoxanthone-I isolated from Maclura amboinensis Bl. roots affect multistep of cancer metastasis processes including proliferation, adhesion, invasion and migration, possibly through induction of apoptosis of highly metastatic B16F10 melanoma cells

  • The inhibitory effects of four extracts and two main compounds isolated from M. amboinensis Bl. roots on cell proliferation as well as cancer metastasis properties such as adhesion, invasion and migration which play a crucial role in the pathogenesis of cancer metastasis on a highly metastastic B16F10 melanoma cells in vitro were evaluated

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Summary

Introduction

Cancer metastasis is the most important cause of cancer death in patients. During the metastatic cascade, metastasizing tumor cells interact with various host cells, extracellular matrices and basement membrane components. The decoction of roots and cortex are locally used in the treatment of malaria, fever, diuretic, hepatitis, liver disease and cancers (Lee et al, 2010) This plant is well known as the source of xanthones, flavonoids, triterpenoids and stilbenes (Lee et al, 2005). The inhibitory effects of four extracts and two main compounds isolated from M. amboinensis Bl. roots on cell proliferation as well as cancer metastasis properties such as adhesion, invasion and migration which play a crucial role in the pathogenesis of cancer metastasis on a highly metastastic B16F10 melanoma cells in vitro were evaluated. Mechanistic of apoptosis- inducing by these drugs was explored

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