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Published on: May 3, 2018
Furowanin A Exhibits Antiproliferative and Pro-Apoptotic Activities by Targeting Sphingosine Kinase 1 in Osteosarcoma
Ke Wei1, Haixia Sun1, Xinhui Chen1
1Department of Orthopedics, Ningbo No. 9 Hospital, Ningbo, Zhejiang, China.
Abstract:
Osteosarcoma (OS) is one of the most common malignant bone tumors among children and young adults. Furowanin A (Fur A), one of the active ingredients of Millettia pachycarpa Benth, has been found to exert pro-apoptotic activity in human leukemia cells. This study is designed to evaluate the efficacy of Fur A against OS. The effect of Fur A on cell viability was assessed by Cell Counting Kit-8 (CCK-8) assay. Western blotting and quantitative real-time PCR (qRT-PCR) were performed to determine the protein and mRNA level of sphingosine kinase 1 (SphK1), respectively. To validate the role of SphK1 in the pro-apoptotic activity of Fur A, overexpressing SphK1 vector and siRNA targeting SphK1 were utilized to transfect OS cells. Moreover, an OS xenograft murine model was used to analyze the therapeutic efficacy of Fur A in vivo. Fur A treatment led to a dose-dependent decrease in the number of viable cells. It also exhibited antiproliferative activity and significantly promoted apoptotic cell death in OS cell lines. Our results showed that the anticancer activity of Fur A was associated with downregulation of SphK1 and inactivation of its downstream signaling. The mediatory role of SphK1 was validated when the pro-apoptotic activity of Fur A was significantly blocked by SphK1 overexpression, while SphK1 knockdown sensitized the OS cells to Fur A. We concluded that Fur A can exhibit anti-growth and pro-apoptotic activities in vitro and in vivo in OS by downregulating SphK1. Our study highlights the possibility of utilizing Fur A as a chemotherapeutic agent in the treatment of OS. Anat Rec, 302:1941-1949, 2019. © 2019 American Association for Anatomy.
Insights
Furowanin A (Fur A), derived from Millettia pachycarpa Benth, demonstrates significant anti-cancer effects against osteosarcoma (OS). This compound inhibits OS cell growth and promotes apoptosis by downregulating sphingosine kinase 1 (SphK1).
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Osteosarcoma (OS) is a prevalent bone cancer in young individuals.
- Furowanin A (Fur A), from Millettia pachycarpa Benth, shows prior pro-apoptotic effects in leukemia cells.
Purpose of the Study:
- To investigate the anti-cancer efficacy of Furowanin A (Fur A) against osteosarcoma (OS).
- To elucidate the role of sphingosine kinase 1 (SphK1) in Fur A's anti-OS activity.
Main Methods:
- Cell viability assessed using Cell Counting Kit-8 (CCK-8) assay.
- Protein and mRNA levels of SphK1 determined by Western blotting and qRT-PCR.
- In vitro studies involved SphK1 overexpression and knockdown in OS cells.
- In vivo efficacy evaluated using an OS xenograft murine model.
Main Results:
- Fur A treatment reduced OS cell viability in a dose-dependent manner.
- Fur A demonstrated antiproliferative activity and induced apoptosis in OS cell lines.
- Anticancer effects correlated with SphK1 downregulation and inactivation of its signaling pathways.
- SphK1 overexpression blocked Fur A's pro-apoptotic effects, while knockdown enhanced sensitivity.
Conclusions:
- Furowanin A exhibits significant anti-growth and pro-apoptotic properties against osteosarcoma in vitro and in vivo.
- The mechanism involves the downregulation of SphK1.
- Fur A shows potential as a novel chemotherapeutic agent for osteosarcoma treatment.
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