Geiparvarin Inhibits OS Metastasis through Upregulation of ANGPTL4 Expression by Inhibiting miRNA-3912-3p Expression

Author:

Jiang Fuling1,Wang Guang-Jie2,Huang Ping3,Chen Shu4,Xiao He4,Zhang Liang4,Zou Hua4ORCID

Affiliation:

1. Department of Spine Surgery, Center of Orthopedics, Daping Hospital, Army Medical University, Chongqing 400042, China

2. Department of Oncology, The General Hospital of Western Theater Command, Chengdu, Sichuan 610083, China

3. Department of Radiation Oncology, Chongqing University Cancer Hospital, Chongqing 400033, China

4. Cancer Center, Daping Hospital, Army Medical University, Chongqing 400042, China

Abstract

Background. Geiparvarin (GN) is a natural compound with anticancer activity. However, the effect of GN on osteosarcoma (OS) and the anticancer mechanism of GN are still unclear. Methods. Cell viability was measured by MTT assay. Invasion and migration were measured by transwell assay. The miRNAs, genes, and signaling pathways affected by GN were confirmed by whole-genome sequencing and bioinformatics analysis. The expression level of mRNA and protein was measured by qRT-PCR and western blot. Animal experiment was performed for confirming the GN anticancer effect and side effect in vivo. Results. Our results show that GN significantly inhibits OS cell growth and metastasis in vitro. In vivo experiment also showed that GN dramatically suppressed OS lung metastasis and no side effects were found. GN treatment inhibited OS metastasis through upregulating the ANGPTL4 expression. In addition, GN inhibited the expression of miR-3912-3p, which targets ANGPTL4. Conclusion. Our data clearly indicate that GN is a candidate drug for OS treatment, and GN plays its role through miR-3912-3p/ANGPTL4 in OS.

Funder

Chongqing Natural Science Foundation

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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