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Lung Cancer Derived Circulating miR-21 Promotes Bone Metastasis by Activating Differentiation of Monocytes to Osteoclasts

26 Pages Posted: 11 Jun 2019

See all articles by Qian Zhao

Qian Zhao

Sichuan University - West China Hospital

Chang Liu

Sichuan University - Laboratory of Endocrinology and Metabolism

Ying Xie

Sichuan University - Laboratory of Endocrinology and Metabolism

Mengjia Tang

Sichuan University - Laboratory of Endocrinology and Metabolism

Guojing Luo

Sichuan University - Laboratory of Endocrinology and Metabolism

Xiang Chen

Sichuan University - Laboratory of Endocrinology and Metabolism

Li Tian

Sichuan University - Laboratory of Endocrinology and Metabolism

Xijie Yu

Sichuan University - Laboratory of Endocrinology and Metabolism

More...

Abstract

Background: Osteoclastogenesis is a key process in osteolytic bone metastasis (BM). Previous studies indicated that miRNAs could regulate cancer progression and osteoclastogenesis. Our purpose was to investigate the roles of lung cancer cells-derived circulating miR-21 on osteoclastogenesis and its clinical significance in BM patients.

Methods: The difference of miRNA expression in two lung cancer cell lines SBC-5 (with characteristic BM ability) and SBC-3 (without BM ability) were analyzed. Circulating miR-21 levels of lung cancer patients with or without BM were compared. The effects of conditioned media from lung cancer cell lines or patients' plasma with different miR-21 levels on osteoclastogenesis were investigated. The diagnostic performance of circulating miR-21 in BM patients was evaluated.

Findings: We found that miR-21 expression was specifically higher in SBC-5 than that in SBC-3 cells. The supernatants of SBC-5 cells with higher level miR-21 promoted osteoclastogenesis. Moreover, we demonstrated that the circulating miR-21 level was significantly higher in BM patients than that in non-BM patients. The plasma from BM patients with higher level miR-21 could also promot osteoclastogenesis. Mechanistically, lung cancer cells-derived circulating miR-21 could be transferred into osteoclast precursor cells and promot osteoclastogenesis probably by inhibiting PTEN (Phosphatase and tensin homologue). Finally, we indecated that circulating miR-21 had a potential for the diagnosis of BM.

Interpretation: Our findings suggested circulating miR-21 played important roles in BM of lung cancer and may service as a biomarker to diagnose BM in lung cancer patients.

Funding: This work was supported by grants from the National Natural Science Foundation of China (No. 81572639, 81770875, 81370969), Department of Science and Technology of Sichuan Province (2018SZ0142), and Sichuan University (2018SCUH0093).

Declaration of Interest: No potential conflicts of interest were disclosed.

Ethical Approval: The study was approved by the hospital research ethics committee of West China Hospital of Sichuan University and conducted in accordance with the International Ethical Guidelines for Biomedical Research Involving Human Subjects. All patients included in this study had signed the informed consent form.

Keywords: MicroRNA; Bone metastasis; Lung cancer; Osteoclast; Biomarker

Suggested Citation

Zhao, Qian and Liu, Chang and Xie, Ying and Tang, Mengjia and Luo, Guojing and Chen, Xiang and Tian, Li and Yu, Xijie, Lung Cancer Derived Circulating miR-21 Promotes Bone Metastasis by Activating Differentiation of Monocytes to Osteoclasts (June 10, 2019). Available at SSRN: https://ssrn.com/abstract=3401958 or http://dx.doi.org/10.2139/ssrn.3401958

Qian Zhao

Sichuan University - West China Hospital

No 37, Guoxue Road
Wuhou District
Chengdu, Sichuan Province 610041
China

Chang Liu

Sichuan University - Laboratory of Endocrinology and Metabolism

China

Ying Xie

Sichuan University - Laboratory of Endocrinology and Metabolism

China

Mengjia Tang

Sichuan University - Laboratory of Endocrinology and Metabolism

China

Guojing Luo

Sichuan University - Laboratory of Endocrinology and Metabolism

China

Xiang Chen

Sichuan University - Laboratory of Endocrinology and Metabolism

China

Li Tian

Sichuan University - Laboratory of Endocrinology and Metabolism

China

Xijie Yu (Contact Author)

Sichuan University - Laboratory of Endocrinology and Metabolism ( email )

China

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