Received:17 February 2018,
Published:30 August 2018
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Chang YU, Yang WANG, Mei XIONG, et al. Capsaicin enhances cisplatin sensitivity of osteosarcoma by inhibiting expression and nuclear-translocation of inhibitor of differentiation 1[J]. Journal of Third Military Medical University, 2018, 40(16): 1492-1499.
Chang YU, Yang WANG, Mei XIONG, et al. Capsaicin enhances cisplatin sensitivity of osteosarcoma by inhibiting expression and nuclear-translocation of inhibitor of differentiation 1[J]. Journal of Third Military Medical University, 2018, 40(16): 1492-1499. DOI: 10.16016/j.1000-5404.201802097.
Objective
2
To investigate the expression of inhibitor of differentiation 1 (Id1) in osteosarcoma tissues and evaluate the effect of capsaicin to enhance the chemosensitivity of osteosarcoma to cisplatin.
Methods
2
Immunohistochemistry was used to investigate Id1 expression levels in 12 osteosacroma tissue specimens and bone tissues from 12 patients with osteoarthritis.Three osteosarcoma cell lines (MG63
HOS and 143B) were treated with cisplatin and capsaicin
alone or in combination
and the expression levels of Id1
p-p65 and p-Smad1/5 in the cells were detected with Western blotting; immunofluorescence assay was used to investigate the location of Id1
and flow cytometry was used to analyze cell apoptosis in the treated cells.
Results
2
Osteosarcoma tissues expressed high levels of Id1 compared with osteoarthritis tissues.In the osteosarcoma cell lines
cisplain treatment induced an obvious up-regulation of Id1 expression (
P
<
0.05) and nuclear translocation of Id1
while treatment with capsaicin significantly reduced Id1 expression by suppressing p65 and Smad1/5 (
P
<
0.05).In cells treated with both capsaicin and cisplatin
capsaicin obviously reduced cisplatin-induced nuclear translocation of Id1 (
P
<
0.05) and significantly enhanced cisplatin-mediated cell apoptosis (
P
<
0.05).
Conclusion
2
Capsaicin can inhibit cisplatin-induced up-regulation and nuclear-translocation of Id1 and enhance cisplatin-mediated osteosarcoma cell apoptosis
and may thus serve as a potential agent for adjuvant chemotherapy of osteosarcoma.
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