张晓娟, 王慧娟, 张米娜. Role of HMGB1/TLR4 pathway in the process of Fibulin-5 inhibiting lung cancer cells proliferation and metastasis[J]. China Oncology, 2017, 27(10): 761-769.
张晓娟, 王慧娟, 张米娜. Role of HMGB1/TLR4 pathway in the process of Fibulin-5 inhibiting lung cancer cells proliferation and metastasis[J]. China Oncology, 2017, 27(10): 761-769. DOI: 10.19401/j.cnki.1007-3639.2017.10.001.
Background and purpose: The expression of Fibulin-5
a tumor suppressor
is reduced in lung cancer tissues. High mobility group box 1 (HMGB1)
overexpressed in lung cancer
can promote the invasion and metastasis of the tumor. This study aimed to investigate the molecular mechanism of Fibulin-5 inhibiting the proliferation and metastasis of lung cancer cells. Method: Firstly the expressions of Fibulin-5 and HMGB1 in lung epithelial cells and lung cancer cells were detected. Then transfection reagents were used to transfect Fibulin-5 plasmid and HMGB1 siRNA into A549 cells
which achieved Fibulin-5 overexpression and HMGB1 down-regulation. MTT was used to detect the cell proliferation. Transwell was used to examine the ability of cell invasion and migration. HMGB1 mRNA expression was detected by real-time fluorescence quantitative polymerase chain reaction (RTFQ-PCR). The secretion of HMGB1 protein was analyzed by enzyme-linked immunosorbent assay (ELISA). Western blot was used to detect the levels of HMGB1
cyclin D1
matrix metalloproteinases (MMPs)
and TLR4/NF-κB pathway related proteins. Results: In A549 cell
Fibulin-5 expression was down-regulated and HMGB1 expression was up-regulated. After overexpression of Fibulin-5 or knockdown of HMGB1 in A549 cells
the levels of HMGB1
cyclin D1
MMP2
MMP7 and MMP9 were significantly reduced; the abilities of lung cancer cell proliferation
invasion and migration were notably suppressed (P0.05). In addition
Fibulin-5 overexpression decreased the protein expressions of TLR4
MyD88
p-p65
increased the expression of IκBα (P0.05). Conclusion: Fibulin-5 may inhibit lung cancer cell proliferation
invasion and migration via inhibiting the expression of HMGB1 and its downstream TLR4/NF-κB pathway.