TY - JOUR
T1 - Antimicrobial peptide LL-37 promotes the proliferation and invasion of skin squamous cell carcinoma by upregulating DNA-binding protein A
AU - Wang, Wei
AU - Jia, Jinjing
AU - Li, Changji
AU - Duan, Qiqi
AU - Yang, Jiao
AU - Wang, Xin
AU - Li, Ruilian
AU - Chen, Caifeng
AU - Yan, Huling
AU - Zheng, Yan
N1 - Publisher Copyright:
© 2016, Spandidos Publications. All rights reserved.
PY - 2016/9
Y1 - 2016/9
N2 - The antimicrobial peptide LL-37 not only contributes to the host defence against microbial invasion but also regulates immune activity, angiogenesis and cell proliferation. Studies have shown that LL-37 participates in the development of a variety of tumours, such as lung cancer, ovarian cancer, breast cancer and melanoma. However, the role of LL-37 in the development of skin squamous cell carcinoma (SCC) is not clear. The present study used immunohistochem- istry to confirm that the expression of human DNA-binding protein A (dbpA) was increased in SCC tissues. After stimulating SCC A341 cells, LL-37 was shown promote the proliferation, migration and invasion of these malignant cells. LL-37 also promoted the upregulation of dbpA mRNA and protein expression. In addition, after using small interfering RNA to silence the normal dbpA expression in these malignant cells, the proliferation and invasion of the tumor cells were significantly reduced. When the NF-κB inhibitor PDTC was used to inhibit the process of LL-37-stimulated cells, it was found that the original upregulated expression of dbpA was downregulated. Overall, the present demonstrated that by upregulating the expression of dbpA, LL-37 can promote the proliferation and invasion of tumour cells, and that this process depends on the NF-κB signalling pathway.
AB - The antimicrobial peptide LL-37 not only contributes to the host defence against microbial invasion but also regulates immune activity, angiogenesis and cell proliferation. Studies have shown that LL-37 participates in the development of a variety of tumours, such as lung cancer, ovarian cancer, breast cancer and melanoma. However, the role of LL-37 in the development of skin squamous cell carcinoma (SCC) is not clear. The present study used immunohistochem- istry to confirm that the expression of human DNA-binding protein A (dbpA) was increased in SCC tissues. After stimulating SCC A341 cells, LL-37 was shown promote the proliferation, migration and invasion of these malignant cells. LL-37 also promoted the upregulation of dbpA mRNA and protein expression. In addition, after using small interfering RNA to silence the normal dbpA expression in these malignant cells, the proliferation and invasion of the tumor cells were significantly reduced. When the NF-κB inhibitor PDTC was used to inhibit the process of LL-37-stimulated cells, it was found that the original upregulated expression of dbpA was downregulated. Overall, the present demonstrated that by upregulating the expression of dbpA, LL-37 can promote the proliferation and invasion of tumour cells, and that this process depends on the NF-κB signalling pathway.
KW - DNA-binding protein A
KW - Epidermal growth factor receptor
KW - LL-37
KW - Nuclear factor-κB
KW - Squamous cell carcinoma
KW - Y-box
UR - https://www.scopus.com/pages/publications/84979710805
U2 - 10.3892/ol.2016.4865
DO - 10.3892/ol.2016.4865
M3 - 文章
AN - SCOPUS:84979710805
SN - 1792-1074
VL - 12
SP - 1745
EP - 1752
JO - Oncology Letters
JF - Oncology Letters
IS - 3
ER -