Oncotarget

Research Papers:

Laricitrin ameliorates lung cancer-mediated dendritic cell suppression by inhibiting signal transducer and activator of transcription 3

Wei-An Chang, Jen-Yu Hung, Shu-Fang Jian, Yi-Shiuan Lin, Cheng-Ying Wu, Ya-Ling Hsu and Po-Lin Kuo _

PDF  |  HTML  |  Supplementary Files  |  How to cite

Oncotarget. 2016; 7:85220-85234. https://doi.org/10.18632/oncotarget.13240

Metrics: PDF 1716 views  |   HTML 2717 views  |   ?  


Abstract

Wei-An Chang1,2, Jen-Yu Hung2,3, Shu-Fang Jian1, Yi-Shiuan Lin1, Cheng-Ying Wu1, Ya-Ling Hsu4, Po-Lin Kuo1,4,5

1Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

2Division of Pulmonary and Critical Care Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan

3School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

4Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

5Institute of Medical Science and Technology, National Sun Yat-Sen University, Kaohsiung, Taiwan

Correspondence to:

Po-Lin Kuo, email: [email protected]

Ya-Ling Hsu, email: [email protected]

Keywords: laricitrin, dendritic cell, lung cancer, IL-10, STAT3

Received: August 20, 2016     Accepted: October 24, 2016     Published: November 09, 2016

ABSTRACT

Natural polyphenolic compounds of grapes and their seeds are thought to be therapeutic adjuvants in a variety of diseases, including cancer prevention. This study was carried out to investigate the effect of grape phenolic compounds on the regulation of cancer-mediated immune suppression. Laricitrin exhibits the greatest potential to ameliorate the suppressive effects of lung cancer on dendritic cells’ (DCs’) differentiation, maturation and function. Human lung cancer A549 and CL1-5 cells change the phenotype of DCs that express to high levels of IL-10 and prime T cells towards an immune suppression type-2 response (Th2). Laricitrin treatment stimulated DC differentiation and maturation in the condition media of cancer cells, a finding supported by monocyte marker CD14’s disappearance and DC marker CD1a’s upregulation. Laricitrin decreases expression of IL-10 in cancer-conditioned DCs, and subsequently switches CD4+ T cell response from Th2 to Th1 in vitro and in vivo. Reversal of laricitrin on lung cancer-induced DCs’ paralysis was via inhibiting the phosphorylation of signal transducer and activator of transcription 3 (STAT3). Laricitrin also potentiated the anticancer activity of cisplatin in mouse models. Thus, laricitrin could be an efficacious immunoadjuvant and have a synergistic effect when combined with chemotherapy.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 13240