Zerumbone modulates CD1d expression and lipid antigen presentation pathway in breast cancer cells

被引:20
|
作者
Shyanti, Ritis K. [1 ,4 ]
Sehrawat, Anuradha [2 ,3 ]
Singh, Shivendra V. [2 ,3 ]
Mishra, J. P. N. [1 ]
Singh, Rana P. [1 ,4 ]
机构
[1] Cent Univ Gujarat, Sch Life Sci, Gandhinagar, Gujarat, India
[2] Univ Pittsburgh, Sch Med, Dept Pharmacol & Chem Biol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Canc Inst, Pittsburgh, PA USA
[4] Jawaharlal Nehru Univ, Sch Life Sci, Canc & Radiat Biol Lab, New Delhi, India
关键词
Zerumbone; alpha-Galactosylceramide; CD1d; NKT cells; Anti-CD1d mAb; Breast cancer; KILLER T-CELLS; NKG2D LIGANDS; NKT CELLS; BENZYL ISOTHIOCYANATE; INDUCED APOPTOSIS; UP-REGULATION; INKT CELLS; ACTIVATION; MICE; INNATE;
D O I
10.1016/j.tiv.2017.06.016
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Natural Killer T (NKT) cells based cancer immunotherapy is an evolving area of cancer therapy, but tumors escape from this treatment modality by altering CD1d expression and its antigen presentation pathway. Here, we have studied the relation of CD1d expression in various breast cancer cell lines to their viability and progression. We observed a novel phenomenon that CD1d expression level increases with the progressive stage of the cancer. A small molecule, zerumbone (ZER) caused down-regulation of CD1d that was accompanied by breast cancer cell growth in vitro. The growth inhibitory effect of ZER against breast cancer cells was augmented by treatment with anti-CD1d mAb. This effect was mediated by Gl-phase cell cycle arrest and apoptosis induction coupled with an increase in mitochondrial membrane depolarization. CD1d expression and cell proliferation were inhibited by both CD1d siRNA and ZER. The a-galactosylceramide, a ligand for CD1d, showed increased CD1d expression as well as cell proliferation which was opposite to the effects of ZER. This study shows that, CD1d overexpression is associated with the progressive stages of breast cancer and ZER could be an adjuvant to potentiate cancer immunotherapy.
引用
收藏
页码:74 / 84
页数:11
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