Potential synergistic anti-tumor activity between lenalidomide and sorafenib in hepatocellular carcinoma

被引:20
|
作者
Ou, Da-Liang [1 ]
Chang, Chun-Jung [1 ]
Jeng, Yung-Ming [2 ]
Lin, Yi-Jang [3 ]
Lin, Zhong-Zhe [3 ]
Gandhi, Anita K. [5 ]
Liao, Sheng-Chieh [3 ]
Huang, Zi-Ming [3 ]
Hsu, Chiun [1 ,3 ,4 ]
Cheng, Ann-Lii [1 ,3 ,4 ]
机构
[1] Natl Taiwan Univ, Grad Inst Oncol, Coll Med, Taipei 10764, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Pathol, Taipei 100, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Oncol, Taipei 100, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[5] Celgene Corp, Dept Translat Dev, Summit, NJ USA
关键词
immune modulatory; lenalidomide; sorafenib; tumor-infiltrating lymphocytes; vascular normalization; REGULATORY T-CELLS; POSTOPERATIVE RECURRENCE; CANCER; SUNITINIB; PD-L1; LIVER; ANGIOGENESIS; INCREASE;
D O I
10.1111/jgh.12708
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aim: The immune modulatory drug lenalidomide has shown promising anti-tumor activity in a clinical trial of patients with advanced hepatocellular carcinoma (HCC). The present study explored whether lenalidomide can enhance the anti-tumor activity of sorafenib, the standard molecular targeted therapy for HCC. Methods: The anti-tumor efficacy of single-agent or combination treatment was measured by change in tumor volume and animal survival using an orthotopic liver cancer model. Distribution of T-cell subpopulations in tumor-infiltrating lymphocytes (TILs) and splenocytes derived from tumor-implanted mice was measured by flow cytometry. Depletion of relevant T-cell subpopulations or cytokines was done by co-administration of relevant antibodies with study drug treatment. Tumor cell apoptosis and tumor angiogenesis were measured by transferase deoxytidyl uridine end labeling assay and immunohistochemical study, respectively. Results: Combination of sorafenib and lenalidomide produced significant synergistic anti-tumor efficacy in terms of tumor growth delay and animal survival. This synergistic effect was associated with a significant increase in interferon-gamma expressing CD8(+) lymphocytes in TILs and a significantly higher number of granzyme-or perforin-expressing CD8(+) T cells, compared with vehicle-or single-agent treatment groups. Combination treatment significantly increased apoptotic tumor cells and vascular normalization in tumor tissue. The synergistic anti-tumor effect was abolished after CD8 depletion. Conclusions: Lenalidomide can enhance the anti-tumor effects of sorafenib in HCC through its immune modulatory effects, and CD8(+) TILs play an important role in the anti-tumor synergism.
引用
收藏
页码:2021 / 2031
页数:11
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