Synergistic Enhancement of Lung Cancer Therapy Through Nanocarrier-Mediated Sequential Delivery of Superantigen and Tyrosin Kinase Inhibitor

被引:24
作者
Li, Da [1 ]
Li, Yongbin [2 ]
Xing, Haibo [4 ]
Guo, Junling [3 ]
Ping, Yuan [3 ]
Tang, Guping [2 ]
机构
[1] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Dept Med Oncol, Hangzhou 310016, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Chem Biol & Pharmaceut Chem, Hangzhou 310028, Zhejiang, Peoples R China
[3] Univ Melbourne, Dept Chem & Biomol Engn, Melbourne, Vic 3010, Australia
[4] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Intens Care Unit, Hangzhou 310019, Zhejiang, Peoples R China
关键词
NONSMALL CELL LUNG; GROWTH-FACTOR RECEPTOR; NECROSIS-FACTOR-ALPHA; OVERCOMING ACQUIRED-RESISTANCE; CO-DELIVERY; GENE DELIVERY; TARGETED THERAPIES; BETA-CYCLODEXTRIN; TUMOR-GROWTH; IN-VITRO;
D O I
10.1002/adfm.201400456
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gefitinib (GFT) and other tyrosine kinase inhibitors (TKIs) have been widely used for the treatment of advanced or metastatic lung cancer due to their reduced side effects when compared to classic cytotoxic chemotherapeutic agents. However, both intrinsic and acquired resistance often hinders the effectiveness of TKIs. Based on recent findings that the outcome of chemotherapy can be influenced by the host immune system at multiple levels, an exploration of whether activating antitumor immunity improves the efficacy of the targeted cancer therapy of TKIs is undertaken. To this end, a cationic carrier is used to deliver superantigen and GFT in a simultaneous or sequential manner. The sequential delivery of superantigen and GFT can significantly enhance T cell immunity, promote cytokine production, inhibit tumor growth, and prolong survival time in tumor models with lung carcinoma xenografts. Most importantly, dual sequential treatment reveals a synergistic effect on tumor inhibition, which is much more effective than the monotherapy of either GFT or pTSA, as well as the combined treatment through simultaneous codelivery of pTSA and GFT together. This study demonstrates the important contribution of immunotherapy to targeted molecular therapy and opens up new possibilities for treating a wide spectrum of cancers.
引用
收藏
页码:5482 / 5492
页数:11
相关论文
共 49 条
[1]   Escape from immunotherapy: possible mechanisms that influence tumor regression/progression [J].
Ahmad, M ;
Rees, RC ;
Ali, SA .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2004, 53 (10) :844-854
[2]   Enhancement of sensitivity to tumor necrosis factor α in non-small cell lung cancer cells with acquired resistance to gefitinib [J].
Ando, K ;
Ohmori, T ;
Inoue, F ;
Kadofuku, T ;
Hosaka, T ;
Ishida, H ;
Shirai, T ;
Okuda, K ;
Hirose, T ;
Horichi, N ;
Nishio, K ;
Saijo, N ;
Adachi, M ;
Kuroki, A .
CLINICAL CANCER RESEARCH, 2005, 11 (24) :8872-8879
[3]   Imatinib potentiates antitumor T cell responses in gastrointestinal stromal tumor through the inhibition of Ido [J].
Balachandran, Vinod P. ;
Cavnar, Michael J. ;
Zeng, Shan ;
Bamboat, Zubin M. ;
Ocuin, Lee M. ;
Obaid, Hebroon ;
Sorenson, Eric C. ;
Popow, Rachel ;
Ariyan, Charlotte ;
Rossi, Ferdinand ;
Besmer, Peter ;
Guo, Tianhua ;
Antonescu, Cristina R. ;
Taguchi, Takahiro ;
Yuan, Jianda ;
Wolchok, Jedd D. ;
Allison, James P. ;
DeMatteo, Ronald P. .
NATURE MEDICINE, 2011, 17 (09) :1094-U99
[4]   Correlation of NK T-like CD3+CD56+ cells and CD4+CD25+(hi) regulatory T cells with VEGF and TNFα in ascites from advanced ovarian cancer:: Association with platinum resistance and prognosis in patients receiving first-line, platinum-based chemotherapy [J].
Bamias, Aristotelis ;
Koutsoukou, Vasiliki ;
Terpos, Evangelos ;
Tsiatas, Marinos L. ;
Liakos, Christina ;
Tsitsilonis, Ourania ;
Rodolakis, Alexandros ;
Voulgaris, Zannis ;
Vlahos, G. ;
Papageorgiou, Theocharis ;
Papatheodoridis, G. ;
Archimandritis, A. ;
Antsaklis, A. ;
Dilnopoulos, M. A. .
GYNECOLOGIC ONCOLOGY, 2008, 108 (02) :421-427
[5]   Regulation of tumor growth by IFN-γ in cancer immunotherapy [J].
Beatty, GL ;
Paterson, Y .
IMMUNOLOGIC RESEARCH, 2001, 24 (02) :201-210
[6]   Therapeutic live vaccines as a potential anticancer strategy [J].
Bolhassani, Azam ;
Zahedifard, Farnaz .
INTERNATIONAL JOURNAL OF CANCER, 2012, 131 (08) :1733-1743
[7]  
Brivio F, 2008, IN VIVO, V22, P647
[8]   ENDOTOXIN-INDUCED SERUM FACTOR THAT CAUSES NECROSIS OF TUMORS [J].
CARSWELL, EA ;
OLD, LJ ;
KASSEL, RL ;
GREEN, S ;
FIORE, N ;
WILLIAMSON, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (09) :3666-3670
[9]   Co-delivery of Doxorubicin and Bcl-2 siRNA by Mesoporous Silica Nanoparticles Enhances the Efficacy of Chemotherapy in Multidrug-Resistant Cancer Cells [J].
Chen, Alex M. ;
Zhang, Min ;
Wei, Dongguang ;
Stueber, Dirk ;
Taratula, Oleh ;
Minko, Tamara ;
He, Huixin .
SMALL, 2009, 5 (23) :2673-2677
[10]  
Choudhury NN, 2012, CURR PHARM BIOTECHNO, V13, P1317