Curcumin as an Adjuvant to Cancer Immunotherapy

被引:47
作者
Paul, Silpita [1 ]
Sa, Gaurisankar [1 ]
机构
[1] Bose Inst, Div Mol Med, Kolkata, India
关键词
curcumin; dendritic cell; CTLA4; PD1; PD-L1; immune cells; Treg cells; immunotherapy; REGULATORY T-CELLS; NF-KAPPA-B; CHEMOPREVENTIVE AGENT CURCUMIN; DOWN-REGULATION; IMMUNE-SYSTEM; DENDRITIC CELLS; MONOCLONAL-ANTIBODIES; OVARIAN-CANCER; BREAST-CANCER; PRIMARY TUMOR;
D O I
10.3389/fonc.2021.675923
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The components of the immune system play a very sincere and crucial role in combating tumors. However, despite their firm efforts of elimination, tumor cells cleverly escape the surveillance process by adopting several immune evasion mechanisms. The conversion of immunogenicity of tumor microenvironment into tolerogenic is considered as a prime reason for tumor immune escape. Therapeutically, different immunotherapies have been adopted to block such immune escaping routes along with better clinical outcomes. Still, the therapies are haunted by several drawbacks. Over time, curcumin has been considered as a potential anti-cancer molecule. Its potentialities have been recorded against the standard hallmarks of cancer such as continuous proliferation, escaping apoptosis, continuous angiogenesis, insensitivity to growth inhibitors, tissue invasion, and metastasis. Hence, the diversity of curcumin functioning has already been established and exploration of its application with immunotherapies might open up a new avenue for scientists and clinicians. In this review, we briefly discuss the tumor's way of immune escaping, followed by various modern immunotherapies that have been used to encounter the escaping paths and their minute flaws. Finally, the conclusion has been drawn with the application of curcumin as a potential immune-adjuvant, which fearlessly could be used with immunotherapies for best outcomes.
引用
收藏
页数:16
相关论文
共 148 条
[131]   Studies of curcumin and curcuminoids.: XXVII.: Cyclodextrin complexation:: solubility, chemical and photochemical stability [J].
Tonnesen, HH ;
Másson, M ;
Loftsson, T .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 244 (1-2) :127-135
[132]   Inhibition of NAD(P)H:quinone oxidoreductase 1 activity and induction of p53 degradation by the natural phenolic compound curcumin [J].
Tsvetkov, P ;
Asher, G ;
Reiss, V ;
Shaul, Y ;
Sachs, L ;
Lotern, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (15) :5535-5540
[133]   Targeting the tumour stroma to improve cancer therapy [J].
Valkenburg, Kenneth C. ;
de Groot, Amber E. ;
Pienta, Kenneth J. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2018, 15 (06) :366-381
[134]   Curcumin Encapsulated in Milk Exosomes Resists Human Digestion and Possesses Enhanced Intestinal Permeability in Vitro [J].
Vashisht, Monika ;
Rani, Payal ;
Onteru, Suneel Kumar ;
Singh, Dheer .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2017, 183 (03) :993-1007
[135]  
Ventola C Lee, 2017, P T, V42, P514
[136]  
Weiner LM, 2015, CLIN ADV HEMATOL ONC, V13, P299
[137]   Autophagy induction contributes to the resistance to methotrexate treatment in rheumatoid arthritis fibroblast-like synovial cells through high mobility group box chromosomal protein 1 [J].
Xu, Ke ;
Cai, Yong-song ;
Lu, She-Min ;
Li, Xiao-li ;
Liu, Lin ;
Li, Zhong ;
Liu, Hui ;
Xu, Peng .
ARTHRITIS RESEARCH & THERAPY, 2015, 17
[138]   Cancer immunotherapy: harnessing the immune system to battle cancer [J].
Yang, Yiping .
JOURNAL OF CLINICAL INVESTIGATION, 2015, 125 (09) :3335-3337
[139]   Cancer vaccine: learning lessons from immune checkpoint inhibitors [J].
Ye, ZhenLong ;
Qian, Qiming ;
Jin, HuaJun ;
Qian, QiJun .
JOURNAL OF CANCER, 2018, 9 (02) :263-268
[140]   Differential binding properties of B7-H1 and B7-DC to programmed death-1 [J].
Youngnak, P ;
Kozono, Y ;
Kozono, H ;
Iwai, H ;
Otsuki, N ;
Jin, H ;
Omura, K ;
Yagita, H ;
Pardoll, DM ;
Chen, LP ;
Azuma, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 307 (03) :672-677