Curcumin as an Adjuvant to Cancer Immunotherapy

被引:46
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
[1]   Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases [J].
Aggarwal, Bharat B. ;
Harikumar, Kuzhuvelil B. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2009, 41 (01) :40-59
[2]   Human Epidermal Growth Factor Receptor 2 (HER2) -Specific Chimeric Antigen Receptor-Modified T Cells for the Immunotherapy of HER2-Positive Sarcoma [J].
Ahmed, Nabil ;
Brawley, Vita S. ;
Hegde, Meenakshi ;
Robertson, Catherine ;
Ghazi, Alexia ;
Gerken, Claudia ;
Liu, Enli ;
Dakhova, Olga ;
Ashoori, Aidin ;
Corder, Amanda ;
Gray, Tara ;
Wu, Meng-Fen ;
Liu, Hao ;
Hicks, John ;
Rainusso, Nino ;
Dotti, Gianpietro ;
Mei, Zhuyong ;
Grilley, Bambi ;
Gee, Adrian ;
Rooney, Cliona M. ;
Brenner, Malcolm K. ;
Heslop, Helen E. ;
Wels, Winfried S. ;
Wang, Lisa L. ;
Anderson, Peter ;
Gottschalk, Stephen .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15) :1688-+
[3]   Cancer immunotherapies, their safety and toxicity [J].
Alatrash, Gheath ;
Jakher, Haroon ;
Stafford, Patricia D. ;
Mittendorf, Elizabeth A. .
EXPERT OPINION ON DRUG SAFETY, 2013, 12 (05) :631-645
[4]   Contribution to Tumor Angiogenesis From Innate Immune Cells Within the Tumor Microenvironment: Implications for Immunotherapy [J].
Albini, Adriana ;
Bruno, Antonino ;
Noonan, Douglas M. ;
Mortara, Lorenzo .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[5]   Bioavailability of curcumin: Problems and promises [J].
Anand, Preetha ;
Kunnumakkara, Ajaikumar B. ;
Newman, Robert A. ;
Aggarwal, Bharat B. .
MOLECULAR PHARMACEUTICS, 2007, 4 (06) :807-818
[6]   Upcoming innovations in lung cancer immunotherapy: focus on immune checkpoint inhibitors [J].
Aspeslagh, Sandrine ;
Marabelle, Aurelien ;
Soria, Jean-Charles ;
Armand, Jean-Pierre .
CHINESE CLINICAL ONCOLOGY, 2015, 4 (04)
[7]   STAT3 as a potential immunotherapy biomarker in oncogene-addicted non-small cell lung cancer [J].
Attili, Ilaria ;
Karachaliou, Niki ;
Bonanno, Laura ;
Berenguer, Jordi ;
Bracht, Jillian ;
Codony-Servat, Jordi ;
Codony-Servat, Carles ;
Ito, Masaoki ;
Rosell, Rafael .
THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY, 2018, 10
[8]   Regulatory T cells under scrutiny [J].
Bach, JF .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (03) :189-198
[9]  
Barbet Jacques, 2012, Methods Mol Biol, V907, P681, DOI 10.1007/978-1-61779-974-7_38
[10]   Regulatory T cells in ovarian cancer: Biology and therapeutic potential [J].
Barnett, B ;
Kryczek, I ;
Cheng, P ;
Zou, WP ;
Curiel, TJ .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2005, 54 (06) :369-377