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Challenges and opportunities for cancer stem cell-targeted immunotherapies include immune checkpoint inhibitor, cancer stem cell-dendritic cell vaccine, chimeric antigen receptor immune cells, and modified exosomes
被引:2
作者:
Alqarni, Abdullah
[1
]
Jasim, Saade Abdalkareem
[2
]
Altalbawy, Farag M. A.
[3
]
Kaur, Harpreet
[4
,5
]
Kaur, Irwanjot
[6
,7
]
Rodriguez-Benites, Carlos
[8
]
Deorari, Mahamedha
[9
]
Alwaily, Enas R.
[10
]
Al-Ani, Ahmed M.
[11
]
Redhee, Ahmed H.
[12
,13
,14
]
机构:
[1] King Khalid Univ, Coll Dent, Dept Diagnost Dent Sci & Oral Biol, Abha, Saudi Arabia
[2] Al Maarif Univ Coll, Med Lab Tech Dept, Anbar, Iraq
[3] Univ Tabuk, Univ Duba Coll, Dept Chem, Tabuk, Saudi Arabia
[4] Shobhit Univ, Sch Basic & Appl Sci, Gangoh, India
[5] Arka Jain Univ, Dept Hlth & Allied Sci, Jamshedpur, India
[6] Jain Deemed Univ, Dept Biotechnol, Bengaluru, India
[7] Vivekananda Global Univ, Dept Allied Healthcare & Sci, Jaipur, India
[8] Univ Nacl Trujillo, Fac Ciencias Fis & Matemat, Dept Acad Fis, Trujillo, Peru
[9] Uttaranchal Univ, Uttaranchal Inst Pharmaceut Sci, Dehra Dun, India
[10] Al Ayen Univ, Coll Pharm, Microbiol Res Grp, Thi Qar, Iraq
[11] Al Nisour Univ Coll, Dept Med Engn, Baghdad, Iraq
[12] Islamic Univ, Med Lab Tech Coll, Najaf, Iraq
[13] Islamic Univ Al Diwaniyah, Med Lab Tech Coll, Al Diwaniyah, Iraq
[14] Islamic Univ Babylon, Med Lab Tech Coll, Babylon, Iraq
关键词:
cancer stem cell;
cancer vaccine;
chimeric antigen receptor T cell;
exosomes;
immune escape;
immunotherapy;
CAR-T-CELLS;
ANTITUMOR-ACTIVITY;
TUMOR PROGRESSION;
PD-L1;
EXPRESSION;
COLON-CANCER;
GLIOBLASTOMA;
ACTIVATION;
VESICLES;
INFILTRATION;
STRATEGIES;
D O I:
10.1002/jbt.23719
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Cancer stem cells (CSCs) are associated with the tumor microenvironment (TME). CSCs induce tumorigenesis, tumor recurrence and progression, and resistance to standard therapies. Indeed, CSCs pose an increasing challenge to current cancer therapy due to their stemness or self-renewal properties. The molecular and cellular interactions between heterogeneous CSCs and surrounding TME components and tumor-supporting immune cells show synergistic effects toward treatment failure. In the immunosuppressive TME, CSCs express various immunoregulatory proteins, growth factors, metabolites and cytokines, and also produce exosomes, a type of extracellular vesicles, to protect themselves from host immune surveillance. Among these, the identification and application of CSC-derived exosomes could be considered for the development of therapeutic approaches to eliminate CSCs or cancer, in addition to targeting the modulators that remodel the composition of the TME, as reviewed in this study. Here, we introduce the role of CSCs and how their interaction with TME complicates immunotherapies, and then present the CSC-based immunotherapy and the limitation of these therapies. We describe the biology and role of tumor/CSC-derived exosomes that induce immune suppression in the TME, and finally, introduce their potentials for the development of CSC-based targeted immunotherapy in the future. We introduce the role of cancer stem cells (CSCs) and how their interaction with tumor microenvironment (TME) and tumor cell-derived exosomes complicates immunotherapies, and then present CSC-based immunotherapy and the limitations of these therapies. We describe the biology and role of tumor/CSC-derived exosomes that induce immune suppression in the TME, and finally introduce their potentials for the development of CSC-based targeted immunotherapy in the future. image Immunotherapies targeting cancer stem cells (CSCs) require reprogramming of tumor microenvironment to recruit immune cells. Targeting CSCs with novel immunogens may improve treatment of resistant tumors. Targeted exosomes in combination with immunotherapies may improve cancer treatment.
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