TY - JOUR
T1 - CAR-NK cell in cancer immunotherapy; A promising frontier
AU - Marofi, Faroogh
AU - Abdul-Rasheed, Omar F.
AU - Rahman, Heshu Sulaiman
AU - Budi, Hendrik Setia
AU - Jalil, Abduladheem Turki
AU - Yumashev, Alexei Valerievich
AU - Hassanzadeh, Ali
AU - Yazdanifar, Mahboubeh
AU - Motavalli, Roza
AU - Chartrand, Max Stanley
AU - Ahmadi, Majid
AU - Cid-Arreguid, Angel
AU - Jarahian, Mostafa
N1 - Publisher Copyright:
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2021/9
Y1 - 2021/9
N2 - Chimeric antigen receptors (CARs) have a unique facet of synthetic biology and offer a paradigm shift in personalized medicine as they can use and redirect the patient's immune cells to attack cancer cells. CAR-natural killer (NK) cells combine the targeted specificity of antigens with the subsequent intracellular signaling ability of the receptors to increase their anti-cancer functions. Importantly, CAR-NK cells can be utilized as universal cell-based therapy without requiring human leukocyte antigen (HLA) matching or earlier contact with tumor-associated antigens (TAAs). Indeed, CAR-NK cells can be adapted to recognize various antigens, hold higher proliferation capacity, and in vivo persistence, show improved infiltration into the tumors, and the ability to overcome the resistant tumor microenvironment leading to sustained cytotoxicity against tumors. Accumulating evidence from recent in vivo studies rendering CAR-NK cell anti-cancer competencies renewed the attention in the context of cancer immunotherapy, as these redirected effector cells can be used in the development of the “off-the-shelf” anti-cancer immunotherapeutic products. In the current review, we focus on the therapeutic efficacy of CAR-NK cell therapies for treating various human malignancies, including hematological malignancies and solid tumors, and will discuss the recent findings in this regard, with a special focus on animal studies.
AB - Chimeric antigen receptors (CARs) have a unique facet of synthetic biology and offer a paradigm shift in personalized medicine as they can use and redirect the patient's immune cells to attack cancer cells. CAR-natural killer (NK) cells combine the targeted specificity of antigens with the subsequent intracellular signaling ability of the receptors to increase their anti-cancer functions. Importantly, CAR-NK cells can be utilized as universal cell-based therapy without requiring human leukocyte antigen (HLA) matching or earlier contact with tumor-associated antigens (TAAs). Indeed, CAR-NK cells can be adapted to recognize various antigens, hold higher proliferation capacity, and in vivo persistence, show improved infiltration into the tumors, and the ability to overcome the resistant tumor microenvironment leading to sustained cytotoxicity against tumors. Accumulating evidence from recent in vivo studies rendering CAR-NK cell anti-cancer competencies renewed the attention in the context of cancer immunotherapy, as these redirected effector cells can be used in the development of the “off-the-shelf” anti-cancer immunotherapeutic products. In the current review, we focus on the therapeutic efficacy of CAR-NK cell therapies for treating various human malignancies, including hematological malignancies and solid tumors, and will discuss the recent findings in this regard, with a special focus on animal studies.
KW - CAR-NK
KW - cancer
KW - chimeric antigen receptors
KW - immunotherapy
KW - natural killer cells
UR - http://www.scopus.com/inward/record.url?scp=85109147432&partnerID=8YFLogxK
U2 - 10.1111/cas.14993
DO - 10.1111/cas.14993
M3 - Review article
C2 - 34050690
AN - SCOPUS:85109147432
SN - 1347-9032
VL - 112
SP - 3427
EP - 3436
JO - Cancer Science
JF - Cancer Science
IS - 9
ER -