Unraveling the Role of Innate Lymphoid Cells in AcuteMyeloid Leukemia.

AHR AML ILC NK immunotherapy

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
17 Jan 2021
Historique:
received: 12 12 2020
revised: 07 01 2021
accepted: 07 01 2021
entrez: 22 1 2021
pubmed: 23 1 2021
medline: 23 1 2021
Statut: epublish

Résumé

Over the past 50 years, few therapeutic advances have been made in treating acute myeloid leukemia (AML), an aggressive form of blood cancer, despite vast improvements in our ability to classify the disease. Emerging evidence suggests the immune system is important in controlling AML progression and in determining prognosis. Natural killer (NK) cells are important cytotoxic effector cells of the innate lymphoid cell (ILC) family that have been shown to have potent anti-leukemic functions. Recent studies are now revealing impairment or dysregulation of other ILCs in various types of cancers, including AML, which limits the effectiveness of NK cells in controlling cancer progression. NK cell development and function are inhibited in AML patients, which results in worse clinical outcomes; however, the specific roles of other ILC populations in AML are just now beginning to be unraveled. In this review, we summarize what is known about the role of ILC populations in AML.

Identifiants

pubmed: 33477248
pii: cancers13020320
doi: 10.3390/cancers13020320
pmc: PMC7830843
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : K22 CA218466
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS106170
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA223400
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA068458
Pays : United States
Organisme : NIH HHS
ID : CA068458
Pays : United States
Organisme : NCI NIH HHS
ID : F30 CA250244
Pays : United States
Organisme : NIH HHS
ID : 5K22CA218466-02
Pays : United States
Organisme : American Cancer Society
ID : RSG-20-051-01-LIB
Organisme : NCI NIH HHS
ID : R01 CA247550
Pays : United States
Organisme : NIH HHS
ID : CA208353
Pays : United States
Organisme : NIH HHS
ID : CA199447
Pays : United States
Organisme : NIH HHS
ID : CA210087
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI129582
Pays : United States
Organisme : American Association for Cancer Research
ID : 17-20-46-MUND
Organisme : NCI NIH HHS
ID : R35 CA210087
Pays : United States

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Auteurs

Matthew R Lordo (MR)

Biomedical Sciences Graduate Program, Medical Scientist Training Program, Columbus, OH 43210, USA.
Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.

Steven D Scoville (SD)

Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Department of Surgery, The Ohio State University, Columbus, OH 43210, USA.

Akul Goel (A)

Department of Hematology & Hematopoietic Cell Transplantation, City of Hope National Medical Center, Los Angeles, CA 91010, USA.

Jianhua Yu (J)

Department of Hematology & Hematopoietic Cell Transplantation, City of Hope National Medical Center, Los Angeles, CA 91010, USA.

Aharon G Freud (AG)

Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.

Michael A Caligiuri (MA)

Department of Hematology & Hematopoietic Cell Transplantation, City of Hope National Medical Center, Los Angeles, CA 91010, USA.

Bethany L Mundy-Bosse (BL)

Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Division of Hematology, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.

Classifications MeSH