Effects of epigenetic therapy on natural killer cell function and development in hematologic malignancy

被引:1
作者
Lordo, Matthew R. [1 ,2 ]
Stiff, Andrew R. [1 ,3 ,4 ]
Oakes, Christopher C. [1 ,4 ]
Mundy-Bosse, Bethany L. [1 ,4 ,5 ]
机构
[1] Ohio State Univ, Comprehens Canc Ctr, 460 W 10th Ave, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Scientist Training Program, Biomed Sci Grad Program, 370 W 9th Ave, Columbus, OH 43210 USA
[3] Ohio State Univ, Phys Scientist Training Program, 370 W 9th Ave, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Internal Med, Div Hematol, Wexner Med Ctr, 460 W 12th Ave, Columbus, OH 43210 USA
[5] Ohio State Univ, Dept Internal Med, Div Hematol, 882 Biomed Res Tower,460 W 12th Ave, Columbus, OH 43210 USA
关键词
epigenetic therapy; natural killer cell; NK cell; AML; ALL; leukemia; HISTONE DEACETYLASE INHIBITORS; MYELODYSPLASTIC SYNDROMES; DNA METHYLATION; OPEN-LABEL; NK CELLS; CHAIN-A; EXPRESSION; DECITABINE; MUTATIONS; CANCER;
D O I
10.1093/jleuko/qiad026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epigenetic therapy is an emerging field in the treatment of human cancer, including hematologic malignancies. This class of therapeutic agents approved by the US Food and Drug Administration for cancer treatment includes DNA hypomethylating agents, histone deacetylase inhibitors, IDH1/2 inhibitors, EZH2 inhibitors, and numerous preclinical targets/agents. Most studies measuring the biological effects of epigenetic therapy focus their attention on either their direct cytotoxic effects on malignant cells or their effects on modifying tumor cell antigen expression, exposing them to immune surveillance mechanisms. However, a growing body of evidence suggests that epigenetic therapy also has effects on the development and function of the immune system, including natural killer cells, which can alter their response to cancer cells. In this review, we summarize the body of literature studying the effects of different classes of epigenetic therapy on the development and/or function of natural killer cells. Epigenetic therapies for hematologic malignancies affect not only leukemia cells but also modify natural killer cell development and function.
引用
收藏
页码:518 / 524
页数:7
相关论文
共 50 条
  • [21] Gene-Based Natural Killer Cell Therapies for the Treatment of Pediatric Hematologic Malignancies
    Rahnama, Ruyan
    Christodoulou, Ilias
    Bonifant, Challice L.
    HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2022, 36 (04) : 745 - 768
  • [22] Regulation of natural killer cell function
    Makrigiannis, AP
    Anderson, SK
    CANCER BIOLOGY & THERAPY, 2003, 2 (06) : 610 - 616
  • [23] Allogeneic natural killer cell therapy
    Berrien-Elliott, Melissa M.
    Jacobs, Miriam T.
    Fehniger, Todd A.
    BLOOD, 2023, 141 (08) : 856 - 868
  • [24] Evolution of natural killer cell-targeted therapy for acute myeloid leukemia
    Kaito, Yuta
    Imai, Yoichi
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2024, 120 (01) : 34 - 43
  • [25] Transcriptional regulation of natural killer cell development and maturation
    Kee, Barbara L.
    Morman, Rosmary E.
    Sun, Mengxi
    ADVANCES IN IMMUNOLOGY, VOL 146, 2020, 146 : 1 - 28
  • [26] Transcriptional Regulation of Natural Killer Cell Development and Functions
    Wang, Dandan
    Malarkannan, Subramaniam
    CANCERS, 2020, 12 (06) : 1 - 33
  • [27] Human natural killer cell development
    Freud, Aharon G.
    Caligiuri, Michael A.
    IMMUNOLOGICAL REVIEWS, 2006, 214 : 56 - 72
  • [28] Emerging Themes in Uterine Natural Killer Cell Heterogeneity and Function
    Hatta, Kota
    MacLeod, R. John
    Gerber, Scott A.
    Croy, B. Anne
    AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2012, 68 (04) : 282 - 289
  • [29] Alteration of Natural Killer cell phenotype and function in obese individuals
    Viel, Sebastien
    Besson, Laurie
    Charrier, Emily
    Marcais, Antoine
    Disse, Emmanuel
    Bienvenu, Jacques
    Walzer, Thierry
    Dumontet, Charles
    CLINICAL IMMUNOLOGY, 2017, 177 : 12 - 17
  • [30] Natural killer lymphocytes: biology, development, and function
    Papamichail, M
    Perez, SA
    Gritzapis, AD
    Baxevanis, CN
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 2004, 53 (03) : 176 - 186