New strategies to treat AML: novel insights into AML survival pathways and combination therapies

被引:59
|
作者
Nair, Ramya [1 ,2 ]
Salinas-Illarena, Alejandro [1 ,2 ]
Baldauf, Hanna-Mari [1 ,2 ]
机构
[1] LMU Munchen, Fac Med, Natl Reference Ctr Retroviruses, Max Von Pettenkofer Inst, Munich, Germany
[2] LMU Munchen, Fac Med, Natl Reference Ctr Retroviruses, Gene Ctr,Virol, Munich, Germany
关键词
ACUTE MYELOID-LEUKEMIA; MARROW STROMAL CELLS; TRANS-RETINOIC ACID; DRUG-RESISTANCE; MITOCHONDRIAL TRANSFER; OXIDATIVE STRESS; SAMHD1; DIFFERENTIATION; CYTARABINE; CERAMIDE;
D O I
10.1038/s41375-020-01069-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effective treatment of acute myeloid leukemia (AML) is very challenging. Due to the immense heterogeneity of this disease, treating it using a "one size fits all" approach is ineffective and only benefits a subset of patients. Instead, there is a shift towards more personalized treatment based on the patients' genomic signature. This shift has facilitated the increased revelation of novel insights into pathways that lead to the survival and propagation of AML cells. These AML survival pathways are involved in drug resistance, evasion of the immune system, reprogramming metabolism, and impairing differentiation. In addition, based on the reports of enhanced clinical efficiencies when combining drugs or treatments, deeper investigation into possible pathways, which can be targeted together to increase treatment response in a wider group of patients, is warranted. In this review, not only is a comprehensive summary of targets involved in these pathways provided, but also insights into the potential of targeting these molecules in combination therapy will be discussed.
引用
收藏
页码:299 / 311
页数:13
相关论文
共 50 条
  • [31] Identification of Novel Combination Therapies Active in BCL2 Inhibitor-Resistant Patient-Derived AML Models
    Andersen, Courtney L.
    Christie, Amanda L.
    Rosen, Alan
    Maratea, Kim
    Hattersley, Maureen
    Travers, Jon
    Cidado, Justin
    Pulukuri, Sai
    Saeh, Jamal
    Clark, Edwin
    Reimer, Corinne
    Mettetal, Jerome
    BLOOD, 2019, 134
  • [32] Xenograft models of human acute myeloid leukemia (AML) with biomarker strategies are valuable in development of new drugs targeting AML
    Zhang, Lan
    Chen, Taiping
    Shil, Qian
    Zhang, Juan
    CANCER RESEARCH, 2012, 72
  • [33] NEW STRATEGIES FOR THE DEVELOPMENT OF ANTIVENOM THERAPIES TO TREAT SNAKEBITE
    Casewell, Nicholas
    Whiteley, Gareth
    Renjifo, Camila
    King, Sarah
    Bolton, Fiona
    Wagstaff, Simon
    Harrison, Robert
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2017, 95 (05): : 148 - 148
  • [34] Evolving racial/ethnic disparities in AML survival in the novel therapy era
    Wang, Xin
    Gimotty, Phyllis A.
    Matthews, Andrew H.
    Mamtani, Ronac
    Luger, Selina M.
    Hexner, Elizabeth O.
    V. Babushok, Daria
    Mccurdy, Shannon R.
    V. Frey, Noelle
    Bruno, Ximena Jordan
    Gill, Saar
    Martin, Mary Ellen
    Paralkar, Vikram R.
    Maillard, Ivan
    Porter, David L.
    Loren, Alison W.
    Perl, Alexander E.
    Pratz, Keith W.
    Getz, Kelly D.
    Lai, Catherine
    BLOOD ADVANCES, 2025, 9 (03) : 533 - 544
  • [35] New therapeutic options for older unfit AML patients (excluding targeted therapies)
    Cerrano, Marco
    Itzykson, Raphael
    HEMATOLOGIE, 2021, 27 : 24 - 35
  • [36] New therapeutic options in elderly unfit AML patients: focus on targeted therapies
    Dumas, Pierre-Yves
    HEMATOLOGIE, 2021, 27 : 13 - 23
  • [37] The EBMT activity survey 2007 with focus on allogeneic HSCT for AML and novel cellular therapies
    A Gratwohl
    H Baldomero
    A Schwendener
    V Rocha
    J Apperley
    K Frauendorfer
    D Niederwieser
    Bone Marrow Transplantation, 2009, 43 : 275 - 291
  • [38] A novel differentiation response with combination IDH inhibitor and intensive induction therapy for AML
    Mason, Emily F.
    Pozdnyakova, Olga
    Roshal, Mikhail
    Fathi, Amir T.
    Stein, Eytan M.
    Ferrell, P. Brent
    Shaver, Aaron C.
    Frattini, Mark
    Wang, Hongfang
    Hua, Lei
    Mu, Jimmy
    Choe, Sung
    Xu, Rengyi
    Almon, Caroline
    Cooper, Michael
    Stone, Richard M.
    Hasserjian, Robert P.
    Savona, Michael R.
    BLOOD ADVANCES, 2021, 5 (08) : 2279 - 2283
  • [39] The EBMT activity survey 2007 with focus on allogeneic HSCT for AML and novel cellular therapies
    Gratwohl, A.
    Baldomero, H.
    Schwendener, A.
    Rocha, V.
    Apperley, J.
    Frauendorfer, K.
    Niederwieser, D.
    BONE MARROW TRANSPLANTATION, 2009, 43 (04) : 275 - 291
  • [40] Identifying novel therapies from unbiased screens in AML with MECOM re-arrangement
    Birdwell, Christine E.
    Fiskus, Warren C.
    Mill, Christopher P.
    Kadia, Tapan M.
    Daver, Naval
    DiNardo, Courtney D.
    Sasaki, Koji
    Davis, John A.
    Das, Kaberi
    Hou, Hanxi
    Cerebelli, Michele
    Bhalla, Kapil N.
    CANCER RESEARCH, 2024, 84 (06)