Hedgehog Pathway Inhibitors: A New Therapeutic Class for the Treatment of Acute Myeloid Leukemia

被引:57
|
作者
Jamieson, Catriona [1 ,2 ]
Martinelli, Giovanni [3 ]
Papayannidis, Cristina [4 ]
Cortes, Jorge E. [5 ]
机构
[1] UC San Diego Moores Canc Ctr, Div Hematol Oncol, La Jolla, CA 92037 USA
[2] Sanford Stem Cell Clin Ctr, La Jolla, CA 92093 USA
[3] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Clin & Res Leukemia Program, Meldola, Italy
[4] Univ Hosp S Orsola Malpighi, Inst Hematol & Med Oncol L & A Seragnoli, Bologna, Italy
[5] Augusta Univ, Georgia Canc Ctr, Augusta, GA USA
来源
BLOOD CANCER DISCOVERY | 2020年 / 1卷 / 02期
关键词
ORAL SMOOTHENED INHIBITOR; CANCER STEM-CELLS; DRUG-RESISTANCE; SONIC HEDGEHOG; PHASE-I; ACTIVATION; ANTAGONIST; VISMODEGIB; MUTATIONS; GLASDEGIB;
D O I
10.1158/2643-3230.BCD-20-0007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeting Hedgehog (Hh) pathway components, such as Smoothened (SMO), is a developing strategy for the treatment of acute myeloid leukemia (AML) and for overcoming relapsed/refractory forms of this disease. Several SMO inhibitors are in clinical development for the treatment of various tumor types and the results from some clinical trials in AML have been reported. This review will discuss the role of Hh signaling in AML pathogenesis, describe the preclinical and clinical development of Hh pathway inhibitors for the treatment of AML, and examine the current evidence on Hh pathway inhibitor resistance and the implications for treatment selection in AML. Significance: In acute myeloid leukemia (AML), components of the Hedgehog (Hh) signaling pathway, such as Smoothened (SMO), have been implicated in the development, maintenance, and expansion of leukemic stem cells (LSC), as well as sensitization to chemotherapy and the development of drug resistance in AML. Observations in preclinical studies of AML, as well as from samples of patients with AML, demonstrate that Hh pathway inhibitors act primarily on the stem cell pathway as differentiation agents. The current data for hematologic malignancies indicate the potential for a synergistic effect when a Hh pathway inhibitor is administered in combination with chemotherapy or investigational agents. It is thought that Hh pathway inhibitors act as agents that reduce LSC dormancy and promote LSC differentiation, thus the newly dividing LSCs can then be targeted by other chemotherapeutic drugs.
引用
收藏
页码:134 / 145
页数:12
相关论文
共 50 条
  • [41] HDAC Inhibitors in Acute Myeloid Leukemia
    San Jose-Eneriz, Edurne
    Gimenez-Camino, Naroa
    Agirre, Xabier
    Prosper, Felipe
    CANCERS, 2019, 11 (11)
  • [42] Bromodomain Inhibitors in Acute Myeloid Leukemia
    Roboz, Gail J.
    ANNALS OF HEMATOLOGY, 2017, 96 : S33 - S34
  • [43] New opportunities and new problems for acute myeloid leukemia treatment
    Lahortiga, Idoya
    Cools, Jan
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2012, 97 (06): : 796 - 796
  • [44] Therapeutic Advances in Acute Myeloid Leukemia
    Burnett, Alan
    Wetzler, Meir
    Loewenberg, Bob
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (05) : 487 - 494
  • [45] Acute myeloid leukemia: therapeutic indications
    Burnett, AK
    Kell, J
    Rowntree, C
    CURRENT OPINION IN HEMATOLOGY, 2000, 7 (06) : 333 - 338
  • [46] Acute Myeloid Leukemia and the Wnt Pathway
    Eaves, Connie J.
    Humphries, R. Keith
    NEW ENGLAND JOURNAL OF MEDICINE, 2010, 362 (24): : 2326 - 2327
  • [47] New Treatment Options for Acute Myeloid Leukemia in 2019
    Cerrano, Marco
    Itzykson, Raphael
    CURRENT ONCOLOGY REPORTS, 2019, 21 (02)
  • [48] NEW AGENTS IN THE TREATMENT OF ACUTE MYELOID-LEUKEMIA
    WIERNIK, PH
    SEMINARS IN HEMATOLOGY, 1991, 28 (03) : 95 - 98
  • [49] Perifosine - a new option in treatment of acute myeloid leukemia?
    Krawczyk, Janusz
    Keane, Niamh
    Swords, Ronan
    O'Dwyer, Michael
    Freeman, Ciara L.
    Giles, Francis J.
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2013, 22 (10) : 1315 - 1327
  • [50] Treatment for relapsed acute myeloid leukemia: what is new?
    Ofran, Yishai
    Rowe, Jacob M.
    CURRENT OPINION IN HEMATOLOGY, 2012, 19 (02) : 89 - 94