Bone marrow niches in haematological malignancies

被引:355
作者
Mendez-Ferrer, Simon [1 ,2 ,3 ]
Bonnet, Dominique [4 ]
Steensma, David P. [5 ,6 ]
Hasserjian, Robert P. [5 ,7 ]
Ghobrial, Irene M. [5 ,6 ]
Gribben, John G. [8 ]
Andreeff, Michael [9 ]
Krause, Daniela S. [10 ,11 ]
机构
[1] Wellcome Trust Res Labs, Med Res Council, Cambridge Stem Cell Inst, Cambridge, England
[2] Natl Hlth Serv Blood & Transplant, Cambridge, England
[3] Univ Cambridge, Dept Haematol, Cambridge, England
[4] Francis Crick Inst, Haematopoiet Stem Cell Lab, London, England
[5] Harvard Med Sch, Boston, MA 02115 USA
[6] Harvard Med Sch, Dana Farber Canc Inst, Dept Med Oncol, Ctr Prevent Progress Blood Canc, Boston, MA 02115 USA
[7] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[8] Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, England
[9] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Sect Mol Hematol & Therapy, Houston, TX 77030 USA
[10] Georg Speyer Haus Inst Tumor Biol & Expt Med, Frankfurt, Germany
[11] Goethe Univ Frankfurt, Frankfurt, Germany
基金
英国医学研究理事会; 英国惠康基金;
关键词
ACUTE MYELOID-LEUKEMIA; HEMATOPOIETIC STEM-CELLS; CHRONIC LYMPHOCYTIC-LEUKEMIA; MESENCHYMAL STROMAL CELLS; ENDOTHELIAL GROWTH-FACTOR; NF-KAPPA-B; HEALTH-ORGANIZATION CLASSIFICATION; NEUTROPHIL EXTRACELLULAR TRAPS; ACUTE LYMPHOBLASTIC-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA;
D O I
10.1038/s41568-020-0245-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Haematological malignancies were previously thought to be driven solely by genetic or epigenetic lesions within haematopoietic cells. However, the niches that maintain and regulate daily production of blood and immune cells are now increasingly being recognized as having an important role in the pathogenesis and chemoresistance of haematological malignancies. Within haematopoietic cells, the accumulation of a small number of recurrent mutations initiates malignancy. Concomitantly, specific alterations of the niches, which support haematopoietic stem cells and their progeny, can act as predisposition events, facilitating mutant haematopoietic cell survival and expansion as well as contributing to malignancy progression and providing protection of malignant cells from chemotherapy, ultimately leading to relapse. In this Perspective, we summarize our current understanding of the composition and function of the specialized haematopoietic niches of the bone marrow during health and disease. We discuss disease mechanisms (rather than malignancy subtypes) to provide a comprehensive description of key niche-associated pathways that are shared across multiple haematological malignancies. These mechanisms include primary driver mutations in bone marrow niche cells, changes associated with increased hypoxia, angiogenesis and inflammation as well as metabolic reprogramming by stromal niche cells. Consequently, remodelling of bone marrow niches can facilitate immune evasion and activation of survival pathways favouring malignant haematopoietic cell maintenance, defence against excessive reactive oxygen species and protection from chemotherapy. Lastly, we suggest guidelines for the handling and biobanking of patient samples and analysis of the niche to ensure that basic research identifying therapeutic targets can be more efficiently translated to the clinic. The hope is that integrating knowledge of how bone marrow niches contribute to haematological disease predisposition, initiation, progression and response to therapy into future clinical practice will likely improve the treatment of these disorders. This Perspective outlines our current understanding of how the bone marrow niche contributes to both the initiation and the progression of haematological malignancies and suggests guidelines for the field which might help to overcome existing research challenges.
引用
收藏
页码:285 / 298
页数:14
相关论文
共 243 条
[1]
Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches [J].
Abarrategi, Ander ;
Mian, Syed A. ;
Passaro, Diana ;
Rouault-Pierre, Kevin ;
Grey, William ;
Bonnet, Dominique .
JOURNAL OF EXPERIMENTAL MEDICINE, 2018, 215 (03) :729-743
[2]
Prediction of acute myeloid leukaemia risk in healthy individuals [J].
Abelson, Sagi ;
Collord, Grace ;
Ng, Stanley W. K. ;
Weissbrod, Omer ;
Cohen, Netta Mendelson ;
Niemeyer, Elisabeth ;
Barda, Noam ;
Zuzarte, Philip C. ;
Heisler, Lawrence ;
Sundaravadanam, Yogi ;
Luben, Robert ;
Hayat, Shabina ;
Wang, Ting Ting ;
Zhao, Zhen ;
Cirlan, Julia ;
Pugh, Trevor J. ;
Soave, David ;
Ng, Karen ;
Latimer, Calli ;
Hardy, Claire ;
Raine, Keiran ;
Jones, David ;
Hoult, Diana ;
Britten, Abigail ;
McPherson, John D. ;
Johansson, Mattias ;
Mbabaali, Faridah ;
Eagles, Jenna ;
Millers, Jessica K. ;
Pasternack, Danielle ;
Timms, Lee ;
Krzyzanowski, Paul ;
Awadalla, Philip ;
Costa, Rui ;
Segal, Eran ;
Bratman, Scott, V ;
Beer, Philip ;
Behjati, Sam ;
Martincorena, Inigo ;
Wang, Jean C. Y. ;
Bowles, Kristian M. ;
Ramon Quiros, J. ;
Karakatsani, Anna ;
La Vecchia, Carlo ;
Trichopoulou, Antonia ;
Salamanca-Fernandez, Elena ;
Huerta, Jose M. ;
Barricarte, Aurelio ;
Travis, Ruth C. ;
Tumino, Rosario .
NATURE, 2018, 559 (7714) :400-+
[3]
The CXCR4 inhibitor BL-8040 induces the apoptosis of AML blasts by downregulating ERK, BCL-2, MCL-1 and cyclin-D1 via altered miR-15a/16-1 expression [J].
Abraham, M. ;
Klein, S. ;
Bulvik, B. ;
Wald, H. ;
Weiss, I. D. ;
Olam, D. ;
Weiss, L. ;
Beider, K. ;
Eizenberg, O. ;
Wald, O. ;
Galun, E. ;
Avigdor, A. ;
Benjamini, O. ;
Nagler, A. ;
Pereg, Y. ;
Tavor, S. ;
Peled, A. .
LEUKEMIA, 2017, 31 (11) :2336-2346
[4]
Single Dose of the CXCR4 Antagonist BL-8040 Induces Rapid Mobilization for the Collection of Human CD34+ Cells in Healthy Volunteers [J].
Abraham, Michal ;
Pereg, Yaron ;
Bulvik, Baruch ;
Klein, Shiri ;
Mishalian, Inbal ;
Wald, Hana ;
Eizenberg, Orly ;
Beider, Katia ;
Nagler, Arnon ;
Golan, Rottem ;
Vainstein, Abi ;
Aharon, Arnon ;
Galun, Eithan ;
Caraco, Yoseph ;
Or, Reuven ;
Peled, Amnon .
CLINICAL CANCER RESEARCH, 2017, 23 (22) :6790-6801
[5]
Deep imaging of bone marrow shows non-dividing stem cells are mainly perisinusoidal [J].
Acar, Melih ;
Kocherlakota, Kiranmai S. ;
Murphy, Malea M. ;
Peyer, James G. ;
Oguro, Hideyuki ;
Inra, Christopher N. ;
Jaiyeola, Christabel ;
Zhao, Zhiyu ;
Luby-Phelps, Katherine ;
Morrison, Sean J. .
NATURE, 2015, 526 (7571) :126-+
[6]
Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor [J].
Center for Regenerative Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, United States ;
不详 ;
不详 ;
不详 ;
不详 ;
不详 .
Nature, 2006, 7076 (599-603) :599-603
[7]
Angiogenesis in acute and chronic leukemias and myelodysplastic syndromes [J].
Aguayo, A ;
Kantarjian, H ;
Manshouri, T ;
Gidel, C ;
Estey, E ;
Thomas, D ;
Koller, C ;
Estrov, Z ;
O'Brien, S ;
Keating, M ;
Freireich, E ;
Albitar, M .
BLOOD, 2000, 96 (06) :2240-2245
[8]
Proliferation dynamics of acute myeloid leukaemia and haematopoietic progenitors competing for bone marrow space [J].
Akinduro, O. ;
Weber, T. S. ;
Ang, H. ;
Haltalli, M. L. R. ;
Ruivo, N. ;
Duarte, D. ;
Rashidi, N. M. ;
Hawkins, E. D. ;
Duffy, K. R. ;
Lo Celso, C. .
NATURE COMMUNICATIONS, 2018, 9
[9]
Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche [J].
Arai, F ;
Hirao, A ;
Ohmura, M ;
Sato, H ;
Matsuoka, S ;
Takubo, K ;
Ito, K ;
Koh, GY ;
Suda, T .
CELL, 2004, 118 (02) :149-161
[10]
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia [J].
Arber, Daniel A. ;
Orazi, Attilio ;
Hasserjian, Robert ;
Thiele, Jurgen ;
Borowitz, Michael J. ;
Le Beau, Michelle M. ;
Bloomfield, Clara D. ;
Cazzola, Mario ;
Vardiman, James W. .
BLOOD, 2016, 127 (20) :2391-2405