All-trans retinoic acid induces differentiation in primary acute myeloid leukemia blasts carrying an inversion of chromosome 16

被引:7
作者
Dembitz, Vilma [1 ,2 ]
Lalic, Hrvoje [1 ,2 ]
Tomic, Barbara [1 ,2 ]
Smoljo, Tomislav [1 ,2 ]
Batinic, Josip [3 ]
Dubravcic, Klara [4 ]
Batinic, Drago [2 ,4 ]
Bedalov, Antonio [5 ]
Visnjic, Dora [1 ,2 ]
机构
[1] Univ Zagreb, Sch Med, Croatian Inst Brain Res, Lab Cell Biol, Zagreb, Croatia
[2] Univ Zagreb, Sch Med, Dept Physiol, Salata 3, Zagreb 10000, Croatia
[3] Univ Hosp Ctr Zagreb, Dept Internal Med, Div Hematol, Zagreb, Croatia
[4] Univ Hosp Ctr Zagreb, Dept Lab Immunol, Zagreb, Croatia
[5] Fred Hutchinson Canc Res Ctr, Clin Res Div, 1124 Columbia St, Seattle, WA 98104 USA
关键词
ATRA(1); Acute myeloid leukemia(2); Differentiation(3); Inversion of chromosome 16(4); CBFB-MYH11(5); ARSENIC TRIOXIDE; AML; INHIBITION; MUTATIONS; NPM1; CHEMOTHERAPY; COMBINATION; APOPTOSIS; CELLS; GENE;
D O I
10.1007/s12185-021-03224-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
All-trans retinoic acid (ATRA)-based therapy for acute promyelocytic leukemia (APL), a subtype of acute myeloid leukemia (AML), is the most successful example of differentiation therapy. Although ATRA can induce differentiation in some non-APL AML cell lines and primary blasts, clinical results of adding ATRA to standard therapy in non-APL AML patients have been inconsistent, probably due to use of different regimens and lack of diagnostic tools for identifying which patients may be sensitive to ATRA. In this study, we exposed primary blasts obtained from non-APL AML patients to ATRA to test for differentiation potential in vitro. We observed increased expression of differentiation markers, indicating a response to ATRA, in four out of fifteen primary AML samples. Three samples in which CD11b increased in response to ATRA had an inversion of chromosome 16 as well as the CBFB-MYH11 fusion gene, and the fourth sample was from a patient with KMT2A-rearranged, therapy-related AML. In conclusion, we identified a subgroup of non-APL AML patients with inv(16) and CBFB-MYH11 as the most sensitive to ATRA-mediated differentiation in vitro, and our results can help identify patients who may benefit from ATRA treatment.
引用
收藏
页码:43 / 53
页数:11
相关论文
共 31 条
[11]   Retinoic acid and arsenic trioxide trigger degradation of mutated NPM1, resulting in apoptosis of AML cells [J].
El Hajj, Hiba ;
Dassouki, Zeina ;
Berthier, Caroline ;
Raffoux, Emmanuel ;
Ades, Lionel ;
Legrand, Olivier ;
Hleihel, Rita ;
Sahin, Umut ;
Tawil, Nadim ;
Salameh, Ala ;
Zibara, Kazem ;
Darwiche, Nadine ;
Mohty, Mohamad ;
Dombret, Herve ;
Fenaux, Pierre ;
de The, Hugues ;
Bazarbachi, Ali .
BLOOD, 2015, 125 (22) :3447-3454
[12]   All-trans retinoic acid combined with 5-Aza-2′-deoxycitidine induces C/EBPα expression and growth inhibition in MLL-AF9-positive leukemic cells [J].
Fujiki, Atsushi ;
Imamura, Toshihiko ;
Sakamoto, Kenichi ;
Kawashima, Sachiko ;
Yoshida, Hideki ;
Hirashima, Yoshifumi ;
Miyachi, Mitsuru ;
Yagyu, Shigeki ;
Nakatani, Takuya ;
Sugita, Kanji ;
Hosoi, Hajime .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 428 (02) :216-223
[13]   5-Aminoimidazole-4-carboxamide ribonucleoside induces differentiation of acute myeloid leukemia cells [J].
Lalic, Hrvoje ;
Dembitz, Vilma ;
Lukinovic-Skudar, Vesna ;
Banfic, Hrvoje ;
Visnjic, Dora .
LEUKEMIA & LYMPHOMA, 2014, 55 (10) :2375-2383
[14]   Valproate and Retinoic Acid in Combination With Decitabine in Elderly Nonfit Patients With Acute Myeloid Leukemia: Results of a Multicenter, Randomized, 2 x 2, Phase II Trial [J].
Luebbert, Michael ;
Grishina, Olga ;
Schmoor, Claudia ;
Schlenk, Richard F. ;
Jost, Edgar ;
Crysandt, Martina ;
Heuser, Michael ;
Thol, Felicitas ;
Salih, Helmut R. ;
Schittenhelm, Marcus M. ;
Germing, Ulrich ;
Kuendgen, Andrea ;
Goetze, Katharina S. ;
Lindemann, Hans-Walter ;
Mueller-Tidow, Carsten ;
Heil, Gerhard ;
Scholl, Sebastian ;
Bug, Gesine ;
Schwaenen, Carsten ;
Giagounidis, Aristoteles ;
Neubauer, Andreas ;
Krauter, Juergen ;
Brugger, Wolfram ;
De Wit, Maike ;
Waesch, Ralph ;
Becker, Heiko ;
May, Annette M. ;
Duyster, Justus ;
Doehner, Konstanze ;
Ganser, Arnold ;
Hackanson, Bjoern ;
Doehner, Hartmut .
JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (03) :257-+
[15]   All-trans retinoic acid synergizes with FLT3 inhibition to eliminate FLT3/ITD+ leukemia stem cells in vitro and in vivo [J].
Ma, Hayley S. ;
Greenblatt, Sarah M. ;
Shirley, Courtney M. ;
Duffield, Amy S. ;
Bruner, J. Kyle ;
Li, Li ;
Bao Nguyen ;
Jung, Eric ;
Aplan, Peter D. ;
Ghiaur, Gabriel ;
Jones, Richard J. ;
Small, Donald .
BLOOD, 2016, 127 (23) :2867-2878
[16]   Arsenic trioxide and all-trans retinoic acid target NPM1 mutant oncoprotein levels and induce apoptosis in NPM1-mutated AML cells [J].
Martelli, Maria Paola ;
Gionfriddo, Ilaria ;
Mezzasoma, Federica ;
Milano, Francesca ;
Pierangeli, Sara ;
Mulas, Floriana ;
Pacini, Roberta ;
Tabarrini, Alessia ;
Pettirossi, Valentina ;
Rossi, Roberta ;
Vetro, Calogero ;
Brunetti, Lorenzo ;
Sportoletti, Paolo ;
Tiacci, Enrico ;
Di Raimondo, Francesco ;
Falini, Brunangelo .
BLOOD, 2015, 125 (22) :3455-3465
[17]   Fludarabine and cytosine are less effective than standard ADE chemotherapy in high-risk acute myeloid leukemia, and addition of G-CSF and ATRA are not beneficial: results of the MRC AML-HR randomized trial [J].
Milligan, Donald W. ;
Wheatley, Keith ;
Littlewood, Timothy ;
Craig, Jenny I. O. ;
Burnett, Alan K. .
BLOOD, 2006, 107 (12) :4614-4622
[18]   A novel, myeloid transcription factor, C/EBP epsilon, is upregulated during granulocytic, but not monocytic, differentiation [J].
Morosetti, R ;
Park, DJ ;
Chumakov, AM ;
Grillier, I ;
Shiohara, M ;
Gombart, AF ;
Nakamaki, T ;
Weinberg, K ;
Koeffler, HP .
BLOOD, 1997, 90 (07) :2591-2600
[19]   All-transretinoic acid in non-promyelocytic acute myeloid leukemia: driver lesion dependent effects on leukemic stem cells [J].
Nguyen, Chi H. ;
Grandits, Alexander M. ;
Purton, Louise E. ;
Sill, Heinz ;
Wieser, Rotraud .
CELL CYCLE, 2020, 19 (20) :2573-2588
[20]   Evi1 Counteracts Anti-Leukemic and Stem Cell Inhibitory Effects of All-Trans Retinoic Acid on Flt3-ITD/Npm1c-Driven Acute Myeloid Leukemia Cells [J].
Nguyen, Chi Huu ;
Grandits, Alexander M. ;
Vassiliou, George S. ;
Staber, Philipp B. ;
Heller, Gerwin ;
Wieser, Rotraud .
BIOMEDICINES, 2020, 8 (10)