Correction
28 Mar 2017: Yang L, Sun H, Cao Y, Xuan B, Fan Y, et al. (2017) Correction: GATA2 Inhibition Sensitizes Acute Myeloid Leukemia Cells to Chemotherapy. PLOS ONE 12(3): e0175005. https://doi.org/10.1371/journal.pone.0175005 View correction
Figures
Abstract
Drug resistance constitutes one of the main obstacles for clinical recovery of acute myeloid leukemia (AML) patients. Therefore, the treatment of AML requires new strategies, such as adding a third drug. To address whether GATA2 could act as a regulator of chemotherapy resistance in human leukemia cells, we observed KG1a cells and clinical patients’ AML cells with a classic drug (Cerubidine) and Gefitinib. After utilizing chemotherapy, the expression of GATA2 and its target genes (EVI, SCL and WT1) in surviving AML cells and KG1a cells were significantly enhanced to double and quadrupled compared to its original level respectively. Furthermore, with continuous chemotherapeutics, AML cells with GATA2 knockdown or treated with GATA2 inhibitor (K1747) almost eliminated with dramatically reduced expression of WT1, SCL, EVI, and significantly increased apoptotic population. Therefore, we propose that reducing GATA2 expression or inhibition of its transcription activity can relieve the drug resistance of acute myeloid leukemia cells and it would be helpful for eliminating the leukemia cells in patients.
Citation: Yang L, Sun H, Cao Y, Xuan B, Fan Y, Sheng H, et al. (2017) GATA2 Inhibition Sensitizes Acute Myeloid Leukemia Cells to Chemotherapy. PLoS ONE 12(1): e0170630. https://doi.org/10.1371/journal.pone.0170630
Editor: Javier S. Castresana, University of Navarra, SPAIN
Received: October 14, 2016; Accepted: January 6, 2017; Published: January 23, 2017
Copyright: © 2017 Yang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by the Shanghai Municipal Health Bureau Project (15ZR1437900), Natural Science Research Project of Changning District (CNKW2014Z01), Leading Disciplines of Medical Laboratory in Changning District (2012QZK01) and Tongren Hospital grant (grant TR201407, TRYJ201506). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Acute myeloid leukemia (AML) is a clinically and biologically heterogeneous malignancy that is primarily treated with chemotherapy, targeted therapy, immune regulation therapy and bone marrow transplant [1, 2]. Considerable progresses have been made in the treatment of AML with application of combined chemotherapies during recent years, which manifested as improved complete remission and long-term survival rates. However, problems such as the resistance to chemotherapies and serious adverse reaction during the process of chemotherapies remain to be tackled in AML treatment[2], in which major cause of treatment failure is resistance to cytarabine (ara-C) and anthracycline [e.g., daunorubicin (DNR)]-based chemotherapy[3]. Thus, novel strategies such small molecular medicines and addition of a third drug are needed to overcome chemoresistance and improve the overall survival of AML patients[4].
GATA2 is a transcription factor crucial for hematopoietic differentiation and lymphatic formation. More specifically, GATA2 plays an essential role in maintaining the proliferation and survival of early hematopoietic cells, as well as preferential differentiation to erythroid or megakaryocytic lineages [5, 6]. Also, the expression of GATA2 is significantly higher in AML compared to normal bone marrow, and recently Maaike Luesink and his colleagues found that high GATA2 expression was a poor prognostic marker in acute myeloid leukemia [7, 8] as well as other transcription factors EVI [9, 10],WT1 [11, 12]. As for GATA2 mutations, in sporadic AML, the majority of acquired GATA2 variations were located within codon 362 in the C-terminal zinc-finger domain, which suggested that this location might be a mutation hot spot and zinc-finger domain relates to the transcriptional activity, promote the downstream genes’ expression[13, 14]. Both loss and gain of function experiments demonstrate that GATA-2 level regulates adult HSC quiescence and modulates HSC apoptosis[15], which could affect the responses to chemotherapy and contribute to poor prognosis in AML.
Our study found that GATA2 expression was associated with the resistance of AML cells to chemotherapeutic medicines. With several repeated chemotherapies, the AML cells with low GATA2 expression were almost killed, which presented a promising potential for clinical treatment. Our founding suggests that suppression of GATA2 expression or its transcriptional activity inhibition could be cooperated with the chemotherapy medicines in the treatment of AML patients.
Materials and Methods
Cell lines and preparation of primary AML cells
KG1a cells (human acute myeloid leukemia cell line) were cultured in RIPM1640 plus 10% FBS, and were collected at day 0, 3, 5, 7 and 9, with or without different treatments. Then cell pellets were washed twice with PBS and RIPA lysis buffer was added to get the cell lysates. Eight consecutive and unselected AML patients were investigated and the peripheral blood blast counts of these patients were more than 7×109/L. Primary AML cells were isolated by density gradient separation alone (Lymphoprep, Axis-Shield, Oslo, Norway) and contained at least 95% leukemic blasts. AML cells were stored in liquid nitrogen until used in experiments[16]. The study protocol was approved by the institutional review board of the Tongren Hospital, Shanghai Jiao-tong University School of Medicine. Before the study, informed consent was obtained from each participant.
RNA extraction
RNA from KG1a and primary AML cells was extracted using the TRIzol® Reagent (Invitrogen) according to the manufacturer’s instruction. To avoid DNA contamination, RNase-free DNase I was applied. DNA/Protein Analyzer (NanoDrop, Invitrogen) assessed the RNA concentration and quantity.
Quantitative real-time PCR
Reverse transcript was performed in a 20 μl reaction system with a total of 1 μg of RNA with M-MLV Reverse Transcriptase (TOYOBO, JAPAN). Quantitative RT-PCR was performed using ABI PCR Thermal Cycler Dice Detection System and SYBR green dye (TOYOBO, JAPAN) according to the manufacturer’s recommended protocol. The PCR primer sequences are listed in Table 1.
Generate stable cell lines with GATA2 knockdown
The online software (http://rnaidesigner.lifetechnologies.com/rnaiexpress/setOption.do?designOption=shrna&pid=-1447534201472129460) was used to design shRNAs of GATA2. The shRNA sequences were listed as follows: 132 GGTGGACGTCTTCTTCAATCA; 654GGAGAGCATGAAGATGGAAAG; 1187 GGAACCGGAAGATGTCCAACA. shRNAs were selected by realtime PCR and western blot, then lentivirus particle was packaged and secreted by 293T cells transfected with the shRNA, VSVG and delta8.9 package plasmids.
KG1a cells were incubated with the lentivirus mixture for 72 h, in the presence of polybrene (Sigma) at a final concentration of 8 μg/ml. Then cells were detached by trypsin and sorted with green fluorescence to get the stable knockdown cell lines. Constructed stable cell lines were amplified and stored in liquid nitrogen for future use.
Cell viability
Cells were seeded in 96-well plates and treated with drugs (Erltinib,5μM; Geftinib,10μM; Cerubidine,1μM; Adriamycine,5μM; Idamycin,5μM; Ara-C,1μg/ml) once every day for 11 days. Cell viability was measured by the CCK-8 assay (CCK-8, Dojindo Laboratories, Kumamoto, Japan) according to the manufacturer’s instruction. All experiments were independently repeated at least 3 times. The survival rate was evaluated by cell counting kit-8 (CCK-8; Dojindo Molecular Technologies Inc., Gaithersburg, MD, USA). Cells were seeded in 48-well plates with RIPM1640 plus 10% FBS. The IC50 value was calculated using Statistical Package of the Social Sciences (SPSS) software version 12 (SPSS Inc., Chicago, IL, USA).
Flow cytometry with annexin V-FITC and PI staining
The cells were divided into two groups: scramble (Scr) KG1a cells and KG1a cells stably knocking down of hGATA2. Each group was treated with DMSO, Geftinib (10μM) or Cerubidine(1μM). The KG1a cells were collected at day 0,3,5,7,9, after washed twice with PBS, and then stained with propidium iodide and annexin V. Apoptotic analyses were performed by flow cytometer (FCM) as described above using an FACS Calibur system. Apoptotic cells were analyzed by quadrant statistics of the propidium iodide negative and annexin V-positive cells.
Western blotting
The whole cell lysates were extracted in 1×SDS, equally loaded to 8% to 12% SDS–polyacrylamide gel, electrophoresed, and transferred to nitrocellulose membrane (Bio-Rad) and stained with 0.4% Ponceau S red to ensure equal protein loading. After blocking with 5% nonfat milk in PBS, the membranes were incubated with antibodies. GATA2 antibody was purchased from Abcam (ab22849, Abcam, MA, USA). GAPDH antibody was purchased from Santa Cruz (SC-365062, Santa Cruz, CA, USA). β-actin was used to measure the amount of protein loaded of each sample. The signals were detected with a chemiluminescence HRP kit (Cell Signaling Technology) according to manufacturer’s instructions.
Statistical analysis
Data are presented as the mean ± SD. Statistical analysis was performed with the Statistical Package for the Social Sciences (SPSS) software version 12 for Windows (SPSS Inc., Chicago, IL, USA). Student t-tests were used to determine the statistical significance of the differences between the experimental groups. P-value of <0.05 was considered significant.
Results
KG1a cells survived from sequential chemotherapies
KG1a cells derived from AML patients that be used as an in vitro model to study the mechanism of AML cells tolerance towards chemo-treatment. In order to determine the exact dosages of chemotherapy drugs used in KG1a cells, half maximal inhibitory concentration (IC50) was performed. According to our study, the IC50s of Erltinib, Geftinib, Cerubidine, Adriamycine, Idamycin and Ara-C in KG1a cells were 4.93μM, 8.92μM, 1.27μM, 4.51μM and 1.27μg/ml (S1 Fig). As shown in Fig 1A, six chemotherapy drugs: Gefitinib, Erlotinib, Cerubidine, Adriamycine, Idamycin and Ara-C were applied to treat KG1a cells respectively for 11 days. The mortality rate of these six drugs was similar except Ara-C whose ability was weaker compared with another 5 drugs. What’s more, the mortality rate of KG1a cells reached the maximum value at 80% at the fifth day. After that, the number of cells increased under continuous administration, which means that the remaining cells were capable of survival during the chemotherapies.
(A) Cell viability was measured using the Cell Counting Kit-8, the work solution concentration of these six medicines listed as follows: Erltinib, 5 μM; Geftinib, 10 μM; Cerubidine, 1 μM; Adriamycine, 5 μM; Idamycin, 5 μM; Ara-C, 1 μg/ml. (B) The survival KG1a cells displayed higher intensity of CD34 after chemotherapy. (C and D) The survival cells from chemotherapy displayed stronger resistance to Geftinib or Cerubidine. All experiments were independently repeated at least 3 times. ***P <0.001.
LSCs are commonly considered to be a kind of cells that could hardly be eliminated by chemotherapy drugs and performed as the quiescent cell in patients. KG1a cell line, which we further studied on, were proved to contain (54.167 ± 6.57)% LSCs [17, 18]. After 11 days treatment of six chemo-drugs, the intensity of CD34 fluorescence significantly increased over than 100 times in the survival KG1a cells, what’s more, cells treated with Cerubidine had the highest intensity and the ones with Gefitinib had similar fluorescence intensity (Fig 1B). Thus, these two drugs were selected for the further study.
To determine the tolerance ability of the survival cells, cells that had treated with Gefitinib and Cerubidine (pre-Gefitinib, pre-Cerubidine) were cultured with same drugs at the same concentrations for another 11 days. As shown in Fig 1C and 1D, the survival cells became much more resistant to Gefitinib and Cerubidine treatment compared with those treated first time (fresh).
GATA2 is upregulated during the progression of clinical patients’ AML cells and KG1a treated with drugs
To evaluate the potential effect of GATA2 in survival cells, we selected 8 patients who were diagnosed as untreated AML with CD34 positive or partly positive in the hospital, whose characteristics were shown in S1 Table. The peripheral primary AML cells were selected before chemotherapy and after 3 months of chemotherapy which named “before” and “after” respectively. We found that the mRNA levels of GATA2 increased about four folds in “after” samples compared with “before” samples (Fig 2A), while similar results were observated in GATA2 protein expression in peripheral AML cells (Fig 2B). All the patients were received the classic remission induction therapy, thus we intended to observe the GATA2 expression in KG1a cells treated with Gefitinib and Cerubidine respectively. As shown in Fig 2C and 2D, both the mRNA and protein expression level of GATA2 in the survival KG1a cells were kept rising trend during the second treated with Gefitinib and Cerubidine, and the statistic significant appeared one day after treatment.
(A) GATA2 mRNA expression in peripheral primary AML cells and chemo treatment AML cells were determined by real time PCR. (B) Western blot detected the GATA2 protein level in two groups as described in Fig 2A. (C) Real time PCR identified GATA2 mRNA expression level with Geftinib(10 μM) or Cerubidine(1 μM) treatment in KG1a cells. (D) GATA2 protein expression after KG1a cells were treated by Geftinib(10 μM) or Cerubidine(1 μM) at different times. ***P <0.001.
GATA2 targeting genes were unregulated during chemotherapy
GATA2 targeting multiple genes are associated with the onset of AML, such as EVI[9, 19], SCL[20, 21] and WT1[11], even including itself[22]. We observed that the expression levels of EVI, SCL and WT1 in peripheral primary AML cells of the same patient were surged to 3 fold after chemotherapy (Fig 3A–3C). The similar results were also detected in KG1a cells treated with Gefitinib, whose expression of these three genes were 2–4 folds higher after 11 days (Fig 3D).
(A-C) Real time PCR identified GATA2 targeting genes: EVI, SCL and WT1 in patients’ primary AML samples. (D) Real time PCR identified the same genes in KG1a cells. Primers used to detect EVI, SCL and WT1 mRNA level were listed in materials and methods. **P <0.01, ***P <0.001.
Knocking down GATA2 reduced cell viability and increased apoptosis during chemo-treatment
Thus, is it possible that the KG1a cells could be sensitize to chemotherapy by blocking the expression of GATA2? We delivered shRNA sequence specifically targeting GATA2 into KG1a cells (Fig 4A). Furthermore, chemotherapies almost completely removed the KG1a cells with depressed GATA2 expression after 11 days of continuous chemotherapies (Fig 4B). After knocking down GATA2 in KG1a cells, Gefitinib or Cerubidine treatment showed a significant increase in the rate of apoptosis (Fig 4C). These results showed that GATA2 contributed to drug resistance in the chemo treatment of AML patients.
(A) The GATA2 knockdown efficiency was identified by western blot in KG1a cells. The sequences used to RNA interference was listed in materials and methods. (B) Cell viabilities after treatment of Gefitinib or Cerubidine between scramble and GATA2 knockdown cells were measured by CCK8 assay at different times. (C) Annexin V-FITC and PI staining determined apoptosis cells at 11 day. ***P<0.001.
GATA2 inhibitor reduced gefitinib-induced GATA2 and its targeting genes expression in clinical primary AML cells
The expressions of GATA2, WT1, SCL and EVI were evaluated in clinical primary AML cells treated with or without GATA2 inhibitor (K1747) and Gefitinib. Results showed that EVI, GATA2, SCL and WT1 were upregulated after Gefitinib treated, while the combination of K1747 and Gefitinib dramatically reduced the expression of them (Fig 5A–5D). What’s more, we observed that the EVI, SCL and WT1 expression reduced in different extent when K1747 was added with six drugs mentioned above (S2 Fig). However, EVI and WT1 levels were the lowest in KG1a cells with K1747 and Gefitinib, compared with the ones with other drugs. Therefore, it is possible to clean up either the AML cell line or the primary AML cells by combining certain chemotherapy drugs and GATA2 inhibitor together, especially Gefitinib.
(A-D) Combination of GATA2 inhibitor and chemotherapies (Gefitinib) dramatically reduced AML related-genes expression as described in Fig 3. Geftinib = 10 μM; K7174 (GATA2 inhibitor) = 20 μM.**P<0.01, ***P<0.001.
Discussion
Recently, GATA2 is proved to be required for the survival of RAS pathway mutated non-small cell lung cancer (NSCLC) cells [23], and it has identified that GATA2 as a regulator of chemotherapy resistance and tumorigenicity in lethal prostate cancer through experimental models and clinical databases [24]. While GATA2 has long been implicated as a hematopoietic transcription factor and its dysregulated expression is associated with human immunodeficiency syndromes and vascular integrity [25], thus, the regulate effect of GATA2 observed in solid tumors may have similar effect on human leukemia cells to chemotherapy. To address whether the effect could be replicated in human leukemia cells, we oberserved KG1a cells and clinical patients’ AML cells with a classic drug (Cerubidine) and Gefitinib [26, 27].
Studies have clearly demonstrated that AML cells are propagated by a subpopulation of leukemia stem cells (LSCs) [28]. Initial reports described a specific cell surface phenotype for LSCs that allowed primitive leukemia cells to be distinguished from normal stem and progenitor cells (CD34+, CD38-, CD123+ and so on)[29]. It has been reported that LSCs are substantially more tolerated to multiple chemotherapies than bulk leukemia populations [28]. Laboratory studies have specifically examined challenge with cytarabine and daunorubicin and have demonstrated preferential survival of functionally defined LSCs [30]. Our data proved that the survival leukemia cells from chemotherapies presented much higher level of CD34+, indicating that there are a higher proportion of stem / progenitor cells in these residual population cells. Unfortunately, we failed to make this result more reliable because no other cell surface phenotype was observed. Thus, there is no solid evidence to prove the relationship between high expression of GATA2 and the progress of LSCs.
In the current study, we found that human leukemia cells that resistant to traditional chemotherapy demonstrated upregulated GATA2. This finding echoes the results reported from human hematopoietic stem and progenitor cell study showing that sustaining high GATA-2 expression confers increased quiescence and consequently limits their performance[31]. Our research confirmed GATA2 expression in the survival cells dramatically increased to 2–4 folds comparing to the control group after the second treatment, which suggested GATA2 might involve to the drug resistance. What’s more, our research suggested that the combination with suppression of GATA2 expression or transcriptional activity and chemotherapies could be a novel strategy to improve the complete remission rate and benefit long-term survival of patients, such as reducing the expression of GATA2 by GATA2 5 'mirRNA UTR, or applying the method of crisper/cas9 to knock out GATA2' UTR [32].
Apoptosis is a form of cell death that could eliminate cells without releasing inflammatory substances into the surrounding area. Previous report showed that TIM3+ HSCs with higher GATA2 displayed overproliferation and decreased apoptosis [33]. Our result confirmed that the increased apoptosis appeared in KG1a cells with knocking down GATA2. However, the fact that we did not explore the underlying mechanism is a limitation of the current study; thus, it is not clear the exact pathway that cause GATA2 gene expression surge after chemotherapy and affect apoptosis. We make a hypothesis that there is a positive feedback mechanism to regulate GATA2 expression: GATA2 expression is upregulated by targeting to itself promoter while chemotherapy promotes GATA2 transcriptional activity. There is evidence that GATA2 targets to its own promoter [34], but under what conditions, such as extracellular stress or intracellular stimuli are still elusive. Thus, the hypothesis is that during the process of chemotherapy with AML cells, GATA2 is activated and binds to its own promoter which in turn enhanced the expression of GATA2 itself. After a series of chemotherapies, a high level of activated GATA2 might confer a strong resistance to the chemotherapy, which eventually leads to failed chemotherapies.
Our study remains to be validated in clinical trials, but it offers an appealing orientation: several nodes of the GATA2 signaling pathway are amenable to existing approved clinical agents, in turn facilitating translation to clinical therapies. Furthermore, the challenge to identify the optimal combinations of chemo-medicines to suppress the proliferation and survival of AML cells remains to be solved.
Supporting Information
S1 Fig. IC50 values of the six drugs in KG1a cells.
KG1a cells were treated with various doses of six drugs for 48 hours and IC50 was determined by CCK8 assay.
https://doi.org/10.1371/journal.pone.0170630.s001
(TIF)
S2 Fig. Combination K1747 and chemotherapeutic drugs affect EVI, SCL and WT1 mRNA expression.
After KGla cells were treated with K1747 and chemotherapeutic drugs for 48 hours, EVI, SCL and WT1 mRNA expression was measured by real-time PCR. The drug concentrations were described as Fig 1.
https://doi.org/10.1371/journal.pone.0170630.s002
(TIF)
S1 Table. Characteristics of clinical patients.
https://doi.org/10.1371/journal.pone.0170630.s003
(XLSX)
Acknowledgments
All authors were involved in the design, conduct and analyses of the study. Wenfang Zhuang for study design, technical assistance, lab management; Wenfang Zhuang, Li Yang, Yanan Cao, and Binbin Xuan for general experimental techniques; Li Yang and Hanxiao Sun for manuscript preparation; for general experimental techniques; Wenfang Zhuang and Huiming Sheng for final approval of the version to be published. We are grateful to Mr. Kai Zhang, Ms. Xiaohui Wu and Ms. Yu Hua for their excellent assistance. The authors thank Shanghai Tuzhu biotechnology, the Flow Cytometry Core, Light Microscopy Core, and the Animal Facility of the SLAC Company in Shanghai for the technical support. This work was supported by the Shanghai Municipal Health Bureau Project (15ZR1437900), Natural Science Research Project of Changning District (CNKW2014Z01), Leading Disciplines of Medical Laboratory in Changning District (2012QZK01) and Tongren Hospital grant (grant TR201407, TRYJ201506). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Author Contributions
- Conceptualization: WZ HS.
- Data curation: LY HS.
- Formal analysis: LY HS.
- Funding acquisition: LY HS.
- Investigation: LY HS.
- Methodology: LY HS.
- Project administration: LY HS.
- Resources: LY HS.
- Software: LY HS.
- Supervision: YC BX YF.
- Validation: LY HS.
- Visualization: LY HS.
- Writing – original draft: LY HS.
- Writing – review & editing: LY HS.
References
- 1. Guzman ML, Swiderski CF, Howard DS, Grimes BA, Rossi RM, Szilvassy SJ, et al. Preferential induction of apoptosis for primary human leukemic stem cells. Proceedings of the National Academy of Sciences of the United States of America. 2002;99(25):16220–5. pmid:12451177
- 2. Perry JM, Li L. Disrupting the stem cell niche: good seeds in bad soil. Cell. 2007;129(6):1045–7. pmid:17574018
- 3. Lichtman MA. A historical perspective on the development of the cytarabine (7days) and daunorubicin (3days) treatment regimen for acute myelogenous leukemia: 2013 the 40th anniversary of 7+3. Blood Cells Mol Dis. 2013;50(2):119–30. pmid:23154039
- 4. Dombret H, Gardin C. An update of current treatments for adult acute myeloid leukemia. Blood. 2016;127(1):53–61. pmid:26660429
- 5. Tsai FY, Orkin SH. Transcription factor GATA-2 is required for proliferation/survival of early hematopoietic cells and mast cell formation, but not for erythroid and myeloid terminal differentiation. Blood. 1997;89(10):3636–43. pmid:9160668
- 6. Kitajima K, Tanaka M, Zheng J, Yen H, Sato A, Sugiyama D, et al. Redirecting differentiation of hematopoietic progenitors by a transcription factor, GATA-2. Blood. 2006;107(5):1857–63. pmid:16254139
- 7. Bullinger L, Dohner K, Bair E, Frohling S, Schlenk RF, Tibshirani R, et al. Use of gene-expression profiling to identify prognostic subclasses in adult acute myeloid leukemia. The New England journal of medicine. 2004;350(16):1605–16. pmid:15084693
- 8. Luesink M, Hollink IH, van der Velden VH, Knops RH, Boezeman JB, de Haas V, et al. High GATA2 expression is a poor prognostic marker in pediatric acute myeloid leukemia. Blood. 2012;120(10):2064–75. pmid:22786876
- 9. Goyama S, Yamamoto G, Shimabe M, Sato T, Ichikawa M, Ogawa S, et al. Evi-1 is a critical regulator for hematopoietic stem cells and transformed leukemic cells. Cell stem cell. 2008;3(2):207–20. pmid:18682242
- 10. Takeshita M, Ichikawa M, Nitta E, Goyama S, Asai T, Ogawa S, et al. AML1-Evi-1 specifically transforms hematopoietic stem cells through fusion of the entire Evi-1 sequence to AML1. Leukemia. 2008;22(6):1241–9. pmid:18337762
- 11. Furuhata A, Murakami M, Ito H, Gao S, Yoshida K, Sobue S, et al. GATA-1 and GATA-2 binding to 3' enhancer of WT1 gene is essential for its transcription in acute leukemia and solid tumor cell lines. Leukemia. 2009;23(7):1270–7. pmid:19212333
- 12. Miwa H, Beran M, Saunders GF. Expression of the Wilms' tumor gene (WT1) in human leukemias. Leukemia. 1992;6(5):405–9. pmid:1317488
- 13. Greif PA, Dufour A, Konstandin NP, Ksienzyk B, Zellmeier E, Tizazu B, et al. GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia. Blood. 2012;120(2):395–403. pmid:22649106
- 14. Celton M, Forest A, Gosse G, Lemieux S, Hebert J, Sauvageau G, et al. Epigenetic regulation of GATA2 and its impact on normal karyotype acute myeloid leukemia. Leukemia. 2014;28(8):1617–26. pmid:24514424
- 15. Rodrigues NP, Tipping AJ, Wang Z, Enver T. GATA-2 mediated regulation of normal hematopoietic stem/progenitor cell function, myelodysplasia and myeloid leukemia. Int J Biochem Cell Biol. 2012;44(3):457–60. pmid:22192845
- 16. Bruserud O, Hovland R, Wergeland L, Huang TS, Gjertsen BT. Flt3-mediated signaling in human acute myelogenous leukemia (AML) blasts: a functional characterization of Flt3-ligand effects in AML cell populations with and without genetic Flt3 abnormalities. Haematologica. 2003;88(4):416–28. pmid:12681969
- 17. She M, Niu X, Chen X, Li J, Zhou M, He Y, et al. Resistance of leukemic stem-like cells in AML cell line KG1a to natural killer cell-mediated cytotoxicity. Cancer letters. 2012;318(2):173–9. pmid:22198207
- 18. Ding Y, Gao H, Zhang Y, Li Y, Vasdev N, Gao Y, et al. Alantolactone selectively ablates acute myeloid leukemia stem and progenitor cells. J Hematol Oncol. 2016;9(1):93. pmid:27658462
- 19. Sato T, Goyama S, Nitta E, Takeshita M, Yoshimi M, Nakagawa M, et al. Evi-1 promotes para-aortic splanchnopleural hematopoiesis through up-regulation of GATA-2 and repression of TGF-b signaling. Cancer science. 2008;99(7):1407–13. pmid:18452556
- 20. Gottgens B, Nastos A, Kinston S, Piltz S, Delabesse EC, Stanley M, et al. Establishing the transcriptional programme for blood: the SCL stem cell enhancer is regulated by a multiprotein complex containing Ets and GATA factors. The EMBO journal. 2002;21(12):3039–50. pmid:12065417
- 21. Ghatpande S, Ghatpande A, Sher J, Zile MH, Evans T. Retinoid signaling regulates primitive (yolk sac) hematopoiesis. Blood. 2002;99(7):2379–86. pmid:11895770
- 22. Huang Z, Dore LC, Li Z, Orkin SH, Feng G, Lin S, et al. GATA-2 reinforces megakaryocyte development in the absence of GATA-1. Molecular and cellular biology. 2009;29(18):5168–80. pmid:19620289
- 23. Kumar MS, Hancock DC, Molina-Arcas M, Steckel M, East P, Diefenbacher M, et al. The GATA2 transcriptional network is requisite for RAS oncogene-driven non-small cell lung cancer. Cell. 2012;149(3):642–55. pmid:22541434
- 24. Vidal SJ, Rodriguez-Bravo V, Quinn SA, Rodriguez-Barrueco R, Lujambio A, Williams E, et al. A targetable GATA2-IGF2 axis confers aggressiveness in lethal prostate cancer. Cancer Cell. 2015;27(2):223–39. pmid:25670080
- 25. de Pater E, Kaimakis P, Vink CS, Yokomizo T, Yamada-Inagawa T, van der Linden R, et al. Gata2 is required for HSC generation and survival. The Journal of experimental medicine. 2013;210(13):2843–50. pmid:24297996
- 26. Deangelo DJ, Neuberg D, Amrein PC, Berchuck J, Wadleigh M, Sirulnik LA, et al. A phase II study of the EGFR inhibitor gefitinib in patients with acute myeloid leukemia. Leuk Res. 2014;38(4):430–4. pmid:24522247
- 27. Boehrer S, Ades L, Galluzzi L, Tajeddine N, Tailler M, Gardin C, et al. Erlotinib and gefitinib for the treatment of myelodysplastic syndrome and acute myeloid leukemia: a preclinical comparison. Biochem Pharmacol. 2008;76(11):1417–25. pmid:18617157
- 28. Corces-Zimmerman MR, Majeti R. Pre-leukemic evolution of hematopoietic stem cells: the importance of early mutations in leukemogenesis. Leukemia. 2014;28(12):2276–82. pmid:25005245
- 29. Haase D, Feuring-Buske M, Konemann S, Fonatsch C, Troff C, Verbeek W, et al. Evidence for malignant transformation in acute myeloid leukemia at the level of early hematopoietic stem cells by cytogenetic analysis of CD34+ subpopulations. Blood. 1995;86(8):2906–12. pmid:7579382
- 30. Shlush LI, Zandi S, Mitchell A, Chen WC, Brandwein JM, Gupta V, et al. Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia. Nature. 2014;506(7488):328–33. pmid:24522528
- 31. Tipping AJ, Pina C, Castor A, Hong D, Rodrigues NP, Lazzari L, et al. High GATA-2 expression inhibits human hematopoietic stem and progenitor cell function by effects on cell cycle. Blood. 2009;113(12):2661–72. pmid:19168794
- 32. Dang Y, Jia G, Choi J, Ma H, Anaya E, Ye C, et al. Optimizing sgRNA structure to improve CRISPR-Cas9 knockout efficiency. Genome biology. 2015;16:280. pmid:26671237
- 33. Tao JL, Li LJ, Fu R, Wang HQ, Jiang HJ, Yue LZ, et al. Elevated TIM3+ hematopoietic stem cells in untreated myelodysplastic syndrome displayed aberrant differentiation, overproliferation and decreased apoptosis. Leuk Res. 2014;38(6):714–21. pmid:24746294
- 34. Gao X, Johnson KD, Chang YI, Boyer ME, Dewey CN, Zhang J, et al. Gata2 cis-element is required for hematopoietic stem cell generation in the mammalian embryo. The Journal of experimental medicine. 2013;210(13):2833–42. pmid:24297994