The DOI matches its Crossref record; 59 of the 60 references it cites were found in a registry or an index.
Requirement for CDK6 in MLL-rearranged acute myeloid leukemia
Open accessAbstract
Key Points: CDK6 is a critical effector of MLL fusions in myeloid leukemogenesis. Genetic and pharmacologic inhibition of CDK6 overcome the differentiation block associated with MLL-rearranged AML.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Multiple types of leukemia cells are dependent on CDK6 for survival, including mixed-lineage leukemia (MLL) [123] and Philadelphia chromosome-positive ALL (Ph+ ALL) [9].”
From Proteolysis targeting chimeras (PROTACs) are emerging therapeutics for hematologic malignancies (2020) · cites this paper as [123]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1
Barbie, D. A., Tamayo, P., Boehm, J. S., Kim, S. Y., Moody, S. E., Dunn, I. F., Schinzel, A. C., Sandy, P., Meylan, E., Scholl, C., et al. (2009) · Nature · doi:10.1038/nature08460 · Cited by 3,922
Self-citationDöhner, H., Estey, E. H., Amadori, S., Appelbaum, F. R., Büchner, T., Burnett, A. K., Dombret, H., Fenaux, P., Grimwade, D. J., Larson, R. A., et al. (2009) · Blood · doi:10.1182/blood-2009-07-235358 · Cited by 3,438
Distinct Sets of Genetic Alterations in Melanoma
Curtin, J. A., Fridlyand, J., Kageshita, T., Patel, H. N., Busam, K. J., Kutzner, H., Cho, K.-H., Aiba, S., Bröcker, E.-B., LeBoit, P. E., et al. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa050092 · Cited by 2,747
Grimwade, D. J., Hills, R. K., Moorman, A. V., Walker, H., Chatters, S., Goldstone, A. H., Wheatley, K., Harrison, C. J., & Burnett, A. K. (2010) · Blood · doi:10.1182/blood-2009-11-254441 · Cited by 1,936
RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia
Zuber, J., Shi, J., Wang, E., Rappaport, A. R., Herrmann, H., Sison, E. A., Magoon, D., Qi, J., Blatt, K., Wunderlich, M., et al. (2011) · Nature · doi:10.1038/nature10334 · Cited by 1,870
Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia
Dawson, M. A., Prinjha, R. K., Dittmann, A., Giotopoulos, G., Bantscheff, M., Chan, W.-I., Robson, S. C., Chung, C., Hopf, C., Savitski, M. M., et al. (2011) · Nature · doi:10.1038/nature10509 · Cited by 1,530
Self-citationTransformation from committed progenitor to leukaemia stem cell initiated by MLL–AF9
Krivtsov, A. V., Twomey, D., Feng, Z., Stubbs, M. C., Wang, Y., Faber, J., Levine, J. E., Wang, J., Hahn, W. C., Gilliland, D. G., et al. (2006) · Nature · doi:10.1038/nature04980 · Cited by 1,513 · cited 1×
“A key functional feature of mixed-lineage leukemia (MLL) rearrangements is their ability to confer leukemia-initiating activity to hematopoietic stem and progenitor cells (HSPC).(5,6) MLL fusions are characterized by loss of the C-terminal H3K4 methyltransferase domain, and their leukemogenic activity is dependent on…”
Self-citationA p16 INK4a -Insensitive CDK4 Mutant Targeted by Cytolytic T Lymphocytes in a Human Melanoma
Wölfel, T., Hauer, M., Schneider, J., Serrano, M., Wölfel, C., Klehmann, E., Plaen, E. D., Hankeln, T., Büschenfelde, K. M. Z., & Beach, D. (1995) · Science · doi:10.1126/science.7652577 · Cited by 1,171
Selective Killing of Mixed Lineage Leukemia Cells by a Potent Small-Molecule DOT1L Inhibitor
Daigle, S. R., Olhava, E. J., Therkelsen, C. A., Majer, C. R., Sneeringer, C. J., Song, J. J., Johnston, L. D., Scott, M. P., Smith, J. J., Xiao, Y., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.06.009 · Cited by 926
Self-citationMLL-Rearranged Leukemia Is Dependent on Aberrant H3K79 Methylation by DOT1L
Bernt, K. M., Zhu, N., Sinha, A. U., Vempati, S., Faber, J., Krivtsov, A. V., Feng, Z., Punt, N., Kedaigle, A. J., Bullinger, L., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.06.010 · Cited by 872
Self-citation
Cited by
Sorted by citations
Döhner, H., Estey, E. H., Grimwade, D. J., Amadori, S., Appelbaum, F. R., Büchner, T., Dombret, H., Ebert, B. L., Fenaux, P., Larson, R. A., et al. (2016) · Blood · doi:10.1182/blood-2016-08-733196 · Cited by 5,938
Genomics of Acute Myeloid Leukemia Diagnosis and Pathways
Bullinger, L., Döhner, K., & Döhner, H. (2017) · Journal of Clinical Oncology · doi:10.1200/jco.2016.71.2208 · Cited by 570
Quality control, modeling, and visualization of CRISPR screens with MAGeCK-VISPR
Li, W., Köster, J., Xu, H., Chen, C.-H., Xiao, T., Liu, J. S., Brown, M. A., & Liu, X. S. (2015) · Genome biology · doi:10.1186/s13059-015-0843-6 · Cited by 503
Krivtsov, A. V., Evans, K., Gadrey, J. Y., Eschle, B. K., Hatton, C., Uckelmann, H. J., Ross, K. N., Perner, F., Olsen, S. N., Pritchard, T., et al. (2019) · Cancer Cell · doi:10.1016/j.ccell.2019.11.001 · Cited by 460
Self-citationMolecular landscape of acute myeloid leukemia in younger adults and its clinical relevance
Grimwade, D. J., Ivey, A., & Huntly, B. J. P. (2015) · Blood · doi:10.1182/blood-2015-07-604496 · Cited by 475
Self-citationMLL-Rearranged Leukemias—An Update on Science and Clinical Approaches
Winters, A. C., & Bernt, K. M. (2017) · Frontiers in Pediatrics · doi:10.3389/fped.2017.00004 · Cited by 402
CDK6 Levels Regulate Quiescence Exit in Human Hematopoietic Stem Cells
Laurenti, E., Frelin, C., Xie, S. Z.-J., Ferrari, R., Dunant, C. F., Zandi, S., Neumann, A. L., Plumb, I., Doulatov, S. R., Chen, J., et al. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.01.017 · Cited by 339
Cyclin-dependent protein kinases and cell cycle regulation in biology and disease
Pellarin, I., Dall’Acqua, A., Favero, A., Segatto, I., Rossi, V., Crestan, N., Karimbayli, J., Belletti, B., & Baldassarre, G. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02080-z · Cited by 381
How I treat refractory and early relapsed acute myeloid leukemia
Thol, F. R., Schlenk, R. F., Heuser, M., & Ganser, A. (2015) · Blood · doi:10.1182/blood-2014-10-551911 · Cited by 307
CDK6 as a key regulator of hematopoietic and leukemic stem cell activation
Scheicher, R., Hoelbl‐Kovacic, A., Bellutti, F., Tigan, A.-S., Prchal‐Murphy, M., Heller, G., Schneckenleithner, C., Salazar‐Roa, M., Zöchbauer‐Müller, S., Zuber, J. A., et al. (2014) · Blood · doi:10.1182/blood-2014-06-584417 · Cited by 265
Tigan, A.-S., Bellutti, F., Kollmann, K., Tebb, G., & Sexl, V (2016) · Oncogene · doi:10.1038/onc.2015.407 · Cited by 204
Nebenfuehr, S., Kollmann, K., & Sexl, V. (2020) · International Journal of Cancer · doi:10.1002/ijc.33054 · Cited by 187
Dysregulated haematopoietic stem cell behaviour in myeloid leukaemogenesis
Yamashita, M., Dellorusso, P. V., Olson, O. C., & Passegue, E. A. (2020) · Nature reviews. Cancer · doi:10.1038/s41568-020-0260-3 · Cited by 197
Palanichamy, J. K., Tran, T. M., Howard, J. M., Contreras, J. R., Fernando, T. R., Sterne-Weiler, T., Katzman, S. J., Toloue, M., Yan, W., Basso, G., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci80046 · Cited by 171
Targeting CDK6 in cancer: State of the art and new insights
Tadesse, S., Yu, M., Kumarasiri, M., Le, B. T., & Wang, S. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1084445 · Cited by 168
LKB1, Salt-Inducible Kinases, and MEF2C Are Linked Dependencies in Acute Myeloid Leukemia
Tarumoto, Y., Lu, B., Somerville, T. D. D., Huang, Y., Milazzo, J. P., Wu, X., Klingbeil, O., Demerdash, O. E., Shi, J., & Vakoc, C. R. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.02.011 · Cited by 154
Uras, I. Z., Walter, G. J., Scheicher, R., Bellutti, F., Prchal‐Murphy, M., Tigan, A.-S., Valent, P., Heidel, F. H., Kubicek, S., Scholl, C., et al. (2016) · Blood · doi:10.1182/blood-2015-11-683581 · Cited by 138
Self-citationmiR-22 has a potent anti-tumour role with therapeutic potential in acute myeloid leukaemia
Jiang, X., Hu, C., Arnovitz, S., Bugno, J., Yu, M., Zuo, Z., Chen, P., Huang, H., Ulrich, B. C., Gurbuxani, S. K., et al. (2016) · Nature Communications · doi:10.1038/ncomms11452 · Cited by 143
Synergistic targeting of FLT3 mutations in AML via combined menin-MLL and FLT3 inhibition
Dzama, M. M., Steiner, M., Rausch, J., Sasca, D., Schönfeld, J., Kunz, K., Taubert, M. C., McGeehan, G. M., Chen, C.-W. D., Mupo, A., et al. (2020) · Blood · doi:10.1182/blood.2020005037 · Cited by 135
Self-citationProteolysis targeting chimeras (PROTACs) are emerging therapeutics for hematologic malignancies
He, Y., Khan, S., Huo, Z., Lv, D., Zhang, X., Liu, X., Yuan, Y., Hromas, R., Xu, M., Zheng, G., et al. (2020) · Journal of Hematology & Oncology · doi:10.1186/s13045-020-00924-z · Cited by 126
Kuntimaddi, A., Achille, N. J., Thorpe, J., Lokken, A. A., Singh, R., Hemenway, C. S., Adli, M., Zeleznik‐Le, N. J., & Bushweller, J. H. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.004 · Cited by 120
Targeting cell cycle regulators in hematologic malignancies
Aleem, E. A., & Arceci, R. J. (2015) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2015.00016 · Cited by 128
Martinez-Soria, N., McKenzie, L., Draper, J. E., Ptasinska, A., Issa, H., Potluri, S., Blair, H. J., Pickin, A., Isa, A., Chin, P. S., et al. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.08.015 · Cited by 115
岩崎, 正., Liedtke, M., Gentles, A. J., & Cleary, M. L. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.08.008 · Cited by 123
Baker, A., Gregory, G. P., Verbrugge, I., Kats, L. M., Hilton, J. J., Vidacs, E., Lee, E. M., Lock, R. B., Zuber, J. A., Shortt, J., et al. (2015) · Cancer Research · doi:10.1158/0008-5472.can-15-1070 · Cited by 117
Complementary activities of DOT1L and Menin inhibitors in MLL-rearranged leukemia
Dafflon, C., Craig, V. J., Méreau, H., Gräsel, J., Engstler, B. S., Hoffman, G., Nigsch, F., Gaulis, S., Barys, L., Ito, M., et al. (2016) · Leukemia · doi:10.1038/leu.2016.327 · Cited by 115
Synergistic Drug Combinations with a CDK4/6 Inhibitor in T-cell Acute Lymphoblastic Leukemia
Pikman, Y., Alexe, G., Roti, G., Conway, A. S., Furman, A. A., Lee, E. S., Place, A. E., Kim, S., Saran, C., Modiste, R., et al. (2016) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-15-2869 · Cited by 115
LncRNA Expression Discriminates Karyotype and Predicts Survival in B-Lymphoblastic Leukemia
Fernando, T. R., Rodriguez-Malave, N. I., Waters, E. V., Yan, W., Casero, D., Basso, G., Pigazzi, M., & Rao, D. S. (2015) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-15-0006-t · Cited by 107
Ying, M., Shao, X., Jing, H., Liu, Y., Qi, X., Cao, J., Chen, Y., Xiang, S., Song, H., Hu, R., et al. (2018) · Blood · doi:10.1182/blood-2017-10-813139 · Cited by 105
NCAM1 (CD56) promotes leukemogenesis and confers drug resistance in AML.
Sasca, D., Szybinski, J., Schüler, A., Shah, V., Heidelberger, J. B., Haehnel, P. S., Dolnik, A., Kriege, O., Fehr, E.-M., Gebhardt, W., et al. (2019) · Blood · doi:10.1182/blood-2018-12-889725 · Cited by 93
Self-citationMLL-Rearranged Acute Lymphoblastic Leukemia
Chaer, F. E., Keng, M. K., & Ballen, K. K. (2020) · Current Hematologic Malignancy Reports · doi:10.1007/s11899-020-00582-5 · Cited by 100
Brenner, A. K., Reikvam, H., Lavecchia, A., & Bruserud, Ø. (2014) · Molecules · doi:10.3390/molecules191118414 · Cited by 91
A Molecular Switch between Mammalian MLL Complexes Dictates Response to Menin–MLL Inhibition
Soto‐Feliciano, Y. M., Rivera, F. J. S., Perner, F., Barrows, D., Kastenhuber, E. R., Ho, Y.-J., Carroll, T., Xiong, Y., Anand, D., Soshnev, A. A., et al. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-22-0416 · Cited by 85
Self-citationUpdate on rational targeted therapy in AML
Shafer, D. A., & Grant, S. (2016) · Blood Reviews · doi:10.1016/j.blre.2016.02.001 · Cited by 79
Lee, D. J., & Zeidner, J. F. (2019) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2019.1678583 · Cited by 78
Distinct CDK6 complexes determine tumor cell response to CDK4/6 inhibitors and degraders
Wu, X., Yang, X., Xiong, Y., Li, R., Ito, T., Ahmed, T. A., Karoulia, Z., Adamopoulos, C., Wang, H., Wang, L., et al. (2021) · Nature Cancer · doi:10.1038/s43018-021-00174-z · Cited by 75
Dual PI3K/mTOR inhibition shows antileukemic activity in MLL-rearranged acute myeloid leukemia
Sandhöfer, N., Metzeler, K. H., Rothenberg, M., Herold, T., Tiedt, S., Groiß, V., Carlet, M., Walter, G., Hinrichsen, T., Wachter, O., et al. (2014) · Leukemia · doi:10.1038/leu.2014.305 · Cited by 75
Self-citationThe molecular mechanics of mixed lineage leukemia
Slany, R. K. (2016) · Oncogene · doi:10.1038/onc.2016.30 · Cited by 72
CDK6 is an essential direct target of NUP98 fusion proteins in acute myeloid leukemia
Schmoellerl, J., Barbosa, I. A. M., Eder, T., Brandstoetter, T., Schmidt, L., Maurer, B., Troester, S., Pham, H. T. T., Mohanty, S., Ebner, J., et al. (2020) · Blood · doi:10.1182/blood.2019003267 · Cited by 74
ZFP36L1 promotes monocyte/macrophage differentiation by repressing CDK6
Chen, M., Dong, L., Zhang, X., Yin, X.-L., Ning, H., Shen, C., Su, R. J., Li, F., Li, S., Ma, Y., et al. (2015) · Scientific Reports · doi:10.1038/srep16229 · Cited by 71
Differentiation therapy of myeloid leukemia: four decades of development
Madan, V., & Koeffler, H. P. (2020) · Haematologica · doi:10.3324/haematol.2020.262121 · Cited by 72
Ng, Y. L. D., Ramberger, E., Bohl, S., Dolnik, A., Steinebach, C., Conrad, T., Müller, S., Popp, O., Kull, M., Haji, M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28515-1 · Cited by 68
RET-mediated autophagy suppression as targetable co-dependence in acute myeloid leukemia
Rudat, S., Pfaus, A., Cheng, Y., Holtmann, J., Ellegast, J. M., Bühler, C., Marcantonio, D. D., Martı́nez, E., Göllner, S., Wickenhauser, C., et al. (2018) · Leukemia · doi:10.1038/s41375-018-0102-4 · Cited by 71
Self-citationHandschuh, L. (2019) · Journal of Oncology · doi:10.1155/2019/7239206 · Cited by 66
CDK6 Inhibition: A Novel Approach in AML Management
Uras, I. Z., Sexl, V., & Kollmann, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072528 · Cited by 65
miR-139-5p controls translation in myeloid leukemia through EIF4G2
Emmrich, S., Engeland, F., El-Khatib, M., Henke, K., Obulkasim, A., Schöning, J., Katsman-Kuipers, J. E., Zwaan, C. M., Pich, A., Starý, J., et al. (2015) · Oncogene · doi:10.1038/onc.2015.247 · Cited by 64
Recent Advances of Cell-Cycle Inhibitor Therapies for Pediatric Cancer
Mills, C. C., Kolb, E. A., & Sampson, V. B. (2017) · Cancer Research · doi:10.1158/0008-5472.can-17-2066 · Cited by 59
MLL-AF9 initiates transformation from fast-proliferating myeloid progenitors
Chen, X., Burkhardt, D. B., Hartman, A. A., Hu, X., Eastman, A. E., Sun, C., Wang, X., Zhong, M., Krishnaswamy, S., & Guo, S. (2019) · Nature Communications · doi:10.1038/s41467-019-13666-5 · Cited by 58
Gao, S.-M., Zhou, B., Li, H.-Y., Huang, X., Wu, Y.-F., Xing, C.-Y., Yu, X.-Z., & Ji, Y.-H. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.08.005 · Cited by 59
Aubrey, B. J., Cutler, J. A., Bourgeois, W., Donovan, K. A., Gu, S. S., Hatton, C., Perlee, S. C., Perner, F., Rahnamoun, H., Theall, A. C. P., et al. (2022) · Nature Cancer · doi:10.1038/s43018-022-00366-1 · Cited by 58
Self-citationRNA-Binding Proteins in Acute Leukemias
Schuschel, K., Helwig, M., Hüttelmaier, S., Heckl, D., Klusmann, J., & Hoell, J. I. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103409 · Cited by 57
Functional Genomic Analysis of CDK4 and CDK6 Gene Dependency across Human Cancer Cell Lines
Zhang, Z., Golomb, L., & Meyerson, M. M. (2022) · Cancer Research · doi:10.1158/0008-5472.can-21-2428 · Cited by 57
Cierpicki, T., & Grembecka, J. (2015) · Immunological Reviews · doi:10.1111/imr.12244 · Cited by 53
Targeting cell cycle and apoptosis to overcome chemotherapy resistance in acute myeloid leukemia
Ling, V., Straube, J., Godfrey, W. A., Haldar, R., Janardhanan, Y., Cooper, L. T., Bruedigam, C., Cooper, E., Shirazi, P. T., Jacquelin, S., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01755-2 · Cited by 49
Long non-coding RNAs defining major subtypes of B cell precursor acute lymphoblastic leukemia
James, A. R., Schroeder, M. P., Neumann, M., Bastian, L., Eckert, C., Gökbuget, N., Tanchez, J. O., Schlee, C., Isaakidis, K., Schwartz, S., et al. (2019) · Journal of Hematology & Oncology · doi:10.1186/s13045-018-0692-3 · Cited by 50
H19 derived microRNA-675 regulates cell proliferation and migration through CDK6 in glioma.
Li, C., Lei, B., Huang, S., Zheng, M., Liu, Z., Li, Z., & Deng, Y. (2015) · Europe PMC (PubMed Central) · Cited by 48
CDK4/6 and MAPK—Crosstalk as Opportunity for Cancer Treatment
Scheiblecker, L., Kollmann, K., & Sexl, V. (2020) · Pharmaceuticals · doi:10.3390/ph13120418 · Cited by 48
Maurer, B., Brandstoetter, T., Kollmann, S., Sexl, V., & Prchal‐Murphy, M. (2020) · Haematologica · doi:10.3324/haematol.2020.256313 · Cited by 48
Cell cycle regulation and hematologic malignancies
Dai, Y., Jin, F., Wu, W., & Kumar, S. K. (2019) · Blood Science · doi:10.1097/bs9.0000000000000009 · Cited by 46
CDKI-73: an orally bioavailable and highly efficacious CDK9 inhibitor against acute myeloid leukemia
Rahaman, M. H., Yu, Y., Zhong, L., Adams, J., Lam, F., Li, P., Noll, B., Milne, R. W., Peng, J., & Wang, S. (2018) · Investigational New Drugs · doi:10.1007/s10637-018-0661-2 · Cited by 42
An essential pathway links FLT3-ITD, HCK and CDK6 in acute myeloid leukemia
Lopez, S., Voisset, E., Tisserand, J. C., Mosca, C., Prébet, T., Santamarı́a, D., Dubreuil, P. C., & Sepulveda, P. D. (2016) · Oncotarget · doi:10.18632/oncotarget.9965 · Cited by 39
Transcriptional activation by MLL fusion proteins in leukemogenesis.
Yokoyama, A. (2017) · Experimental Hematology · doi:10.1016/j.exphem.2016.10.014 · Cited by 35
Wang, X., Jin, P., Zhang, Y., & Wang, K. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03566-2 · Cited by 33
The IRX1/HOXA connection: insights into a novel t(4;11)- specific cancer mechanism
Kühn, A., Löscher, D., & Marschalek, R. (2016) · Oncotarget · doi:10.18632/oncotarget.9241 · Cited by 33
The RUNX1/RUNX1T1 network: translating insights into therapeutic options
Swart, L. E., & Heidenreich, O. T. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.11.005 · Cited by 32
Bortolozzi, R., Mattiuzzo, E., Trentin, L., Accordi, B., Basso, G., & Viola, G. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.01.050 · Cited by 31
miR-196b target screen reveals mechanisms maintaining leukemia stemness with therapeutic potential
Meyer, S. E., Muench, D. E., Rogers, A. M., Newkold, T. J., Orr, E., O'Brien, E. J., Perentesis, J. P., Doench, J. G., Lal, A., Morris, P. J., et al. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20171312 · Cited by 30
Cdk6 contributes to cytoskeletal stability in erythroid cells
Uras, I. Z., Scheicher, R., Kollmann, K., Glösmann, M., Prchal‐Murphy, M., Tigan, A.-S., Fux, D. A., Altamura, S., Neves, J., Muckenthaler, M. U., et al. (2017) · Haematologica · doi:10.3324/haematol.2016.159947 · Cited by 31
CDC25A governs proliferation and differentiation of FLT3-ITD acute myeloid leukemia
Bertoli, S., Boutzen, H., David, L., Larrue, C., Vergez, F., Fernandez-Vidal, A., Yuan, L., Tamburini, J., Demur, C., Delabesse, É., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5706 · Cited by 31
p16 promotes proliferation in cervical carcinoma cells through CDK6-HuR-IL1A axis
Li, M., Yang, J., Liu, K., Yang, J., Zhan, X., Wang, L., Shen, X., Chen, J., & Mao, Z. (2020) · Journal of Cancer · doi:10.7150/jca.35479 · Cited by 32
Deciphering the Therapeutic Resistance in Acute Myeloid Leukemia
Gurnari, C., Pagliuca, S., & Visconte, V. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228505 · Cited by 31
Antileukemic Efficacy of BET Inhibitor in a Preclinical Mouse Model of MLL-AF4+ Infant ALL
Bardini, M., Trentin, L., Rizzo, F., Vieri, M., Savino, A. M., Castro, P. G., Fazio, G., Roon, E. H. J. V., Kerstjens, M. J., Smithers, N. N., et al. (2018) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-17-1123 · Cited by 29
Numata, A., Kwok, H. S., Kawasaki, A., Li, J., Zhou, Q.-L., Kerry, J., Benoukraf, T., Bararia, D., Li, F., Ballabio, E., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03854-0 · Cited by 28
Targeting CDK6 and BCL2 Exploits the “MYB Addiction” of Ph+ Acute Lymphoblastic Leukemia
Dominici, M. D., Porazzi, P., Soliera, A. R., Mariani, S. A., Addya, S., Fortina, P. M., Peterson, L. F., Spinelli, O., Rambaldi, A., Martinelli, G., et al. (2017) · Cancer Research · doi:10.1158/0008-5472.can-17-2644 · Cited by 27
TBP loading by AF4 through SL1 is the major rate-limiting step in MLL fusion-dependent transcription
Okuda, H., Takahashi, S., Takaori-Kondo, A., & Yokoyama, A. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1222337 · Cited by 26
High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia
Othman, M. A. K., Melo, J. B., Carreira, I. M., Rinčić, M., Glaser, A., Grygalewicz, B., Gruhn, B., Wilhelm, K., Rittscher, K., Meyer, B., et al. (2015) · Molecular Cytogenetics · doi:10.1186/s13039-015-0153-4 · Cited by 26
Hernandez Maganhi, S., Jensen, P., Caracelli, I., Zukerman Schpector, J., Fröhling, S., & Friedman, R. (2017) · Protein Science · doi:10.1002/pro.3135 · Cited by 25
Self-citationGiovanni, C. D., Novellino, E., Chilin, A., Lavecchia, A., & Marzaro, G. (2016) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2016.1234603 · Cited by 25
Tomić, B., Smoljo, T., Lalić, H., Dembitz, V., Batinić, J., Batinić, D., Bedalov, A., & Višnjić, D. (2022) · Scientific Reports · doi:10.1038/s41598-022-15520-z · Cited by 25
Richter, A., Schoenwaelder, N., Sender, S., Junghanss, C., & Maletzki, C. (2021) · Cancers · doi:10.3390/cancers13102497 · Cited by 24
Murine Models of Acute Myeloid Leukemia
Kurtz, K. J., Conneely, S. E., O'Keefe, M. B., Wohlan, K., & Rau, R. E. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.854973 · Cited by 25
ZNF521 sustains the differentiation block in MLL-rearranged acute myeloid leukemia
Germanò, G., Morello, G., Aveic, S., Pinazza, M., Minuzzo, S. A., Frasson, C., Persano, L., Bonvini, P., Viola, G., Bresolin, S., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.15387 · Cited by 21
Zhou, B., Jin, X.-H., Jin, W., Huang, X., Wu, Y.-F., Li, H.-Y., Zhu, W., Qin, X., Ye, H.-G., & Gao, S.-M. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02384-y · Cited by 27
Rasouli, M., Troester, S., Grebien, F., Goemans, B. F., Zwaan, C. M., & Heidenreich, O. T. (2024) · HemaSphere · doi:10.1002/hem3.70013 · Cited by 24
Adriaanse, F. R. S., Schneider, P., Arentsen-Peters, S. T. C. J. M., da Fonseca, A. M. N., Stutterheim, J., Pieters, R., Zwaan, C. M., & Stam, R. W. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25116020 · Cited by 22
Emerging cell cycle inhibitors for acute myeloid leukemia
Zahr, A. A., & Borthakur, G. M. (2017) · Expert Opinion on Emerging Drugs · doi:10.1080/14728214.2017.1330885 · Cited by 21
CDK6 Is a Therapeutic Target in Myelofibrosis
Dutta, A., Nath, D., Yang, Y., Le, B. T., & Mohi, G. (2021) · Cancer Research · doi:10.1158/0008-5472.can-21-0590 · Cited by 24
Kumarasamy, V. M., Gao, Z., Zhao, B., Jiang, B., Rubin, S. M., Burgess, K., Witkiewicz, A. K., & Knudsen, E. S. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02399-4 · Cited by 20
Targeting chromatin modifying complexes in acute myeloid leukemia
Schurer, A., Glushakow-Smith, S. G., & Gritsman, K. (2024) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szae089 · Cited by 20
Differential role of Id1 in MLL-AF9-driven leukemia based on cell of origin.
Man, N., Sun, X.-J., Tan, Y., Garcia-Cao, M., Liu, F., Cheng, G.-Y., Hatlen, M. A., Xu, H.-M., Shah, R., Chastain, N., et al. (2016) · Blood · doi:10.1182/blood-2015-11-677708 · Cited by 22
Therapeutic Vulnerabilities in FLT3-Mutant AML Unmasked by Palbociclib
Uras, I. Z., Maurer, B., Nebenfuehr, S., Zojer, M., Valent, P., & Sexl, V. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123987 · Cited by 19
CDK6 Degradation Is Counteracted by p16INK4A and p18INK4C in AML
Schmalzbauer, B. S., Thondanpallil, T., Heller, G., Schirripa, A., Sperl, C.-M., Mayer, I. M., Knab, V. M., Nebenfuehr, S., Zojer, M., Müller, A. C., et al. (2022) · Cancers · doi:10.3390/cancers14061554 · Cited by 17
HCK maintains the self-renewal of leukaemia stem cells via CDK6 in AML
Li, Z., Wang, F., Tian, X., Long, J., Ling, B., Zhang, W., Xu, J., & Liang, A. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02007-4 · Cited by 17
Xu, J. J., Chalk, A. M., Nikolić, I., Simpson, K. J., Smeets, M. F. M. A., & Walkley, C. R. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021004571 · Cited by 19
NFkB is activated by multiple mechanisms in hairy cell leukemia
Nagel, S., Ehrentraut, S., Meyer, C., Kaufmann, M., Drexler, H. G., & MacLeod, R. A. F. (2015) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22253 · Cited by 18
Li, J., & Kalev‐Zylinska, M. L. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1170622 · Cited by 16
Buetti‐Dinh, A., & Friedman, R. (2018) · BMC Bioinformatics · doi:10.1186/s12859-018-2145-y · Cited by 16
Palbociclib—The First of a New Class of Cell Cycle Inhibitors
Schmidt, M., & Sebastian, M. (2018) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-319-91442-8_11 · Cited by 18
Learning from mouse models of MLL fusion gene-driven acute leukemia.
Schwaller, J. (2020) · Biochimica et Biophysica Acta. Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2020.194550 · Cited by 16
Reikvam, H., Hauge, M., Brenner, A. K., Hatfield, K. J., & Bruserud, Ø. (2015) · Expert Review of Hematology · doi:10.1586/17474086.2015.1032935 · Cited by 16
Metadata
- Authors
- Placke, T., Faber, K., Nonami, A., Putwain, S. L., Salih, H. R., Heidel, F. H., Krämer, A., Root, D. E., Barbie, D. A., Krivtsov, A. V., Armstrong, S. A., Hahn, W. C., Huntly, B. J., Sykes, S. M., Milsom, M. D., Scholl, C., & Fröhling, S.
- Affiliations
- German Cancer Research Center (DE)
- Universität Ulm (DE)
- Dana-Farber Cancer Institute (US)
- Wellcome/MRC Cambridge Stem Cell Institute (GB)
- Deutsches Konsortium für Translationale Krebsforschung (DE)
- Otto-von-Guericke-Universität Magdeburg (DE)
- Broad Institute (US)
- Memorial Sloan Kettering Cancer Center (US)
- Fox Chase Cancer Center (US)
- ORCID
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2014-07-03
- Volume
- 124
- Issue
- 1
- Pages
- 13-23
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- PMC
- PMC4190617
- OpenAlex
- W1990966504
- Cited by
- 170
- References
- 60
- Citations by year
- 2026: 6 · 2025: 9 · 2024: 6 · 2023: 11 · 2022: 16 · 2021: 19 · 2020: 24 · 2019: 10 · 2018: 14 · 2017: 9 · 2016: 17 · 2015: 23 · 2014: 6
- FWCI
- 13.00
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Blood (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (R00CA158461, U01CA176058, K08CA138918, P30CA008748)
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
- Keywords
- CDK6, MLL rearrangement, acute myeloid leukemia, MLL-AF9, CDK4, cell cycle regulators, myeloid differentiation, leukemogenesis, MLL fusion proteins, CDK6 inhibitors, leukemia mouse model
- MeSH terms
- Animals, Flow Cytometry, Humans, Mice, Inbred C57BL, Transduction, Genetic, Immunoblotting, Leukemia, Myeloid, Acute, Oncogene Proteins, Fusion, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Profiling, RNA, Small Interfering, Cell Line, Tumor, Cyclin-Dependent Kinase 6, Mice, Myeloid-Lymphoid Leukemia Protein
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review