TP53 mutations in myelodysplastic syndromes and secondary AML confer an immunosuppressive phenotype
Open accessAbstract
Somatic gene mutations are key determinants of outcome in patients with myelodysplastic syndromes (MDS) and secondary AML (sAML). In particular, patients with TP53 mutations represent a distinct molecular cohort with uniformly poor prognosis. The precise pathogenetic mechanisms underlying these inferior outcomes have not been delineated. In this study, we characterized the immunological features of the malignant clone and alterations in the immune microenvironment in patients with TP53-mutant and wild-type MDS or sAML. Notably, PDL1 expression is significantly increased in hematopoietic stem cells of patients with TP53 mutations, which is associated with MYC upregulation and marked downregulation of MYC’s negative regulator miR-34a, a p53 transcription target. Notably, patients with TP53 mutations display significantly reduced numbers of bone marrow–infiltrating OX40+ cytotoxic T cells and helper T cells, as well as decreased ICOS+ and 4-1BB+ natural killer cells. Further, highly immunosuppressive regulatory T cells (Tregs) (ie, ICOShigh/PD-1−) and myeloid-derived suppressor cells (PD-1low) are expanded in cases with TP53 mutations. Finally, a higher proportion of bone marrow–infiltrating ICOShigh/PD-1− Treg cells is a highly significant independent predictor of overall survival. We conclude that the microenvironment of TP53 mutant MDS and sAML has an immune-privileged, evasive phenotype that may be a primary driver of poor outcomes and submit that immunomodulatory therapeutic strategies may offer a benefit for this molecularly defined subpopulation.
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
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?
TP53 mutant MDS/AML patients have significant upregulation of PDL1 in leukemic stem cells as well as a highly immunosuppressive microenvironment.
“data in TP53 mutant MDS/AML patients with significant upregulation of PDL1 in leukemic stem cells as well as a highly immunosuppressive microenvironment.”
From Long‐term follow‐up and combined Phase 2 results of eprenetapopt and azacitidine in patients with <i>TP53</i> mutant MDS/AML (2025) · cites this paper as [51]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
PD-1 and PD-L1 Immune Checkpoint Blockade to Treat Breast Cancer
Hartkopf, A. D., Taran, F., Wallwiener, M., Walter, C. B., Krämer, B., Grischke, E., & Brucker, S. Y. (2016) · Breast Care · doi:10.1159/000453569 · Cited by 30,989 · see citing works
Safety, activity, and immune correlates of anti–PD-1 antibody in cancer
Topalian, S. L., Hodi, F. S., Brahmer, J. R., Gettinger, S. N., Smith, D. C., McDermott, D. F., Powderly, J. D., Carvajal, R. D., Sosman, J. A., Atkins, M. B., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1200690 · Cited by 12,628 · see citing works
Arber, D. A., Orazi, A., Hasserjian, R., Thiele, J., Borowitz, M. J., Le Beau, M. M., Bloomfield, C. D., Cazzola, M., & Vardiman, J. W. (2016) · Blood · doi:10.1182/blood-2016-03-643544 · Cited by 10,119 · see citing works
Safety and activity of anti-PD-L1 antibody in patients with advanced cancer
Brahmer, J. R., Tykodi, S. S., Chow, L. Q. M., Hwu, W.-J., Topalian, S. L., Hwu, P., Drake, C. G., Camacho, L. H., Kauh, J., Odunsi, K., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1200694 · Cited by 7,945 · see citing works
Freeman, G. J., Long, A. J., Iwai, Y., Bourque, K., Chernova, T., Nishimura, H., Fitz, L. J., Malenkovich, N., Okazaki, T., Byrne, M. C., et al. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.7.1027 · Cited by 5,294 · see citing works
Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia
The Cancer Genome Atlas Research Network (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1301689 · Cited by 5,078 · see citing works
Tumor-associated B7-H1 promotes T-cell apoptosis: A potential mechanism of immune evasion
Dong, H., Strome, S. E., Salomao, D. R., Tamura, H., Hirano, F., Flies, D. B., Roche, P. C., Lu, J., Zhu, G., Tamada, K., et al. (2002) · Nature Medicine · doi:10.1038/nm730 · Cited by 5,025 · see citing works
Revised International Prognostic Scoring System for Myelodysplastic Syndromes
Greenberg, P. L., Tuechler, H., Schanz, J., Sanz, G. F., Garcia‐Manero, G., Solé, F. G., Bennett, J. M., Bowen, D., Fenaux, P., Dreyfus, F., et al. (2012) · Blood · doi:10.1182/blood-2012-03-420489 · Cited by 3,181 · see citing works
Mechanism-driven biomarkers to guide immune checkpoint blockade in cancer therapy
Topalian, S. L., Taube, J. M., Anders, R. A., & Pardoll, D. M. (2016) · Nature Reviews Cancer · doi:10.1038/nrc.2016.36 · Cited by 2,733 · see citing works
MYC regulates the antitumor immune response through CD47 and PD-L1
Casey, S. C., Tong, L., Li, Y., Do, R., Walz, S., Fitzgerald, K. N., Gouw, A. M., Baylot, V., Gütgemann, I., Eilers, M., et al. (2016) · Science · doi:10.1126/science.aac9935 · Cited by 1,403 · see citing works
Gros, A., Parkhurst, M. R., Tran, E., Pasetto, A., Robbins, P. F., Ilyas, S., Prickett, T. D., Gartner, J. J., Crystal, J. S., Roberts, I. M., et al. (2016) · Nature Medicine · doi:10.1038/nm.4051 · Cited by 830 · see citing works
<i>TP53</i> and Decitabine in Acute Myeloid Leukemia and Myelodysplastic Syndromes
Welch, J. S., Petti, A. A., Miller, C. A., Fronick, C. C., O’Laughlin, M., Fulton, R. S., Wilson, R. K., Baty, J. D., Duncavage, E. J., Tandon, B., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1605949 · Cited by 796 · see citing works
Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation
Lindsley, R. C., Saber, W., Mar, B. G., Redd, R., Wang, T., Haagenson, M. D., Grauman, P. V., Hu, Z.-H., Spellman, S. R., Lee, S. J., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1611604 · Cited by 776 · see citing works
Self-citationProgrammed death ligand-1 expression in non-small cell lung cancer
Velcheti, V., Schalper, K. A., Carvajal, D. E., Anagnostou, V., Syrigos, K. N., Sznol, M., Herbst, R. S., Gettinger, S. N., Chen, L., & Rimm, D. L. (2013) · Laboratory Investigation · doi:10.1038/labinvest.2013.130 · Cited by 752 · see citing works
Yang, H., Bueso-Ramos, C., DiNardo, C., Estecio, M. R., Davanlou, M., Geng, Q.-R., Fang, Z., Nguyen, M., Pierce, S., Wei, Y., et al. (2014) · Leukemia · doi:10.1038/leu.2013.355 · Cited by 688 · see citing works
PDL1 Regulation by p53 via miR-34
Cortez, M. A., Ivan, C., Valdecanas, D., Wang, X., Peltier, H. J., Ye, Y., Araujo, L., Carbone, D. P., Shilo, K., Giri, D. K., et al. (2016) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/djv303 · Cited by 683 · see citing works
Haferlach, T., Kohlmann, A., Wieczorek, L., Basso, G., Kronnie, G. T., Béné, M. C., Vos, J. D., Hernández‐Rivas, J. M., Hofmann, W., Mills, K., et al. (2010) · Journal of Clinical Oncology · doi:10.1200/jco.2009.23.4732 · Cited by 657 · see citing works
Self-citationIpilimumab for Patients with Relapse after Allogeneic Transplantation
Davids, M. S., Kim, H. T., Bachireddy, P., Costello, C. L., Liguori, R., Savell, A., Lukez, A. P., Avigan, D., Chen, Y., McSweeney, P. A., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1601202 · Cited by 595 · see citing works
Boettcher, S., Miller, P. G., Sharma, R., McConkey, M., Leventhal, M., Krivtsov, A. V., Giacomelli, A. O., Wong, W., Kim, J., Chao, S., et al. (2019) · Science · doi:10.1126/science.aax3649 · Cited by 441 · see citing works
Self-citationBejar, R. L., Stevenson, K. E., Caughey, B. A., Lindsley, R. C., Mar, B. G., Stojanov, P., Getz, G. A., Steensma, D. P., Ritz, J., Soiffer, R. J., et al. (2014) · Journal of Clinical Oncology · doi:10.1200/jco.2013.52.3381 · Cited by 396 · see citing works
Self-citationmiR-34 miRNAs provide a barrier for somatic cell reprogramming
Choi, Y. J., Lin, C., Ho, J. J., He, X., Okada, N., Bu, P., Zhong, Y., Kim, S. Y., Bennett, M. J., Chen, C., et al. (2011) · Nature Cell Biology · doi:10.1038/ncb2366 · Cited by 381 · see citing works
Yoshizato, T., Nannya, Y., Atsuta, Y., Shiozawa, Y., Iijima‐Yamashita, Y., Yoshida, K., Shiraishi, Y., Suzuki, H., Nagata, Y., Sato, Y., et al. (2017) · Blood · doi:10.1182/blood-2016-12-754796 · Cited by 351 · see citing works
Self-citationWilliams, P., Basu, S., Garcia‐Manero, G., Hourigan, C. S., Oetjen, K. A., Cortes, J. E., Ravandi, F., Jabbour, E. J., Al‐Hamal, Z., Konopleva, M., et al. (2019) · Cancer · doi:10.1002/cncr.31896 · Cited by 330 · see citing works
Wang, X., Li, J., Dong, K., Fang, L., Long, M., Ouyang, Y., Wei, J., Chen, X., Weng, Y., He, T., et al. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.12.003 · Cited by 313 · see citing works
Szczepański, M. J., Szajnik, M. E., Czystowska, M., Mandapathil, M., Strauss, L., Welsh, A., Foon, K. A., Whiteside, T. L., & Boyiadzis, M. M. (2009) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-08-3010 · Cited by 304 · see citing works
The immunobiology of CD27 and OX40 and their potential as targets for cancer immunotherapy
Buchan, S. L., Rogel, A., & Al‐Shamkhani, A. (2017) · Blood · doi:10.1182/blood-2017-07-741025 · Cited by 276 · see citing works
Kikushige, Y., Miyamoto, T., Yuda, J., Jabbarzadeh-Tabrizi, S., Shima, T., Takayanagi, S.-I., Niiro, H., Yurino, A., Miyawaki, K., Takenaka, K., et al. (2015) · Cell Stem Cell · doi:10.1016/j.stem.2015.07.011 · Cited by 262 · see citing works
for the International Working Group for MDS Molecular Prognostic Committee, Haase, D., Stevenson, K. E., Neuberg, D., Maciejewski, J. P., Nazha, A., Sekeres, M. A., Ebert, B. L., Garcia-Manero, G., Haferlach, C., et al. (2019) · Leukemia · doi:10.1038/s41375-018-0351-2 · Cited by 259 · see citing works
Self-citationPorta, M. G. D., Gallì, A., Bacigalupo, A. P., Zibellini, S., Bernardi, M., Rizzo, E., Allione, B., Lint, M. T. V., Pioltelli, P. E., Marenco, P., et al. (2016) · Journal of Clinical Oncology · doi:10.1200/jco.2016.67.3616 · Cited by 255 · see citing works
PD-1 marks dysfunctional regulatory T cells in malignant gliomas
Lowther, D. E., Goods, B. A., Lucca, L. E., Lerner, B., Raddassi, K., van Dijk, D., Hernandez, A. L., Duan, X.-G., Gunel, M., Coric, V., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.85935 · Cited by 237 · see citing works
Sallman, D. A., Komrokji, R., Vaupel, C., Cluzeau, T., Geyer, S. M., McGraw, K. L., Al Ali, N. H., Lancet, J., McGinniss, M. J., Nahas, S., et al. (2016) · Leukemia · doi:10.1038/leu.2015.304 · Cited by 231 · see citing works
Self-citationRegulation of PD-L1: Emerging Routes for Targeting Tumor Immune Evasion
Wang, Y., Wang, H., Yao, H., Li, C., Fang, J., & Xu, J. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00536 · Cited by 209 · see citing works
Kondo, A., Yamashita, T., Tamura, H., Zhao, W., Tsuji, T., Shimizu, M., Shinya, E., Takahashi, H., Tamada, K., Chen, L., et al. (2010) · Blood · doi:10.1182/blood-2009-12-255125 · Cited by 201 · see citing works
Frazier, M. W., He, X., Wang, J., Gu, Z., Cleveland, J. L., & Zambetti, G. P. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.7.3735 · Cited by 194 · see citing works
Self-citationZhang, B., Chikuma, S., Hori, S., Fagarasan, S., & Honjo, T. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608873113 · Cited by 166 · see citing works
Vadakekolathu, J. N., Lai, C., Reeder, S., Church, S., Hood, T., Lourdusamy, A., Rettig, M. P., Aldoss, I. T., Advani, A. S., Godwin, J. E., et al. (2020) · Blood Advances · doi:10.1182/bloodadvances.2020002512 · Cited by 156 · see citing works
Yamamura, S., Saini, S., Majid, S., Hirata, H., Ueno, K., Deng, G., & Dahiya, R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029722 · Cited by 152 · see citing works
Wang, X., Zheng, J., Liu, J., Yao, J., He, Y., Li, X., Yu, J., Yang, J. X., Liu, Z., & Huang, S. (2005) · European Journal Of Haematology · doi:10.1111/j.1600-0609.2005.00537.x · Cited by 147 · see citing works
Tu, J., Ding, Y., Ying, X., Wu, F., Zhou, X.-M., Zhang, D.-K., Zou, H., & Ji, J. (2016) · Scientific Reports · doi:10.1038/srep35056 · Cited by 144 · see citing works
Saft, L., Karimi, M., Ghaderi, M., Matolcsy, A., Mufti, G. J., Kulasekararaj, A. G., Göhring, G., Giagounidis, A. A. N., Selleslag, D., Muus, P., et al. (2014) · Haematologica · doi:10.3324/haematol.2013.098103 · Cited by 137 · see citing works
Self-citationClinical significance of B7-H1(PD-L1)expression in human acute leukemia
Chen, X., Liu, S., Wang, L., Zhang, W., Ji, Y., & Ma, X. (2008) · Cancer Biology & Therapy · doi:10.4161/cbt.7.5.5689 · Cited by 122 · see citing works
Cheng, P., Eksioglu, E. A., Chen, X., Kandell, W. M., Trinh, T. L., Cen, L., Qi, J., Sallman, D. A., Zhang, Y., Tu, N., et al. (2019) · Leukemia · doi:10.1038/s41375-019-0397-9 · Cited by 103 · see citing works
Self-citationInducible Co-Stimulator (ICOS) as a potential therapeutic target for anti-cancer therapy
Amatore, F., Gorvel, L., & Olive, D. (2018) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2018.1444753 · Cited by 95 · see citing works
Yamamura, S., Saini, S., Majid, S., Hirata, H., Ueno, K., Chang, I., Tanaka, Y., Gupta, A. K., & Dahiya, R. (2011) · Carcinogenesis · doi:10.1093/carcin/bgr286 · Cited by 90 · see citing works
PD-1 checkpoint blockade in patients with relapsed AML after allogeneic stem cell transplantation
Albring, J. C., Inselmann, S., Sauer, T., Schliemann, C., Altvater, B., Kailayangiri, S., Rössig, C., Hartmann, W., Knorrenschild, J. R., Sohlbach, K., et al. (2016) · Bone Marrow Transplantation · doi:10.1038/bmt.2016.274 · Cited by 84 · see citing works
Garcia‐Manero, G., Sasaki, K., Bravo, G. M., Daver, N. G., Jabbour, E. J., Alvarado, Y., Dinardo, C. D., Ravandi, F., Borthakur, G. M., Bose, P., et al. (2018) · Blood · doi:10.1182/blood-2018-99-119424 · Cited by 68 · see citing works
Welch, J. S., Petti, A. A., & Ley, T. J. (2017) · New England Journal of Medicine · doi:10.1056/nejmc1616062 · Cited by 56 · see citing works
Mo, L., Chen, Q., Zhang, X., Shi, X., Wei, L., Zheng, D., Li, H., Gao, J., Li, J., & Hu, Z. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.08.093 · Cited by 50 · see citing works
Expression of CD 274 ( PD ‐L1) is associated with unfavourable recurrent mutations in AML
Zajac, M., Zaleska, J., Dolnik, A., Bullinger, L., & Giannopoulos, K. (2017) · British Journal of Haematology · doi:10.1111/bjh.15040 · Cited by 20 · see citing works
Garcia‐Manero, G., Bravo, G. M., Sasaki, K., Daver, N. G., Jabbour, E. J., Alvarado, Y., Dinardo, C. D., Ravandi, F., Borthakur, G. M., Bose, P., et al. (2018) · Blood · doi:10.1182/blood-2018-99-118948 · Cited by 14 · see citing works
Daver, N. G., Kantarjian, H. M., Mackay, S., Flynn, B., Basu, S., Garcia‐Manero, G., Alfayez, M., Konopleva, M. Y., Matthews, J. A., Kornblau, S. M., et al. (2019) · Cancer Research · doi:10.1158/1538-7445.am2019-lb-222 · Cited by 6 · see citing works
Lai, C., Vadakekolathu, J. N., Reeder, S., Church, S., Hood, T., Aldoss, I. T., Godwin, J. E., Wieduwilt, M. J., Arellano, M. L., MUTH, J. B., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.28.961391 · Cited by 3 · see citing works
Flagged first, then by citations
1 of the 53 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- [6]Montalban-Bravo G, Takahashi K, Garcia-Manero G. Decitabine in TP53-Mutated AML. N Engl J Med. 2017;376(8):796-797. [DOI] [PubMed] [Google Scholar]
- [41]Sallman DA, Asch AS, Al Malki MM, et al. The First-in-Class Anti-CD47 Antibody Magrolimab (5F9) in Combination with Azacitidine Is Effective in MDS and AML Patients: Ongoing Phase 1b Results [abstract]. Blood. 2019;134(suppl 1). Abstract 569. [Google Scholar]
Cited by
Sorted by citations
Li, W., Wang, Y., Liu, R., Kasinski, A. L., Shen, H., Slack, F. J., & Tang, D. G. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.640587 · Cited by 195 · see citing works
Daver, N. G., Maiti, A., Kadia, T. M., Vyas, P., Majeti, R., Wei, A. H., Garcia‐Manero, G., Craddock, C., Sallman, D. A., & Kantarjian, H. M. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-22-0332 · Cited by 173 · see citing works
Self-citationSallman, D. A., Kerre, T. C. C., Havelange, V., Poiré, X., Lewalle, P., Wang, E. S., Brayer, J. B., Davila, M. L., Moors, I., Machiels, J., et al. (2023) · The Lancet Haematology · doi:10.1016/s2352-3026(22)00378-7 · Cited by 102 · see citing works
Self-citationRutella, S., Vadakekolathu, J. N., Mazziotta, F., Reeder, S., Yau, T. O., Mukhopadhyay, R., Dickins, B., Altmann, H., Krämer, M., Knaus, H. A., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci159579 · Cited by 96 · see citing works
Targeting PD-1/PD-L1 pathway in myelodysplastic syndromes and acute myeloid leukemia
Yang, X., Ma, L., Zhang, X., Huang, L., & Wei, J. (2022) · Experimental Hematology and Oncology · doi:10.1186/s40164-022-00263-4 · Cited by 98 · see citing works
The role of p53 in anti-tumor immunity and response to immunotherapy
Carlsen, L., Zhang, S., Tian, X., Cruz, A. D. L., George, A., Arnoff, T. E., & El‐Deiry, W. S. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1148389 · Cited by 92 · see citing works
Versluis, J., Saber, W., Tsai, H. K., Gibson, C. J., Dillon, L. W., Mishra, A., McGuirk, J., Maziarz, R. T., Westervelt, P., Hegde, P., et al. (2023) · Journal of Clinical Oncology · doi:10.1200/jco.23.00866 · Cited by 78 · see citing works
Escape from T-cell–targeting immunotherapies in acute myeloid leukemia
Vadakekolathu, J. N., & Rutella, S. (2023) · Blood · doi:10.1182/blood.2023019961 · Cited by 73 · see citing works
Immune Checkpoint Inhibition in Acute Myeloid Leukemia and Myelodysplastic Syndromes
Abaza, Y., & Zeidan, A. M. (2022) · Cells · doi:10.3390/cells11142249 · Cited by 73 · see citing works
Corradi, G., Bassani, B., Simonetti, G., Sangaletti, S., Vadakekolathu, J. N., Fontana, M. C., Pazzaglia, M., Gulino, A., Tripodo, C., Cristiano, G., et al. (2022) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-21-3594 · Cited by 70 · see citing works
Chien, K. S., Kim, K., Nogueras‐González, G. M., Borthakur, G. M., Naqvi, K., Daver, N. G., Bravo, G. M., Cortes, J. E., Dinardo, C. D., Jabbour, E. J., et al. (2021) · British Journal of Haematology · doi:10.1111/bjh.17689 · Cited by 62 · see citing works
Fiorenza, S., & Turtle, C. J. (2021) · BioDrugs · doi:10.1007/s40259-021-00477-8 · Cited by 57 · see citing works
BiTEs, DARTS, BiKEs and TriKEs—Are Antibody Based Therapies Changing the Future Treatment of AML?
Allen, C., Zeidan, A. M., & Bewersdorf, J. P. (2021) · Life · doi:10.3390/life11060465 · Cited by 57 · see citing works
Loke, J. C. T., Labopin, M., Craddock, C., Cornelissen, J. J., Labussière‐Wallet, H., Wagner-Drouet, E., van Gorkom, G. N. Y., Schaap, N. P., Kröger, N. M., Veelken, J. H., et al. (2022) · Cancer · doi:10.1002/cncr.34268 · Cited by 54 · see citing works
Translating recent advances in the pathogenesis of acute myeloid leukemia to the clinicPreprint
Bewersdorf, J. P., & Abdel-Wahab, O. I. (2022) · Genes & Development · doi:10.1101/gad.349368.122 · Cited by 52 · see citing works
Targeting the innate immune system in pediatric and adult AML
Perzolli, A., Koedijk, J. B., Zwaan, C. M., & Heidenreich, O. T. (2024) · Leukemia · doi:10.1038/s41375-024-02217-7 · Cited by 51 · see citing works
What’s new in the pathogenesis and treatment of therapy-related myeloid neoplasms
Voso, M. T., Falconi, G., & Fabiani, E. (2021) · Blood · doi:10.1182/blood.2021010764 · Cited by 55 · see citing works
TP53 in Acute Myeloid Leukemia: Molecular Aspects and Patterns of Mutation
George, B., Kantarjian, H. M., Baran, N., Krocker, J. D., & Rios, A. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910782 · Cited by 50 · see citing works
Inflammation and myeloid malignancy: quenching the flame
Stubbins, R. J., Platzbecker, U., & Karsan, A. (2022) · Blood · doi:10.1182/blood.2021015162 · Cited by 46 · see citing works
CCR8: a promising therapeutic target against tumor-infiltrating regulatory T cells
Wen, Y., Xia, Y., Yang, X., Li, H., & Gao, Q. (2025) · Trends in Immunology · doi:10.1016/j.it.2025.01.001 · Cited by 44 · see citing works
TP53 in MDS and AML: Biological and clinical advances
Zhao, Y., Chen, W., Yu, J., Pei, S., Zhang, Q., Shi, J., Huang, H., & Zhao, Y. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.216767 · Cited by 44 · see citing works
TP53 Mutations in Acute Leukemias and Myelodysplastic Syndromes: Insights and Treatment Updates
Santini, V., Stahl, M. F., & Sallman, D. A. (2024) · American Society of Clinical Oncology Educational Book · doi:10.1200/edbk_432650 · Cited by 43 · see citing works
Self-citationTP53 ‐Mutated Myeloid Neoplasms: 2024 Update on Diagnosis, Risk‐Stratification, and Management
Shah, M. V., Arber, D. A., & Hiwase, D. (2025) · American Journal of Hematology · doi:10.1002/ajh.27655 · Cited by 41 · see citing works
Chen, E. C., Liu, Y., Harris, C. E., Winer, E. S., Wadleigh, M., Lane, A. A., Vedula, R. S., Lindsley, R. C., Copson, K. M., Charles, A. L., et al. (2022) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2022.2047964 · Cited by 36 · see citing works
Mohty, R., Hamed, R. A., Brissot, É., Bazarbachi, A. A., & Mohty, M. (2023) · Haematologica · doi:10.3324/haematol.2022.280798 · Cited by 36 · see citing works
Targeting the mevalonate or Wnt pathways to overcome CAR T-cell resistance in TP53-mutant AML cells
Mueller, J., Schimmer, R. R., Koch, C., Schneiter, F., Fullin, J., Lysenko, V., Pellegrino, C. E., Klemm, N., Russkamp, N. F., Myburgh, R., et al. (2024) · EMBO Molecular Medicine · doi:10.1038/s44321-024-00024-2 · Cited by 33 · see citing works
Self-citationGallazzi, M., Ucciero, M. A. M., Faraci, D., Mahmoud, A. M., Essa, W. A., Gaïdano, G., Mouhssine, S., & Crisà, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147542 · Cited by 32 · see citing works
TP53-mutated acute myeloid leukemia: how can we improve outcomes?
Sallman, D. A., & Stahl, M. F. (2024) · Blood · doi:10.1182/blood.2024024245 · Cited by 31 · see citing works
Self-citationTP53 to mediate immune escape in tumor microenvironment: an overview of the research progress
Zhu, K., Su, F., Yang, J., Xiao, R., Wu, R.-Y., Cao, M.-Y., Ling, X., & Zhang, T. (2024) · Molecular Biology Reports · doi:10.1007/s11033-023-09097-7 · Cited by 30 · see citing works
Mannelli, F. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030436 · Cited by 30 · see citing works
Transplant for TP53-mutated MDS and AML: because we can or because we should?
Versluis, J., & Lindsley, R. C. (2022) · Hematology · doi:10.1182/hematology.2022000354 · Cited by 30 · see citing works
p53 mutation and deletion contribute to tumor immune evasion
Liu, S. M., Liu, T., Jiang, J., Guo, H., & Yang, R. L. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1088455 · Cited by 28 · see citing works
Application of omics in the diagnosis, prognosis, and treatment of acute myeloid leukemia
Zhang, Z., Huang, J., Zhang, Z., Shen, H., Tang, X., Wu, D., Bao, X., Xu, G., & Chen, S. (2024) · Biomarker Research · doi:10.1186/s40364-024-00600-1 · Cited by 30 · see citing works
An IDO1-related immune gene signature predicts overall survival in acute myeloid leukemia
Ragaini, S., Wagner, S., Marconi, G., Parisi, S., Sartor, C., Nanni, J., Cristiano, G., Talami, A., Olivi, M., Očadlíková, D., et al. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021004878 · Cited by 28 · see citing works
Serroukh, Y. I. M., Hébert, J., Busque, L., Mercier, F., Rudd, C. E., Assouline, S. E., Lachance, S., & Delisle, J. (2022) · Blood Reviews · doi:10.1016/j.blre.2022.100991 · Cited by 27 · see citing works
Mascarenhas, J. O., Passamonti, F., Burbury, K., El‐Galaly, T. C., Gerds, A. T., Gupta, V. K., Higgins, B., Wonde, K., Jamois, C., Kovic, B., et al. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021006043 · Cited by 26 · see citing works
Gagelmann, N., Badbaran, A., Salit, R. B., Schroeder, T. A., Gurnari, C., Pagliuca, S., Panagiota, V., Rautenberg, C., Cassinat, B., Thol, F. R., et al. (2023) · Blood · doi:10.1182/blood.2023019630 · Cited by 27 · see citing works
The promise of macrophage directed checkpoint inhibitors in myeloid malignancies
Swoboda, D. M., & Sallman, D. A. (2020) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2020.101221 · Cited by 25 · see citing works
Self-citationVenetoclax combination therapy in acute myeloid leukemia and myelodysplastic syndromes
Shimony, S. O., Stone, R. M., & Stahl, M. F. (2021) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000698 · Cited by 24 · see citing works
Immune Dysfunction, Cytokine Disruption, and Stromal Changes in Myelodysplastic Syndrome: A Review
Lynch, O. F., & Calvi, L. M. (2022) · Cells · doi:10.3390/cells11030580 · Cited by 26 · see citing works
Herrera, D. A., Sparks, A. D., Singh, R., Alejos, D., Batra, A., Glushakow-Smith, S. G., Pradhan, K., Shastri, A., & Zakai, N. A. (2023) · Blood Advances · doi:10.1182/bloodadvances.2023011050 · Cited by 22 · see citing works
Barakos, G. P., & Hatzimichael, E. C. (2022) · Diseases · doi:10.3390/diseases10020033 · Cited by 22 · see citing works
A perspective of immunotherapy for acute myeloid leukemia: Current advances and challenges
Chen, Y., Wang, J., Zhang, F., & Liu, P. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1151032 · Cited by 22 · see citing works
Fan, T. T., Liu, Y., Liu, H., Wang, L., Tian, H., Zheng, Y., Zheng, B. J., Xue, L., Li, C., & He, J. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.828814 · Cited by 21 · see citing works
Ikeda, D., Chi, S., Uchiyama, S., Nakamura, H., Guo, Y., Yamauchi, N., Yuda, J., & Minami, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23115950 · Cited by 21 · see citing works
Bruserud, Ø., Selheim, F., Hernandez-Valladares, M., & Reikvam, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126356 · Cited by 21 · see citing works
Sallman, D. A., Komrokji, R. S., Dezern, A. E., Sebert, M., Garcia‐Manero, G., Rahmé, R., Winer, E. S., Lehmann‐Che, J., Roboz, G. J., Madelaine, I., et al. (2025) · HemaSphere · doi:10.1002/hem3.70164 · Cited by 20 · see citing works
“51,52 With targeted agents for mutations that may have one or more significant hot spots, there is an art to further drug development in terms of thoughtful trial design, patient eligibility by target, and applicability of results to varied populations.”
Self-citationZha, C., Yang, X., Yang, J., Zhang, Y., & Huang, R. (2024) · Annals of Hematology · doi:10.1007/s00277-024-06117-9 · Cited by 22 · see citing works
Zampini, M., Riva, E., Lanino, L., Sauta, E., Reis, R. A. D., Ejarque, R. A., Maggioni, G., Termanini, A., Merlotti, A., Campagna, A., et al. (2025) · Journal of Clinical Oncology · doi:10.1200/jco-24-02394 · Cited by 21 · see citing works
Self-citationTP53 in Myelodysplastic Syndromes
Jiang, Y., Gao, S., Soubise, B., Douet‐Guilbert, N., Liu, Z., & Troadec, M. (2021) · Cancers · doi:10.3390/cancers13215392 · Cited by 21 · see citing works
CD155 and CD112 as possible therapeutic targets of FLT3 inhibitors for acute myeloid leukemia
Kaito, Y., Hirano, M., Futami, M., Nojima, M., Tamura, H., Tojo, A., & Imai, Y. (2021) · Oncology Letters · doi:10.3892/ol.2021.13169 · Cited by 20 · see citing works
Myeloid-Derived Suppressor Cells: New Insights into the Pathogenesis and Therapy of MDS
Velegraki, M., Stiff, A. R., Papadaki, H. Α., & Li, Z. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11164908 · Cited by 20 · see citing works
Zhong, F., Yao, F., Liu, J., Zhang, H., Zhang, J., Zhang, N., Jin, L., Li, S., Li, M., Jiang, J., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.888570 · Cited by 20 · see citing works
Bewersdorf, J. P., Xie, Z., Bejar, R. L., Borate, U., Boultwood, J., Brunner, A. M., Buckstein, R. J., Carraway, H. E., Churpek, J. E., Daver, N. G., et al. (2023) · Blood Reviews · doi:10.1016/j.blre.2023.101072 · Cited by 20 · see citing works
Self-citationFrom Clonal Hematopoiesis to Therapy-Related Myeloid Neoplasms: The Silent Way of Cancer Progression
Gurnari, C., Fabiani, E., Falconi, G., Travaglini, S., Ottone, T., Cristiano, A., & Voso, M. T. (2021) · Biology · doi:10.3390/biology10020128 · Cited by 21 · see citing works
Myelodysplasia Syndrome, Clonal Hematopoiesis and Cardiovascular Disease
Veiga, C. B., Lawrence, E., Murphy, A. J., Herold, M. J., & Dragoljevic, D. (2021) · Cancers · doi:10.3390/cancers13081968 · Cited by 19 · see citing works
Personalized Medicine for TP53 Mutated Myelodysplastic Syndromes and Acute Myeloid Leukemia
Cluzeau, T., Loschi, M. L., Fenaux, P., Komrokji, R. S., & Sallman, D. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810105 · Cited by 19 · see citing works
Self-citationBone Marrow Niches and Tumour Cells: Lights and Shadows of a Mutual Relationship
Granata, V., Crisafulli, L., Nastasi, C., Ficara, F., & Sobacchi, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.884024 · Cited by 19 · see citing works
Diagnosis of TP53-mutated myeloid disease by the ICC and WHO fifth edition classifications
Hart, S. A., Lee, L. A., Seegmiller, A. C., & Mason, E. F. (2024) · Blood Advances · doi:10.1182/bloodadvances.2024014140 · Cited by 19 · see citing works
Molecular Targeted Therapy in Myelodysplastic Syndromes: New Options for Tailored Treatments
Pagliuca, S., Gurnari, C., & Visconte, V. (2021) · Cancers · doi:10.3390/cancers13040784 · Cited by 18 · see citing works
Progress toward Better Treatment of Therapy-Related AML
Kotsiafti, A., Giannakas, K., Christoforou, P., & Liapis, K. (2023) · Cancers · doi:10.3390/cancers15061658 · Cited by 17 · see citing works
Wang, P., Zhang, Y., Cai, Q., Long, Q., Pan, S., Zhou, W., Deng, T., Mo, W., Wang, S., Zhang, Y., et al. (2023) · Annals of Medicine · doi:10.1080/07853890.2023.2201507 · Cited by 17 · see citing works
Jambhekar, A., Ackerman, E. E., Alpay, B. A., Lahav, G., & Lovitch, S. B. (2024) · Blood Neoplasia · doi:10.1016/j.bneo.2024.100004 · Cited by 17 · see citing works
Assouline, S. E., Michaelis, L. C., Othus, M. K. D., Hay, A. E., Walter, R. B., Jacoby, M. A., Schroeder, M. A., Uy, G. L., Law, L. Y., Cheema, F. E., et al. (2022) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2022.2148212 · Cited by 15 · see citing works
Luo, D., Liu, S., Luo, J., Chen, H., He, Z., Gao, Z., Wen, Z., Liu, X., & Xu, N. (2023) · Clinical & Translational Oncology · doi:10.1007/s12094-023-03118-4 · Cited by 15 · see citing works
The Role of BCL-2 and PD-1/PD-L1 Pathway in Pathogenesis of Myelodysplastic Syndromes
Kuszczak, B., Wróbel, T., Wicherska‐Pawłowska, K., & Rybka, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054708 · Cited by 15 · see citing works
Patel, S. A. (2024) · Leukemia · doi:10.1038/s41375-024-02417-1 · Cited by 15 · see citing works
Zeidan, A. M., Bewersdorf, J. P., Hasle, V., Shallis, R. M., Thompson, E. G., Menezes, D. L. D., Rose, S., Boss, I. W., Halene, S., Haferlach, T., et al. (2024) · Therapeutic Advances in Hematology · doi:10.1177/20406207241257904 · Cited by 15 · see citing works
Self-citationKállai, A., Ungvari, A., Csabán, D., Őrfi, Z., Lehoczki, A., Harasztdombi, J., Yabluchanskiy, A., Benyó, Z., Szappanos, Á., Tarantini, S., et al. (2025) · GeroScience · doi:10.1007/s11357-025-01654-1 · Cited by 14 · see citing works
Schwind, S., Jentzsch, M., Kubasch, A. S., Metzeler, K. H., & Platzbecker, U. (2021) · Neoplasia · doi:10.1016/j.neo.2021.09.002 · Cited by 14 · see citing works
Mohty, R., Hamed, R. A., Bazarbachi, A. A., Brissot, É., Nagler, A., Zeidan, A. M., & Mohty, M. (2022) · Journal of Hematology & Oncology · doi:10.1186/s13045-022-01346-9 · Cited by 14 · see citing works
How I Treat TP53-Mutated Acute Myeloid Leukemia and Myelodysplastic Syndromes
Loschi, M. L., Fenaux, P., & Cluzeau, T. (2022) · Cancers · doi:10.3390/cancers14184519 · Cited by 15 · see citing works
Therapy-related myelodysplastic syndromes in the genomics era
Renneville, A., Bernard, E., & Micol, J. (2023) · Bulletin du Cancer · doi:10.1016/j.bulcan.2023.02.022 · Cited by 14 · see citing works
Targeting Menin and CD47 to Address Unmet Needs in Acute Myeloid Leukemia
Matthews, A. H., Pratz, K., & Carroll, M. (2022) · Cancers · doi:10.3390/cancers14235906 · Cited by 11 · see citing works
Myeloid-derived suppressor cells: a grey eminence in the AML tumor microenvironment?
Bewersdorf, J. P., & Zeidan, A. M. (2022) · Expert Review of Anticancer Therapy · doi:10.1080/14737140.2022.2030227 · Cited by 13 · see citing works
Xu, T., Yang, T., Yuan, B., Yang, Y., Liu, J., Wang, X., Wang, Y., Ma, T., Yin, X. H., Yu, H., et al. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1177133 · Cited by 12 · see citing works
Quattrocchi, A., Cappelli, L. V., Simone, G. D., Marinis, E. D., Gentile, M., Gasperi, T., Pulsoni, A., Ascenzi, P., & Nervi, C. (2023) · Aspects of Molecular Medicine · doi:10.1016/j.amolm.2023.100023 · Cited by 12 · see citing works
Marvin‐Peek, J., Mason, E. F., Kishtagari, A., Jayani, R., Dholaria, B., Kim, T. K., Engelhardt, B. G., Chen, H., Strickland, S. A., Savani, B. N., et al. (2023) · Transplantation and Cellular Therapy · doi:10.1016/j.jtct.2023.03.008 · Cited by 12 · see citing works
Ma, B., Jiang, H., Luo, Y., Liao, T., Xu, W., Wang, X., Dong, C., Ji, Q., & Wang, Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.692079 · Cited by 12 · see citing works
Precision Medicine Approaches in Acute Myeloid Leukemia with Adverse Genetics
Santoro, N., Salutari, P., Ianni, M. D., & Marra, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084259 · Cited by 10 · see citing works
New Treatment Options for Older Patients with Acute Myeloid Leukemia
Saxena, K., & Konopleva, M. Y. (2021) · Current Treatment Options in Oncology · doi:10.1007/s11864-021-00841-4 · Cited by 11 · see citing works
TP53 -mutant myelodysplastic syndrome and acute myeloid leukemia: the black hole of hematology
Patel, S. A., & Černý, J. (2022) · Blood Advances · doi:10.1182/bloodadvances.2021006580 · Cited by 11 · see citing works
Bauer, M., Vaxevanis, C., Al‐Ali, H. K., Jaekel, N., Naumann, C. L. H., Schaffrath, J., Rau, A., Seliger, B., & Wickenhauser, C. (2021) · Cancers · doi:10.3390/cancers13020186 · Cited by 10 · see citing works
Extracellular Vesicles and MicroRNA in Myelodysplastic Syndromes
Meunier, M., Laurin, D., & Park, S. (2023) · Cells · doi:10.3390/cells12040658 · Cited by 10 · see citing works
Lu, Y., Li, D., Cao, Y., Ying, L., Qing, T., Xiong, F., Hu, Z., Yang, Y., Qiao, X., Chen, P., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.862294 · Cited by 10 · see citing works
Are We Moving the Needle for Patients with TP53-Mutated Acute Myeloid Leukemia?
Shallis, R. M., Bewersdorf, J. P., Stahl, M. F., Halene, S., & Zeidan, A. M. (2022) · Cancers · doi:10.3390/cancers14102434 · Cited by 11 · see citing works
From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
Comont, T., Treiner, E., & Vergez, F. (2021) · Diagnostics · doi:10.3390/diagnostics11111982 · Cited by 10 · see citing works
Immunity in acute myeloid leukemia: Where the immune response and targeted therapy meet
Fink, A., Hung, E., Singh, I., & Ben‐Neriah, Y. (2021) · European Journal of Immunology · doi:10.1002/eji.202048945 · Cited by 9 · see citing works
Diagnosis of Myelodysplastic Syndromes: From Immunological Observations to Clinical Applications
Simoni, Y., & Chapuis, N. (2022) · Diagnostics · doi:10.3390/diagnostics12071659 · Cited by 9 · see citing works
Gut Microbiota in Acute Myeloid Leukemia: From Biomarkers to Interventions
Ji, M., Ji, M., Zhong, Y., & Shao, L. (2025) · Metabolites · doi:10.3390/metabo15090568 · Cited by 9 · see citing works
Prediction of Adrenocortical Carcinoma Relapse and Prognosis with a Set of Novel Multigene Panels
Lin, X., Gu, Y. J., Su, Y., Dong, Y., Major, P. P., Kapoor, A., & Tang, D. (2022) · Cancers · doi:10.3390/cancers14112805 · Cited by 9 · see citing works
Verigou, E., Chatzilygeroudi, T., Lazaris, V., de Lastic, A.-L., & Symeonidis, A. S. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1447001 · Cited by 8 · see citing works
Biology of post-transplant relapse: actionable features
Orofino, G., & Vago, L. (2024) · Hematology · doi:10.1182/hematology.2024000588 · Cited by 8 · see citing works
TP53 ‐Mutated Acute Myeloid Leukemia: Unanswered Questions
Bruzzese, A., Vigna, E., Martino, E. A., Labanca, C., Caridà, G., Mendicino, F., Lucia, E., Olivito, V., Puccio, N., Neri, A., et al. (2025) · Hematological Oncology · doi:10.1002/hon.70106 · Cited by 10 · see citing works
Zanwar, S., Jacob, E. K., Greiner, C. W., Pavelko, K. D., Strausbauch, M. A., Anderson, E., Arsana, A., Weivoda, M. M., Shah, M. V., & Kourelis, T. (2023) · Blood Cancer Journal · doi:10.1038/s41408-023-00920-9 · Cited by 8 · see citing works
Zhang, P., Whipp, E. C., Skuli, S. J., Gharghabi, M., Saygin, C., Sher, S., Carroll, M. P., Pan, X., Eisenmann, E. D., Lai, T.-H., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci184021 · Cited by 8 · see citing works
da Cruz, L. C., Lee, Y.-J., Paik, J. Y., Park, J., Diederich, M., & Cerella, C. (2025) · Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · doi:10.1016/j.biopha.2025.118287 · Cited by 9 · see citing works
Molecular and Clinical Insights into TP53-Mutated MDS and AML
Georgantzinos, E., & Karantanos, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262210818 · Cited by 7 · see citing works
Menezes, D. L. D., See, W. L., Risueño, A., Tsai, K.-T., Lee, J. K., Ma, J., Khan, R., Prébet, T., Skikne, B., Beach, C. L., et al. (2023) · British Journal of Haematology · doi:10.1111/bjh.18783 · Cited by 7 · see citing works
Musil, J., Ptacek, A., & Vaníková, Š. (2024) · Cytometry Part A · doi:10.1002/cyto.a.24892 · Cited by 7 · see citing works
- Authors
- Sallman, D. A., McLemore, A. F., Aldrich, A. L., Komrokji, R. S., McGraw, K. L., Dhawan, A., Geyer, S., Hou, H.-A., Eksioglu, E. A., Sullivan, A., Warren, S., MacBeth, K. J., Meggendorfer, M., Haferlach, T., Boettcher, S., Ebert, B. L., Al Ali, N. H., Lancet, J. E., Cleveland, J. L., Padron, E., & List, A. F.
- Affiliations
- Moffitt Cancer Center (US)
- University of South Florida (US)
- National Taiwan University Hospital (TW)
- Nanostring Technologies (United States) (US)
- Celgene Corporation, San Francisco, CA;
- Munich Leukemia Laboratory (Germany) (DE)
- University of Zurich (CH)
- Broad Institute (US)
- Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL;
- ORCID
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2020-12-10
- Volume
- 136
- Issue
- 24
- Pages
- 2812-2823
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- PMC
- PMC7731792
- OpenAlex
- W3046762554
- Cited by
- 196
- References
- 53
- Citations by year
- 2026: 26 · 2025: 31 · 2024: 30 · 2023: 38 · 2022: 39 · 2021: 30 · 2020: 2
- FWCI
- 17.21
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Blood (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (R35CA253125, P30CA076292)
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- TP53 mutation, myelodysplastic syndrome, secondary acute myeloid leukemia, tumor immune microenvironment, immunosuppression, PD-L1 expression, hematopoietic stem cells, miR-34a, regulatory T cells, myeloid-derived suppressor cells, cytotoxic T lymphocytes, natural killer cells, ICOS, 4-1BB, prognostic factors, overall survival, immunomodulatory therapy
- MeSH terms
- Myeloid-Derived Suppressor Cells, Adult, Aged, Aged, 80 and over, Female, Humans, Immunosuppression Therapy, Male, Middle Aged, Mutation, Myelodysplastic Syndromes, RNA, Neoplasm, Leukemia, Myeloid, Acute, Tumor Suppressor Protein p53, MicroRNAs, T-Lymphocytes, Regulatory
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