Targeting myeloid chemotaxis to reverse prostate cancer therapy resistance.
Humans
Male
Chemotaxis
/ drug effects
Disease Progression
Drug Resistance, Neoplasm
Inflammation
/ drug therapy
Lewis X Antigen
/ metabolism
Myeloid Cells
/ drug effects
Neoplasm Metastasis
Prostate
/ drug effects
Prostatic Neoplasms, Castration-Resistant
/ drug therapy
Receptors, Androgen
/ metabolism
Androgen Receptor Antagonists
/ pharmacology
Antineoplastic Agents
/ pharmacology
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
received:
23
05
2023
accepted:
28
09
2023
medline:
1
12
2023
pubmed:
17
10
2023
entrez:
16
10
2023
Statut:
ppublish
Résumé
Inflammation is a hallmark of cancer
Identifiants
pubmed: 37844613
doi: 10.1038/s41586-023-06696-z
pii: 10.1038/s41586-023-06696-z
pmc: PMC10686834
doi:
Substances chimiques
CD14 protein, human
0
enzalutamide
93T0T9GKNU
ITGAM protein, human
0
Lewis X Antigen
0
N-(2-(2,3-difluoro-6-benzylthio)-6-(3,4-dihydroxybutan-2-yloxy)pyrimidin-4-yl)azetidine-1-sulfonamide
0
Receptors, Androgen
0
Androgen Receptor Antagonists
0
Antineoplastic Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1053-1061Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Informations de copyright
© 2023. The Author(s).
Références
Hanahan, D. Hallmarks of cancer: new dimensions. Cancer Discov. 12, 31–46 (2022).
pubmed: 35022204
doi: 10.1158/2159-8290.CD-21-1059
Templeton, A. J. et al. Simple prognostic score for metastatic castration-resistant prostate cancer with incorporation of neutrophil-to-lymphocyte ratio. Cancer 120, 3346–3352 (2014).
pubmed: 24995769
doi: 10.1002/cncr.28890
Leibowitz-Amit, R. et al. Clinical variables associated with PSA response to abiraterone acetate in patients with metastatic castration-resistant prostate cancer. Ann. Oncol. 25, 657–662 (2014).
pubmed: 24458472
pmcid: 4433513
doi: 10.1093/annonc/mdt581
Valero, C. et al. Pretreatment neutrophil-to-lymphocyte ratio and mutational burden as biomarkers of tumor response to immune checkpoint inhibitors. Nat. Commun. 12, 729 (2021).
pubmed: 33526794
pmcid: 7851155
doi: 10.1038/s41467-021-20935-9
Howard, R., Kanetsky, P. A. & Egan, K. M. Exploring the prognostic value of the neutrophil-to-lymphocyte ratio in cancer. Sci. Rep. 9, 19673 (2019).
pubmed: 31873162
pmcid: 6928022
doi: 10.1038/s41598-019-56218-z
Sung, H. et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 71, 209–249 (2021).
pubmed: 33538338
doi: 10.3322/caac.21660
Beer, T. M. et al. Randomized, double-blind, phase III trial of ipilimumab versus placebo in asymptomatic or minimally symptomatic patients with metastatic chemotherapy-naive castration-resistant prostate cancer. J. Clin. Oncol. 35, 40–47 (2017).
pubmed: 28034081
doi: 10.1200/JCO.2016.69.1584
Kwon, E. D. et al. Ipilimumab versus placebo after radiotherapy in patients with metastatic castration-resistant prostate cancer that had progressed after docetaxel chemotherapy (CA184-043): a multicentre, randomised, double-blind, phase 3 trial. Lancet Oncol. 15, 700–712 (2014).
pubmed: 24831977
pmcid: 4418935
doi: 10.1016/S1470-2045(14)70189-5
Antonarakis, E. S. et al. Pembrolizumab for treatment-refractory metastatic castration-resistant prostate cancer: multicohort, open-label phase II KEYNOTE-199 study. J. Clin. Oncol. 38, 395–405 (2020).
pubmed: 31774688
doi: 10.1200/JCO.19.01638
Calcinotto, A. et al. IL-23 secreted by myeloid cells drives castration-resistant prostate cancer. Nature https://doi.org/10.1038/s41586-018-0266-0 (2018).
doi: 10.1038/s41586-018-0266-0
pubmed: 29950727
pmcid: 6461206
Garcia, A. J. et al. Pten null prostate epithelium promotes localized myeloid-derived suppressor cell expansion and immune suppression during tumor initiation and progression. Mol. Cell. Biol. 34, 2017–2028 (2014).
pubmed: 24662052
pmcid: 4019050
doi: 10.1128/MCB.00090-14
Di Mitri, D. et al. Tumour-infiltrating Gr-1
pubmed: 25156255
doi: 10.1038/nature13638
Guo, C. et al. CD38 in advanced prostate cancers. Eur. Urol. 79, 736–746 (2021).
pubmed: 33678520
pmcid: 8175332
doi: 10.1016/j.eururo.2021.01.017
Lopez-Bujanda, Z. A. et al. Castration-mediated IL-8 promotes myeloid infiltration and prostate cancer progression. Nat. Cancer 2, 803–818 (2021).
pubmed: 35122025
pmcid: 9169571
doi: 10.1038/s43018-021-00227-3
Wang, G. et al. Targeting YAP-dependent MDSC infiltration impairs tumor progression. Cancer Discov. 6, 80–95 (2016).
pubmed: 26701088
doi: 10.1158/2159-8290.CD-15-0224
Di Mitri, D. et al. Re-education of tumor-associated macrophages by CXCR2 blockade drives senescence and tumor inhibition in advanced prostate cancer. Cell Rep. 28, 2156–2168 (2019).
pubmed: 31433989
pmcid: 6715643
doi: 10.1016/j.celrep.2019.07.068
Gil, V. et al. HER3 is an actionable target in advanced prostate cancer. Cancer Res. 81, 6207–6218 (2021).
pubmed: 34753775
pmcid: 8932336
doi: 10.1158/0008-5472.CAN-21-3360
Wang, L. et al. A robust blood gene expression-based prognostic model for castration-resistant prostate cancer. BMC Med. 13, 201 (2015).
pubmed: 26297150
pmcid: 4546313
doi: 10.1186/s12916-015-0442-0
Olmos, D. et al. Prognostic value of blood mRNA expression signatures in castration-resistant prostate cancer: a prospective, two-stage study. Lancet Oncol. 13, 1114–1124 (2012).
pubmed: 23059046
pmcid: 4878433
doi: 10.1016/S1470-2045(12)70372-8
Maxwell, P. J. et al. Potentiation of inflammatory CXCL8 signalling sustains cell survival in PTEN-deficient prostate carcinoma. Eur. Urol. 64, 177–188 (2013).
pubmed: 22939387
doi: 10.1016/j.eururo.2012.08.032
Acosta, J. C. et al. Chemokine signaling via the CXCR2 receptor reinforces senescence. Cell 133, 1006–1018 (2008).
pubmed: 18555777
doi: 10.1016/j.cell.2008.03.038
Toso, A. et al. Enhancing chemotherapy efficacy in Pten-deficient prostate tumors by activating the senescence-associated antitumor immunity. Cell Rep. 9, 75–89 (2014).
pubmed: 25263564
doi: 10.1016/j.celrep.2014.08.044
Armstrong, C. W. D. et al. Clinical and functional characterization of CXCR1/CXCR2 biology in the relapse and radiotherapy resistance of primary PTEN-deficient prostate carcinoma. NAR Cancer 2, zcaa012 (2020).
pubmed: 32743555
pmcid: 7380483
doi: 10.1093/narcan/zcaa012
Katoh, H. et al. CXCR2-expressing myeloid-derived suppressor cells are essential to promote colitis-associated tumorigenesis. Cancer Cell 24, 631–644 (2013).
pubmed: 24229710
pmcid: 3928012
doi: 10.1016/j.ccr.2013.10.009
Highfill, S. L. et al. Disruption of CXCR2-mediated MDSC tumor trafficking enhances anti-PD1 efficacy. Sci. Transl. Med. 6, 237ra267 (2014).
doi: 10.1126/scitranslmed.3007974
Cesano, A. nCounter
pubmed: 26674611
pmcid: 4678588
doi: 10.1186/s40425-015-0088-7
Fenor de la Maza, M. D. et al. Immune biomarkers in metastatic castration-resistant prostate cancer. Eur. Urol. Oncol. 5, 659–667 (2022).
pubmed: 35491356
doi: 10.1016/j.euo.2022.04.004
Proudfoot, A. E. I. Chemokine receptors: multifaceted therapeutic targets. Nat. Rev. Immunol. 2, 106–115 (2002).
pubmed: 11910892
pmcid: 7097668
doi: 10.1038/nri722
Eash, K. J., Greenbaum, A. M., Gopalan, P. K. & Link, D. C. CXCR2 and CXCR4 antagonistically regulate neutrophil trafficking from murine bone marrow. J. Clin. Invest. 120, 2423–2431 (2010).
pubmed: 20516641
pmcid: 2898597
doi: 10.1172/JCI41649
Matsusaka, T. et al. Transcription factors NF-IL6 and NF-kappa B synergistically activate transcription of the inflammatory cytokines, interleukin 6 and interleukin 8. Proc. Natl Acad. Sci. USA 90, 10193–10197 (1993).
pubmed: 8234276
pmcid: 47740
doi: 10.1073/pnas.90.21.10193
Stein, B., Cogswell, P. C. & Baldwin, A. S. Jr Functional and physical associations between NF-kappa B and C/EBP family members: a Rel domain-bZIP interaction. Mol. Cell. Biol. 13, 3964–3974 (1993).
pubmed: 8321203
pmcid: 359940
Burke, S. J. et al. NF-κB and STAT1 control CXCL1 and CXCL2 gene transcription. Am. J. Physiol. Endocrinol. Metab. 306, E131–E149 (2014).
pubmed: 24280128
doi: 10.1152/ajpendo.00347.2013
Alshetaiwi, H. et al. Defining the emergence of myeloid-derived suppressor cells in breast cancer using single-cell transcriptomics. Sci. Immunol. 5, eaay6017 (2020).
pubmed: 32086381
pmcid: 7219211
doi: 10.1126/sciimmunol.aay6017
Abida, W. et al. Genomic correlates of clinical outcome in advanced prostate cancer. Proc. Natl Acad. Sci. USA 116, 11428–11436 (2019).
pubmed: 31061129
pmcid: 6561293
doi: 10.1073/pnas.1902651116
He, M. X. et al. Transcriptional mediators of treatment resistance in lethal prostate cancer. Nat. Med. 27, 426–433 (2021).
pubmed: 33664492
pmcid: 7960507
doi: 10.1038/s41591-021-01244-6
Song, H. et al. Single-cell analysis of human primary prostate cancer reveals the heterogeneity of tumor-associated epithelial cell states. Nat. Commun. 13, 141 (2022).
pubmed: 35013146
pmcid: 8748675
doi: 10.1038/s41467-021-27322-4
Antonarakis, E. S. et al. AR-V7 and resistance to enzalutamide and abiraterone in prostate cancer. New Engl. J. Med. 371, 1028–1038 (2014).
pubmed: 25184630
doi: 10.1056/NEJMoa1315815
Mateo, J. et al. DNA-repair defects and olaparib in metastatic prostate cancer. N. Engl. J. Med. 373, 1697–1708 (2015).
pubmed: 26510020
pmcid: 5228595
doi: 10.1056/NEJMoa1506859
Welti, J. et al. Targeting bromodomain and extra-terminal (BET) family proteins in castration-resistant prostate cancer (CRPC). Clin. Cancer Res. 24, 3149–3162 (2018).
pubmed: 29555663
doi: 10.1158/1078-0432.CCR-17-3571
Sharp, A. et al. Androgen receptor splice variant-7 expression emerges with castration resistance in prostate cancer. J. Clin. Investig. 129, 192–208 (2019).
pubmed: 30334814
doi: 10.1172/JCI122819
Schaefer, C. F. et al. PID: the Pathway Interaction Database. Nucleic Acids Res. 37, D674–D679 (2009).
pubmed: 18832364
doi: 10.1093/nar/gkn653
Liberzon, A. et al. The Molecular Signatures Database (MSigDB) hallmark gene set collection. Cell Syst. 1, 417–425 (2015).
pubmed: 26771021
pmcid: 4707969
doi: 10.1016/j.cels.2015.12.004
Li, Y. et al. Targeting cellular heterogeneity with CXCR2 blockade for the treatment of therapy-resistant prostate cancer. Sci. Transl. Med. 11, eaax0428 (2019).
pubmed: 31801883
pmcid: 7238624
doi: 10.1126/scitranslmed.aax0428
Bronte, V. et al. Recommendations for myeloid-derived suppressor cell nomenclature and characterization standards. Nat. Commun. 7, 12150 (2016).
pubmed: 27381735
pmcid: 4935811
doi: 10.1038/ncomms12150
Tonnessen-Murray, C. A., Lozano, G. & Jackson, J. G. The regulation of cellular functions by the p53 protein: cellular senescence. Cold Spring Harb. Perspect. Med. 7, a026112 (2017).
pubmed: 27881444
pmcid: 5287062
doi: 10.1101/cshperspect.a026112
Razavipour, S. F., Harikumar, K. B. & Slingerland, J. M. p27 as a transcriptional regulator: new roles in development and cancer. Cancer Res. 80, 3451–3458 (2020).
Rajagopalan, L. & Rajarathnam, K. Ligand selectivity and affinity of chemokine receptor CXCR1. Role of N-terminal domain. J. Biol. Chem. 279, 30000–30008 (2004).
pubmed: 15133028
doi: 10.1074/jbc.M313883200
Nasser, M. W. et al. Differential activation and regulation of CXCR1 and CXCR2 by CXCL8 monomer and dimer. J. Immunol. 183, 3425–3432 (2009).
pubmed: 19667085
doi: 10.4049/jimmunol.0900305
Moussouras, N. A. et al. Differences in sulfotyrosine binding amongst CXCR1 and CXCR2 chemokine ligands. Int. J. Mol. Sci. 18, 1894 (2017).
pubmed: 28869519
pmcid: 5618543
doi: 10.3390/ijms18091894
Ferraldeschi, R. et al. PTEN protein loss and clinical outcome from castration-resistant prostate cancer treated with abiraterone acetate. Eur. Urol. 67, 795–802 (2015).
pubmed: 25454616
pmcid: 4410287
doi: 10.1016/j.eururo.2014.10.027
Rescigno, P. et al. Characterizing CDK12-mutated prostate cancers. Clin. Cancer Res. https://doi.org/10.1158/1078-0432.Ccr-20-2371 (2020).
doi: 10.1158/1078-0432.Ccr-20-2371
pubmed: 32988971
pmcid: 7855716
Migliozzi, D. et al. Microfluidics-assisted multiplexed biomarker detection for in situ mapping of immune cells in tumor sections. Microsyst. Nanoeng. 5, 59 (2019).
pubmed: 31700674
pmcid: 6831597
doi: 10.1038/s41378-019-0104-z
Goodall, J. et al. Circulating cell-free DNA to guide prostate cancer treatment with PARP inhibition. Cancer Discov. 7, 1006–1017 (2017).
pubmed: 28450425
pmcid: 6143169
doi: 10.1158/2159-8290.CD-17-0261
Hothorn, T. & Lausen, B. On the exact distribution of maximally selected rank statistics. Comput. Stat. Data Anal. 43, 121–137 (2003).
doi: 10.1016/S0167-9473(02)00225-6
Lausen, B., Hothorn, T., Bretz, F. & Schumacher, M. Assessment of optimal selected prognostic factors. Biom. J. 46, 364–374 (2004).
doi: 10.1002/bimj.200310030