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Autonomic Nerve Development Contributes to Prostate Cancer Progression
Abstract
Cancer Hits a Nerve: Solid tumors sculpt their microenvironment to maximize their growth and metastatic potential. This concept is illustrated most famously by tumor angiogenesis, a process whereby tumors induce the growth of new blood vessels to boost their supply of oxygen and blood-borne nutrients. Magnon et al. (p. 10.1126/science.1236361 ; see the Perspective by Isaacs ) now highlight the important contribution made by another microenvironmental component—developing autonomic nerve fibers—to tumor growth and metastasis. In mouse models of prostate cancer, surgical or chemical destruction of sympathetic nerves prevented early-stage growth of tumors, whereas pharmacological inhibition of parasympathetic nerves inhibited tumor dissemination. In a small study of human prostate cancer specimens, the presence of a high density of nerve fibers in and around the tumor tissue was found to correlate with poor clinical outcome. These results raise the possibility that drugs targeting the autonomic nervous system may have therapeutic potential for prostate cancer.
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“SNS dysfunction is closely associated with metabolic syndrome, oncogenic activation, neoplastic growth and tumor initiation (Lee et al., 2010; Magnon et al., 2013; Tentolouris et al., 2006).”
From Circadian Homeostasis of Liver Metabolism Suppresses Hepatocarcinogenesis (2016) · cites this paper as Magnon et al., 2013
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“both of which have been linked to oncogenic activation and increased risk of cancer (Kettner NM, 2016; Lee et al., 2010; Magnon et al., 2013).”
From Circadian Homeostasis of Liver Metabolism Suppresses Hepatocarcinogenesis (2016) · cites this paper as Magnon et al., 2013
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Cites
D'Amico, A., Whittington, R., Malkowicz, S., Schultz, D., Blank, K., Broderick, G., Tomaszewski, J., Renshaw, A., Kaplan, I., Beard, C., et al. (1998) · Journal of the American Medical Association (JAMA) · doi:10.1001/jama.280.11.969 · Cited by 2,697
Christakis, D., Richards, J. A., Zimmerman, F. J., Garrison, M. M., Xu, D., & Yapanel, U. H. (2009) · Cited by 2,290
Radical Prostatectomy versus Observation for Localized Prostate Cancer
Wilt, T. J., Brawer, M. K., Jones, K. M., Barry, M. J., Aronson, W. J., Fox, S., Gingrich, J. R., Wei, J. T., Gilhooly, P. E., Grob, B. M., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1113162 · Cited by 1,767
Signals from the Sympathetic Nervous System Regulate Hematopoietic Stem Cell Egress from Bone Marrow
Katayama, Y., Battista, M., Kao, W.-M., Hidalgo, A., Peired, A. J., Thomas, S. A., & Frenette, P. S. (2006) · Cell · doi:10.1016/j.cell.2005.10.041 · Cited by 1,412
Self-citationChronic stress promotes tumor growth and angiogenesis in a mouse model of ovarian carcinoma
Thaker, P. H., Han, L. Y., Kamat, A. A., Arevalo, J. M., Takahashi, R., Lu, C., Jennings, N. B., Armaiz-Pena, G., Bankson, J. A., Ravoori, M., et al. (2006) · Nature Medicine · doi:10.1038/nm1447 · Cited by 1,320
Haematopoietic stem cell release is regulated by circadian oscillations
Méndez‐Ferrer, S., Lucas, D., Battista, M., & Frenette, P. S. (2008) · Nature · doi:10.1038/nature06685 · Cited by 1,310
Self-citationMuscarinic Receptors—Characterization, coupling and function
Caulfield, M. P. (1993) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(93)90027-b · Cited by 1,284
Liebig, C., Ayala, G., Wilks, J. A., Berger, D. H., & Albo, D. (2009) · Cancer · doi:10.1002/cncr.24396 · Cited by 1,243
Common mechanisms of nerve and blood vessel wiring
Carmeliet, P., & Tessier-Lavigne, M. (2005) · Nature · doi:10.1038/nature03875 · Cited by 1,085
TNM classification of malignant tumors, fifth edition (1997)
Sobin, L. H., & Fleming, I. D. (1997) · Cancer · doi:10.1002/(sici)1097-0142(19971101)80:9 · Cited by 996
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- 10.1200/JCO.2010.33.4441 · DOI
- 10.1016/j.cell.2005.10.041 · DOI · Paper page
- L. Wecker L. Crespo G. Dunaway S. Watts Brody’s Human Pharmacology (Mosby Elsevier Philadelphia ed. 5 2010).
- 10.1016/0024-3205(88)90345-1 · DOI
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Items 401–500 of 1,000
Sympathetic nerve signaling rewires the tumor microenvironment: a shift in “microenvironmental-ity”
Sattler, A. L., Korzun, T., Gupta, K. R., Diba, P., Kyprianou, N., & Eksi, S. E. (2025) · Cancer and Metastasis Reviews · doi:10.1007/s10555-025-10241-x · Cited by 36
Jansen, L., Weberpals, J. G., Kuiper, J. G., Vissers, P. A. J., Wolkewitz, M., Hoffmeister, M., & Brenner, H. (2017) · International Journal of Cancer · doi:10.1002/ijc.30717 · Cited by 34
Hara, M., Takeba, Y., Iiri, T., Ohta, Y., Ootaki, M., Watanabe, M., Watanabe, D., Koizumi, S., Otsubo, T., & Matsumoto, N. (2018) · Cancer Science · doi:10.1111/cas.13861 · Cited by 34
Role of Muscarinic Acetylcholine Signaling in Gastrointestinal Cancers
Konishi, M., Hayakawa, Y., & Koike, K. (2019) · Biomedicines · doi:10.3390/biomedicines7030058 · Cited by 35
Clinically Actionable Strategies for Studying Neural Influences in Cancer
Demir, İ. E., Reyes, C. M., Alrawashdeh, W., Ceyhan, G. O., Deborde, S., Friess, H., Görgülü, K., Istvánffy, R., Jungwirth, D., Kuner, R., et al. (2020) · Cancer Cell · doi:10.1016/j.ccell.2020.05.023 · Cited by 34
Self-citationJiang, S., Zhang, X.-X., Hu, L.-P., Wang, X., Li, Q., Zhang, X., Li, J., Gu, J., & Zhang, Z. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.586757 · Cited by 34
Neuroimmunology of cancer and associated symptomology
Scheff, N. N., & Saloman, J. L. (2021) · Immunology and Cell Biology · doi:10.1111/imcb.12496 · Cited by 33
Yaman, İ., Çobanoğlu, D. A., Xie, T., Ye, Y., & Amit, M. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108199 · Cited by 35
Li, J., Che, M., Zhang, B., Zhao, K., Wan, C., & Yang, K. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.189007 · Cited by 33
Neurobiology of cancer: Adrenergic signaling and drug repurposing
Dong, Z.-K., Wang, Y., Li, W., & Jin, W. (2024) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2024.108750 · Cited by 33
Gururajan, M., Cavassani, K. A., Sievert, M. F., Duan, P., Lichterman, J. N., Huang, J.-M., Smith, B., You, S., Nandana, S., Chu, G. C., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6398 · Cited by 33
Unintended Effects of GPCR-Targeted Drugs on the Cancer Phenotype
Cornwell, A. C., & Feigin, M. E. (2020) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2020.10.001 · Cited by 34
Rademakers, G., Massen, M., Koch, A., Draht, M. X. G., Buekers, N., Wouters, K., Vaes, N., Meyer, T. D., Carvalho, B. G., Meijer, G. A., et al. (2021) · Clinical Epigenetics · doi:10.1186/s13148-021-01067-9 · Cited by 33
Hiller, J. G., Brodner, G., & Gottschalk, A. (2013) · Best practice & research. Clinical anaesthesiology · doi:10.1016/j.bpa.2013.10.003 · Cited by 33
Jurca, G., Addam, O., Aksaç, A., Gao, S. B., Özyer, T., Demetrick, D. J., & Alhajj, R. (2016) · BMC Research Notes · doi:10.1186/s13104-016-2023-5 · Cited by 33
The Central Nervous Mechanism of Stress-Promoting Cancer Progression
Hong, Y., Zhang, L., Liu, N., Xu, X., Liu, D., & Tu, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012653 · Cited by 33
Dong, W., Fekete, Á., Chen, X. F., Liu, H., Beilhartz, G. L., Chen, X., Bahrampour, S., Xiong, Y., Yang, Q., Zhao, H., et al. (2023) · Nature Cancer · doi:10.1038/s43018-023-00626-8 · Cited by 33
Neuroscience in peripheral cancers: tumors hijacking nerves and neuroimmune crosstalk
Fan, H., Liang, X., & Tang, Y. (2024) · MedComm · doi:10.1002/mco2.784 · Cited by 33
Neurodevelopmental hijacking of oligodendrocyte lineage programs drives glioblastoma infiltration
Wu, Y., Wu, B. Z., Ellenbogen, Y., Kant, J. A., Yu, P., Li, X., Caloren, L. C., Sotov, V., Tran, C. N., Restrepo, M., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.04.022 · Cited by 35
Androgen-Regulated SPARCL1 in the Tumor Microenvironment Inhibits Metastatic Progression
Hurley, P. J., Hughes, R. M., Simons, B. W., Huang, J., Miller, R. M., Shinder, B. M., Haffner, M. C., Esopi, D., Kimura, Y., Jabbari, J., et al. (2015) · Cancer Research · doi:10.1158/0008-5472.can-15-0024 · Cited by 32
Cardiac autonomic modulation impairments in advanced breast cancer patients
Arab, C., Vanderlei, L. C. M., Paiva, L. D. S., Fulghum, K., Fristachi, C. E., Nazário, A. C. P., Elias, S., Gebrim, L. H., Filho, C. F., Gidron, Y., et al. (2018) · Clinical Research in Cardiology · doi:10.1007/s00392-018-1264-9 · Cited by 34
Antitumoral Effects of Tricyclic Antidepressants: Beyond Neuropathic Pain Treatment
Cantó, A. A., López-Abellán, M. D., Guardiola, V. C., Hurtado, A. M., PENELLA, M. M., Luengo‐Gil, G., & Conesa‐Zamora, P. (2022) · Cancers · doi:10.3390/cancers14133248 · Cited by 32
What pain tells us about cancer
Schmidt, B. L. (2015) · Pain · doi:10.1097/j.pain.0000000000000099 · Cited by 32
Stress-Related Signaling Pathways in Lethal and Nonlethal Prostate Cancer
Lu, D., Sinnott, J. A., Valdimarsdóttir, U. A., Fang, F., Gerke, T. A., Tyekucheva, S., Fiorentino, M., Lambe, M. P., Sesso, H. D., Sweeney, C. J., et al. (2015) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-15-0101 · Cited by 32
Hylander, B. L., Eng, J. W. ‐., & Repasky, E. A. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-67577-0_12 · Cited by 33
Schwann Cells as Orchestrators of Nerve Repair: Implications for Tissue Regeneration and PathologiesPreprint
Stassart, R. M., Gomez-Sanchez, J. A., & Lloyd, A. C. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041363 · Cited by 32
Kruglov, O., Vats, K., Soman, V., Tyurin, V. A., Tyurina, Y. Y., Wang, J., Williams, L., Zhang, J., Carey, C. D., Jaklitsch, E. L., et al. (2023) · OncoImmunology · doi:10.1080/2162402x.2023.2192098 · Cited by 32
Pancreatic Schwann cell reprogramming supports cancer-associated neuronal remodeling
Rangel-Sosa, M. M., Mann, F., & Chauvet, S. (2023) · bioRxiv · doi:10.1002/glia.24586 · Cited by 27
Wang, X., Fan, Y., Wang, Q., Shu, X., Lin, J., Guo, J., Li, Z., & Xu, J. (2025) · Discover Oncology · doi:10.1007/s12672-025-02827-2 · Cited by 31
Self-citationCancer neuroscience: The past, the present, and the road ahead
Winkler, F., Heuer, S., Althammer, F., Augustin, H. G., Beleggia, F., Demir, İ. E., Koenig, J., Kuner, R., Kuner, T., Loges, S., et al. (2026) · Cell · doi:10.1016/j.cell.2026.03.018 · Cited by 33
Clinicopathological Significance of Nerves in Esophageal Cancer
Griffin, N., Rowe, C. W., Gao, F., Jobling, P., Wills, V. L., Walker, M. M., Faulkner, S., & Hondermarck, H. (2020) · American Journal Of Pathology · doi:10.1016/j.ajpath.2020.05.012 · Cited by 31
The Role of Extracellular Vesicles in Cancer–Nerve Crosstalk of the Peripheral Nervous System
Guo, Y., & Gil, Z. (2022) · Cells · doi:10.3390/cells11081294 · Cited by 31
The Role of Nerve Fibers in the Tumor Immune Microenvironment of Solid Tumors
Hernandez, S. D., Serrano, A. G., & Soto, L. M. S. (2022) · Advanced Biology · doi:10.1002/adbi.202200046 · Cited by 31
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Malik, J. A., Ahmed, S., Momin, S. S., Shaikh, S., Alafnan, A., Alanazi, J., Almermesh, M. H. S., & Anwar, S. (2022) · ACS Omega · doi:10.1021/acsomega.2c05821 · Cited by 31
Perrot, C. Y., Sawada, J., & Komatsu, M. (2018) · The FASEB Journal · doi:10.1096/fj.201700818rrr · Cited by 31
Zhu, Y., Zhang, G., Shi, Y., Cui, L., Leng, X., & Huang, J. (2019) · Annals of Translational Medicine · doi:10.21037/atm.2019.04.35 · Cited by 31
Tumor-Induced T Cell Polarization by Schwann Cells
Shurin, G. V., Vats, K., Kruglov, O., Bunimovich, Y. L., & Shurin, M. R. (2022) · Cells · doi:10.3390/cells11223541 · Cited by 31
Crosstalk Between Peripheral Innervation and Pancreatic Ductal Adenocarcinoma
Ni, B., Yin, Y., Li, Z., Wang, J., Wang, X., & Wang, K. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01082-1 · Cited by 31
Wang, Y., Dong, Z.-K., & Jin, W. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02396-6 · Cited by 32
Braadland, P. R., Ramberg, H., Grytli, H. H., Urbanucci, A., Nielsen, H. K., Guldvik, I. J., Engedal, A., Ketola, K., Wang, W., Svindland, A., et al. (2019) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-18-0605 · Cited by 30
β3-Adrenoreceptor Blockade Induces Stem Cells Differentiation in Melanoma Microenvironment
Calvani, M., Bruno, G., Dabraio, A., Subbiani, A., Bianchini, F., Fontani, F., Casazza, G., Vignoli, M., Logu, F. D., Frenos, S., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041420 · Cited by 30
β3-Adrenoceptors as Putative Regulator of Immune Tolerance in Cancer and Pregnancy
Calvani, M., Dabraio, A., Subbiani, A., Buonvicino, D., Gregorio, V. D., Mannurita, S. C., Pini, A., Nardini, P., Favre, C., & Filippi, L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.02098 · Cited by 30
Sensory nerves in the spotlight of the stem cell niche
Picoli, C. C., Costa, A. C., Rocha, B. G. S., da Silva, W. N., Santos, G. S. P., Prazeres, P. H. D. M., Costa, P. A. C., Oropeza, A., da Silva, R. A., Azevedo, V., et al. (2020) · Stem Cells Translational Medicine · doi:10.1002/sctm.20-0284 · Cited by 30
Liu, T., Li, J., Li, Q., Liang, Y., Gao, J. J., Meng, Z., Li, P., Yao, M., Gu, J., Tu, H., et al. (2023) · Hepatology · doi:10.1097/hep.0000000000000239 · Cited by 30
Schwann cells as a target cell for the treatment of cancer pain
Zhang, W.-J., Wu, C., & Liu, J. (2023) · Glia · doi:10.1002/glia.24391 · Cited by 30
Wu, S., Lin, X., Lin, S. X. H., Lu, M., Deng, T., Wang, Z., Olumi, A. F., Dahl, D. M., Wang, D., Blute, M. L., et al. (2019) · Scandinavian Journal of Urology · doi:10.1080/21681805.2019.1643913 · Cited by 29
Gregorio, V. D., Urciuolo, F., Netti, P. A., & Imparato, G. (2020) · Cancers · doi:10.3390/cancers12051150 · Cited by 30
Shi, Y., Luo, J., Wang, X., Zhang, Y., Zhu, H., Su, D., Yu, W., & Tian, J. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.800499 · Cited by 29
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Liu, D., Deng, Q., Sun, L., Wang, T., Yang, Z., Chen, H., Guo, L., Liu, Y., Yuan-fang Ma, A., Guo, N., et al. (2015) · BMC Cancer · doi:10.1186/s12885-015-1869-6 · Cited by 29
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Xu, G., Feng, F., Liu, Z., Liu, S., Zheng, G., Xiao, S., Cai, L., Yang, X., Li, G., Lian, X., et al. (2017) · Scientific Reports · doi:10.1038/srep43828 · Cited by 29
Li, W., & Zhao, Y. (2018) · Asian Journal of Andrology · doi:10.4103/aja.aja_32_18 · Cited by 29
Norepinephrine induces anoikis resistance in high-grade serous ovarian cancer precursor cells
Reavis, H. D., Gysler, S. M., McKenney, G. B., Knarr, M., Lusk, H. J., Rawat, P., Rendulich, H. S., Mitchell, M. A., Berger, D. S., Moon, J. S., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.170961 · Cited by 31
Remodeling the tumor dormancy ecosystem to prevent recurrence and metastasis
Liang, Y., Chen, W., Zhang, Y., & Li, L. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02328-2 · Cited by 29
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Maly, I. V., & Hofmann, W. A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041237 · Cited by 31
Ion Channels in Cancer: Orchestrators of Electrical Signaling and Cellular Crosstalk
Fan, J. J., & Huang, X. (2020) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2020_48 · Cited by 31
Neural signaling modulates metabolism of gastric cancer
Rabben, H.-L., Andersen, G. T., Olsen, M. K., Øverby, A., Ianevski, A., Kainov, D. E., Wang, T. C., Lundgren, S., Grønbech, J. E., Chen, D., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102091 · Cited by 28
Novel Combinatorial Approaches to Tackle the Immunosuppressive Microenvironment of Prostate Cancer
Shackleton, E. G., Ali, H. Y., Khan, M. A., Pockley, A. G., & McArdle, S. (2021) · Cancers · doi:10.3390/cancers13051145 · Cited by 29
Blood Vessels and Peripheral Nerves as Key Players in Cancer Progression and Therapy Resistance
Roda, N., Blandano, G., & Pelicci, P. G. (2021) · Cancers · doi:10.3390/cancers13174471 · Cited by 29
Sæter, T., Bogaard, M., Vlatkovic, L., Waaler, G., Servoll, E., Nesland, J. M., Axcrona, K., & Axcrona, U. (2015) · The Prostate · doi:10.1002/pros.23112 · Cited by 28
Differential receptor dependencies
Baig, A. M., Khan, N. A., Effendi, V., Rana, Z., Ahmad, H. R., & Abbas, F. (2016) · Anti-Cancer Drugs · doi:10.1097/cad.0000000000000432 · Cited by 28
Role of the Bone Microenvironment in the Development of Painful Complications of Skeletal Metastases
Park, S. H., Eber, M. R., Widner, D. B., & Shiozawa, Y. (2018) · Cancers · doi:10.3390/cancers10050141 · Cited by 28
Inside the Biology of the β3-Adrenoceptor
Pasha, A., Tondo, A., Favre, C., & Calvani, M. (2024) · Biomolecules · doi:10.3390/biom14020159 · Cited by 30
Integrating priorities at the intersection of cancer and neuroscience
Hwang, W. L., Perrault, E. N., Birbrair, A., Mattson, B. J., Gutmann, D. H., Mabbott, D., Cukierman, E., Repasky, E. A., Sloan, E. K., Zong, H., et al. (2024) · Cancer Cell · doi:10.1016/j.ccell.2024.09.014 · Cited by 29
The neuro-immune oncology axis
Abeele, F. V., & Salzet, M. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.218070 · Cited by 27
Cancer–nerve interplay in cancer progression and cancer-induced bone pain
Yoneda, T., Hiasa, M., Okui, T., & Hata, K. (2023) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-023-01401-6 · Cited by 27
Xu, W., Liu, J., Zhang, J., Lu, J., & Guo, J. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.189032 · Cited by 27
Characterization of prostate cancer using diffusion tensor imaging: A new perspective
Gholizadeh, N., Greer, P. B., Simpson, J., Denham, J. W., Lau, P., Dowling, J., Hondermarck, H., & Ramadan, S. A. (2018) · European Journal of Radiology · doi:10.1016/j.ejrad.2018.11.026 · Cited by 28
Calcitonin Related Polypeptide Alpha Mediates Oral Cancer Pain
Tu, N. H., Inoue, K., Lewis, P. K., Khan, A., Hwang, J. H., Chokshi, V., Dabovic, B., Selvaraj, S., Bhattacharya, A., Dubeykovskaya, Z. A., et al. (2023) · Cells · doi:10.3390/cells12131675 · Cited by 26
Zhang, Z., Lv, Z. G., Lu, M., Li, H., & Zhou, J. (2024) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2024.189121 · Cited by 27
The Intersection of the Nervous System and Breast Cancer.
Liu, Y.-T., Yin, S., Lu, G.-Y., & Du, Y. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.217132 · Cited by 26
Li, Y., Yu, H., Li, Z., Yin, K.-W., Jin, S., Chen, C.-C., Tan, M.-S., Zhang, C.-J., Liu, X.-H., Li, W.-P., et al. (2025) · Nature Cancer · doi:10.1038/s43018-025-01033-x · Cited by 28
β-adrenergic signaling blockade attenuates metastasis through activation of cytotoxic CD4 T cells
Fjæstad, K. Y., Johansen, A. Z., Linder, H., Baker, K. J., Schattefor, M., Czajkowski, N. K., Thorseth, M., Siersbæk, M. S., Kurzay, A., Perez-Penco, M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65048-9 · Cited by 27
Cancer neuroscience: signaling pathways and new therapeutic strategies for cancer
Zhang, S., Yuan, L., Lin, P., Yang, G., Zhou, X., Jinfu, X., Wu, M., & Huang, Y. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02364-y · Cited by 29
Alshalalfa, M., Nguyen, P. L., Beltran, H., Chen, W. S., Davicioni, E., Zhao, S. G., Rebbeck, T. R., Schaeffer, E. M., Lotan, T. L., Feng, F. Y.-C., et al. (2019) · European Urology Oncology · doi:10.1016/j.euo.2019.05.001 · Cited by 27
Use of beta-blocker types and risk of incident prostate cancer in a multiethnic population
Zahalka, A. H., Fram, E., Lin, W., Mohn, L., Frenette, P. S., Agalliu, I., & Watts, K. L. (2020) · Urologic Oncology Seminars and Original Investigations · doi:10.1016/j.urolonc.2020.03.024 · Cited by 26
Self-citationWu, S., Xie, L., Lin, S. X. H., Wirth, G. J., Lu, M., Zhang, Y., Blute, M. L., Dahl, D. M., & Wu, C. (2020) · Human Pathology · doi:10.1016/j.humpath.2020.07.005 · Cited by 26
Bruno, G., Nastasi, N., Subbiani, A., Boaretto, A., Mannurita, S. C., Mattei, G., Nardini, P., Bella, C. D., Magi, A., Pini, A., et al. (2023) · Cancer Gene Therapy · doi:10.1038/s41417-023-00599-x · Cited by 27
Kaapu, K. J., Ahti, J., Tammela, T. L. J., Auvinen, A. P., & Murtola, T. J. (2015) · International Journal of Cancer · doi:10.1002/ijc.29470 · Cited by 26
Yao, J., Zhang, L.-L., Huang, X.-M., Li, W.-Y., & Gao, S. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i21.3907 · Cited by 26
The contribution of the nervous system in the cancer progression
Park, H., & Lee, C. H. (2024) · BMB Reports · doi:10.5483/bmbrep.2024-0019 · Cited by 25
Itami, T., Kurokawa, Y., Hagi, T., Nagano, S., Nakamoto, R., Kamakura, Y., Takahashi, T., Saito, T., Yamamoto, K., Momose, K., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-87492-9 · Cited by 25
Liu, B., Li, C., He, S., Li, Z., Wang, H., Feng, C., Xiong, Z., Tu, C., Song, D., & Li, Z. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114545 · Cited by 25
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Monje, M. (2017) · Cancer Cell · doi:10.1016/j.ccell.2016.12.008 · Cited by 25
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da Rosa, M. M., Sampaio, M. C. P. D., Santos, R. V. C., Sharjeel, M., Araújo, C., Pitta, M. G. D. R., Pereira, M. C., & Rêgo, M. J. B. D. M. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114547 · Cited by 25
Maru, Y. (2021) · Springer eBooks · doi:10.1007/978-981-16-1757-7_11 · Cited by 25
Regan, J. L., Schumacher, D., Staudte, S., Steffen, A., Lesche, R., Toedling, J., Jourdan, T., Haybaeck, J., Golob‐Schwarzl, N., Mumberg, D., et al. (2022) · iScience · doi:10.1016/j.isci.2022.104498 · Cited by 27
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Chang, A., Kim-Fuchs, C., Le, C. P., Hollande, F., & Sloan, E. K. (2015) · Cancers · doi:10.3390/cancers7030838 · Cited by 25
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Toro, R. D., & Méndez‐Ferrer, S. (2013) · Haematologica · doi:10.3324/haematol.2013.084764 · Cited by 25
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Abdel‐Hamid, N. M., Shehata, D. E., Abdel-ghany, A. A., Ragaa, A., & Wahid, A. M. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.07.005 · Cited by 25
Zhang, L., Xiu, D., Zhan, J., He, X., Guo, L., Wang, J., Tao, M., Fu, W., & Zhang, H. (2016) · OncoTargets and Therapy · doi:10.2147/ott.s111382 · Cited by 25
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Pagella, P., Catón, J., Meisel, C. T., & Mitsiadis, T. A. (2020) · Cells · doi:10.3390/cells9030644 · Cited by 26
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Fernández‐Nogueira, P., Linzoain-Agos, P., Cueto‐Remacha, M., la Guia-Lopez, I. D., Recalde‐Percaz, L., Parcerisas, A., Gascón, P., Carbó, N., Gutiérrez-Uzquiza, Á., Fuster, G., et al. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.217308 · Cited by 24
Prostatic nerve subtypes independently predict biochemical recurrence in prostate cancer
Reeves, F., Battye, S., Roth, H. S., Peters, J. S., Hovens, C. M., Costello, A. J., & Corcoran, N. M. (2019) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2019.01.052 · Cited by 24
Ein, L., Mei, C., Bracho, O. R., Bas, E., Monje, P. V., Weed, D. T., Sargi, Z., Thomas, G. R., & Dinh, C. T. (2019) · Anticancer Research · doi:10.21873/anticanres.13798 · Cited by 24
Neuroimmune Regulation of Surgery-Associated Metastases
Shurin, M. R., Baraldi, J. H., & Shurin, G. V. (2021) · Cells · doi:10.3390/cells10020454 · Cited by 24
Plavá, J., Buríková, M., Cihova, M., Trnkova, L., Smolková, B., Babál, P., Krivošíková, L., Janega, P., Rojikova, L., Drahošová, S., et al. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02087-2 · Cited by 24
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Doepner, M., Lee, I., Natale, C. A., Brathwaite, R., Venkat, S., Kim, S. H., Wei, Y., Vakoc, C. R., Capell, B. C., Katzenellenbogen, J. A., et al. (2022) · Science Advances · doi:10.1126/sciadv.abn4007 · Cited by 25
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Metadata
- Authors
- Magnon, C., Hall, S. J., Lin, J., Xue, X., Gerber, L., Freedland, S. J., & Frenette, P. S.
- Affiliations
- Albert Einstein College of Medicine (US)
- Icahn School of Medicine at Mount Sinai (US)
- Duke University (US)
- Corresponding author
- Magnon, Claire
- Frenette, Paul S.
- Venue
- Science
- Published
- 2013-07-12
- Volume
- 341
- Issue
- 6142
- Pages
- 1236361-1236361
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2049959255
- Cited by
- 1,287
- References
- 36
- Citations by year
- 2026: 136 · 2025: 128 · 2024: 127 · 2023: 119 · 2022: 116 · 2021: 120 · 2020: 120 · 2019: 85 · 2018: 78 · 2017: 66 · 2016: 66 · 2015: 56 · 2014: 46 · 2013: 23
- FWCI
- 45.11
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL069438, HL097819, R01HL069438, R01HL097819)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK056638, DK056638)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Stress, Anesthesia, and Immune Response
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Prostate Cancer Treatment and Research
- Life Sciences › Neuroscience › Neurology › Vagus Nerve Stimulation Research
- Keywords
- prostate cancer, autonomic nerves, tumor microenvironment, sympathetic nerves, parasympathetic nerves, cholinergic fibers, adrenergic receptors, muscarinic receptors, metastasis, tumor invasion
- MeSH terms
- Adenocarcinoma, Adrenergic Fibers, Animals, Autonomic Nervous System, Cell Transformation, Neoplastic, Cholinergic Fibers, Humans, Male, Mice, Transgenic, Neoplasm Invasiveness, Neoplasm Transplantation, Nerve Net, Parasympathetic Nervous System, Promoter Regions, Genetic, Prostate, Prostatic Neoplasms, Genes, myc, Disease Progression, Cell Line, Tumor, Mice, Neurogenesis
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