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https://doi.org/10.2139/ssrn.4679863

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cam4.1614openalex-extracted
The pivotal role of DNA methylation in the radio‐sensitivity of tumor radiotherapy
inferredcites →https://doi.org/10.1002/em.20361openalex-extracted
Epigenetic changes and nontargeted radiation effects—Is there a link?
inferredcites →https://doi.org/10.1002/gcc.22757openalex-extracted
Radiation‐induced genomic instability in breast carcinomas of the Swedish hemangioma cohort
inferredcites →https://doi.org/10.1007/s12253-016-0185-zopenalex-extracted
Exosomes Derived from Irradiated Esophageal Carcinoma-Infiltrating T Cells Promote Metastasis by Inducing the Epithelial–Mesenchymal Transition in Esophageal Cancer Cells
inferredcites →https://doi.org/10.1016/b978-0-12-814879-2.00003-0openalex-extracted
Histone Modifications
inferredcites →https://doi.org/10.1016/j.bbagen.2023.130386openalex-extracted
Epigenetic modifications in radiation-induced non-targeted effects and their clinical significance
inferredcites →https://doi.org/10.1016/j.bbrc.2016.07.124openalex-extracted
Exosome cargo reflects TGF-β1-mediated epithelial-to-mesenchymal transition (EMT) status in A549 human lung adenocarcinoma cells
inferredcites →https://doi.org/10.1016/j.biomaterials.2020.119925openalex-extracted
Bioinspired exosome-like therapeutics and delivery nanoplatforms
inferredcites →https://doi.org/10.1016/j.ejphar.2009.07.028openalex-extracted
Ionizing radiation-induced bystander effects, potential targets for modulation of radiotherapy
inferredcites →https://doi.org/10.1016/j.eururo.2016.02.046openalex-extracted
Extracellular Vesicles and Their Role in Urologic Malignancies
inferredcites →https://doi.org/10.1016/j.ijpharm.2017.02.038openalex-extracted
Exosomes as novel bio-carriers for gene and drug delivery
inferredcites →https://doi.org/10.1016/j.ijrobp.2022.01.036openalex-extracted
Irradiated Cell-Derived Exosomes Transmit Essential Molecules Inducing Radiation Therapy Resistance
inferredcites →https://doi.org/10.1016/j.matbio.2018.08.004openalex-extracted
Prostate cancer sheds the αvβ3 integrin in vivo through exosomes
inferredcites →https://doi.org/10.1016/j.mrfmmm.2014.12.007openalex-extracted
The non-targeted effects of radiation are perpetuated by exosomes
inferredcites →https://doi.org/10.1016/j.mrrev.2012.12.001openalex-extracted
Non-targeted effects of ionising radiation—Implications for low dose risk
inferredcites →https://doi.org/10.1016/j.neuroscience.2018.04.003openalex-extracted
Cell-to-cell Communication by Extracellular Vesicles: Focus on Microglia
inferredcites →https://doi.org/10.1016/j.rpor.2014.08.004openalex-extracted
Bystander effects and radiotherapy
inferredcites →https://doi.org/10.1021/acs.molpharmaceut.8b00059openalex-extracted
Exosomes from Irradiated Nonsmall Cell Lung Cancer Cells Reduced Sensitivity of Recipient Cells to Anaplastic Lymphoma Kinase Inhibitors
inferredcites →https://doi.org/10.1038/aps.2017.178openalex-extracted
Exosomal cargo-loading and synthetic exosome-mimics as potential therapeutic tools
inferredcites →https://doi.org/10.1038/ncomms15016openalex-extracted
Exosome-delivered EGFR regulates liver microenvironment to promote gastric cancer liver metastasis
inferredcites →https://doi.org/10.1038/nrg2540openalex-extracted
Linking DNA methylation and histone modification: patterns and paradigms
inferredcites →https://doi.org/10.1038/nrm.2017.125openalex-extracted
Shedding light on the cell biology of extracellular vesicles
inferredcites →https://doi.org/10.1038/s41388-020-1250-3openalex-extracted
Radiation resistance in head and neck squamous cell carcinoma: dire need for an appropriate sensitizer
inferredcites →https://doi.org/10.1038/s41416-020-0942-3openalex-extracted
Radiation-induced bystander and abscopal effects: important lessons from preclinical models
inferredcites →https://doi.org/10.1038/s41598-017-12403-6openalex-extracted
Radiation alters the cargo of exosomes released from squamous head and neck cancer cells to promote migration of recipient cells
inferredcites →https://doi.org/10.1038/sj.onc.1206961openalex-extracted
Oxidative metabolism, gap junctions and the ionizing radiation-induced bystander effect
inferredcites →https://doi.org/10.1073/pnas.0804549105openalex-extracted
Circulating microRNAs as stable blood-based markers for cancer detection
inferredcites →https://doi.org/10.1074/jbc.m506591200openalex-extracted
Radiation-induced Epidermal Growth Factor Receptor Nuclear Import Is Linked to Activation of DNA-dependent Protein Kinase
inferredcites →https://doi.org/10.1080/09553002.2018.1434323openalex-extracted
Intercellular communication of DNA damage and oxidative status underpin bystander effects
inferredcites →https://doi.org/10.1080/09553002.2018.1549757openalex-extracted
Radiation-induced genomic instability, epigenetic mechanisms and the mitochondria: a dysfunctional ménage a trois?
inferredcites →https://doi.org/10.1080/15476286.2015.1100795openalex-extracted
Exosome-mediated microRNA transfer plays a role in radiation-induced bystander effect
inferredcites →https://doi.org/10.1089/ars.2017.7267openalex-extracted
Targeted and Off-Target (Bystander and Abscopal) Effects of Radiation Therapy: Redox Mechanisms and Risk/Benefit Analysis
inferredcites →https://doi.org/10.1093/jrr/rrz001openalex-extracted
Ionizing radiation affects the composition of the proteome of extracellular vesicles released by head-and-neck cancer cells in vitro
inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00920.xopenalex-extracted
Multivesicular Endosome Biogenesis in the Absence of ESCRTs
inferredcites →https://doi.org/10.1113/jp282799openalex-extracted
Exosome engineering for efficient and targeted drug delivery: Current status and future perspective
inferredcites →https://doi.org/10.1126/sciadv.abh4050openalex-extracted
Radiotherapy orchestrates natural killer cell dependent antitumor immune responses through CXCL8
inferredcites →https://doi.org/10.1158/1078-0432.ccr-10-2639openalex-extracted
Cancer Stem Cells: Targets and Potential Biomarkers for Radiotherapy
inferredcites →https://doi.org/10.1161/circulationaha.110.956839openalex-extracted
Epigenetic Modifications
inferredcites →https://doi.org/10.1186/s12964-022-00986-1openalex-extracted
The emerging role of exosomes in radiotherapy
inferredcites →https://doi.org/10.1186/s40779-018-0167-4openalex-extracted
Biological effects of radiation on cancer cells
inferredcites →https://doi.org/10.1371/journal.pone.0152213openalex-extracted
Exosomes Derived from Squamous Head and Neck Cancer Promote Cell Survival after Ionizing Radiation
inferredcites →https://doi.org/10.1371/journal.pone.0205496openalex-extracted
Harmonization of exosome isolation from culture supernatants for optimized proteomics analysis
inferredcites →https://doi.org/10.14740/wjon996wopenalex-extracted
Radiation-Induced Malignancies Making Radiotherapy a “Two-Edged Sword”: A Review of Literature
inferredcites →https://doi.org/10.1615/critrevoncog.2018025946openalex-extracted
Profiles of Radioresistance Mechanisms in Prostate Cancer
inferredcites →https://doi.org/10.1667/rr1141.1openalex-extracted
Dilution of Irradiated Cell Conditioned Medium and the Bystander Effect
inferredcites →https://doi.org/10.1667/rr14201.1openalex-extracted
Exosome-Mediated Telomere Instability in Human Breast Epithelial Cancer Cells after X Irradiation
inferredcites →https://doi.org/10.1667/rr15489.1openalex-extracted
The Radiation-Induced Bystander Effect (RIBE) and its Connections with the Hallmarks of Cancer
inferredcites →https://doi.org/10.1667/rr2868.1openalex-extracted
Possible Role of Exosomes Containing RNA in Mediating Nontargeted Effect of Ionizing Radiation
inferredcites →https://doi.org/10.18388/abp.2015_970openalex-extracted
Ionizing radiation affects protein composition of exosomes secreted in vitro from head and neck squamous cell carcinoma
inferredcites →https://doi.org/10.2147/cmar.s220976openalex-extracted
Benefits and Limitations of a Multidisciplinary Approach in Cancer Patient Management
inferredcites →https://doi.org/10.22038/ijbms.2016.7725openalex-extracted
The role of exosomes contents on genetic and epigenetic alterations of recipient cancer cells.
inferredcites →https://doi.org/10.2217/epi-2019-0193openalex-extracted
Radiotherapy-Induced Overexpression of Exosomal Mirna-378A-3P in Cancer Cells Limits Natural Killer Cells Cytotoxicity
inferredcites →https://doi.org/10.3109/09553002.2010.522686openalex-extracted
Radiation-induced genomic instability: Are epigenetic mechanisms the missing link?
inferredcites →https://doi.org/10.3389/fcell.2018.00018openalex-extracted
Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
inferredcites →https://doi.org/10.3389/fcell.2021.624312openalex-extracted
A Perspective of Epigenetic Regulation in Radiotherapy
inferredcites →https://doi.org/10.3389/fgene.2018.00611openalex-extracted
Long Noncoding RNA FAM201A Mediates the Radiosensitivity of Esophageal Squamous Cell Cancer by Regulating ATM and mTOR Expression via miR-101
inferredcites →https://doi.org/10.3389/fonc.2020.00874openalex-extracted
Immunomodulation of NK Cells by Ionizing Radiation
inferredcites →https://doi.org/10.3389/fonc.2023.1124412openalex-extracted
Radiation-induced bystander effect and its clinical implications
inferredcites →https://doi.org/10.3390/cancers11091236openalex-extracted
Relevance of Non-Targeted Effects for Radiotherapy and Diagnostic Radiology; A Historical and Conceptual Analysis of Key Players
inferredcites →https://doi.org/10.3390/cells9061419openalex-extracted
Exosome-Derived LINC00960 and LINC02470 Promote the Epithelial-Mesenchymal Transition and Aggressiveness of Bladder Cancer Cells
inferredcites →https://doi.org/10.3390/ijms19041183openalex-extracted
The Double Face of Exosome-Carried MicroRNAs in Cancer Immunomodulation
inferredcites →https://doi.org/10.3390/ijms20153649openalex-extracted
Ionizing Radiation Increases the Activity of Exosomal Secretory Pathway in MCF-7 Human Breast Cancer Cells: A Possible Way to Communicate Resistance against Radiotherapy
inferredcites →https://doi.org/10.3390/ijms20225527openalex-extracted
Extracellular Vesicles in Modifying the Effects of Ionizing Radiation
inferredcites →https://doi.org/10.3390/ijms21010052openalex-extracted
Extracellular Vesicles and Epigenetic Modifications Are Hallmarks of Melanoma Progression
inferredcites →https://doi.org/10.3390/ijms21175993openalex-extracted
Ionizing Radiation-Induced Epigenetic Modifications and Their Relevance to Radiation Protection
inferredcites →https://doi.org/10.3390/ijms222111570openalex-extracted
Ionising Radiation Promotes Invasive Potential of Breast Cancer Cells: The Role of Exosomes in the Process
inferredcites →https://doi.org/10.3390/ijms23084169openalex-extracted
Radiation-Induced Bystander Effect Mediated by Exosomes Involves the Replication Stress in Recipient Cells
inferredcites →https://doi.org/10.3390/ncrna4040033openalex-extracted
lncRNA Expression after Irradiation and Chemoexposure of HNSCC Cell Lines
inferredcites →https://doi.org/10.4103/ijmr.ijmr_3335_21openalex-extracted
Improving outcomes of women’s cancer in India
inferredcites →https://doi.org/10.4161/cc.9.17.12884openalex-extracted
H2AX post-translational modifications in the ionizing radiation response and homologous recombination
inferredcites →https://doi.org/10.7150/ijbs.18890openalex-extracted
Exosomal miR-7 Mediates Bystander Autophagy in Lung after Focal Brain Irradiation in Mice
inferredcites →https://doi.org/10.7150/ijms.3635openalex-extracted
Cancer and Radiation Therapy: Current Advances and Future Directions
inferredcites →https://doi.org/10.7150/thno.21945openalex-extracted
Exosome Theranostics: Biology and Translational Medicine
inferredcites →https://doi.org/10.7150/thno.30853openalex-extracted
Design strategies and application progress of therapeutic exosomes
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