Exosome-derived miR-339-5p mediates radiosensitivity by targeting Cdc25A in locally advanced esophageal squamous cell carcinoma

Concise Review: MSC-Derived Exosomes for Cell-Free Therapy

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Cancer statistics, 2016

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Circulating exosomes and exosomal microRNAs as biomarkers in gastrointestinal cancer

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miR-339-3p Is a Tumor Suppressor in Melanoma

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miR-196b Is Epigenetically Silenced during the Premalignant Stage of Lung Carcinogenesis

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DNA damage response regulation by microRNAs as a therapeutic target in cancer

(2016) Maryam Majidinia et al.   DNA REPAIR

Stem Cell-Derived Exosomes, Autophagy, Extracellular Matrix Turnover, and miRNAs in Cardiac Regeneration during Stem Cell Therapy

(2016) Priyanka Prathipati et al.   Stem Cell Reviews and Reports

Stem Cell-Derived Exosomes, Autophagy, Extracellular Matrix Turnover, and miRNAs in Cardiac Regeneration during Stem Cell Therapy

(2016) Priyanka Prathipati et al.   Stem Cell Reviews and Reports

Molecular Pathways: Overcoming Radiation Resistance by Targeting DNA Damage Response Pathways

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MicroRNA-339, an epigenetic modulating target is involved in human gastric carcinogenesis through targeting NOVA1

(2015) Bo Shen et al.   FEBS LETTERS

Exosome-Mediated Transfer of microRNAs Within the Tumor Microenvironment and Neuroblastoma Resistance to Chemotherapy

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Neoadjuvant chemoradiotherapy plus surgery versus surgery alone for oesophageal or junctional cancer (CROSS): long-term results of a randomised controlled trial

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Exosome-Mediated Transfer of microRNAs Within the Tumor Microenvironment and Neuroblastoma Resistance to Chemotherapy

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Cancer Exosomes Perform Cell-Independent MicroRNA Biogenesis and Promote Tumorigenesis

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MicroRNA silencing for cancer therapy targeted to the tumour microenvironment

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Clinical relevance of circulating cell-free microRNAs in cancer

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miR-339-5p regulates the p53 tumor-suppressor pathway by targeting MDM2

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miR-205 acts as a tumour radiosensitizer by targeting ZEB1 and Ubc13

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Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma

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MicroRNA profiling in locally advanced esophageal cancer indicates a high potential of miR-192 in prediction of multimodality therapy response

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MicroRNA-339-5p Down-regulates Protein Expression of β-Site Amyloid Precursor Protein-Cleaving Enzyme 1 (BACE1) in Human Primary Brain Cultures and Is Reduced in Brain Tissue Specimens of Alzheimer Disease Subjects

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Oesophageal carcinoma

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Charity begins at home: non-coding RNA functions in DNA repair

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Sumoylated hnRNPA2B1 controls the sorting of miRNAs into exosomes through binding to specific motifs

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Clinical impact of serum exosomal microRNA-21 as a clinical biomarker in human esophageal squamous cell carcinoma

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MicroRNAs and their targets: recognition, regulation and an emerging reciprocal relationship

(2012) Amy E. Pasquinelli   NATURE REVIEWS GENETICS

Survival after neoadjuvant chemotherapy or chemoradiotherapy for resectable oesophageal carcinoma: an updated meta-analysis

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MiR-339-5p inhibits breast cancer cell migration and invasion in vitro and may be a potential biomarker for breast cancer prognosis

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Downregulation of p53-inducible microRNAs 192, 194, and 215 Impairs the p53/MDM2 Autoregulatory Loop in Multiple Myeloma Development

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Prognostic Significance of Age in the Radical Treatment of Oesophageal Cancer with Surgery or Chemoradiotherapy: a Prospective Observational Cohort Study

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RUNX3 Modulates DNA Damage-mediated Phosphorylation of Tumor Suppressor p53 at Ser-15 and Acts as a Co-activator for p53

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Secretory Mechanisms and Intercellular Transfer of MicroRNAs in Living Cells

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Robust one-day in situ hybridization protocol for detection of microRNAs in paraffin samples using LNA probes

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Radiation-induced cell death mechanisms

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Dicer-regulated microRNAs 222 and 339 promote resistance of cancer cells to cytotoxic T-lymphocytes by down-regulation of ICAM-1

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Coordinated Regulation of Cell Cycle Transcripts by p53-Inducible microRNAs, miR-192 and miR-215

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MicroRNAmiR-199a*Regulates theMETProto-oncogene and the Downstream Extracellular Signal-regulated Kinase 2 (ERK2)

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