MicroRNA and Cancer

• Autore: Tucci Paola
• Pubblicazione: Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
• Descrizione fisica: 1 online resource (298 p.)
• Soggetto topico: Biology, life sciences; Research & information: general
• Soggetto non controllato: 2'-O-methylation; adipokines; B-CLL; bioinformatics analysis; biomarker; blood biomarker; brain tumour; breast cancer; Breast cancer; cancer stem cell; cancer stem cells; ccRCC; circulating biomarkers; circulating microRNA; colon cancer; Cyclooxygenase-2 (COX-2); deformability; diagnosis; endometrial cancer; estrogens; exosome; head and neck squamous cell carcinoma; hepatocellular carcinoma; hyperinsulinemia; Hypoxia inducible factor 1-alpha (HIF-1α); immune checkpoint inhibitors; immunotherapy; insulin; insulin resistance; insulin signaling; insulin-like growth factors; malignant melanoma; medulloblastoma; meta-analysis; metastasis; metastatic melanoma; methylation; microRNA; MicroRNA (miRNA); microRNAs; Migration; miR-584-5p; miR526b; miR655; miRNA; miRNA-transcription factor network; miRNAs; n/a; non-small cell lung cancer; normal B-cell development; ovarian cancer; Oxidative stress; PARP; PI3K/Akt; plasma; prediction; prognosis; prognostic factor; progression; Prostaglandin E2 receptor 4 (EP4); pseudouridylation; RCC; regulation; renal cancer; replication stress; serum LDH; smoking; snoRNA; stem cells; stemness; subgroups; survival; targeted therapy; therapy; YKT6
• Persona (resp. second.): TucciPaola
• Sommario/riassunto: MicroRNAs (miRs) are small noncoding RNAs that function as post-transcriptional regulators of gene expression and have important roles in almost all biological pathways. Deregulated miR expression has been detected in numerous cancers, where miRs act as both oncogene and tumor suppressors. Due to their important roles in tumorigenesis, miRs have been investigated as prognostic and diagnostic biomarkers and as useful targets for therapeutic intervention. From a therapeutic point of view, two modalities can serve to rectify gene networks in cancer cells. For oncomiRs, a rational means is downregulation through antagomirs. Moreover, observations of the pathological reductions in tumor-suppressive miRs have inspired the concept of "miR replacement therapy" to enhance the amount of these miRs, thereby restoring them to normal levels. However, the clinical applicability of miR-based therapies is severely limited by the lack of effective delivery systems. Therefore, to understand the role of this new class of regulators, we need to identify the mRNA targets regulated by individual miRs as well as to develop specific, efficient, and safe delivery systems for therapeutic miRs.
• Titolo autorizzato: MicroRNA and Cancer
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910580213503321
• Lo trovi qui: Univ. Federico II