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Status: Bibliographieeintrag

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Verfasst von:Misir, Sema [VerfasserIn]   i
 Ozer Yaman, Serap [VerfasserIn]   i
 Petrović, Nina [VerfasserIn]   i
 Šami, Ahmad [VerfasserIn]   i
 Akidan, Osman [VerfasserIn]   i
 Hepokur, Ceylan [VerfasserIn]   i
 Aliyazicioglu, Yuksel [VerfasserIn]   i
Titel:Identification of a novel hsa_circ_0058058/miR-324-5p axis and prognostic/predictive molecules for acute myeloid leukemia outcome by bioinformatics-based analysis
Verf.angabe:Sema Misir, Serap Ozer Yaman, Nina Petrović, Ahmad Šami, Osman Akidan, Ceylan Hepokur and Yuksel Aliyazicioglu
E-Jahr:2024
Jahr:20 June 2024
Umfang:19 S.
Fussnoten:Gesehen am 24.02.2024
Titel Quelle:Enthalten in: Biology
Ort Quelle:Basel : MDPI, 2012
Jahr Quelle:2024
Band/Heft Quelle:13(2024), 7, Artikel-ID 487, Seite 1-19
ISSN Quelle:2079-7737
Abstract:Acute myeloid leukemia (LAML) is one of the most prevalent hematological malignancies. In recent years, while targeted approaches have shown promise in the fight against cancer, the treatability and prognosis of patients remain inadequate due to the shortage of drugs. Noncoding RNAs, especially circular RNA (circRNA) and microRNA (miRNA), have been shown to play a unique role in tumor development. This study aims to identify the disease-associated circRNA-miRNA-mRNA network by bioinformatic analysis and investigate the mechanisms in the development and progression of LAML. Additionally, it reveals the promising roles of these molecules as a diagnostic biomarker and therapeutic target for LAML treatment. Using various bioinformatics approaches, we identified the hsa_circ_0058058/miR-324-5p axis in LAML and its possible functions in LAML development. According to our results, hsa circ-0058058 can regulate the expression of AP1G1 and SP1 through miR-324-5p to support angiogenesis, the cell cycle, and DNA replication processes. Downregulation of hsa circ-0058058 may contribute to the anticancer functions of miR-324-5p on LAML tumorigenesis, and upregulation of miR-324-5p can abolish the oncogenic effects of AP1G1 and SP1 on LAML tumorigenesis. Additionally, highly enriched pathways indicated possible interactions between molecules underlying LAML pathology. Targeted molecules within this network may be able to function as therapeutic and diagnostic biomarkers for disease, while more research and clinical confirmation are needed.
DOI:doi:10.3390/biology13070487
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.3390/biology13070487
 kostenfrei: Volltext: https://www.mdpi.com/2079-7737/13/7/487
 DOI: https://doi.org/10.3390/biology13070487
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:acute myeloid leukemia
 circRNA
 miRNA
 non-coding RNAs
K10plus-PPN:1917911246
Verknüpfungen:→ Zeitschrift

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