Exosomal circular RNA: a signature for lung cancer progression

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作者
Bashdar Mahmud Hussen
Snur Rasool Abdullah
Goran Sedeeq Hama Faraj
Mohammed Fatih Rasul
Abbas Salihi
Soudeh Ghafouri-Fard
Mohammad Taheri
Majid Mokhtari
机构
[1] Hawler Medical University,Department of Pharmacognosy, College of Pharmacy
[2] Lebanese French University,Medical Laboratory Science
[3] Komar University of Science and Technology,Department of Medical Laboratory Science
[4] Tishk International University,Department of Pharmaceutical Basic Science, Faculty of Pharmacy
[5] Salahaddin University-Erbil,Department of Biology, College of Science
[6] Cihan University-Erbil,Department of Biomedical Sciences
[7] Shahid Beheshti University of Medical Sciences,Department of Medical Genetics
[8] Shahid Beheshti University of Medical Sciences,Urology and Nephrology Research Center
[9] Jena University Hospital,Institute of Human Genetics
[10] Shahid Beheshti University of Medical Sciences,Tracheal Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD)
来源
关键词
Lung Cancer (LC); Circular RNA (circRNA); Exosomal circular RNA (exo-circRNA);
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摘要
Membrane vesicles having a diameter of 30–150 nm are known as exosomes. Several cancer types secrete exosomes, which may contain proteins, circular RNAs (circRNAs), microRNAs, or DNA. CircRNAs are endogenous RNAs that do not code for proteins and can create continuous and covalently closed loops. In cancer pathogenesis, especially metastasis, exosomal circRNAs (exo-circRNAs) have a crucial role mainly due to the frequently aberrant expression levels within tumors. However, neither the activities nor the regulatory mechanisms of exo-circRNAs in advancing lung cancer (LC) are obvious. A better understanding of the regulation and network connections of exo-circRNAs will lead to better treatment for LCs. The main objective of the current review is to highlight the functions and mechanisms of exo-circRNAs in LC and assess the relationships between exo-circRNA dysregulation and LC progression. In addition, underline the possible therapeutic targets based on exo-circRNA modulating.
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