Interplay between SOX9 transcription factor and microRNAs in cancer.

M. Ashrafizadeh,A. Zarrabi,Sima Orouei,Amirhossein Zabolian,Hossein Saleki,Negar Azami,A. K. Bejandi,Sepideh Mirzaei,Milad Nemati Janaghard,K. Hushmandi,N. Nabavi,B. Baradaran,A. Kumar,Pooyan Makvandi,S. Samarghandian,H. Khan,Michael R Hamblin

Published 2021 in International Journal of Biological Macromolecules

ABSTRACT

SOX transcription factors are critical regulators of development, homeostasis and disease progression and their dysregulation is a common finding in various cancers. SOX9 belongs to SOXE family located on chromosome 17. MicroRNAs (miRNAs) possess the capacity of regulating different transcription factors in cancer cells by binding to 3'-UTR. Since miRNAs can affect differentiation, migration, proliferation and other physiological mechanisms, disturbances in their expression have been associated with cancer development. In this review, we evaluate the relationship between miRNAs and SOX9 in different cancers to reveal how this interaction can affect proliferation, metastasis and therapy response of cancer cells. The tumor-suppressor miRNAs can decrease the expression of SOX9 by binding to the 3'-UTR of mRNAs. Furthermore, the expression of downstream targets of SOX9, such as c-Myc, Wnt, PI3K/Akt can be affected by miRNAs. It is noteworthy that other non-coding RNAs including lncRNAs and circRNAs regulate miRNA/SOX9 expression to promote/inhibit cancer progression and malignancy. The pre-clinical findings can be applied as biomarkers for diagnosis and prognosis of cancer patients.

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