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Therapeutic Targeting of Overexpressed MiRNAs in Cancer Progression
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Abstract:
MicroRNAs (miRNAs) are non-coding RNAs involved in the modulation of various bio-logical processes, and their dysregulation is greatly associated with cancer progression as miRNAs can act as either tumour suppressors or oncogenes, depending on their intended target, mechanism of actions, and expression levels. This review paper aims to shed light on the role of overexpressed miRNAs in cancer progression. Cancer cells are known to upregulate specific miRNAs to inhibit the expression of genes regulating the cell cycle, such as PTEN, FOXO1, SOX7, caspases, KLF4, TRIM8, and ZBTB4. Inhibition of these genes promotes cancer development and survival by indu-cing cell growth, migration, and invasion while evading apoptosis, which leads to poor cancer sur-vival rates. Therefore, the potential of antisense miRNAs in treating cancer is also explored in this review. Antisense miRNAs are chemically modified oligonucleotides that can reverse the action of overexpressed miRNAs. Currently, the therapeutic potential of antisense miRNAs is being validated in both in vitro and in vivo models. Studies have shown that antisense miRNAs could slow down the progression of cancer while enhancing the action of conventional anticancer drugs. These fin-dings provide hope for future oncologic care as this novel intervention is in the process of clinical translation.
Title: Therapeutic Targeting of Overexpressed MiRNAs in Cancer Progression
Description:
Abstract:
MicroRNAs (miRNAs) are non-coding RNAs involved in the modulation of various bio-logical processes, and their dysregulation is greatly associated with cancer progression as miRNAs can act as either tumour suppressors or oncogenes, depending on their intended target, mechanism of actions, and expression levels.
This review paper aims to shed light on the role of overexpressed miRNAs in cancer progression.
Cancer cells are known to upregulate specific miRNAs to inhibit the expression of genes regulating the cell cycle, such as PTEN, FOXO1, SOX7, caspases, KLF4, TRIM8, and ZBTB4.
Inhibition of these genes promotes cancer development and survival by indu-cing cell growth, migration, and invasion while evading apoptosis, which leads to poor cancer sur-vival rates.
Therefore, the potential of antisense miRNAs in treating cancer is also explored in this review.
Antisense miRNAs are chemically modified oligonucleotides that can reverse the action of overexpressed miRNAs.
Currently, the therapeutic potential of antisense miRNAs is being validated in both in vitro and in vivo models.
Studies have shown that antisense miRNAs could slow down the progression of cancer while enhancing the action of conventional anticancer drugs.
These fin-dings provide hope for future oncologic care as this novel intervention is in the process of clinical translation.
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