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An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
Therapeutic Targeting of Overexpressed MiRNAs in Cancer Progression
Sau Har Lee1,2, Brianna Brianna3
1Faculty of Health and Medical Sciences, School of Biosciences, Taylor's University, Subang Jaya, Selangor, Malaysia.
Abstract:
MicroRNAs (miRNAs) are non-coding RNAs involved in the modulation of various biological 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 inducing cell growth, migration, and invasion while evading apoptosis, which leads to poor cancer survival 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 findings provide hope for future oncologic care as this novel intervention is in the process of clinical translation.
Insights
Overexpressed microRNAs (miRNAs) drive cancer progression by inhibiting tumor suppressor genes. Antisense miRNAs offer a promising therapeutic strategy to reverse this effect and improve cancer treatment outcomes.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression, with dysregulation implicated in cancer development.
- Aberrant miRNA expression can promote tumorigenesis by targeting tumor suppressor genes, impacting cell cycle control and apoptosis.
- Overexpressed miRNAs in cancer cells often inhibit critical genes like PTEN, FOXO1, and caspases, fostering tumor growth and survival.
Approach:
- This review examines the role of overexpressed microRNAs in promoting cancer progression.
- It explores how cancer cells utilize specific miRNAs to suppress tumor-suppressing genes, facilitating uncontrolled cell proliferation and metastasis.
- The therapeutic potential of antisense microRNAs (oligonucleotides) designed to counteract oncogenic miRNA activity is investigated.
Key Points:
- Upregulation of specific miRNAs in cancer inhibits tumor suppressor genes (e.g., PTEN, FOXO1, caspases), promoting cell growth, migration, and invasion.
- This inhibition leads to evasion of apoptosis and contributes to poor patient survival rates.
- Antisense microRNAs can reverse the effects of overexpressed oncogenic miRNAs.
Conclusions:
- Antisense microRNAs represent a novel therapeutic approach for cancer treatment, with ongoing validation in preclinical models.
- These agents show potential in slowing cancer progression and potentiating conventional chemotherapy.
- The clinical translation of antisense microRNA therapy offers hope for improved oncologic care.
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