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MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR qPCR
Published on: May 16, 2012
Exploring the Potential of MicroRNA Let-7c as a Therapeutic for Prostate Cancer
Eoghan J Mulholland1, William P Green2, Niamh E Buckley2
1Gastrointestinal Stem Cell Biology Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
Abstract:
Prostate cancer (PCa) is one of the leading causes of mortality worldwide and often presents with aberrant microRNA (miRNA) expression. Identifying and understanding the unique expression profiles could aid in the detection and treatment of this disease. This review aims to identify miRNAs as potential therapeutic targets for PCa. Three bio-informatic searches were conducted to identify miRNAs that are reportedly implicated in the pathogenesis of PCa. Only hsa-Lethal-7 (let-7c), recognized for its role in PCa pathogenesis, was common to all three databases. Three further database searches were conducted to identify known targets of hsa-let-7c. Four targets were identified, HMGA2, c-Myc (MYC), TRAIL, and CASP3. An extensive review of the literature was undertaken to assess the role of hsa-let-7c in the progression of other malignancies and to evaluate its potential as a therapeutic target for PCa. The heterogeneous nature of cancer makes it logical to develop mechanisms by which the treatment of malignancies is tailored to an individual, harnessing specific knowledge of the underlying biology of the disease. Resetting cellular miRNA levels is an exciting prospect that will allow this ambition to be realized.
Insights
MicroRNAs (miRNAs) show altered expression in prostate cancer (PCa). This review highlights hsa-Lethal-7 (let-7c) as a potential therapeutic target for PCa due to its role in disease pathogenesis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Prostate cancer (PCa) is a major global health concern.
- Aberrant microRNA (miRNA) expression is frequently observed in PCa.
- Understanding miRNA profiles is crucial for PCa detection and treatment.
Purpose of the Study:
- To identify specific microRNAs (miRNAs) as potential therapeutic targets for prostate cancer (PCa).
- To investigate the role of hsa-Lethal-7 (let-7c) in PCa pathogenesis.
- To evaluate hsa-let-7c as a therapeutic strategy for PCa.
Main Methods:
- Conducted three bioinformatic searches to identify miRNAs implicated in PCa pathogenesis.
- Performed three database searches to identify known targets of hsa-let-7c.
- Undertook an extensive literature review on hsa-let-7c in other malignancies and its therapeutic potential.
Main Results:
- hsa-Lethal-7 (let-7c) was the only miRNA consistently identified across all three bioinformatic searches for PCa pathogenesis.
- Identified four key targets of hsa-let-7c: HMGA2, c-Myc (MYC), TRAIL, and CASP3.
- Assessed the role of hsa-let-7c in various cancers, supporting its potential therapeutic relevance.
Conclusions:
- hsa-let-7c is a promising candidate for targeted therapy in prostate cancer.
- Modulating miRNA levels, such as hsa-let-7c, offers a novel approach for personalized cancer treatment.
- Resetting cellular miRNA levels presents an exciting prospect for realizing tailored cancer therapies.
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