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Updated: Feb 14, 2026

Clinicopathological Analysis of miRNA Expression in Breast Cancer Tissues by Using miRNA In Situ Hybridization
Published on: June 7, 2016
Expression analysis of AFAP1-AS1 and AFAP1 in breast cancer
Ali Dianatpour1, Sepideh Faramarzi1, Lobat Geranpayeh2
1Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
Long non-coding RNAs (lncRNA) constitute a significant percentage of RNAs with no translation to proteins. Their participation in fundamental aspects of cell physiology as well as their dysregulation in a number of pathologic conditions such as cancer have been documented. Among lncRNAs is actin filament associated protein 1 antisense RNA1 (AFAP1-AS1) whose elevated expression levels have been demonstrated in different cancers. In the in the present study we evaluated expression levels of AFAP1-AS1 and its antisense protein coding gene AFAP1 in breast cancer samples compare with adjacent non-cancerous tissues (ANCTs) as well as breast cancer cell lines with special focus on the assessment of the association between their transcript levels and patients' clinicopathological data. AFAP1-AS1 has shown significant up-regulation in both MDA-MB-231 and MCF-7 compared with control sample. AFAP1-AS1 has been shown to be expressed in all of tumor tissues but 76% (39 out of 51) ANCTs. AFAP1 expression was not significantly different between tumor samples and ANCTs. AFAP1-AS1 has been demonstrated to be significantly up-regulated in tumor tissues compared with ANCTs (fold change = 4.65, P= 0.028). No significant correlation has been detected between the levels of these two transcripts in tumor tissues (R=2 0.081) or ANCTs (R=2 0.115). No significant associations have been found between expression levels of these genes and patients' characteristics. However, both genes were significantly down-regulated in Ki-67 negative tumor samples. The observed up-regulation of AFAP1-AS1 in tumor samples compared with ANCTs implies its involvement in breast cancer pathogenesis and potentiates it as a biomarker or therapeutic target.
Insights
Long non-coding RNA AFAP1-AS1 is significantly upregulated in breast cancer tissues, suggesting its role in cancer development. This finding highlights AFAP1-AS1 as a potential biomarker and therapeutic target for breast cancer.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) are key regulators of cellular processes.
- Dysregulation of lncRNAs is implicated in various pathologies, including cancer.
- Actin filament associated protein 1 antisense RNA1 (AFAP1-AS1) is a lncRNA found at elevated levels in several cancers.
Purpose of the Study:
- To evaluate AFAP1-AS1 and AFAP1 expression in breast cancer.
- To compare transcript levels in tumor tissues versus adjacent non-cancerous tissues (ANCTs).
- To assess the association between transcript levels and clinicopathological data.
Main Methods:
- Quantitative real-time PCR was used to measure AFAP1-AS1 and AFAP1 expression.
- Expression levels were analyzed in breast cancer tissues, ANCTs, and cell lines (MDA-MB-231, MCF-7).
- Statistical analyses were performed to correlate expression with clinicopathological features.
Main Results:
- AFAP1-AS1 was significantly upregulated in breast tumor tissues compared to ANCTs (fold change = 4.65, P= 0.028).
- AFAP1-AS1 showed significant upregulation in MDA-MB-231 and MCF-7 cell lines.
- AFAP1 expression did not differ significantly between tumor and ANCTs.
- No significant correlation was found between AFAP1-AS1/AFAP1 levels and patient characteristics.
- Both genes were downregulated in Ki-67 negative tumor samples.
Conclusions:
- AFAP1-AS1 is significantly upregulated in breast cancer, indicating its involvement in pathogenesis.
- AFAP1-AS1 presents potential as a diagnostic biomarker and therapeutic target for breast cancer.
- Further research is warranted to elucidate the precise role of AFAP1-AS1 in breast cancer.
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