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Updated: Jan 3, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Long noncoding RNA LINC00899 suppresses breast cancer progression by inhibiting miR-425
Wenying Zhou1, Jiao Gong1, Yaqiong Chen1
1Department of Laboratory Medicine, Key Laboratory of Liver Disease of Guangdong Province, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, P.R. China.
Abstract:
Long non-coding RNAs (lncRNAs) have emerged as important regulators in cancer, including breast cancer. The precise expression pattern of long noncoding RNA 00899 (LINC00899) in breast cancer and its mechanisms of action have not been reported. Here, we found that LINC00899 is downregulated in breast cancer tissues and cell lines. Kaplan-Meier analysis showed that elevated LINC00899 expression is closely associated with better relapse-free survival (RFS) in breast cancer, including the basal, luminal A or luminal B breast cancer subtypes. Gene Ontology terms and Kyoto Encyclopedia of Genes and Genomes pathway analysis suggested that LINC00899 is closely related to several cancer associated processes, including tight junction- and metabolism-associated pathways. Functional assays indicated that LINC00899 overexpression suppresses proliferation, migration and invasion of breast cancer cells in vitro. Moreover, LINC00899 was found to competitively bind miR-425, thereby functioning as a tumor suppressor by enhancing DICER1. Overexpression of miR-425 attenuated the LINC00899-induced inhibition of breast cancer cell proliferation and invasion. These findings highlight the important role of the LINC00899-miR-425-DICER1 axis in breast cancer cell proliferation and invasion, and could potentially lead to new lncRNA-based diagnostics or therapeutics for breast cancer.
Insights
Long non-coding RNA 00899 (LINC00899) is downregulated in breast cancer and linked to better survival. Its overexpression suppresses tumor growth by regulating the LINC00899-miR-425-DICER1 axis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) are key regulators in cancer development.
- The role of LINC00899 in breast cancer remains largely uncharacterized.
Purpose of the Study:
- To investigate the expression pattern and functional role of LINC00899 in breast cancer.
- To elucidate the underlying molecular mechanisms of LINC00899 action in breast cancer.
Main Methods:
- Analysis of LINC00899 expression in breast cancer tissues and cell lines.
- Kaplan-Meier survival analysis.
- Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis.
- In vitro functional assays (proliferation, migration, invasion).
- Mechanism studies involving miR-425 and DICER1.
Main Results:
- LINC00899 is significantly downregulated in breast cancer.
- Lower LINC00899 expression correlates with poorer relapse-free survival across breast cancer subtypes.
- LINC00899 overexpression inhibits breast cancer cell proliferation, migration, and invasion.
- LINC00899 acts as a tumor suppressor by sponging miR-425, leading to enhanced DICER1 expression.
Conclusions:
- The LINC00899-miR-425-DICER1 axis plays a critical role in regulating breast cancer cell proliferation and invasion.
- LINC00899 functions as a tumor suppressor in breast cancer.
- LINC00899 holds potential as a diagnostic biomarker or therapeutic target for breast cancer.
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