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Circular RNA MALAT1 as a potential target for antimetastatic therapy
1Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 12 R. Weigla Street, 53-114, Wroclaw, Poland.
Abstract:
Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) is a long non-coding RNA (lncRNA) located in the nucleus that is involved in the regulation of gene expression and alternative splicing of gene transcription products. MALAT1 has also been implicated in processes leading to metastasis in various types of cancer. On the other hand, during the epithelial-to-mesenchymal transition (EMT) process of cancer cells, which allows the invasion and migration of cancer cells outside the primary tumor, increases in the levels of the Quaking RNA-binding protein (QKI) were found, which also led to the formation of circular RNA molecules (circRNA), including MALAT1-derived circRNAs. It was also found that at least some MALAT1-derived circRNAs could support processes leading to the spread of cancer cells outside the primary tumor. Due to the unique back-splicing junction in a given circRNA, it is possible to therapeutically target specific circRNA molecules in cancer cells while protecting linear RNAs in normal cells. Without questioning the aberrant involvement of lncRNA MALAT1 in promoting cancer cell migration and invasion, it appears that MALAT1-derived circRNAs, especially the circRNA known as circ-MALAT1 or circ2082 (hsa_circ_0002082), among other circRNAs, may be considered for further study as potential targets for anti-metastatic therapy.
Insights
Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) derived circular RNAs (circRNAs) may promote cancer metastasis. Targeting these specific circRNAs offers a potential anti-metastatic therapy strategy.
Area of Science:
- Molecular Biology
- Cancer Research
- RNA Biology
Background:
- Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) is a long non-coding RNA (lncRNA) involved in gene regulation and cancer metastasis.
- Increased Quaking RNA-binding protein (QKI) during epithelial-to-mesenchymal transition (EMT) promotes circular RNA (circRNA) formation, including MALAT1-derived circRNAs.
Purpose of the Study:
- To investigate the role of MALAT1-derived circRNAs in cancer metastasis.
- To explore the potential of targeting MALAT1-derived circRNAs as an anti-metastatic therapeutic strategy.
Main Methods:
- Analysis of MALAT1 and its derived circRNAs during cancer cell EMT.
- Investigating the function of MALAT1-derived circRNAs in cancer cell migration and invasion.
Main Results:
- MALAT1-derived circRNAs, such as circ-MALAT1 (hsa_circ_0002082), were found to support cancer cell spread.
- The unique back-splicing junction of circRNAs allows for targeted therapeutic intervention.
Conclusions:
- MALAT1-derived circRNAs are implicated in promoting cancer metastasis.
- Specific MALAT1-derived circRNAs represent promising targets for novel anti-metastatic therapies.
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