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Updated: Nov 30, 2025

An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
Mitotically associated long non-coding RNA is a tumor promoter in anaplastic thyroid cancer
Nai-Si Huang1,2, Bo-Wen Lei1,2, Li-Cheng Tan1,2
1Department of Head and Neck Surgery, Fudan University, Shanghai Cancer Center, Shanghai, China.
Background:
Patients with anaplastic thyroid cancer (ATC), which is among the deadliest of all cancers, often have a poor response to traditional therapies. Currently, the role of long non-coding RNAs (lncRNAs) in ATC carcinogenesis is unclear. In this study, we analyzed the lncRNA expression profile of ATC with the aim of identifying potential molecular targets for treatment of the disease.
Methods:
Whole transcriptome sequencing of three ATC and two normal thyroid (NT) samples was performed, and the lncRNA expression profile of ATC was analyzed. Original data as well as datasets deposited in the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) were used for clinical validation. Cell proliferation, Transwell, and apoptosis assays were performed using ATC cell lines. Gene Ontology (GO) and gene set enrichment analyses (GSEA) were performed to determine the dysregulated pathways.
Results:
Whole transcriptome sequencing revealed 182 lncRNAs to be differentially expressed in ATC. One of the lncRNAs, mitotically associated long non-coding RNA (MANCR; LINC00704), was significantly overexpressed in ATC cell lines and patient samples compared with NT and papillary thyroid cancer (PTC). MANCR depletion in ATC cells significantly inhibited cancer cell proliferation and invasion, and induced apoptosis. By further analyzing the transcriptome data, we identified 451 genes co-expressed with MANCR. GO and GSEA showed that the top dysregulated pathways were related to mitosis and cell cycle.
Conclusions:
MANCR is a tumor promoter in ATC, and its role in carcinogenesis is possibly associated with cell cycle regulation. Because MANCR expression is minimal in most normal tissues, it may serve as a potential target in the future treatment of ATC.
Insights
Mitotically associated long non-coding RNA (MANCR) promotes anaplastic thyroid cancer (ATC) growth and invasion. MANCR may be a potential therapeutic target for treating this deadly cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Anaplastic thyroid cancer (ATC) is a deadly malignancy with poor therapeutic response.
- The role of long non-coding RNAs (lncRNAs) in ATC development is not well understood.
- Identifying novel molecular targets is crucial for effective ATC treatment.
Purpose of the Study:
- To investigate the lncRNA expression profile in ATC.
- To identify potential lncRNAs as therapeutic targets for ATC.
- To elucidate the function of dysregulated lncRNAs in ATC carcinogenesis.
Main Methods:
- Whole transcriptome sequencing of ATC and normal thyroid samples.
- Analysis of public datasets (GEO, TCGA) for clinical validation.
- In vitro assays (proliferation, Transwell, apoptosis) in ATC cell lines.
- Gene Ontology (GO) and gene set enrichment analysis (GSEA) for pathway identification.
Main Results:
- 182 differentially expressed lncRNAs identified in ATC.
- Mitotically associated long non-coding RNA (MANCR) was significantly overexpressed in ATC.
- MANCR depletion inhibited ATC cell proliferation and invasion, and induced apoptosis.
- MANCR co-expressed genes were primarily involved in mitosis and cell cycle regulation.
Conclusions:
- MANCR acts as a tumor promoter in ATC, potentially through cell cycle regulation.
- MANCR's minimal expression in normal tissues suggests its potential as a targeted therapy for ATC.
- Further research into MANCR's role could lead to novel treatment strategies for anaplastic thyroid cancer.
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