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Updated: Feb 22, 2026

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Published on: August 23, 2019
RDM1 gene overexpression represents a therapeutic target in papillary thyroid carcinoma
Wei Li1, Qing Huang2, Danyang Sun3
1Department of Nuclear MedicineTianjin Medical University General Hospital, Tianjin, People's Republic of China liwei01@tmu.edu.cn.
Abstract:
RAD52 motif containing 1 (RDM1) encodes the RAD52 protein involved in DNA double-strand break repair and recombination events. However, the importance of RDM1 in papillary thyroid carcinoma (PTC) is largely unknown. In the present study, we examined the role of RDM1 in thyroid cancer. The RDM1 expression in PTC patients was examined using immunohistochemistry. The expression levels of RDM1 mRNA in thyroid cancer cells were measured by quantitative real-time PCR (qRT-PCR). Lentivirus-mediated small interfering RNAs (siRNAs) were used to knock down the RDM1 expression in the K1 and TPC1 cells. Then, changes in the RDM1 target gene expression were determined by qRT-PCR and Western blot. Cell proliferation was examined by a high content screening assay. Cell cycle distribution and apoptosis were detected by flow cytometric analysis and MTT analysis. We showed that the RDM1 expression was higher in PTC tissue compared to pericarcinous tissue. RDM1 mRNA was found to be expressed by qRT-PCR. Using a lentivirus-based RNA interference (RNAi) approach, the RDM1 expression was significantly inhibited. The inhibition of RDM1 expression by RNAi significantly impaired cell proliferation, increased apoptosis and arrested cells in the G2/M phase. These data showed that RDM1 was highly expressed in PTC tissue and thyroid cancer cell lines. Moreover, RDM1 may play an important role in cell proliferation, cell cycle distribution and apoptosis of human PTC cells.
Insights
RAD52 motif containing 1 (RDM1) is highly expressed in papillary thyroid carcinoma (PTC). Inhibiting RDM1 impairs cell proliferation, increases apoptosis, and arrests the cell cycle in PTC, suggesting its role in thyroid cancer progression.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- RAD52 motif containing 1 (RDM1) encodes a protein crucial for DNA repair and recombination.
- The specific role of RDM1 in papillary thyroid carcinoma (PTC) remains largely uninvestigated.
- Understanding RDM1's function in PTC is vital for potential therapeutic strategies.
Purpose of the Study:
- To investigate the expression and functional significance of RDM1 in papillary thyroid carcinoma.
- To determine the impact of RDM1 knockdown on PTC cell behavior, including proliferation, cell cycle, and apoptosis.
Main Methods:
- Immunohistochemistry and quantitative real-time PCR (qRT-PCR) were used to assess RDM1 expression in PTC tissues and cell lines.
- Lentivirus-mediated small interfering RNAs (siRNAs) were employed to achieve RDM1 knockdown in K1 and TPC1 cells.
- Cell proliferation, cell cycle distribution, and apoptosis were analyzed using high-content screening, flow cytometry, and MTT assays.
Main Results:
- RDM1 expression was significantly elevated in PTC tissues compared to adjacent non-cancerous tissues.
- RDM1 mRNA was detected in thyroid cancer cell lines.
- RDM1 knockdown led to impaired cell proliferation, increased apoptosis, and G2/M phase cell cycle arrest.
Conclusions:
- RDM1 is highly expressed in papillary thyroid carcinoma and its cell lines.
- RDM1 plays a significant role in regulating cell proliferation, cell cycle progression, and apoptosis in human PTC.
- Targeting RDM1 may represent a potential therapeutic avenue for papillary thyroid carcinoma.
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