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Published on: August 2, 2024
RDM1 plays an oncogenic role in human ovarian carcinoma cells
Lu Tong1,2, Wenjiao Cao1, Jun Sheng3
1International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, The China Welfare Institute, Shanghai, China.
Abstract:
Ovarian cancer is one of the deadliest gynecological cancer, with a low overall 5-year survival rate. RDM1, RAD52 motif-containing protein 1, is sensitive to cisplatin, a common chemotherapy drug and it has an important role inDNA damage repair pathway. Until now, the effect of RDM1 in ovarian cancer is undiscovered. Here, clinical data shows that the tumour tissues of ovarian carcinoma patients with higher mRNA and protein expression of RDM1. Knockdown of RDM1 in ovarian carcinoma cells reduces cell proliferation and promotes apoptosis, consistent with the role RDM1 in the overexpression experiments. The research of xenograft mouse model shows stable knockdown of RDM1 significantly inhibits ovarian cancer tumour growth. These in vitro and in vivo results conclude that RDM1 plays an oncogenic role in human ovarian carcinoma. Interestingly, p53/RAD51/RAD52 signalling pathway can be regulated by RDM1, and the negative regulation of p53 by RDM1 may be one of major mechanisms for RDM1 to accomplish its oncogenic functions in ovarian carcinoma. Therefore, RDM1 may be a new target for the treatment of ovarian carcinoma.
Insights
RAD52 motif-containing protein 1 (RDM1) promotes ovarian cancer growth and may be a new therapeutic target. Silencing RDM1 inhibits tumor progression and enhances apoptosis in ovarian cancer models.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Ovarian cancer has a low 5-year survival rate, necessitating new therapeutic strategies.
- RAD52 motif-containing protein 1 (RDM1) is involved in DNA damage repair and its role in ovarian cancer is unknown.
- RDM1 is sensitive to cisplatin, a common chemotherapy agent.
Purpose of the Study:
- To investigate the role of RDM1 in the development and progression of ovarian cancer.
- To explore RDM1 as a potential therapeutic target for ovarian carcinoma.
Main Methods:
- Analysis of RDM1 mRNA and protein expression in clinical ovarian carcinoma tissues.
- In vitro studies involving RDM1 knockdown in ovarian carcinoma cell lines to assess proliferation and apoptosis.
- In vivo studies using a xenograft mouse model to evaluate the effect of RDM1 knockdown on tumor growth.
Main Results:
- RDM1 expression is upregulated in ovarian carcinoma tissues.
- RDM1 knockdown reduces ovarian carcinoma cell proliferation and induces apoptosis in vitro.
- Stable knockdown of RDM1 significantly inhibits ovarian cancer tumor growth in vivo.
- RDM1 regulates the p53/RAD51/RAD52 signaling pathway, potentially by negatively regulating p53.
Conclusions:
- RDM1 plays an oncogenic role in human ovarian carcinoma.
- RDM1 may serve as a novel therapeutic target for ovarian cancer treatment.
- RDM1's oncogenic function may be mediated through the regulation of the p53/RAD51/RAD52 pathway.
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