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Updated: Feb 8, 2026

Quantitation of Intra-peritoneal Ovarian Cancer Metastasis
Published on: July 18, 2016
Cancer-related transcription regulator protein NAC1 forms a protein complex with CARM1 for ovarian cancer progression
Naomi Nakayama1, Gyosuke Sakashita1, Yuko Nariai1
1Department of Biochemistry, Shimane University School of Medicine, Izumo, Japan.
Abstract:
NAC1 is a cancer-related transcription regulator protein that is overexpressed in various carcinomas, including ovarian, cervical, breast, and pancreatic carcinomas. NAC1 knock-down was previously shown to result in the apoptosis of ovarian cancer cell lines and to rescue their sensitivity to chemotherapy, suggesting that NAC1 may be a potential therapeutic target, but protein complex formation of intranuclear NAC1 in ovarian cancer cells remain poorly understood. In this study, analysis of ovarian cancer cell lysates by fast protein liquid chromatography on a sizing column showed that the NAC1 peak corresponded to an apparent molecular mass of 300-500 kDa, which is larger than the estimated molecular mass (58 kDa) of the protein. Liquid chromatography-tandem mass spectrometry analysis identified CARM1 as interacting with NAC1 in the protein complex. Furthermore, tissue microarray analysis revealed a significant correlation between CARM1 and NAC1 expression levels. Ovarian cancer patients expressing high levels of NAC1 and CARM1 exhibited poor prognosis after adjuvant chemotherapy. Collectively, our results demonstrate that high expression levels of NAC1 and its novel binding partner CARM1 may serve as an informative prognostic biomarker for predicting resistance to chemotherapy for ovarian cancer.
Insights
Nuclear Factor NAC1 (NAC1) and CARM1 protein complex formation in ovarian cancer cells is linked to poor prognosis. High NAC1 and CARM1 expression predicts chemotherapy resistance, identifying them as potential prognostic biomarkers.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Nuclear Factor NAC1 (NAC1) is a transcription regulator overexpressed in multiple carcinomas.
- NAC1 overexpression correlates with poor outcomes and chemotherapy resistance in ovarian cancer.
- The protein complex formation of intranuclear NAC1 in ovarian cancer cells is not well understood.
Purpose of the Study:
- To investigate the protein complex formation of NAC1 in ovarian cancer cells.
- To identify NAC1 interacting partners.
- To evaluate the prognostic significance of NAC1 and its interacting partners in ovarian cancer.
Main Methods:
- Ovarian cancer cell lysates were analyzed using Fast Protein Liquid Chromatography (FPLC).
- Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to identify interacting proteins.
- Tissue microarray analysis was performed to correlate protein expression with patient prognosis.
Main Results:
- NAC1 was found to exist in a larger protein complex (300-500 kDa) than its individual molecular mass (58 kDa).
- CARM1 was identified as a novel binding partner of NAC1 within this complex.
- High expression levels of both NAC1 and CARM1 significantly correlated with poor prognosis in ovarian cancer patients receiving chemotherapy.
Conclusions:
- NAC1 forms a larger protein complex with CARM1 in ovarian cancer cells.
- The combined high expression of NAC1 and CARM1 serves as a prognostic biomarker for chemotherapy resistance in ovarian cancer.
- Targeting NAC1 and CARM1 may offer therapeutic strategies for overcoming chemotherapy resistance.
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