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Updated: Nov 16, 2025

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues
Published on: December 5, 2016
DNA N6-Methyladenine (6mA) Modification Regulates Drug Resistance in Triple Negative Breast Cancer
Xianneng Sheng1, Jinqiu Wang1, Yu Guo1
1Department of Breast and Thyroid Surgery, Ningbo First Hospital, Ningbo, China.
Abstract:
Triple negative breast cancer (TNBC) is a subtype of breast cancer with strong aggressiveness and poor clinical treatment effect, accounting for about 10-20% of breast cancer cases. N(6)-methyldeoxyadenosine (6mA) is the most conservative DNA modification in prokaryotes and eukaryotes. It is widely found in bacteria and has such functions as DNA mismatch repair, chromosome separation and virulence regulation. We determined that 6mA was modified in TNBC cell line MDA-MB-231 and the TNBC tissue. Meanwhile, compared with normal tissues, the expression level of 6mA and its methylase N6AMT1 was significantly decreased in TNBC tissue. MDA-MB-231cells were cultured with 8μM Olaparib for 2 months to construct drug-resistant cell line 231-RO. It was found that the level of 6mA also increased significantly, and the expression of N6AMT1 or ALKBH1 could effectively influence the drug resistance. Subsequently, we found that LINP1 was highly expressed in 231-RO, which was involved in DNA repair, and the expression of LINP1 could be positively regulated by 6mA modification. LINP1 expression level is directly related to TNBC drug resistance. The above results indicate that 6mA may be a new biological marker of TNBC. Meanwhile, 6mA modification may be involved in the regulation of Olaparib resistance.
Insights
N(6)-methyldeoxyadenosine (6mA) DNA modification is decreased in triple-negative breast cancer (TNBC) but increases with Olaparib resistance. This suggests 6mA may serve as a biomarker for TNBC and influence treatment resistance.
Area of Science:
- Epigenetics
- Molecular Biology
- Oncology
Background:
- Triple-negative breast cancer (TNBC) presents significant clinical challenges due to its aggressiveness and limited treatment options.
- N(6)-methyldeoxyadenosine (6mA) is a conserved DNA modification with known roles in various cellular processes.
Purpose of the Study:
- To investigate the role of 6mA DNA modification in TNBC.
- To explore the relationship between 6mA and Olaparib resistance in TNBC.
Main Methods:
- Analysis of 6mA levels in TNBC cell lines and tissues.
- Construction of an Olaparib-resistant TNBC cell line (231-RO).
- Assessment of 6mA, N6AMT1, ALKBH1, and LINP1 expression in relation to drug resistance.
Main Results:
- 6mA and its methylase N6AMT1 expression were significantly decreased in TNBC tissues compared to normal tissues.
- 6mA levels increased in Olaparib-resistant TNBC cells.
- LINP1, a DNA repair gene, was highly expressed in resistant cells and positively regulated by 6mA, correlating with drug resistance.
Conclusions:
- 6mA modification may serve as a novel biomarker for TNBC.
- 6mA and LINP1 are implicated in the regulation of Olaparib resistance in TNBC.
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