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Updated: Sep 17, 2025

Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
Published on: June 9, 2023
RLIG1 promotes triple-negative breast cancer proliferation by activating mTORC1 signal pathway by interacting with
Qingqing Wang1, Fengxia Chen2, Bo Pei3
1Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China; Hubei Key Laboratory of Tumor Biological Behaviors, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, China; Hubei Clinical Cancer Study Center, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, China.
Background:
The prognosis of triple-negative breast cancer (TNBC) is notably unfavorable, necessitating the development of novel treatments to enhance therapeutic outcomes. The underlying mechanisms contributing to the pathogenesis of TNBC remain incompletely understood. RNA 5'-phosphate and 3'-OH ligase 1 (RLIG1) was found to be the first RNA ligase in humans and may be related to cancer development, but no reports have been reported. We observe RLIG1 elevated expression levels in TNBC tissues compared to adjacent non-cancerous tissues, with high RLIG1 expression correlating with reduced overall survival in TNBC patients.
Methods:
We investigated RLIG1 in TNBC using bioinformatics tools, cell counting kit-8 (CCK-8), 5-ethynyl-2'-deoxyuridine (EdU), colony formation, flow cytometry, and western blotting. Mechanistic insights were gained via mass spectrometry, co-immunoprecipitation, and immunofluorescence.
Results:
Here, we found that interfering with RLIG1 can effectively hinder tumor cell cycle progression and proliferation in vitro, as well as inhibit tumor growth in vivo. Mechanistically, RLIG1 was identified as an oncogene that stimulates the mTORC1 signaling pathway in TNBC cells. Furthermore, the interaction between RLIG1 and ERK was confirmed, with RLIG1 promoting cell cycle transition and proliferation through mediating ERK phosphorylation.
Conclusions:
Our research offers novel insights into the biological role of RLIG1, indicating its potential as a therapeutic target for TNBC.
Insights
RNA 5'-phosphate and 3'-OH ligase 1 (RLIG1) is elevated in triple-negative breast cancer (TNBC), promoting tumor growth. Inhibiting RLIG1 hinders cancer progression, suggesting it as a potential therapeutic target for TNBC.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Triple-negative breast cancer (TNBC) has a poor prognosis, and its pathogenesis is not fully understood.
- RNA 5'-phosphate and 3'-OH ligase 1 (RLIG1) expression is elevated in TNBC tissues and linked to reduced patient survival.
Purpose of the Study:
- To investigate the role of RLIG1 in TNBC pathogenesis.
- To explore RLIG1 as a potential therapeutic target for TNBC.
Main Methods:
- Bioinformatics analysis, cell counting kit-8 (CCK-8), 5-ethynyl-2'-deoxyuridine (EdU) assays, colony formation, flow cytometry, and western blotting were used.
- Mass spectrometry, co-immunoprecipitation, and immunofluorescence elucidated mechanistic insights.
Main Results:
- RLIG1 inhibition impaired tumor cell proliferation and growth in vitro and in vivo.
- RLIG1 acts as an oncogene, activating the mTORC1 signaling pathway and promoting ERK phosphorylation in TNBC cells.
- RLIG1 interacts with ERK, driving cell cycle transition and proliferation.
Conclusions:
- RLIG1 plays a significant role in TNBC progression.
- RLIG1 represents a promising therapeutic target for triple-negative breast cancer.
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