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Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
Published on: June 9, 2023
NORAD-Regulated Signaling Pathways in Breast Cancer Progression
Ana Maria Capela1, Carlota Tavares-Marcos1, Hugo F Estima-Arede1
1Department of Medical Sciences, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-193 Aveiro, Portugal.
Abstract:
Long non-coding RNA activated by DNA damage (NORAD) has recently been associated with pathologic mechanisms underlying cancer progression. Due to NORAD's extended range of interacting partners, there has been contradictory data on its oncogenic or tumor suppressor roles in BC. This review will summarize the function of NORAD in different BC subtypes and how NORAD impacts crucial signaling pathways in this pathology. Through the preferential binding to pumilio (PUM) proteins PUM1 and PUM2, NORAD has been shown to be involved in the control of cell cycle, angiogenesis, mitosis, DNA replication and transcription and protein translation. More recently, NORAD has been associated with PUM-independent roles, accomplished by interacting with other ncRNAs, mRNAs and proteins. The intricate network of NORAD-mediated signaling pathways may provide insights into the potential design of novel unexplored strategies to overcome chemotherapy resistance in BC treatment.
Insights
Long non-coding RNA NORAD plays a complex role in breast cancer (BC) progression. Understanding NORAD
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Long non-coding RNA activated by DNA damage (NORAD) is implicated in cancer progression.
- NORAD exhibits contradictory roles as either an oncogene or tumor suppressor in breast cancer (BC).
Purpose of the Study:
- To review NORAD's function across different BC subtypes.
- To elucidate NORAD's impact on critical signaling pathways in BC.
- To explore NORAD's potential in overcoming chemotherapy resistance.
Main Methods:
- Literature review summarizing existing research on NORAD in BC.
- Analysis of NORAD's interactions with PUM proteins (PUM1, PUM2) and other molecules.
- Investigation of NORAD's influence on cellular processes like cell cycle and angiogenesis.
Main Results:
- NORAD's binding to PUM proteins regulates cell cycle, angiogenesis, mitosis, DNA replication, transcription, and protein translation.
- Emerging evidence highlights PUM-independent roles of NORAD through interactions with ncRNAs, mRNAs, and proteins.
- NORAD's complex signaling network offers potential therapeutic targets.
Conclusions:
- NORAD's multifaceted roles in BC necessitate further investigation.
- Targeting NORAD-mediated pathways may offer novel strategies for BC treatment, particularly for overcoming chemotherapy resistance.
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