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Updated: Aug 16, 2025

Describing a Transcription Factor Dependent Regulation of the MicroRNA Transcriptome
Published on: June 15, 2016
Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy
Yanjun Tian1, Haiqing Liu2, Mengwei Wang3
1Medical Laboratory of Jining Medical University, Jining Medical University, Jining 272067, China.
Abstract:
Signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid-derived 2-like 2 (NRF2, also known as NFE2L2), are two of the most complicated transcription regulators, which participate in a variety of physiological processes. Numerous studies have shown that they are overactivated in multiple types of tumors. Interestingly, STAT3 and NRF2 can also interact with each other to regulate tumor progression. Hence, these two important transcription factors are considered key targets for developing a new class of antitumor drugs. This review summarizes the pivotal roles of the two transcription regulators and their interactions in the tumor microenvironment to identify potential antitumor drug targets and, ultimately, improve patients' health and survival.
Insights
Signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid-derived 2-like 2 (NRF2) are key regulators overactivated in tumors. Their interactions offer promising targets for novel antitumor drug development to improve patient survival.
Area of Science:
- Molecular Biology
- Oncology
- Drug Discovery
Background:
- Signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid-derived 2-like 2 (NRF2) are complex transcription regulators involved in numerous physiological processes.
- Both STAT3 and NRF2 are frequently overactivated in various types of cancer, indicating their significant role in tumorigenesis.
Purpose of the Study:
- To review the critical roles of STAT3 and NRF2 in the tumor microenvironment.
- To explore the interactions between STAT3 and NRF2 in regulating tumor progression.
- To identify potential antitumor drug targets based on these transcription factors and their interplay.
Main Methods:
- Literature review of existing studies on STAT3 and NRF2 in cancer.
- Analysis of the molecular mechanisms underlying STAT3 and NRF2 functions.
- Examination of the crosstalk between STAT3 and NRF2 in the tumor microenvironment.
Main Results:
- STAT3 and NRF2 play pivotal roles in various aspects of tumor progression.
- The interaction between STAT3 and NRF2 influences tumor development and the tumor microenvironment.
- Dysregulation of these transcription factors is a hallmark of many cancers.
Conclusions:
- STAT3 and NRF2 represent crucial targets for the development of novel anticancer therapeutics.
- Targeting the interaction between STAT3 and NRF2 may offer a promising strategy for cancer treatment.
- Further research into these transcription factors could lead to improved patient outcomes and survival rates.
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