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Updated: Jun 17, 2026

DNA Vector-based RNA Interference to Study Gene Function in Cancer
Published on: June 4, 2012
Yin yang 1 expression in human tumors
Apostolos Zaravinos1, Demetrios A Spandidos
1Department of Clinical Virology, School of Medicine, University of Crete, Heraklio, Greece. azaravinos@gmail.com
Abstract:
The Yin Yang 1 (YY1) transcription factor has been identified to target a plethora of potential target genes, the products of which are important for proliferation and differentiation. The mechanisms of YY1 action are related to its ability to initiate, activate or repress transcription depending on the context in which it binds. This article sheds a light on the role that YY1 plays in different human types of cancer, through the context of its expression levels. Moreover, we concentrate on the most relevant studies that have focused on YY1 regulation. we performed computational analysis on thirty-six publicly available Gene expression Omnibus (GeO) datasets, to further understand whether differences in YY1 transcript levels occur in different cancer types when compared with relative normal tissue, benign tumor or its metastatic counterpart. Our results suggest a dual role of YY1 in cancer development, either through overexpression or under-expression, depending on the tumor type.
Insights
Yin Yang 1 (YY1) transcription factor shows a dual role in human cancers. Its expression levels, whether high or low, influence cancer development differently across various tumor types.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Yin Yang 1 (YY1) is a transcription factor regulating genes crucial for cell proliferation and differentiation.
- YY1's function can activate or repress transcription based on its binding context.
- Dysregulation of YY1 is implicated in various human diseases, including cancer.
Purpose of the Study:
- To investigate the role of YY1 expression levels in different human cancer types.
- To analyze the association between YY1 transcript levels and cancer development, progression, and metastasis.
- To consolidate existing knowledge on YY1 regulation in the context of cancer.
Main Methods:
- Computational analysis of thirty-six publicly available Gene Expression Omnibus (GEO) datasets.
- Comparison of YY1 transcript levels in various cancer types versus normal tissues, benign tumors, and metastatic counterparts.
- Review of relevant literature on YY1 regulation and its role in cancer.
Main Results:
- YY1 transcript levels exhibit significant differences across various human cancer types when compared to normal tissues.
- Overexpression of YY1 is observed in some cancers, while underexpression is noted in others.
- The study identified a context-dependent, dual role for YY1 in cancer development.
Conclusions:
- YY1 plays a significant, albeit complex, role in human tumorigenesis.
- Altered YY1 expression (over or under) is a hallmark of specific cancer types.
- Further research into YY1's regulatory mechanisms is warranted for therapeutic strategies.
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