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- Genta NAGAE
Researcher's Profile

- Project Associate Professor
- Genta NAGAE
- Genome Science & Medicine
- Genome Science & Medicine
- nagaeg-tky
umin.ac.jp
- Tel
- 03-5452-5235
- FAX
- 03-5452-5355
Biography
March 2000 | Medical School, The University of Tokyo (UTokyo) |
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May 2000 | Junior Resident, The University of Tokyo Hospital |
June 2001 | Junior Resident, NTT Medical Center Tokyo |
June 2002 | Senior Resident, Jichi Medical University Hospital |
March 2008 | Medical Doctors Graduate, UTokyo |
April 2008 | Project Researcher, RCAST, UTokyo |
October 2010 | Research Associate, RCAST, UTokyo |
October 2015 | Project Lecturer, RCAST, UTokyo |
July 2017 | Lecturer, RCAST, UTokyo |
April 2021 | Project Associate Professor, RCAST, UTokyo |
Research Interests
The human body is composed of hundreds of diverse cell types and their distinct patterns of gene expression are tightly regulated by epigenetic modifications. Disruption of these regulatory systems is frequently observed in human diseases. Notably, epigenomic disruptions as well as genomic aberrations are deeply associated with cancer development. We would like to approach the mechanism of why epigenomic networks are dysregulated and they may result in disease, for basic research and translational medicine.
1. Profiling the epigenomic information of cancer cells
We are analyzing variable patterns of cancer methylome and studying the aberrant methylations that are associated with biological behaviors of cancer.
2. Understanding how to alter the dynamics of cytosine modification
Epigenetic modifiers are often dysregulated in human cancer. We would like to uncover the landscape of dysregulated networks in cancer cells.
3. Performing epigenetic analysis from the limited number of cells
We are trying to profile the covalent modifications of cytosine (WGBS, TAB-seq) and of histone tails (ChIP-seq), chromatin accessibility and chromatin interactions to elucidate epigenetic heterogeneity during cellular differentiation and cancer development.
1. Profiling the epigenomic information of cancer cells
We are analyzing variable patterns of cancer methylome and studying the aberrant methylations that are associated with biological behaviors of cancer.
2. Understanding how to alter the dynamics of cytosine modification
Epigenetic modifiers are often dysregulated in human cancer. We would like to uncover the landscape of dysregulated networks in cancer cells.
3. Performing epigenetic analysis from the limited number of cells
We are trying to profile the covalent modifications of cytosine (WGBS, TAB-seq) and of histone tails (ChIP-seq), chromatin accessibility and chromatin interactions to elucidate epigenetic heterogeneity during cellular differentiation and cancer development.
Keywords
Epigenetics, DNA methylation, Cancer, Translational research