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S T Lee

Researcher at Agency for Science, Technology and Research

Publications -  22
Citations -  1235

S T Lee is an academic researcher from Agency for Science, Technology and Research. The author has contributed to research in topics: Cancer & Methyltestosterone. The author has an hindex of 14, co-authored 22 publications receiving 1087 citations. Previous affiliations of S T Lee include Singapore General Hospital & Genome Institute of Singapore.

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Context-specific regulation of NF-κB target gene expression by EZH2 in breast cancers.

TL;DR: This work uncovers an unexpected role of EZH2 in conferring the constitutive activation of NF-κB target gene expression in ER-negative basal-like breast cancer cells and functions as a double-facet molecule in breast cancers.
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FOXQ1 Regulates Epithelial-Mesenchymal Transition in Human Cancers

TL;DR: RNAi-mediated suppression of FOXQ1 expression in highly invasive human breast cancer cells reversed EMT, reduced invasive ability, and alleviated other aggressive cancer phenotypes manifested in 3-dimensional Matrigel (BD Biosciences) culture.
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PDK1 Signaling Toward PLK1–MYC Activation Confers Oncogenic Transformation, Tumor-Initiating Cell Activation, and Resistance to mTOR-Targeted Therapy

TL;DR: The findings identify a novel pathway in human cancer and CSC activation and provide a therapeutic strategy for targeting MYC-associated tumorigenesis and therapeutic resistance, and targeted inhibition of PDK1/PLK1 is robust in targeting MyC dependency in cancer cells.
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Blood Concentrations of Lead, Cadmium, Mercury, Zinc, and Copper and Human Semen Parameters

TL;DR: Significant correlations were observed between blood cadmium levels and volume of semen, midpiece defects, and immature forms of spermatozoa, which may have an effect on spermatogenesis.
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Polycomb protein EZH2 regulates cancer cell fate decision in response to DNA damage.

TL;DR: It is shown that EZH2 is an important determinant of cell fate decision in response to genotoxic stress and a crucial role of EZh2 in determining the cancer cell outcome following DNA damage is unraveled, suggesting that therapeutic targeting oncogenic EH2 might serve as a strategy for improving conventional chemotherapy in a given malignancy.