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Chao Wang

Researcher at National University of Singapore

Publications -  5
Citations -  522

Chao Wang is an academic researcher from National University of Singapore. The author has contributed to research in topics: Metastasis & Carcinogenesis. The author has an hindex of 4, co-authored 5 publications receiving 423 citations. Previous affiliations of Chao Wang include Semmelweis University.

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Targeting transcription factor STAT3 for cancer prevention and therapy.

TL;DR: The importance of STAT3 as a potential target for cancer therapy is discussed and novel insights into various classes of existing pharmacological inhibitors of this transcription factor that can be potentially developed as anti-cancer drugs are provided.
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Targeting the PI3K/Akt signaling pathway in gastric carcinoma: A reality for personalized medicine?

TL;DR: The common dysregulation of PI3K/Akt/mTOR pathway in GC and the various types of single or dual pathway inhibitors under development that might have a superior role in GC treatment are reviewed and the recent developments in identification of predictive biomarkers are summarized.
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microRNAs in breast cancer: regulatory roles governing the hallmarks of cancer

TL;DR: This review provides a comprehensive overview of microRNAs with established functional relevance in breast cancer, their established target genes and resulting cellular phenotype, and the role and application of circulating miRNAs in breast cancers.
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Wanted DEAD/H or Alive: Helicases Winding Up in Cancers.

TL;DR: Next-generation sequencing data obtained from public portals and reviewing existing literature are analyzed to provide new insights on the potential of DEAD/H-box helicases to act as pharmacological drug targets in cancers and the potential small molecule inhibitors of helicases and their therapeutic value are discussed.
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DEAD-box RNA Helicases: the microRNA managers of breast cancer

TL;DR: A brief summary of these miRNA-associated hallmarks in breast cancer progression and a highlight on a family of proteins known as DEAD-box RNA helicases, many of which have been found to be associated with mi RNA-associated tumorigenesis.