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Shuang Huang

Researcher at Georgia Regents University

Publications -  53
Citations -  3525

Shuang Huang is an academic researcher from Georgia Regents University. The author has contributed to research in topics: Cancer & Cell migration. The author has an hindex of 35, co-authored 53 publications receiving 3163 citations. Previous affiliations of Shuang Huang include Shanghai University & Charlie Norwood VA Medical Center.

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Journal Article

ATR-Chk2 signaling in p53 activation and DNA damage response during cisplatin-induced apoptosis (Journal of Biological Chemistry (2008) 283, (6572-6583))

TL;DR: It is shown that ATR is specifically activated during cisplatin treatment and co-localizes with H2AX, forming nuclear foci at the site of DNA damage, suggesting an important role for the DNA damage response mediated by ATR-Chk2 in p53 activation and renal cell apoptosis during cisPlatin nephrotoxicity.
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ATR-Chk2 signaling in p53 activation and DNA damage response during cisplatin-induced apoptosis

TL;DR: In this article, the authors demonstrate an early DNA damage response during cisplatin treatment of renal cells and tissues, and demonstrate a critical role for ATR, but not ATM (ataxia telangiectasia mutated) or DNA-PK (DNA-dependent protein kinase), in the activation and apoptosis of kidney cells.
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The Histone H3 Methyltransferase G9A Epigenetically Activates the Serine-Glycine Synthesis Pathway to Sustain Cancer Cell Survival and Proliferation

TL;DR: It is shown that the histone H3 lysine 9 (H3K9) methyltransferase G9A is required for maintaining the pathway enzyme genes in an active state marked by H3K 9 monomethylation and for the transcriptional activation of this pathway in response to serine deprivation.
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Extracellular Signal–Regulated Kinase Signaling Pathway Regulates Breast Cancer Cell Migration by Maintaining slug Expression

TL;DR: The study suggests that the ERK pathway regulates breast cancer cell migration by maintaining slug expression, and an association between ERK-regulated cell migration and slug expression is suggested.
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Ratio of miR-196s to HOXC8 messenger RNA correlates with breast cancer cell migration and metastasis.

TL;DR: The findings identify miRNA-196s as potent metastasis suppressors and reveal that the ratio of miR- 196s to HOXC8 mRNA might be an indicator of the metastatic capability of breast tumors.