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Yaxiong Tang

Researcher at Chinese Academy of Sciences

Publications -  31
Citations -  774

Yaxiong Tang is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 13, co-authored 20 publications receiving 687 citations. Previous affiliations of Yaxiong Tang include University of California, Irvine.

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The Wnt inhibitory factor 1 restoration in prostate cancer cells was associated with reduced tumor growth, decreased capacity of cell migration and invasion and a reversal of epithelial to mesenchymal transition

TL;DR: Analysis of the effect and underlying mechanism of a naturally-occurring Wnt inhibitor, WIF1, on the growth and cellular invasiveness of a bone metastatic PCa cell line, PC3, suggests that Wif1 regulates tumor invasion through EMT process and thus, may play an important role in controlling metastatic disease in PCa patients.
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WIF1, a Wnt pathway inhibitor, regulates SKP2 and c-myc expression leading to G1 arrest and growth inhibition of human invasive urinary bladder cancer cells

TL;DR: Results suggest that mechanisms of WIF1-induced G1 arrest include SKP2 down-regulation leading to p27/Kip1 accumulation and c-myc down- regulation releasing p21/WAF1 transcription and shows that Wif1 inhibits in vivo bladder tumor growth in nude mice.
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Flavokawain B, a kava chalcone, induces apoptosis via up‐regulation of death‐receptor 5 and Bim expression in androgen receptor negative, hormonal refractory prostate cancer cell lines and reduces tumor growth

TL;DR: In this article, the effect of flavokawain B (FKB), a kava chalcone, is shown to be about 4- to 12-fold more effective in reducing the cell viabilities of androgen receptor (AR)-negative, HRPC cell lines DU145 and PC-3 than AR-positive, hormone-sensitive prostate cancer cell lines LAPC4 and LNCaP, with minimal effect on normal prostatic epithelial and stromal cells.
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Effects of the Kava Chalcone Flavokawain A Differ in Bladder Cancer Cells with Wild-type versus Mutant p53

TL;DR: In a p53 wild-type, low-grade, and papillary bladder cancer cell line (RT4), flavokawain A increased p21/WAF1 and p27/KIP1, which resulted in a decrease in cyclin-dependent kinase-2 (CDK2) kinase activity and subsequent G1 arrest, and induced a G2-M arrest in p53-defective cells.
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Frzb, a secreted Wnt antagonist, decreases growth and invasiveness of fibrosarcoma cells associated with inhibition of Met signaling

TL;DR: The data showed that Frzb expression was significantly inversely correlated with Met expression in both STS cell lines and tissues, suggesting the usefulness of Frzb in modulating Met signaling as a new treatment strategy for STS.