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Ping Wei

Researcher at Fudan University

Publications -  54
Citations -  3234

Ping Wei is an academic researcher from Fudan University. The author has contributed to research in topics: Metastasis & Carcinogenesis. The author has an hindex of 26, co-authored 45 publications receiving 2283 citations. Previous affiliations of Ping Wei include University of Texas MD Anderson Cancer Center.

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FoxM1 Promotes β-Catenin Nuclear Localization and Controls Wnt Target-Gene Expression and Glioma Tumorigenesis

TL;DR: FoxM1 is a downstream component of Wnt signaling and is critical for β-catenin transcriptional function in tumor cells, and Wnt3a increases the level and nuclear translocation of FoxM1, which binds directly to β- catenin and enhances β-Catenin nuclear localization and transcriptional activity.
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A peptide encoded by circular form of LINC-PINT suppresses oncogenic transcriptional elongation in glioblastoma

TL;DR: A 87-amino-acid peptide encoded by the circular form of the long intergenic non-protein-coding RNA p53-induced transcript (LINC-PINT) is identified that can reduce glioblastoma proliferation via interaction with PAF1 which sequentially inhibits the transcriptional elongation of some oncogenes.
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Tumor-derived exosomal miR-934 induces macrophage M2 polarization to promote liver metastasis of colorectal cancer

TL;DR: A tumor and TAM interaction in the metastatic microenvironment mediated by tumor-derived exosomes that affects colorectal cancer liver metastasis and the present study provides a theoretical basis for secondary liver cancer.
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The lncRNA NEAT1 activates Wnt/β-catenin signaling and promotes colorectal cancer progression via interacting with DDX5.

TL;DR: The findings indicated that NEAT1 activated Wnt signaling to promote colorectal cancer progression and metastasis and theNEAT1/DDX5/Wnt/β-catenin axis could be a potential therapeutic target of pharmacological strategies.
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A Positive Feedback Loop of lncRNA-PVT1 and FOXM1 Facilitates Gastric Cancer Growth and Invasion.

TL;DR: PVT1 may be a valuable prognostic predictor for gastric cancer, and the positive feedback loop of PVT1-FOXM1 could be a therapeutic target in pharmacologic strategies.