4.4 Article

High Expression of WWP1 Associates with Tumor Progression in Papillary Thyroid Cancer

Journal

CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS
Volume 37, Issue 4, Pages 313-323

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/cbr.2020.4148

Keywords

papillary thyroid cancer; WWP1; PTEN-Akt signaling pathway

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The study found that WWP1 expression is increased in PTC tissues and cells, and its upregulation is closely correlated with clinical parameters. Knockdown of WWP1 suppressed cell proliferation, migration, and invasion in PTC cells, inducing cell cycle arrest and apoptosis. Knockdown of WWP1 also led to decreased levels of p-PI3K and p-Akt, contributing to the understanding of PTC pathogenesis.
Background: WWP1 (WW domain-containing E3 ubiquitin protein ligase 1) is increased in several kinds of carcinomas, but the influence of WWP1 in papillary thyroid cancer (PTC) is not well understood. Materials and Methods: The expression of WWP1 in PTC tissues and cells is detected by real-time reverse transcription PCR. The biological role of WWP1 on PTC cell growth, apoptosis, migration, and invasion ability was assessed with the Cell Counting Kit-8, colony forming, flow cytometry, wound healing, and transwell assays, respectively. Results: The expression of WWP1 mRNA and protein is increased in PTC tissue samples and cells. There is closely correlation between the up expression of WWP1 and clinical parameters, such as tumor size, TNM, and distant metastasis. Knockdown of WWP1 blocks cell proliferation, migration, and invasion, causes cell cycle arrest, and induces apoptosis in PTC cells. Knockdown of WWP1 increases PTEN level and reduces p-PI3K and p-Akt level in PTC cells. Conclusions: Knockdown of WWP1 suppressed cell proliferation, migration, and invasion of PTC cell by downregulating the expression of p-PI3K and p-Akt, contributing to their understanding the pathogenesis of PTC.

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