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Ping Li

Researcher at Anhui Medical University

Publications -  19
Citations -  199

Ping Li is an academic researcher from Anhui Medical University. The author has contributed to research in topics: Medicine & Cancer. The author has an hindex of 5, co-authored 13 publications receiving 63 citations.

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Rationally designed rapamycin-encapsulated ZIF-8 nanosystem for overcoming chemotherapy resistance.

TL;DR: The optimized nanoplatform, Rapa@ZIF-8, provides a proof of concept for intentionally interfering mTOR pathway and utilizing the switch of survival-to death-promoting autophagy for adjunct chemotherapy.
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Brucine Suppresses Vasculogenic Mimicry in Human Triple-Negative Breast Cancer Cell Line MDA-MB-231.

TL;DR: The results for the first time indicated that brucine could disrupt F-actin cytoskeleton and microtubule structure, thereby impairing hallmarks of aggressive tumors, like migration, invasion, and holding a possibility of suppressing vasculogenic mimicry.
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Brucine suppresses breast cancer metastasis via inhibiting epithelial mesenchymal transition and matrix metalloproteinases expressions.

TL;DR: Brucine inhibited triple negative breast cancer cells metastasis potentially through EMT reversion and MMP-2 and M MPs inhibition and decreased the protein and mRNA levels of mesenychmal markers such as vimentin and fibronectin.
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Modeling nonalcoholic fatty liver disease on a liver lobule chip with dual blood supply.

TL;DR: In this article, a biomimetic liver lobule chip (LC) was developed for modeling non-alcoholic fatty liver disease (NAFLD) on a microfluidic chip, achieving self-organized liver microtissue that is similar to in vivo tissue.
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On-Chip Construction of Liver Lobules with Self-Assembled Perfusable Hepatic Sinusoid Networks.

TL;DR: In this article, a lifelike bionic liver lobule chip (LLC) was developed, on which the perfusable hepatic sinusoid networks were achieved using a microflow-guided angiogenesis methodology; additionally, during and after self-assembly, oxygen concentration was regulated to mimic physiologically dissolved levels supplied by actual hepatic arterioles and venules.