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Mengmeng Li

Researcher at Nanjing University of Chinese Medicine

Publications -  6
Citations -  286

Mengmeng Li is an academic researcher from Nanjing University of Chinese Medicine. The author has contributed to research in topics: Hepatic stellate cell & Hepatic fibrosis. The author has an hindex of 6, co-authored 6 publications receiving 144 citations.

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Curcumol induces RIPK1/RIPK3 complex-dependent necroptosis via JNK1/2-ROS signaling in hepatic stellate cells.

TL;DR: A potential clinical use of curcumol-targeted RIPK1/RIPK3 complex-dependent necroptosis via JNK1/2-ROS signaling for the treatment of hepatic fibrosis is suggested.
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P53-dependent induction of ferroptosis is required for artemether to alleviate carbon tetrachloride-induced liver fibrosis and hepatic stellate cell activation

TL;DR: The findings revealed that P53‐dependent induction of ferroptosis is necessary for ART to ameliorate CCl4‐induced hepatic fibrosis and inhibit HSC activation, and determined that tumor suppressor P53 was an upstream molecule in the facilitation of ART‐induced HSC ferroPTosis.
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Blockade of glycolysis-dependent contraction by oroxylin a via inhibition of lactate dehydrogenase-a in hepatic stellate cells

TL;DR: Blockade of aerobic glycolysis by oroxylin A via inhibition of LDH-A reduced HSC contraction and attenuated liver fibrosis, suggesting LDH -A as a promising target for intervention of hepatic fibrosis.
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TPP-related mitochondrial targeting copper (II) complex induces p53-dependent apoptosis in hepatoma cells through ROS-mediated activation of Drp1.

TL;DR: Investigating how CTB affects mitochondrial functions and exerts its anti-tumor activity in hepatoma cells shows that CTB merits further evaluation as a chemotherapeutic agent for the treatment of Hepatocellular carcinoma.
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Novel mitochondrion-targeting copper(II) complex induces HK2 malfunction and inhibits glycolysis via Drp1-mediating mitophagy in HCC.

TL;DR: These findings established a previously unrecognized role for copper complex in aerobic glycolysis of tumour cells, revealing the interaction between mitochondrial HK2‐mediated mitophagy and Drp1‐regulated mitochondrial fission.