Feng Cao
Capital Medical University
26 Papers
4 Citations
Feng Cao is an academic researcher from Capital Medical University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 1, co-authored 1 publications.
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Papers
Ferroptosis: past, present and future
TL;DR: This paper systematically summarizes the latest progress in ferroptosis research, with a focus on providing references for further understanding of its pathogenesis and for proposing new targets for the treatment of related diseases.
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Role of m6A writers, erasers and readers in cancer
TL;DR: The N(6)-methyladenosine (m6A) modification is the most pervasive modification of human RNAs as discussed by the authors and it has been shown that m6A is involved in the biological functions of cancer cells, such as proliferation, invasion, metastasis and drug resistance.
The crosstalk between ferroptosis and mitochondrial dynamic regulatory networks
TL;DR: In this paper , the authors systematically summarized changes in ferroptosis, mitochondrial fission and fusion and mitophagy to promote an in-depth understanding of the mechanism underlying ferro-ptosis and provide a corresponding reference for the treatment of related diseases.
Integration of scRNA-Seq and Bulk RNA-Seq Reveals Molecular Characterization of the Immune Microenvironment in Acute Pancreatitis
Zhen Fang,Jie Li,Feng Cao,Fei Li +3 more
TL;DR: In this article , the authors investigated cell-to-cell communication networks using the CellChat package, and defined AP-specific gene signatures (Clic1, Sat1, Serpina3n, Atf3, Lcn2, Osmr, Ccl9, Hspb1, Anxa2, Krt8, Cd44, Tmsb10, Hmox1, Fxyd5, Plin2, Pnp).
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Acinous cell AR42J-derived exosome miR125b-5p promotes acute pancreatitis exacerbation by inhibiting M2 macrophage polarization via PI3K/AKT signaling pathway
Zhichao Zheng,Feng Cao,Yi-Xuan Ding,Jiong-Di Lu,Y. Fu,Lin Liu,Yulin Guo,Shuang Liu,Haichen Sun,Yeqing Cui,Fei Li +10 more
TL;DR: In this article , exosomes derived from AR42J cells were isolated and extracted in active and inactive states by an exosome extraction kit, and were verified via transmission electron microscopy, nanoparticle tracking analysis, and western blotting.
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