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Haiyan Cao

Researcher at Fourth Military Medical University

Publications -  12
Citations -  625

Haiyan Cao is an academic researcher from Fourth Military Medical University. The author has contributed to research in topics: Mitochondrial fission & Medicine. The author has an hindex of 7, co-authored 8 publications receiving 389 citations.

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Increased mitochondrial fission promotes autophagy and hepatocellular carcinoma cell survival through the ROS-modulated coordinated regulation of the NFKB and TP53 pathways.

TL;DR: It is demonstrated that increased mitochondrial fission plays a critical role in regulation of HCC cell survival, which provides a strong evidence for this process as drug target in HCC treatment.
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MCUR1 facilitates epithelial-mesenchymal transition and metastasis via the mitochondrial calcium dependent ROS/Nrf2/Notch pathway in hepatocellular carcinoma

TL;DR: Evidence supporting a metastasis-promoting role for MCUR1-dependent mitochondrial Ca2+ uptake in HCC is provided and it is suggested thatMCUR1 may be a potential therapeutic target for HCC treatment.
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MICU1 Alleviates Diabetic Cardiomyopathy Through Mitochondrial Ca2+-dependent Antioxidant Response

TL;DR: These findings provide the first direct evidence that upregulated MICU1 preserves cardiac function in diabetic db/db mice, suggesting that increasing the expression or activity of MICU 1 may be a pharmacological approach to ameliorate cardiomyopathy in diabetes.
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Drp1-mediated mitochondrial fission promotes cell proliferation through crosstalk of p53 and NF-κB pathways in hepatocellular carcinoma

TL;DR: It is found that targeting Drp1-dependent mitochondrial fission may provide a novel strategy for suppressing tumor growth of HCC and the crosstalk between p53 and NF-κB pathways was proved to be involved in the regulation of mitochondrial fissions-mediated cell proliferation.
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Mitochondrial fission promotes cell migration by Ca2+/CaMKII/ERK/FAK pathway in hepatocellular carcinoma

TL;DR: It is shown that increased mitochondrial fission significantly promoted the proliferation of hepatocellular carcinoma cells and how these dynamics influence the migration of tumour cells remained largely unknown.