Publications by authors named "Shujian Hu"

Despite extensive scientific efforts directed toward the evolutionary trajectory of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in humans at the beginning of the COVID-19 epidemic, it remains unclear how the virus jumped into and evolved in humans so far. Herein, we recruited almost all adult coronavirus disease 2019 (COVID-19) cases appeared locally or imported from abroad during the first 8 months of the outbreak in Shanghai. From these patients, SARS-CoV-2 genomes occupying the important phylogenetic positions in the virus phylogeny were recovered.

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Bats, rodents, and shrews are the most important animal sources of human infectious diseases. However, the evolution and transmission of viruses among them remain largely unexplored. Through the meta-transcriptomic sequencing of internal organ and fecal samples from 2,443 wild bats, rodents, and shrews sampled from four Chinese habitats, we identified 669 viruses, including 534 novel viruses, thereby greatly expanding the mammalian virome.

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Gastrodiae Rhizoma and its active constituents are known to exhibit neuroprotective effects in Alzheimer's disease (AD). However, the effect of Rhizoma Gastrodiae water extract (WERG) on AD and the detailed mechanism of action remain unclear. In this study, the mechanism of action of WERG was investigated by the microbiome-gut-brain axis using a D-galactose (D-gal)/AlCl-induced AD mouse model.

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Article Synopsis
  • A novel compound called IPM714, derived from 1H-imidazole [4,5-f][1,10] phenanthroline, has shown potential as an effective treatment for colorectal cancer (CRC) by selectively inhibiting CRC cell growth.
  • The research demonstrated that IPM714 had a half maximal inhibitory concentration (IC) of 1.74 μM and 2 μM against HCT116 and SW480 cells, respectively, and induces cell cycle arrest and apoptosis in these cancer cells.
  • Analysis revealed that IPM714 likely targets the PI3K/AKT/mTOR signaling pathway, which plays a key role in regulating cell proliferation and survival, making it a promising candidate for CRC therapy.
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A series of novel derivatives of isaindigotone, which comes from the root of Fort, were synthesised (Compound -). Four human gastrointestinal cancer cells (HCT116, PANC-1, SMMC-7721, and AGS) were employed to evaluate the anti-proliferative activity. Among them, Compound displayed the most effective inhibitory activity on AGS cells with an IC (50% inhibitory concentration) value of 2.

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Article Synopsis
  • - 1H-imidazo[4,5-f][1,10]phenanthroline (IPM713) has shown promising anticancer effects, particularly against the colorectal cancer cell line HCT116, with an IC of 1.7 μM.
  • - The study found that IPM713 works by blocking the cell cycle in the G0/G1 phase and inducing cell death (apoptosis) through the inhibition of the PI3K/AKT/mTOR signaling pathway.
  • - An acute toxicity test revealed that IPM713 has a high safety profile, with a median lethal dose (LD) above 5000 mg/kg, indicating its potential as a therapeutic agent for colorectal cancer. *
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Colorectal cancer (CRC) is a common clinical malignancy globally ranked as the fourth leading cause of cancer mortality. Some microbes are known to contribute to adenoma-carcinoma transition and possess diagnostic potential. Advances in high-throughput sequencing technology and functional studies have provided significant insights into the landscape of the gut microbiome and the fundamental roles of its components in carcinogenesis.

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Colorectal cancer (CRC), a major health threat in the world, ranks third in incidence and second in mortality among cancers. Chemotherapy, an important treatment for colorectal cancer, have be limited in the clinic due to the resistance and side effect. Studies have shown that PI3K-related regulatory pathways play a colossal role in colorectal cancer.

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