Publications by authors named "Xiao-chuan Gu"

nucleotide biosynthesis is essential for maintaining cellular nucleotide pools, the suppression of which leads to genome instability. The metabolic enzyme transketolase (TKT) in the nonoxidative branch of the pentose phosphate pathway (PPP) regulates ribose 5-phosphate (R5P) levels and nucleotide biosynthesis. TKT is required for maintaining cell proliferation in human liver cancer cell lines, yet the role of TKT in liver injury and cancer initiation remains to be elucidated.

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Fracture repair is a complex yet well orchestrated regenerative process involving numerous signaling and cell types including osteoblasts. Here we showed that NPY, a neurotransmitter with regulatory functions in bone homeostasis, may contribute to the post-fracture bone healing in patients with traumatic brain injury-fracture combined injuries. Our results suggested NPY levels were increased in patients with the combined injuries, accomplished by arising of bone healing markers, such as ALP, OC, PICP and ICTP, than in those with simple fractures, and NPY have direct actions on MSCs to promote their osteogenic differentiation.

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Synopsis of recent research by authors named "Xiao-chuan Gu"

  • - Xiao-Chuan Gu's research primarily focuses on the role of metabolic enzymes and neuropeptides in cellular processes related to liver health and bone healing mechanisms.
  • - One significant finding is that Transketolase (TKT) deficiency in the liver can protect against DNA damage by increasing ribose 5-phosphate and nucleotide levels, highlighting its importance in cellular proliferation and genome stability.
  • - Additionally, Gu's studies demonstrate that Neuropeptide Y (NPY) plays a crucial role in enhancing post-fracture bone healing by promoting the osteogenic differentiation of mesenchymal stem cells, particularly in patients with complex injuries.