CHU-CHYN OUJIUNN-LIANG KO2026-10-162026-10-162015-12-01Pure ID: 15281208Pure UUID: 20766a9c-109a-4568-953e-552ddad08c3d10.1016/j.jff.2015.09.042https://www.scopus.com/pages/publications/84946405620https://scholars.csmu.edu.tw/handle/123456789/32947Docetaxel is widely used in the treatment of non-small cell lung cancer. Fungal immunomodulatory proteins of Flammulina velutipes (FIP-. fve) and Ganoderma tsugae (FIP-. gts) possess immunomodulatory and anti-cancer effects. The abilities of FIP-. fve and FIP-. gts to protect against docetaxel-induced adverse effects were investigated. FIP-. gts, but not FIP-. fve, reversed docetaxel-induced decrease in white blood cells (WBCs). On haematoxylin and eosin (H & E), FIP-. fve and FIP-. gts reduced docetaxel-induced empty vacuoles in bone marrow and damage to small intestinal mucosa. On 3D micro-CT analysis, FIP-. fve and FIP-. gts significantly reversed docetaxel-induced decreases in percent bone volume (BV/TV), trabecular number (Tb.N) and bone surface density (BS/TV) in mice. Moreover, monocyte chemoattractant protein-1 (MCP-1) production and mRNA expressions induced by docetaxel in A549 cells were diminished by FIP-. fve and FIP-. gts. Thus, FIP-. fve and FIP-. gts have the potential to mitigate docetaxel-induced adverse effects in patients undergoing chemotherapy and to serve as novel therapeutic protective agents.13enjournal article