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作 者:Zhiwei Zheng Benyu Nan Chang Liu Dongmei Tang Wen Li Liping Zhao Guohui Nie Yingzi He
机构地区:[1]ENT Institute and Department of Otorhinolaryngology,Eye&ENT Hospital,State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science,NHC Key Laboratory of Hearing Medicine(Fudan University),Fudan University,Shanghai,200031,China [2]Department of Otorhinolaryngology-Head and Neck Surgery,The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University,Wenzhou,325000,Zhejiang,China [3]Department of Otolaryngology-Head and Neck Surgery,The Third Affiliated Hospital of Sun Yat-Sen University,Guangzhou,510630,China [4]Department of Otolaryngology,Shenzhen Institute of Translational Medicine,Shenzhen Second People's Hospital,The First Affiliated Hospital of Shenzhen University,Shenzhen,518035,Guangdong,China
出 处:《Journal of Pharmaceutical Analysis》2023年第6期590-602,共13页药物分析学报(英文版)
基 金:supported by grants from the National Natural Science Foundation of China(Grant Nos.:82271158,82192865,and 82071045);Wenzhou Municipal Science and Technology Research Program(Grant No.:2021Y0681).
摘 要:This study aimed to evaluate the therapeutic potential of inhibiting protein arginine methyltransferase 5(PRMT5)in cisplatin-induced hearing loss.The effects of PRMT5 inhibition on cisplatin-induced auditory injury were determined using immunohistochemistry,apoptosis assays,and auditory brainstem response.The mechanism of PRMT5 inhibition on hair cell survival was assessed using RNA-seq and Cleavage Under Targets and Tagment-quantitative polymerase chain reaction(CUT&Tag-qPCR)analyses in the HEI-OC1 cell line.Pharmacological inhibition of PRMT5 significantly alleviated cisplatin-induced damage to hair cells and spiral ganglion neurons in the cochlea and decreased apoptosis by protecting mitochondrial function and preventing the accumulation of reactive oxygen species.CUT&Tag-qPCR analysis demonstrated that inhibition of PRMT5 in HEI-OC1 cells reduced the accumulation of H4R3me2s/H3R8me2s marks at the promoter region of the Pik3ca gene,thus activating the expression of Pik3ca.These findings suggest that PRMT5 inhibitors have strong potential as agents against cisplatininduced ototoxicity and can lay the foundation for further research on treatment strategies of hearing loss.
关 键 词:Protein arginine methyltransferase 5 (PRMT5) LLY-283 CISPLATIN Hearing loss Hair cell Spiral ganglion neuron
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