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miR-199a-3p suppresses neuroinflammation by directly targeting MyD88 in a mouse model of bone cancer pain

Pain is a profoundly debilitating symptom in cancer patients, leading to disability, immobility, and a marked decline in their quality of life. This study aimed to investigate the potential roles of miR-199a-3p in a murine model of bone cancer pain induced by tumor cell implantation in the medullary...

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Published in:Life sciences (1973) 2023-11, Vol.333, p.122139-122139, Article 122139
Main Authors: Saadh, Mohamed J., Rashed, Amera Bekhatroh, Jamal, Azfar, Castillo-Acobo, Roxana Yolanda, Kamal, Mohammad Azhar, Cotrina-Aliaga, Juan Carlos, Gonzáles, José Luis Arias, Alothaim, Abdulaziz S., Alhoqail, Wardah A., Ahmad, Fuzail, Lakshmaiya, Natrayan, Amin, Ali H., Younus, Dhuha Ghassan, Rojas, Gregorio Gilmer Rosales, Bahrami, Abolfazl, Akhavan-Sigari, Reza
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Language:English
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Summary:Pain is a profoundly debilitating symptom in cancer patients, leading to disability, immobility, and a marked decline in their quality of life. This study aimed to investigate the potential roles of miR-199a-3p in a murine model of bone cancer pain induced by tumor cell implantation in the medullary cavity of the femur. We assessed pain-related behaviors, including the paw withdrawal mechanical threshold (PWMT) and the number of spontaneous flinches (NSF). To investigate miRNA expression and its targets in astrocytes, we employed a combination of RNA-seq analysis, qRT-PCR, Western blotting, EdU, TUNEL, ChIP, ELISA, and luciferase reporter assays in mice (C3H/HeJ) with bone cancer pain and control groups. On days 10, 14, 21, and 28 post-surgery, we observed significant differences in PWTL, PWMT, and NSF when compared to the sham group (P 
ISSN:0024-3205
1879-0631
DOI:10.1016/j.lfs.2023.122139