| Literature DB >> 29396379 |
Zongyou Pan1, Heng Sun1, Binbin Xie2, Dongdong Xia3, Xiaoan Zhang1, Dongsheng Yu1, Jun Li1, Yuzi Xu1, Zuhua Wang1, Yan Wu1, Xiaolei Zhang4, Yafei Wang1, Qianbao Fu1, Wei Hu5, Yang Yang5, Varitsara Bunpetch1, Weiliang Shen1, Boon Chin Heng6, Shufang Zhang7, Hongwei Ouyang8.
Abstract
Intervertebral disc (IVD) degeneration is one of the most widespread musculoskeletal diseases worldwide, which remains an intractable clinical challenge. The aim of this study is to investigate the therapeutic potential of the small molecule gefitinib (an epidermal growth factor receptor (EGFR) inhibitor) in ameliorating IVD degeneration. Aberrant EGFR activation levels were detected in both human and rat degenerative IVDs, which prompted us to investigate the functional roles of EGFR by utilizing inducible cartilage-specific EGFR-deficient mice. We demonstrated that conditional EGFR deletion in mice increased nucleus pulposus (NP) extracellular matrix (ECM) production and autophagy marker activation while MMP13 expression decreased. These outcomes are comparable to the use of a controlled-release injectable thermosensitive hydrogel of gefitinib to block EGFR activity in a puncture-induced rat model. We also conducted a case series study involving patients with non-small cell lung cancer and IVD degeneration who received gefitinib treatment from 2010 to 2015. Gefitinib-treated patients displayed a relative slower disc degenerating progression, in contrast to control subjects. These findings thus provide evidence that suppression of EGFR by the FDA-approved drug gefitinib can protect IVD degeneration in rats, implying the potential application of gefitinib as a small molecule drug for treating IVD degeneration.Entities:
Keywords: EGFR; Gefitinib; Intervertebral disc degeneration; Thermosensitive injectable hydrogel
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Year: 2018 PMID: 29396379 DOI: 10.1016/j.biomaterials.2018.01.016
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479