Department of Pathology, Yanbian University Hospital, Yanji, Jilin 133000, China.
Oral Cancer Research Institute, Yonsei University College of Dentistry, Seoul 03722, Korea.
Int J Mol Sci. 2020 Nov 30;21(23):9138. doi: 10.3390/ijms21239138.
Fibrosis is presented in various physiologic and pathologic conditions of the salivary gland. Transforming growth factor beta (TGF-β) pathway has a pivotal role in the pathogenesis of fibrosis in several organs, including the salivary glands. Among the TGF-β superfamily members, TGF-β1 and 2 are pro-fibrotic ligands, whereas TGF-β3 and some bone morphogenetic proteins (BMPs) are anti-fibrotic ligands. TGF-β1 is thought to be associated with the pro-fibrotic pathogenesis of sialadenitis, post-radiation salivary gland dysfunction, and Sjögren's syndrome. Potential therapeutic strategies that target multiple levels in the TGF-β pathway are under preclinical and clinical research for fibrosis. Despite the anti-fibrotic effect of BMPs, their in vivo delivery poses a challenge in terms of adequate clinical efficacy. In this article, we will review the relevance of TGF-β signaling in salivary gland fibrosis and advances of potential therapeutic options in the field.
纤维化存在于唾液腺的各种生理和病理状况中。转化生长因子-β(TGF-β)途径在包括唾液腺在内的多个器官的纤维化发病机制中起着关键作用。在 TGF-β 超家族成员中,TGF-β1 和 2 是促纤维化配体,而 TGF-β3 和一些骨形态发生蛋白(BMPs)是抗纤维化配体。TGF-β1 被认为与唾液腺炎、放射后唾液腺功能障碍和干燥综合征的促纤维化发病机制有关。针对 TGF-β 途径多个水平的潜在治疗策略正在进行临床前和临床研究,以治疗纤维化。尽管 BMPs 具有抗纤维化作用,但它们在体内的传递在获得足够的临床疗效方面存在挑战。本文将综述 TGF-β 信号在唾液腺纤维化中的相关性,以及该领域潜在治疗选择的进展。