Wang Yajie, Zheng Liying, Zhang Lai, Tai Yuncheng, Lin Xuesong, Cai Zhencheng
Department of Burn Surgery, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang, China.
Postgraduate Department, First Affiliated Hospital of Gannan Medical College, Ganzhou, China.
Front Pharmacol. 2024 Nov 25;15:1444653. doi: 10.3389/fphar.2024.1444653. eCollection 2024.
Keloid scars (keloids), a prototypical form of aberrant scar tissue formation, continue to pose a significant therapeutic challenge within dermatology and plastic surgery due to suboptimal treatment outcomes. Gelatinases are a subgroup of matrix metalloproteinases (MMPs), a family of enzymes that play an important role in the degradation and remodeling of the ECM (a pivotal factor for keloids development). Gelatinases include gelatinase A (MMP-2) and gelatinase B (MMP-9). Since accumulating evidence has shown that gelatinases played a crucial role in the process of keloid formation, we summarized the current knowledge on the association between MMP-2 and MMP-9 expression and the pathological process of keloids through a comprehensive review. This review demonstrated that the interplay between MMP-2, MMP-9, and their regulators, such as TGF-β1/Smad, PI3K/AKT, and LncRNA-ZNF252P-AS1/miR-15b-5p/BTF3 signaling cascades, involved in the intricate balance governing ECM homeostasis, collectively driving the excessive collagen deposition and altered tissue architecture observed in keloids. In summary, this review consolidates the current understanding of MMP-2 and MMP-9 in keloid pathogenesis, shedding light on their intricate involvement in the dysregulated keloids processes. The potential for targeted therapeutic interventions presents promising opportunities for advancing keloid management strategies.
瘢痕疙瘩是异常瘢痕组织形成的一种典型形式,由于治疗效果欠佳,在皮肤科和整形外科领域仍然构成重大的治疗挑战。明胶酶是基质金属蛋白酶(MMPs)的一个亚组,基质金属蛋白酶家族的酶在细胞外基质(瘢痕疙瘩形成的关键因素)的降解和重塑中起重要作用。明胶酶包括明胶酶A(MMP-2)和明胶酶B(MMP-9)。由于越来越多的证据表明明胶酶在瘢痕疙瘩形成过程中起关键作用,我们通过全面综述总结了目前关于MMP-2和MMP-9表达与瘢痕疙瘩病理过程之间关联的知识。这篇综述表明,MMP-2、MMP-9及其调节因子(如TGF-β1/Smad、PI3K/AKT和LncRNA-ZNF252P-AS1/miR-15b-5p/BTF3信号级联)之间的相互作用,参与了控制细胞外基质稳态的复杂平衡,共同驱动了瘢痕疙瘩中观察到的过度胶原沉积和组织结构改变。总之,这篇综述巩固了目前对MMP-2和MMP-9在瘢痕疙瘩发病机制中的理解,揭示了它们在瘢痕疙瘩失调过程中的复杂参与情况。靶向治疗干预的潜力为推进瘢痕疙瘩管理策略提供了有前景的机会。