Targeting of keloid with TRAIL and TRAIL-R2/DR5

被引:6
|
作者
Sun, Pengfei [1 ]
Hu, Zhensheng [2 ]
Pan, Bo [3 ]
Lu, Xiaosheng [4 ]
机构
[1] Zibo Cent Hosp, Dept Plast Surg, Zibo, Peoples R China
[2] Shandong Univ, Dept Plast Surg, Qilu Hosp, Jinan, Peoples R China
[3] Chinese Acad Med Sci, Plast Surg Hosp, Peking Union Med Coll, Dept Plast Surg, Beijing, Peoples R China
[4] Weifang Med Univ, Dept Plast Surg, Affiliated Hosp, Weifang, Peoples R China
关键词
Keloid; targeted therapy; TRAIL; DR5; PHASE-I TRIAL; HYPERTROPHIC SCAR; MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; SIGNALING PATHWAY; APOPTOSIS; LIGAND; SUSCEPTIBILITY; IDENTIFICATION; POLYMORPHISMS;
D O I
10.1080/09546634.2020.1714541
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Keloid is a common and frequently-occurring disease in plastic surgery, and its ugly appearance and itching symptoms bring mental and life pain to patients. However, the clinical treatment of keloid, such as drug injection treatment, surgical resection, cryotherapy, laser treatment and other therapeutic effects are poor. Since the discovery of tumor necrosis factor related apoptosis inducing ligand (TRAIL) in 1995, its selective apoptosis on tumor cells makes it have a great prospect in the targeted treatment of tumor. In recent years, it has been found that the formation of keloid is related to the imbalance of apoptosis of fibroblasts in scar and the binding of TRAI to its receptor mediates the apoptosis of fibroblasts. Therefore, the use of TRAIL and TRAIL-R2/death receptor 5 (DR5) in the treatment of keloid has become a hot research topic. In this paper, the present situation, mechanism and development prospect of TRAIL and TRAIL-R2/DR5 targeted treatment of keloid were reviewed, which provided a reference for promoting the development of keloid treatment.
引用
收藏
页码:957 / 964
页数:8
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