LSD1 as a Biomarker and the Outcome of Its Inhibitors in the Clinical Trial: The Therapy Opportunity in Tumor

被引:21
作者
Agboyibor, Clement [1 ,2 ,3 ]
Dong, Jianshu [1 ,2 ,3 ]
Effah, Clement Yaw [4 ]
Drokow, Emmanuel Kwateng [5 ,6 ]
Pervaiz, Waqar [1 ,2 ,3 ]
Liu, Hong-Min [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[2] Coinnovat Ctr Henan Prov New Drug R&D & Preclin, Zhengzhou 450001, Peoples R China
[3] Zhengzhou Univ, Minist Educ China, Key Lab Adv Technol Drug Preparat Technol, Zhengzhou 450001, Peoples R China
[4] Zhengzhou Univ, Coll Publ Hlth, Zhengzhou 450001, Peoples R China
[5] Zhengzhou Univ Peoples Hosp, Dept Oncol, Zhengzhou 450003, Peoples R China
[6] Henan Prov Peoples Hosp Henan, Zhengzhou 450003, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1155/2021/5512524
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumors are the foremost cause of death worldwide. As a result of that, there has been a significant enhancement in the investigation, treatment methods, and good maintenance practices on cancer. However, the sensitivity and specificity of a lot of tumor biomarkers are not adequate. Hence, it is of inordinate significance to ascertain novel biomarkers to forecast the prognosis and therapy targets for tumors. This review characterized LSD1 as a biomarker in different tumors. LSD1 inhibitors in clinical trials were also discussed. The recent pattern advocates that LSD1 is engaged at sauce chromatin zones linking with complexes of multi-protein having an exact DNA-binding transcription factor, establishing LSD1 as a favorable epigenetic target, and also gives a large selection of therapeutic targets to treat different tumors. This review sturdily backing the oncogenic probable of LSD1 in different tumors indicated that LSD1 levels can be used to monitor and identify different tumors and can be a useful biomarker of progression and fair diagnosis in tumor patients. The clinical trials showed that inhibitors of LSD1 have growing evidence of clinical efficacy which is very encouraging and promising. However, for some of the inhibitors such as GSK2879552, though selective, potent, and effective, its disease control was poor as the rate of adverse events (AEs) was high in tumor patients causing clinical trial termination, and continuation could not be supported by the risk-benefit profile. Therefore, we propose that, to attain excellent clinical results of inhibitors of LSD1, much attention is required in designing appropriate dosing regimens, developing in-depth in vitro/in vivo mechanistic works of LSD1 inhibitors, and developing inhibitors of LSD1 that are reversible, safe, potent, and selective which may offer safer profiles.
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页数:11
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