Annexin A5 as a targeting agent for cancer treatment

被引:23
|
作者
Woodward, Alexis [1 ]
Faria, Gabriela N. F. [2 ]
Harrison, Roger G. [2 ,3 ]
机构
[1] Univ Oklahoma, Stephenson Sch Biomed Engn, Norman, OK USA
[2] Univ Oklahoma, Sch Chem Biol & Mat Engn, Norman, OK USA
[3] 100 E Boyd,Room T-301, Norman, OK 73072 USA
关键词
Phosphatidylserine; Annexin A5; Fusion proteins; Carbon nanotubes; Immune modulation; IN-VIVO; PHOSPHOLIPID FLIPPASES; FLUDARABINE PHOSPHATE; TUMOR VASCULATURE; GENE-THERAPY; COLON-CANCER; PROTEIN; 8; PHOSPHATIDYLSERINE; CELLS; EXPRESSION;
D O I
10.1016/j.canlet.2022.215857
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Identifying a universal biomarker for cancer treatment remains a major challenge in cancer therapy. Extracel-lular exposure of phosphatidylserine (PS) is tightly regulated and is an "eat me" signal for phagocytosis in healthy cells. Although cancer cells and vasculature express high levels of externalized PS, they do not undergo apoptosis, making them a promising biomarker for cancer treatment. Annexin A5 (ANXA5) is the native binding partner of PS and can actively target and deliver chemotherapies to the tumor microenvironment (TME) via PS expression. ANXA5 acts as a bridge between the innate and adaptive immune systems and contributes to an immunostimulatory profile in the TME. ANXA5-enzyme prodrug therapies allow for systemic delivery of pro -drugs and targeted killing at the tumor site. ANXA5-carbon nanotube conjugates have been used to physically ablate tumors via photothermal therapy. This review aims to explore the expression of PS in cancer cells and how ANXA5 has been used as a chemotherapeutic and targeting agent for cancer.
引用
收藏
页数:15
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