Proteoglycan signaling in tumor angiogenesis and endothelial cell autophagy

被引:36
|
作者
Gubbiotti, Maria A. [1 ,2 ]
Buraschi, Simone [1 ,2 ]
Kapoor, Aastha [1 ,2 ]
Iozzo, Renato, V [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Sidney Kimmel Med Coll & Canc Ctr, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Sidney Kimmel Med Coll & Canc Ctr, Canc Cell Biol & Signaling Program, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
Proteoglycan; Autophagy; Angiogenesis; Decorin; Perlecan; Biglycan; Endostatin; Tumorigenesis; BASEMENT-MEMBRANE PROTEOGLYCANS; DECORIN-MEDIATED INHIBITION; BREAST-CARCINOMA CELLS; CANCER GROWTH; HEPARAN-SULFATE; IN-VIVO; TARGETED DISRUPTION; BECLIN; BIGLYCAN; ENDOREPELLIN;
D O I
10.1016/j.semcancer.2019.05.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The need for more effective cancer therapies is omnipresent as the ever-complex, and highly adaptive, mechanisms of tumor biology allow this disease to elude even the most stringent treatment options. The expanding field of proteoglycan signaling is enticing as a reservoir of potential drug targets and prospects for novel therapeutic strategies. The newest trend in proteoglycan biology is the interplay between extracellular signaling and autophagy fueled by the close link between autophagy and angiogenesis. Here we summarize the most current evidence surrounding proteoglycan signaling in both of these biological processes featuring the well-known suspects, decorin and perlecan, as well as other up-and-coming neophytes in this evolving signaling web.
引用
收藏
页码:1 / 8
页数:8
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