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Proteoglycan neofunctions: regulation of inflammation and autophagy in cancer biology

期刊

FEBS JOURNAL
卷 284, 期 1, 页码 10-26

出版社

WILEY
DOI: 10.1111/febs.13963

关键词

biglycan; decorin; microtubule-associated protein light chain 3; receptor tyrosine kinase; small leucine-rich proteoglycans; Toll-like receptors

资金

  1. German Research Council [SFB 815, SFB 1039, SFB 1177, SCHA 1082/6-1]
  2. LOEWE Program Ub-Net
  3. National Institutes of Health [RO1 CA39481, RO1 CA47282, RO1 CA164462]
  4. NIH [T32 AA07463]

向作者/读者索取更多资源

Inflammation and autophagy have emerged as prominent issues in the context of proteoglycan signaling. In particular, two small, leucine-rich proteoglycans, biglycan and decorin, play pivotal roles in the regulation of these vital cellular pathways and, as such, are intrinsically involved in cancer initiation and progression. In this minireview, we will address novel functions of biglycan and decorin in inflammation and autophagy, and analyze new emerging signaling events triggered by these proteoglycans, which directly or indirectly modulate these processes. We will critically discuss the dual role of proteoglycan-driven inflammation and autophagy in tumor biology, and delineate the potential mechanisms through which soluble extracellular matrix constituents affect the microenvironment associated with inflammatory and neoplastic diseases.

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