2020
DOI: 10.1007/978-3-030-48457-6_1
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Elastin in the Tumor Microenvironment

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Cited by 26 publications
(21 citation statements)
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“…Tropoelastins are the precursors of elastin; they are bound to a chaperone when they are secreted; they are additionally modified when they come into contact with mature elastin fibers, when then chemically transform into elastin chains. Lack of elastin in the ECM can lead to cutis laxa and Williams syndrome (34)(35)(36).…”
Section: Elastinmentioning
confidence: 99%
See 1 more Smart Citation
“…Tropoelastins are the precursors of elastin; they are bound to a chaperone when they are secreted; they are additionally modified when they come into contact with mature elastin fibers, when then chemically transform into elastin chains. Lack of elastin in the ECM can lead to cutis laxa and Williams syndrome (34)(35)(36).…”
Section: Elastinmentioning
confidence: 99%
“…Studies have shown that elastin-derived peptides have numerous biological activities in cancer cells and their surrounding stroma (36). They enhance tumor cell migration and stromal invasion (39,40).…”
Section: Elastinmentioning
confidence: 99%
“…It regulates several types of cancer cells by activating a multiple-step cell apoptosis process 24,25 . ELN encodes the elastin protein, which is a key protein in the tumor microenvironment 26 . Moreover, the protein encoded by the CHGA gene is a member of the chromogranin/secretogranin family of neuroendocrine secretory proteins 27 .…”
Section: Discussionmentioning
confidence: 99%
“…Collagen fibrils are often found together with elastin and fibulin containing elastic fibrils [25], which, due to their reversible elasticity, allow the resilience of the ECM. Interestingly, most of the body's elastin is formed pre-and early postnatally but hardly in the adult body [26].…”
Section: The Extracellular Matrix As a Key Component Of The Tmementioning
confidence: 99%
“…Interestingly, most of the body's elastin is formed pre-and early postnatally but hardly in the adult body [26]. However, some cancer entities stimulate and reinitiate elastin production and deposition, which is known as elastosis [25]. Similarly noteworthy, elastin degradation peptides (EDPs) are released in the TME, which stimulate tumor cell growth and progression via different receptors [27] (Figure 2).…”
Section: The Extracellular Matrix As a Key Component Of The Tmementioning
confidence: 99%