2017
DOI: 10.1166/asl.2017.9426
|View full text |Cite
|
Sign up to set email alerts
|

mRNA Relative Expression of Cancer Associated Fibroblasts Markers in Keloid Scars

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
3
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 0 publications
0
3
0
Order By: Relevance
“…It has been observed that prolonged treatment with CAP inhibits cell viability and collagen production of murine fibroblasts [93]. A reduction in collagen secretion and the migration behavior was also observed after CAP treatment in keloid fibroblasts, which, like tumor-associated fibroblasts, show an overproduction of collagen [94,95]. Moreover, in vitro studies have shown that CAP is able to destroy collagen [96].…”
Section: Cap Interaction With the Tumor Microenvironmentmentioning
confidence: 99%
“…It has been observed that prolonged treatment with CAP inhibits cell viability and collagen production of murine fibroblasts [93]. A reduction in collagen secretion and the migration behavior was also observed after CAP treatment in keloid fibroblasts, which, like tumor-associated fibroblasts, show an overproduction of collagen [94,95]. Moreover, in vitro studies have shown that CAP is able to destroy collagen [96].…”
Section: Cap Interaction With the Tumor Microenvironmentmentioning
confidence: 99%
“…This outcome may be related to the aforementioned effect of CAP on fibroblasts. Another study showed that CAP inhibited the excessive synthesis of collagen in keloid fibroblasts (KFs) (108), and the activated fibroblasts may have similar characteristics with CAFs (109). An in vitro study on the effect of CAP on dentin surfaces and extracted type I collagen fibrils showed that CAP can destroy the structure of collagen (110).…”
Section: Effects Of Cap On a Cellular Tme Componentsmentioning
confidence: 99%
“…In vitro studies have shown that plasma can destroy dry and dissolved collagen I molecules due to the oxidation of amino acids and breakage of hydrogen bonds [153], which loosen the collagen structure ( Figure 3b) [154]. In addition, plasma decreased the collagen secretion and cell migration in keloid fibroblasts [155], which similarly to CAFs, overproduce collagen [156]. Using Matrigel (matrix extracted from the Engelbreth-Holm-Swarm mouse sarcoma rich in laminin, collagen IV, entactin, proteoglycans, and growth factors) as a surrogate model in vivo, it was shown that high doses of plasma-derived ROS hindered ECM-cell interactions and decreased bone formation, whereas lower ROS doses promoted chondrocyte differentiation, VEGF production and bone formation [157].…”
Section: Acellular Components Of the Tumour Microenvironmentmentioning
confidence: 99%