2014
DOI: 10.1111/boc.201400014
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Revelation of fibroblast protein commonalities and differences and their possible roles in wound healing and tumourigenesis using co‐culture models of cells

Abstract: The findings provide strong support for crucial role of stromal microenvironment in wound healing and tumourigenesis. In particular, epithelia-induced protein changes in fibroblasts offer new potential targets which may lead to novel tailored cancer therapeutic strategies.

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Cited by 11 publications
(6 citation statements)
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“…In both cases, these stimulated fibroblasts significantly elevated expression of keratin 8 in normal human keratinocytes [ 56 ]. These in vitro activated fibroblasts are also remarkably similar to CAFs as demonstrated by proteomic approach [ 94 ]. Interestingly, this stimulation of normal dermal fibroblasts in response to presence of normal/malignant keratinocytes is only transient.…”
Section: Cafs As the Master Cell Type In Tumor Stromamentioning
confidence: 84%
“…In both cases, these stimulated fibroblasts significantly elevated expression of keratin 8 in normal human keratinocytes [ 56 ]. These in vitro activated fibroblasts are also remarkably similar to CAFs as demonstrated by proteomic approach [ 94 ]. Interestingly, this stimulation of normal dermal fibroblasts in response to presence of normal/malignant keratinocytes is only transient.…”
Section: Cafs As the Master Cell Type In Tumor Stromamentioning
confidence: 84%
“…Cytotoxicity of the NaGdF 4 :Yb 3+ /Er 3+ and NaGdF 4 :Yb 3+ /Er 3+ @PEG nanoparticles was evaluated on a cell line derived from human cervical carcinoma (HeLa) and human dermal fibroblast (HF) 46 48 kindly provided by Dr. Mělková and Dr. Dvořánková, respectively, First Faculty of Medicine, Charles University, Prague. 5∙10 3 of HeLa or 8∙10 3 of HF cells were seeded in 100 µl of media into 96-well flat-bottom TPP plates (Merck; Darmstadt, Germany) for 24 h. Subsequently, the nanoparticles (0.4–400 µg/ml) were added, the cells were cultivated at 37 °C for 72 h under 5% CO 2 atmosphere, AlamarBlue cell viability reagent (10 µl) was added to each well, and the incubation continued at 37 °C for 4 h. The active component of the AlamarBlue reagent (resazurin) was reduced to the highly fluorescent resorufin only in viable cells.…”
Section: Methodsmentioning
confidence: 99%
“…Overexpression of CALDESMON, associated with Actin and HSP70, has been previously described in the setting of tissue injury. 49 …”
Section: Discussionmentioning
confidence: 99%