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001-es BibID:BIBFORM084536
035-os BibID:(WOS)000574374700012 (Scopus)85083321686
Első szerző:Retzlerné Medgyesi Barbara (biotechnológus)
Cím:Rosacea is Characterized by a Profoundly Diminished Skin Barrier / Medgyesi B., Dajnoki Zs., Béke G., Gáspár K., Szabó I. L., Janka E. A., Póliska S., Hendrik Z., Méhes G., Törőcsik D., Bíró T., Kapitány A., Szegedi A.
Dátum:2020
ISSN:0022-202X 1523-1747
Megjegyzések:Rosacea is a common, chronic inflammation of sebaceous gland-rich facial skin characterized by severe skin dryness, elevated pH, transepidermal water loss, and decreased hydration levels. Until now, there has been no thorough molecular analysis of permeability barrier alterations in the skin of rosacea patients. Thus, we aimed to investigate the barrier alterations in papulopustular rosacea (PPR) samples compared to healthy sebaceous gland-rich (SGR) skin, using RNASeq analysis (n=8). Pathway analyses by Cytoscape ClueGo revealed 15 significantly enriched pathways related to skin barrier formation. RT-PCR and immunohistochemistry were used to validate the pathway analyses. The results showed significant alterations in barrier components in PPR samples compared to SGR, including the cornified envelope and intercellular lipid lamellae formation, desmosome and tight junction organizations, barrier alarmins, and antimicrobial peptides. Moreover, the barrier damage in PPR was unexpectedly similar to atopic dermatitis (AD); this similarity was confirmed by immunofluorescent staining. In summary, besides the well-known dysregulation of immunological, vascular, and neurological functions, we demonstrated prominent permeability barrier alterations in PPR at the molecular level, which highlight the importance of barrier repair therapies for rosacea.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
antimicrobial peptides
barrier function
cornified envelope
papulopustular rosacea
Megjelenés:The Journal of investigative dermatology. - 140 : 10 (2020), p. 1938-1950. -
További szerzők:Dajnoki Zsolt (1985-) (molekuláris biológus) Béke Gabriella (1987-) (molekuláris biológus) Gáspár Krisztián (1974-) (bőrgyógyász) Szabó Imre Lőrinc (1987-) (általános orvos) Janka Eszter Anna (1989-) (bőrgyógyász, népegészségügyi szakember) Póliska Szilárd (1978-) (biológus) Hendrik Zoltán (1986-) (orvos) Méhes Gábor (1966-) (patológus) Töröcsik Dániel (1979-) (bőrgyógyász) Bíró Tamás (1968-) (élettanász) Kapitány Anikó (1979-) (molekuláris biológus) Szegedi Andrea (1964-) (bőrgyógyász)
Internet cím:DOI
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2.

001-es BibID:BIBFORM117681
035-os BibID:(WoS)001138525600001 (Scopus)85181969555
Első szerző:Szeőcs Dóra (PhD hallgató)
Cím:Cell-free ascites from ovarian cancer patients induces Warburg metabolism and cell proliferation through TGFbeta-ERK signalling / Szeőcs D., Vida B., Petővári G., Póliska Sz., Janka E., Sipos A., Uray K., Sebestyén A., Krasznai Z., Bai P.
Dátum:2024
ISSN:2509-2715 2509-2723
Megjegyzések:Ascites plays a key role in supporting the metastatic potential of ovarian cancer cells. Shear stress and carry-over of cancer cells by ascites flow support carcinogenesis and metastasis formation. In addition, soluble factors may participate in the procarcinogenic effects of ascites in ovarian cancer. This study aimed to determine the biological effects of cell-free ascites on carcinogenesis in ovarian cancer cells. Cell-free ascites from ovarian cancer patients (ASC) non-selectively induced cell proliferation in multiple models of ovarian cancer and untransformed primary human dermal fibroblasts. Furthermore, ASC induced a Warburg-type rearrangement of cellular metabolism in A2780 ovarian cancer cells characterized by increases in cellular oxygen consumption and glycolytic flux; increases in glycolytic flux were dominant. ASC induced mitochondrial uncoupling and fundamentally reduced fatty acid oxidation. Ascites-elicited effects were uniform among ascites specimens. ASC-elicited transcriptomic changes in A2780 ovarian cancer cells included induction of the TGF beta-ERK/MEK pathway, which plays a key role in inducing cell proliferation and oncometabolism. ASC-induced gene expression changes, as well as the overexpression of members of the TGF beta signaling system, were associated with poor survival in ovarian cancer patients. We provided evidence that the activation of the autocrine/paracrine of TGF beta signaling system may be present in bladder urothelial carcinoma and stomach adenocarcinoma. Database analysis suggests that the TGF beta system may feed forward bladder urothelial carcinoma and stomach adenocarcinoma. Soluble components of ASC support the progression of ovarian cancer. These results suggest that reducing ascites production may play an essential role in the treatment of ovarian cancer by inhibiting the progression and reducing the severity of the disease.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:GeroScience. - [Epub ahead of print] (2024). -
További szerzők:Vida Beáta (1994-) (szülészet-nőgyógyászat) Petővári Gábor Póliska Szilárd (1978-) (biológus) Janka Eszter Anna (1989-) (bőrgyógyász, népegészségügyi szakember) Sipos Adrienn (1984-) (biológus, biotechnológus) Uray Karen (1964-) (biokémikus) Sebestyén Anna Krasznai Zoárd Tibor (1973-) (szülész-nőgyógyász, gyermeknőgyógyász) Bai Péter (1976-) (biokémikus)
Pályázati támogatás:K142141
NKFIH
FK128387
NKFIH
FK146852
NKFIH
TKP2021-EGA-19
NKFIH
TKP2021-EGA-20
NKFIH
POST-COVID2021-33
Egyéb
NKM2022-30
Egyéb
Internet cím:DOI
Intézményi repozitóriumban (DEA) tárolt változat
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3.

001-es BibID:BIBFORM094083
035-os BibID:(cikkazonosító)600017 (WoS)000652520500001 (Scopus)85106199263
Első szerző:Töröcsik Dániel (bőrgyógyász)
Cím:Epidermal Growth Factor Modulates Palmitic Acid-Induced Inflammatory and Lipid Signaling Pathways in SZ95 Sebocytes / Dániel Törőcsik, Fruzsina Fazekas, Szilárd Póliska, Andrea Gregus, Eszter Anna Janka, Katalin Dull, Andrea Szegedi, Christos C. Zouboulis, Dóra Kovács
Dátum:2021
ISSN:1664-3224
Megjegyzések:Epidermal growth factor (EGF) acts as a paracrine and autocrine mediator of cell proliferation and differentiation in various types of epithelial cells, such as sebocytes, which produce the lipid-rich sebum to moisturize the skin. However, sebum lipids via direct contact and by penetrating through the epidermis may have regulatory roles on epidermal and dermal cells as well. As EGF receptor (EGFR) is expressed throughout the proliferating and the lipid-producing layers of sebaceous glands (SGs) in healthy and acne-involved skin, we investigated the effect of EGF on SZ95 sebocytes and how it may alter the changes induced by palmitic acid (PA), a major sebum component with bioactive roles. We found that EGF is not only a potent stimulator of sebocyte proliferation, but also induces the secretion of interleukin (IL)6 and down-regulates the expression of genes involved in steroid and retinoid metabolism. Importantly, when applied in combination with PA, the PA-induced lipid accumulation was decreased and the cells secreted increased IL6 levels. Functional clustering of the differentially regulated genes in SZ95 sebocytes treated with EGF, PA or co-treated with EGF+PA further confirmed that EGF may be a potent inducer of hyperproliferative/inflammatory pathways (IL1 signaling), an effect being more pronounced in the presence of PA. However, while a group of inflammatory genes was up-regulated significantly in EGF+PA co-treated sebocytes, PA treatment in the absence of EGF, regulated genes only related to cell homeostasis. Meta-analysis of the gene expression profiles of whole acne tissue samples and EGF- and EGF+PA ?treated SZ95 sebocytes showed that the EGF+PA co-activation of sebocytes may also have implications in disease. Altogether, our results reveal that PA-induced lipid accumulation and inflammation can be modulated by EGF in sebocytes, which also highlights the need for system biological approaches to better understand sebaceous (immuno)biology.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Immunology. - 12 (2021), p. 1-16. -
További szerzők:Fazekas Fruzsina (1993-) (biológus) Póliska Szilárd (1978-) (biológus) Gregus Andrea (1980-) (biológus) Janka Eszter Anna (1989-) (bőrgyógyász, népegészségügyi szakember) Dull Katalin (1983-) (molekuláris biológus, genetikus) Szegedi Andrea (1964-) (bőrgyógyász) Zouboulis, Christos C. (1960-) (bőrgyógyász) Kovács Dóra (1988-) (Biológus)
Pályázati támogatás:FK-132296
OTKA
K-128250
OTKA
Bolyai ösztöndíj
MTA
ÚNKP-20-5
Egyéb
GINOP-2.3.2-15-2016-00005
GINOP
Internet cím:Szerző által megadott URL
DOI
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