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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003975naa a2200373 4500
001oai:DiVA.org:liu-88366
003SwePub
008130204s2012 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-883662 URI
024a https://doi.org/10.1371/journal.pone.00531192 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Vegfors, Jennyu Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet4 aut
2451 0a The Expression of Psoriasin (S100A7) and CD24 Is Linked and Related to the Differentiation of Mammary Epithelial Cells
264 c 2012-12-27
264 1b Public Library of Science,c 2012
338 a electronic2 rdacarrier
500 a Funding Agencies|Ingrid Asp Foundation||Swedish Cancer Society||Swedish Psoriasis Association||Welander Foundation||
520 a Psoriasin (S100A7), a member of the S100 family of calcium-binding proteins, is highly expressed in high-grade ductal carcinoma in situ (DCIS) and in the benign hyperproliferative skin disorder psoriasis. The gene that encodes psoriasin and many other S100 genes are located within a gene cluster on chromosome region 1q21, known as the epidermal differentiation complex. This cluster contains genes for several differentiation markers that play important roles in the terminal differentiation of the epidermis. The purpose of the present study was to evaluate the role of psoriasin in the differentiation process of mammary epithelial cells. Normal mammary epithelial cells (MCF10A) cultured in confluence and suspension, conditions known to induce psoriasin expression, demonstrated a shift towards a more differentiated phenotype indicated by an increase in the expression of the luminal differentiation markers CD24 and MUC1 and the reduced expression of the breast stem cell marker CD44. The expression of psoriasin and MUC1 was most pronounced in the CD24(+)-enriched fraction of confluent MCF10A cells. The shift towards a more differentiated phenotype was abolished upon the downregulation of psoriasin using short hairpin RNA (shRNA) and small interfering RNA (siRNA). Using specific inhibitors, we showed that psoriasin and CD24 expression was regulated by reactive oxygen species (ROS) and the nuclear factor (NF)-kappa B signaling pathways. While immunohistochemical analyses of DCIS showed heterogeneity, the expression of psoriasin and CD24 showed a similar staining pattern. Our findings suggest that the expression of psoriasin is linked to the luminal differentiation marker CD24 in mammary epithelial cells. Psoriasin demonstrated an essential role in the shift towards a more differentiated CD24(+) phenotype, supporting the hypothesis that psoriasin plays a role in the differentiation of luminal mammary epithelial cells.
653 a MEDICINE
653 a MEDICIN
700a Petersson, Stinau Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet4 aut0 (Swepub:liu)stipe45
700a Kovacs, Anikou Sahlgrens University Hospital, Sweden4 aut
700a Polyak, Korneliau Harvard University, USA4 aut
700a Enerbäck, Charlottau Linköpings universitet,Östergötlands Läns Landsting,Hudkliniken i Östergötland,Hälsouniversitetet,Cellbiologi4 aut0 (Swepub:liu)chaen00
710a Linköpings universitetb Institutionen för klinisk och experimentell medicin4 org
773t PLOS ONEd : Public Library of Scienceg 7:12q 7:12x 1932-6203
856u https://liu.diva-portal.org/smash/get/diva2:602877/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0053119&type=printable
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-88366
8564 8u https://doi.org/10.1371/journal.pone.0053119

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