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HDAC9/p300/F-actin immunoexpression and migration analysis for malignant melanoma stem cell

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dc.creator Kurkutçu, Yesim
dc.creator Ozdemir, Merve
dc.creator ÖZDİL BAY, BERRİN
dc.creator Abdikan, Cemile Sinem Asker
dc.creator Erisik, Derya
dc.creator Yesin, Taha Kadir
dc.creator Avci, Cıgır Biray
dc.creator Aktug, Huseyin
dc.creator Guler, Gunnur
dc.date 2023-10-01T00:00:00Z
dc.date.accessioned 2025-02-25T10:18:54Z
dc.date.available 2025-02-25T10:18:54Z
dc.identifier 28f2c52b-ab4f-41b9-b319-6d439191fcb0
dc.identifier 10.1016/j.prp.2023.154829
dc.identifier https://avesis.sdu.edu.tr/publication/details/28f2c52b-ab4f-41b9-b319-6d439191fcb0/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/99144
dc.description Melanoma is an aggressive tumor with a poor prognosis that worsens in the metastatic phase. Distruptions of epigenetic mechanisms is known to effect cancer stem cells (CSCs) activity. Malignant melanoma (MM) progression may be promoted by changes in the genetic structure of CSC. Thus, treatments that target epigenetic modifications could be a promising weapon, especially in melanoma. Here, we compared p300, HDAC9, and F-actin proteins in melanoma CSCs (CD133+), non-CSCs (CD133-) and CHL-1 cell line, as well as cell migration and division rates. At 4 and 6 h, P300 protein levels in CHL-1 and CD133 + were remarkably similar, and the CD133- showed increases in expression levels as the incubation period lengthened. HDAC9 protein intensity decreased in CHL-1, increased in the CD133-, and remained relatively unchanged in the CD133+ as the incubation period lengthened. The mean value of F-actin expression level increased in all cell group with time, when the highest increase observed in CHL-1. In conclusion, our studies contribute to the management of metastatic diseases in the future and offer new insight into the molecular basis of the initiation and progression of MM.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title HDAC9/p300/F-actin immunoexpression and migration analysis for malignant melanoma stem cell
dc.type info:eu-repo/semantics/article


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