Retinoblastoma: a primitive tumor with multipotential characteristics (Journal article)

Kyritsis, A. P./ Tsokos, M./ Triche, T. J./ Chader, G. J.

The histogenesis of retinoblastoma, the most common intraocular tumor of childhood, has been recently attributed to a primitive retinal cell which is capable of differentiation into both neuronal and glial elements. By manipulating the culture medium constituents and using differentiating agents, such as dibutyryl-cyclic AMP and butyrate, we have now been able to differentiate a population of Y-79 human retinoblastoma cells into cells of pigment epithelial character, as well as into cells of neuronal or glial nature. These studies additionally implicate the outer layer of the optic vesicle in retinoblastoma etiology, and introduce a new system for studying the biologic properties of primitive neural tumors as well as the embryonic development of the retina and central nervous system.
Institution and School/Department of submitter: Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής
Keywords: Bucladesine/pharmacology,Butyric Acid,Butyric Acids/pharmacology,Cell Differentiation/drug effects,Cell Line,Eye Neoplasms/metabolism/*pathology/ultrastructure,Humans,Microscopy, Electron,Retinoblastoma/metabolism/*pathology/ultrastructure,Staining and Labeling
ISSN: 0146-0404
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

Files in This Item:
There are no files associated with this item.

 Please use this identifier to cite or link to this item:
  This item is a favorite for 0 people.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.