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Benzyl butyl phthalate influences actin distribution and cell proliferation in rat Py1a osteoblasts.

Abstract
We previously reported that transient administration of phthalates induced actin cytoskeleton disruption in Py1a osteoblasts. However, the mechanism of this transient effect was not elucidated. In this study we provided evidence that the actin cytoskeletal re-established conditions are dependent on new actin expression and synthesis. To assess the role of phthalates in modulating the distribution of actin, confocal and electron microscopy studies were carried out. Results indicated a modification of actin distribution after phthalate administration. In addition, a relation with the nucleoskeletal component lamin A supports the hypothesis that phthalates may participate in regulatory cell processes involving actin in Py1a osteoblasts. The present study also supports the mitogenic effects of phthalates, which involve microfilament disruption, nuclear actin and lamin A. In particular, the increased levels of cyclin D3, which in mammalian cells plays a critical role in G1 to S transition and is a putative proto-oncogene in benzyl butyl phthalate treated cells, suggested a possible effect of the endocrine disruptor in cancer processes.
AuthorsDimitrios Agas, Maria G Sabbieti, Mariolina Capacchietti, Stefano Materazzi, Giovanna Menghi, Giovanni Materazzi, Marja M Hurley, Luigi Marchetti
JournalJournal of cellular biochemistry (J Cell Biochem) Vol. 101 Issue 3 Pg. 543-51 (Jun 01 2007) ISSN: 0730-2312 [Print] United States
PMID17171637 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Actins
  • Phthalic Acids
  • RNA, Messenger
  • butylbenzyl phthalate
Topics
  • Actins (genetics, metabolism)
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Cell Proliferation (drug effects)
  • Cells, Cultured
  • Immunohistochemistry
  • Microscopy, Immunoelectron
  • Osteoblasts (cytology, metabolism, ultrastructure)
  • Phthalic Acids (pharmacology)
  • Protein Biosynthesis (drug effects)
  • RNA, Messenger (genetics, metabolism)
  • Rats

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