論文

国際誌
2009年3月31日

Multinucleation followed by an acytokinetic cell division in myxofibrosarcoma with giant cell proliferation.

Journal of experimental & clinical cancer research : CR
  • Takashi Ariizumi
  • ,
  • Akira Ogose
  • ,
  • Hiroyuki Kawashima
  • ,
  • Tetsuo Hotta
  • ,
  • Hajime Umezu
  • ,
  • Naoto Endo

28
開始ページ
44
終了ページ
44
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1186/1756-9966-28-44

BACKGROUND: Multinucleated cells are frequently seen in association with a malignant neoplasm. Some of these multinucleated cells are considered to be neoplastic. The mechanism of neoplastic multinucleation remains unknown, but is considered to be induced by either cell-cell fusion or acytokinetic cell division. Myxofibrosarcoma consists of spindled and pleomorphic tumor cells and bizarre multinucleated giant cells. Some of these multinucleated cells are considered to be neoplastic. METHODS: We studied the mitotic activity of the multinucleated cells by Ki-67 immunohistochemistry, and the dynamics and differentiation by live-cell video microscopy in the two myxofibrosarcoma cell lines to determine whether the mechanism of multinucleation is cell-cell fusion or acytokinetic cell division RESULTS: A Ki-67 immunohistochemical analysis revealed a high positive rate of multinucleated cells, as well as mononuclear cells, and mitotic ability was shown in the multinucleated cells. In live-cell video microscopy, most of the multinucleated cells were induced via the process of acytokinetic cell division. CONCLUSION: The current study indicates that a vulnerability of the cytoskeleton components, such as the contractile ring, causes multinucleation to occur from the telophase to the cytokinesis of the cell cycle.

リンク情報
DOI
https://doi.org/10.1186/1756-9966-28-44
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/19335880
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669054
ID情報
  • DOI : 10.1186/1756-9966-28-44
  • PubMed ID : 19335880
  • PubMed Central 記事ID : PMC2669054

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