Disruption of Tacc3 function leads to in vivo tumor regression

R. Yao, Y. Natsume, Y. Saiki, H. Shioya, K. Takeuchi, T. Yamori, H. Toki, I. Aoki, T. Saga, T. Noda

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

The formation of the bipolar spindle is responsible for accurate chromosomal segregation during mitosis. The dynamic instability of microtubules has an important role in this process, and has been shown to be an effective target for cancer chemotherapy. Several agents that target non-microtubule mitotic proteins, including the motor protein Eg5, Aurora kinases and Polo-like kinases, are currently being developed as chemotherapeutic drugs. However, because the efficacies of these drugs remain elusive, new molecular targets that have essential roles in tumor cells are desired. Here, we provide in vivo evidence that transforming acidic coiled-coil-3 (Tacc3) is a potential target for cancer chemotherapy. Using MRI, we showed that Tacc3 loss led to the regression of mouse thymic lymphoma in vivo, which was accompanied by massive apoptosis. By contrast, normal tissues, including the thymus, showed no overt abnormalities, despite high Tacc3 expression. in vitro analysis indicated that Tacc3 depletion induced multi-polar spindle formation, which led to mitotic arrest, followed by apoptosis. Similar responses have been observed in Burkitt's lymphoma and T-ALL. These results show that Tacc3 is a vulnerable component of the spindle assembly in lymphoma cells and is a promising cancer chemotherapy target.

Original languageEnglish
Pages (from-to)135-148
Number of pages14
JournalOncogene
Volume31
Issue number2
DOIs
Publication statusPublished - 2012 Jan 12

Keywords

  • TACC3
  • mitosis
  • p53
  • spindle
  • tumor regression

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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  • Cite this

    Yao, R., Natsume, Y., Saiki, Y., Shioya, H., Takeuchi, K., Yamori, T., Toki, H., Aoki, I., Saga, T., & Noda, T. (2012). Disruption of Tacc3 function leads to in vivo tumor regression. Oncogene, 31(2), 135-148. https://doi.org/10.1038/onc.2011.235