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Chemotherapeutic targeting of microtubules causes epidermal growth factor receptor dephosphorylation

Wu, Xuping (author)
Uppsala universitet,Enheten för onkologi
Lennartsson, Johan (author)
Uppsala universitet,Ludwiginstitutet för cancerforskning
Bergström, Stefan (author)
Uppsala universitet,Enheten för onkologi
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Bergqvist, Michael (author)
Uppsala universitet,Enheten för onkologi
Gullbo, Joachim (author)
Uppsala universitet,Institutionen för medicinska vetenskaper
Ekman, Simon (author)
Uppsala universitet,Enheten för onkologi
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  • Microtubules are important structures for a range of cellular functions including cell division. Drugs that interfere with microtubule function can prevent cells from mitosis and various microtubule targeting drugs are used in a clinical setting. In the current study we investigated the sensitivity of oesophageal cancer cells to different microtubule targeting agents. As expected, experiments demonstrated that these agents in a dose-dependent manner inhibited survival and proliferation of oesophageal cancer cells and disrupted the microtubule network. Unexpectedly, experiments showed that microtubule destabilising agents inhibited phosphorylation and activation of the EGF-receptor, and that a tyrosine phosphatase inhibitor, sodium orthovanadate, could reverse the EGFR dephosphorylation. We propose a model in which disruption of the microtubule network leads to activation of a protein tyrosine phosphatase that can regulate EGFR phosphorylation and activation, indicating an additional mechanism of action of microtubule targeting agents.

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