Ovarian Cancer Cells Sensitized To Chemotherapy By Extracellular Protein

Main Category: Cancer / Oncology
Also Included In: Women's Health / Gynecology
Article Date: 11 Dec 2007 - 3:00 PDT

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Scientists have uncovered critical new details about the mechanisms that modulate the response of ovarian cancer cells to chemotherapy. The research, published by Cell Press in the December issue of Cancer Cell, helps to explain why many patients develop resistance to the taxane class of drugs and may lead to improved treatment of ovarian cancer.

Cancer cells divide rapidly and undergo extensive microtubule-driven restructuring as they proliferate. Taxanes, such as paclitaxel (Taxol), interfere with the dynamic growth of microtubules by directly binding to them and making them more stable and, as a result, disrupt the normal process of cell division. Paclitaxel has been used extensively to treat lung, ovarian and breast cancers but drug resistance limits the clinical usefulness of this drug to only about half of breast or ovarian cancer patients.

Although it is clear that taxane resistance is associated with a loss of stable microtubules and that microtubule stability can be influenced by signals from the extracellular matrix (ECM), a role for ECM proteins in the modulation of paclitaxel sensitivity has not been established. To explore the connection between regulation of microtubules and taxane resistance, Dr. James D. Brenton from the Cancer Research UK Cambridge Research Institute in Cambridge, England and colleagues performed an extensive examination of ovarian cancer cell lines that were sensitive or resistant to paclitaxel.

The researchers found that the ECM protein, transforming growth factor beta induced (TGFBI), was significantly reduced in paclitaxel-resistant cells. Importantly, TGFBI mediated sensitization to paclitaxel and loss of TGFBI was sufficient to induce paclitaxel resistance. TGFBI induced microtubule stabilization that was dependent on integrin-mediated FAK and Rho signaling. Further, analysis of ovarian cancer samples taken after treatment with paclitaxel revealed that paclitaxel-induced cell death was associated with high levels of TGFBI expression.

These results identify TGFBI as an ECM protein that induces microtubule stability and modulates sensitivity to paclitaxel in ovarian cell lines and in patients receiving paclitaxel therapy. "Our findings have potentially significant clinical applications as TGFBI protein expression is lost in one third of primary ovarian and lung cancers and FAK is low or absent in one-third of ovarian cancer patients," explains Dr. Brenton. "It is possible that TGFBI could be used as a biomarker for selecting patients likely to respond to taxane therapy. In addition, proteins that activate TGFBI or mimic its action may be an effective strategy for modulating the response to widely used drugs like paclitaxel or docetaxel."

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Article adapted by Medical News Today from original press release.
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The researchers include Ahmed Ashour Ahmed, Cancer Research UK Cambridge Research Institute, Cambridge, UK, and Hutchison/MRC Research Centre, Cambridge, UK, and Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK; Carlos Caldas, Cancer Research UK Cambridge Research Institute, Cambridge, UK, and Hutchison/MRC Research Centre, Cambridge, UK; Ashraf E.K. Ibrahim, Cancer Research UK Cambridge Research Institute, Cambridge, UK; Jillian Temple, Cancer Research UK Cambridge Research Institute, Cambridge, UK, and Hutchison/MRC Research Centre, Cambridge, UK; Cherie Blenkiron, Hutchison/MRC Research Centre, Cambridge, UK; Maria Vias, Hutchison/MRC Research Centre, Cambridge, UK; Charlie E. Massie, Hutchison/MRC Research Centre, Cambridge, UK; N. Gopalakrishna Iyer, Hutchison/MRC Research Centre, Cambridge, UK; Helena M. Earl, Hutchison/MRC Research Centre, Cambridge, UK; James D. Brenton, Cancer Research UK Cambridge Research Institute, Cambridge, UK, and the Hutchison/MRC Research Centre, Cambridge, UK; Anthony D. Mills, Hutchison/MRC Research Centre, Cambridge, UK; Adam McGeoch, Hutchison/MRC Research Centre, Cambridge, UK; Stephen D. Bell, Hutchison/MRC Research Centre, Cambridge, UK; Ronald A. Laskey, Hutchison/MRC Research Centre, Cambridge, UK; Robin Crawford, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK; Barbara Nicke, Cancer Research UK London Research Institute, London, UK; Julian Downward, Cancer Research UK London Research Institute, London, UK; and Charles Swanton, Cancer Research UK London Research Institute, London, UK.

Source: Cathleen Genova
Cell Press