Oncotarget

Research Papers:

Targeting PLK1 as a novel chemopreventive approach to eradicate preneoplastic mucosal changes in the head and neck

D. Vicky de Boer, Sanne R. Martens-de Kemp, Marijke Buijze, Marijke Stigter-van Walsum, Elisabeth Bloemena, Ralf Dietrich, C. René Leemans, Victor W. van Beusechem, Boudewijn J.M. Braakhuis and Ruud H. Brakenhoff _

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Oncotarget. 2017; 8:97928-97940. https://doi.org/10.18632/oncotarget.17880

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Abstract

D. Vicky de Boer1, Sanne R. Martens-de Kemp1, Marijke Buijze1, Marijke Stigter-van Walsum1, Elisabeth Bloemena2,3, Ralf Dietrich4, C. René Leemans1, Victor W. van Beusechem5, Boudewijn J.M. Braakhuis1 and Ruud H. Brakenhoff1

1Department of Otolaryngology-Head and Neck Surgery, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands

2Department of Pathology, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands

3Department of Maxillofacial Surgery/Oral Pathology, Academic Center for Dentistry Amsterdam (ACTA), Amsterdam, The Netherlands

4German Fanconi-Anemia-Help e.V., Unna-Siddinghausen, Germany

5Department of Medical Oncology, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands

Correspondence to:

Ruud H. Brakenhoff, email: [email protected]

Keywords: preneoplastic fields; head and neck squamous cell carcinoma; siRNA screening; targeted treatment; polo-like kinase 1

Received: November 01, 2016    Accepted: March 30, 2017    Published: May 16, 2017

ABSTRACT

Head and neck squamous cell carcinomas (HNSCC) and local relapses thereof develop in preneoplastic fields in the mucosal linings of the upper aerodigestive tract. These fields are characterized by tumor-associated genetic changes, are frequently dysplastic and occasionally macroscopically visible. Currently, no adequate treatment options exist to prevent tumor development. Array-based screening with a panel of tumor-lethal small interfering RNAs (siRNAs) identified Polo-like kinase 1 (PLK1) as essential for survival of preneoplastic cells. Inhibition of PLK1 caused cell death of preneoplastic and HNSCC cells, while primary cells were hardly affected. Both siRNAs and small molecule inhibitors caused a strong G2/M cell cycle arrest accompanied by formation of monopolar spindles. In a xenografted mouse model PLK1 caused a significant tumor growth delay and cures, while chemoradiation had no effect. Thus, PLK1 seems to be a promising target for chemopreventive treatment of preneoplastic cells, and could be applied to prevent HNSCC and local relapses.


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