TCTN2: a novel tumor marker with oncogenic properties
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David Cano-Rodriguez2,*, Susanna Campagnoli1,*, Alberto Grandi1, Matteo Parri1, Elisa De Camilli3, Chaojun Song4, Boquan Jin4, Aurelien Lacombe5, Andrea Pierleoni1,9, Mauro Bombaci7, Chiara Cordiglieri7, Marcel HJ Ruiters2, Giuseppe Viale3,6, Luigi Terracciano5, Paolo Sarmientos1, Sergio Abrignani7, Guido Grandi8, Piero Pileri1, Marianne G. Rots2 and Renata Grifantini1,7
1Externautics SpA, Siena, Italy
2Department of Pathology and Medical Biology, University of Groningen, University Medical Center, Groningen, The Netherlands
3Department of Pathology, European Institute of Oncology, Milan, Italy
4Department of Immunology, The Fourth Military Medical University, Xi’an, China
5Institute of Pathology, University Hospital Basel, Basel, Switzerland
6Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy
7Istituto Nazionale Genetica Molecolare, Padiglione Romeo ed Enrica Invernizzi, IRCCS Ospedale Maggiore Policlinico, Milan, Italy
8Centre for Integrative Biology - CIBIO, University of Trento, Trento, Italy
9Present affiliation: European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge, UK
*These authors have contributed equally to this work
Renata Grifantini, email: firstname.lastname@example.org
Piero Pileri, email: email@example.com
Marianne G. Rots, email: firstname.lastname@example.org
Keywords: TCTN2; cancer; biomarker; oncogene; epigenetic editing
Received: February 17, 2017 Accepted: July 25, 2017 Published: August 24, 2017
Tectonic family member 2 (TCTN2) encodes a transmembrane protein that belongs to the tectonic family, which is involved in ciliary functions. Previous studies have demonstrated the role of tectonics in regulating a variety of signaling pathways at the transition zone of cilia. However, the role of tectonics in cancer is still unclear. Here we identify that TCTN2 is overexpressed in colorectal, lung and ovary cancers. We show that different cancer cell lines express the protein that localizes at the plasma membrane, facing the intracellular milieu. TCTN2 over-expression in cancer cells resulted in an increased ability to form colonies in an anchorage independent way. On the other hand, downregulation of TCTN2 using targeted epigenetic editing in cancer cells significantly reduced colony formation, cell invasiveness, increased apoptosis and impaired assembly of primary cilia. Taken together, our results indicate that TCTN2 acts as an oncogene, making it an interesting cancer-associated protein and a potential candidate for therapeutic applications.
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