Unraveling LINE‐1 retrotransposition in head and neck squamous cell carcinoma

Author:

Brea‐Iglesias Jenifer12,Oitabén Ana12,Zumalave Sonia2,Rodriguez‐Martin Bernardo2,Gallardo‐Gómez María1,Santamarina Martín2,Pequeño‐Valtierra Ana2,Juaneda‐Magdalena Laura1,García‐Escudero Ramón345,López‐Cedrún José Luis6,Fraga Máximo7,Tubio José M. C.2,Martínez‐Fernández Mónica12ORCID

Affiliation:

1. Translational Oncology Research Group, Galicia Sur Health Research Institute (IIS Galicia Sur) SERGAS‐UVIGO, Estrada de Clara Campoamor Vigo Spain

2. Mobile Genomes Lab, Centre for Research in Molecular Medicine and Chronic Diseases (CiMUS) Universidad de Santiago de Compostela Santiago de Compostela Spain

3. Molecular and Translational Oncology Division CIEMAT (ed 70A) Madrid Spain

4. Research Institute Hospital 12 de Octubre (imas12) Madrid Spain

5. Centro de Investigación Biomédica en Red de Cáncer (CIBERONC) Madrid Spain

6. Department of Maxillofacial Surgery University Hospital of A Coruña A Coruña Spain

7. Pathological Anatomy, Faculty of Medicine University Clinical Hospital & Health Research Institute of Santiago de Compostela (IDIS) Santiago de Compostela Spain

Abstract

The relevant role of LINE‐1 (L1) retrotransposition in cancer has been recurrently demonstrated in recent years. However, the repetitive nature of retrotransposons makes their identification and detection inaccessible for clinical practice. Also, its clinical relevance for cancer patients is still limited. Here, we developed RetroTest, a new efficient method to quantify L1 activation based on targeted sequencing and a sophisticated bioinformatic pipeline, allowing its application in tumor biopsies. Firstly, we performed RetroTest benchmarking to confirm its high specificity and reliability. Then, we unraveled L1 activation in head‐and‐neck squamous cell carcinoma (HNSCC) according to an extensive patient cohort including all tumor stages. L1 retrotransposition estimation revealed a surprisingly early activation in HNSCC progression, contrary to its classical association with advanced stages. In addition, L1 activation together with genomic mutational profiling in normal adjacent tissues supported a field cancerization process, a phenomenon where a tissue develops multiple patches of cells with genetic and/or epigenetic alterations, increasing the risk of cancer development in that area. Overall, our results underline an early L1 activation in HNSCC and field characterization, raising L1 as a promising early diagnostic biomarker and supporting the importance of estimating L1 retrotransposition in clinical practice toward a more efficient diagnosis in HNSCC.

Funder

Fundación Científica Asociación Española Contra el Cáncer

Axencia Galega de Innovación

Instituto de Salud Carlos III

Publisher

Wiley

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