Helicase-like transcription factor expression is associated with a poor prognosis in Non-Small-Cell Lung Cancer (NSCLC)

BMC Cancer - Tập 18 - Trang 1-10 - 2018
Ludovic Dhont1,2,3, Melania Pintilie4, Ethan Kaufman2, Roya Navab2, Shirley Tam2, Arsène Burny5, Frances Shepherd6, Alexandra Belayew1, Ming-Sound Tsao2,6,7, Céline Mascaux8,9
1Laboratory of Molecular Biology, Research Institute for Health Sciences and Technology, Université de Mons, Mons, Belgium
2Princess Margaret Research Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
3Cellular and Molecular Epigenetics, Université de Liège-GIGA, Liège, Belgium
4Biostatistics Department, University of Toronto, Toronto, Canada
5Université Libre de Bruxelles (ULB), Bruxelles, Belgium
6Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
7Laboratory of Medicine and Pathobiology, University of Toronto, Toronto, Canada
8Department of Muldisciplinary Oncology and Therapeutic Innovations, Assistance Publique des Hôpitaux de Marseille (AP-HM), Aix-Marseille University, Marseille, Cedex 20, France
9Centre de Recherche en Cancérologie de Marseille (CRCM, Cancer Research Center of Marseille), Inserm UMR1068, CNRS UMR7258 and Aix-Marseille University UM105, Marseille, France

Tóm tắt

The relapse rate in early stage non-small cell lung cancer (NSCLC) after surgical resection is high. Prognostic biomarkers may help identify patients who may benefit from additional therapy. The Helicase-like Transcription Factor (HLTF) is a tumor suppressor, altered in cancer either by gene hypermethylation or mRNA alternative splicing. This study assessed the expression and the clinical relevance of wild-type (WT) and variant forms of HLTF RNAs in NSCLC. We analyzed online databases (TCGA, COSMIC) for HLTF alterations in NSCLC and assessed WT and spliced HLTF mRNAs expression by RT-ddPCR in 39 lung cancer cell lines and 171 patients with resected stage I-II NSCLC. In silico analyses identified HLTF gene alterations more frequently in lung squamous cell carcinoma than in adenocarcinoma. In cell lines and in patients, WT and I21R HLTF mRNAs were detected, but the latter at lower level. The subgroup of 25 patients presenting a combined low WT HLTF expression and a high I21R HLTF expression had a significantly worse disease-free survival than the other 146 patients in univariate (HR 1.96, CI 1.17–3.30; p = 0.011) and multivariate analyses (HR 1.98, CI 1.15–3.40; p = 0.014). A low WT HLTF expression with a high I21R HLTF expression is associated with a poor DFS.

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