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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

5604 - An expression signature characterizes cancer stem cells from lung adenocarcinoma patients

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Presenters

Alejandro Herreros-Pomares

Citation

Annals of Oncology (2018) 29 (suppl_8): viii649-viii669. 10.1093/annonc/mdy303

Authors

A. Herreros-Pomares1, S. Calabuig Fariñas2, J.D. de Maya3, E. Escorihuela1, E. Durendez-Saez1, A. Blasco Cordellat4, A. Navarro5, E. García-Del-Olmo6, R. Lucas7, R. Farràs8, E. Jantus-Lewintre9, C. Camps10

Author affiliations

  • 1 Molecular Oncology, Fundación de Investigación Hospital General Universitario de Valencia-CIBERONC, 46014 - valencia/ES
  • 2 Dep. Of Pathology, Universitat De València, MOLECULAR ONCOLOGY Fundación Investigación Hospital General Universitario Valencia-CIBERONC;, 46014 - Valencia/ES
  • 3 Lab De Señalización Oncogénica, Centro de Investigación Príncipe Felipe, 46012 - Valencia/ES
  • 4 Medical Oncology Service, Hospital General Universitario Valencia - CIBERONC, 46014 - Valencia/ES
  • 5 Pathology Service, Hospital General Universitario Valencia, 46014 - Valencia/ES
  • 6 Thoracic Surgery Service, Hospital General Universitario Valencia, 46014 - Valencia/ES
  • 7 Dep. Of History Of Science And Documentation, Universitat de València, 46014 - Valencia/ES
  • 8 Oncogenic Signalling Lab., Centro de Investigación Príncipe Felipe, 46012 - Valencia/ES
  • 9 Molecular Oncology Laboratory, Fundación Para La Investigación Hospital General Universitario De Valencia-ciberonc., Biotechnology Department, Universitat Politécnica de València, 46014 - Valencia/ES
  • 10 Molecular Oncology Laboratory, Fundación Para La Investigación, Hospital General Universitario De Valencia-ciberonc, Valencia, Spain., Medical Oncology Service, Hospital General Universitario de Valencia - CIBERONC Valencia, Spain; Medicine Department, Universitat de València, Valencia, Spain, 46014 - Valencia/ES

Resources

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Abstract 5604

Background

Treatment resistance in cancer has been linked to a population of tumor cells with self-renewal properties called cancer stem cells (CSCs). The aim of this study was to isolate and characterize CSCs from lung cancer cell lines and tumor tissue from resected non-small cell lung cancer (NSCLC) patients.

Methods

The study was performed on tumor cells from 8 resected NSCLC patients and 12 NSCLC cell lines. Suspension cultures were established for CSC isolation (3D tumorspheres), whereas differentiated tumor cells were cultured under adherent conditions (2D). In vitro differentiation, proliferation and chemotherapy resistance and in vivo tumor initiation capacity were tested. 60 CSC-related genes were evaluated by RTqPCR. Gene expression results were validated at protein level by immunoblot and IF.

Results

8 out of 20 primary NSCLC cultures were successfully established, forming 3D tight spheroids or loose aggregates. Tumorspheres showed proper differentiation capacity, unlimited exponential growth, high resistance to cisplatin, paclitaxel, vinorelbine and pemetrexed, and great tumor initiation potential. Gene expression analysis revealed high variability between cell lines and patient cultures and that 2D cultures were more homogenous than 3D. Tight tumorspheres expressed more ECAD than loose ones. Lung tumorspheres had significantly higher expression of CSC-related genes (ALDH1A1, KLF4, NANOG, CD44, CD90, CDKN1A, JUNB, MDM2), invasion promoters (MMP9, SNAI1, ITGA6), ligands and receptors of Notch (NOTCH1, NOTCH3, DLL4, JAG1) and Wnt components (CTNNB1 and GSK3B) than their corresponding 2D cultures cells. Based on their significant and consistent overexpression in all tumorspheres: CD44, NANOG, CDKN1A, SNAI1, ITGA6 and NOTCH3 were selected to constitute a gene signature. Protein expression analyses showed overexpression of proteins encoded by the gene signature on tumorspheres from ADC patients.

Conclusions

Lung tumorspheres are a useful platform for CSCs characterization. The expression signature proposed could provide the basis for developing novel therapies for the treatment of lung ADC. Supported by grants RD12/0036/0025 from RTICC-FEDER, PI12-02838 and PI15-00753 from ISCIII.

Clinical trial identification

Legal entity responsible for the study

Laboratorio de Oncología Molecular, Fundación de Investigación Hospital General Universitario de Valencia.

Funding

RTICC-FEDER and Instituto de Salud Carlos III.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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