E. Marshall
BC Cancer Research Centre
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Publication
Featured researches published by E. Marshall.
Clinical Cancer Research | 2018
E. Marshall; Emily A. Vucic; Victor D. Martinez; Raymond T. Ng; Wan Lam
Background: Patients with chronic obstructive pulmonary disease (COPD) are at increased risk of developing lung cancer. COPD, clinically defined by reduced lung function measurements, is characterized by chronic airway inflammation, remodeling and loss as well as destruction of alveoli (emphysema). While this disease is an important lung cancer risk factor independent of smoking, the molecular progression from COPD to lung cancer tumourigenesis is relatively understudied. Method: We first analyzed small-airway epithelial gene expression profiles obtained from bronchial brushings from 127 COPD and 140 non-COPD ever-smoker patients. We performed weighted gene correlation network analysis (WGCNA) on these gene expression profiles to discover deregulated gene modules (“metagenes”) associated with reduced lung function (Forced Expiratory Volume at 1 second, FEV-1)—a clinical measure of COPD severity most robustly negatively correlated with lung cancer risk. We then assessed the preservation of these modules in two non-small cell lung cancer (NSCLC) tumor/normal data sets (lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC), n= 887 tumors total) to examine the molecular overlap between COPD and lung cancer. Airway and tumor patient cohorts were matched for age, gender, tumor stage, and smoking status. Result: We discovered 10 distinct small-airway gene expression modules, two of which were significantly negatively correlated (p Conclusion: Coordinated gene expression changes associated with COPD severity measures in small airways and preserved in NSCLC tumors are enriched for G2/M phase transition genes. These genes are further disrupted in tumors, where co-occurring mutations to gatekeeper genes are present. Progression of mitosis during abnormal aneuploidy in lung tissues of COPD patients may confer increased risk of oncogenic transformation in this population, and may underlie the molecular progression from COPD to lung cancer. Citation Format: Erin A. Marshall, Emily A. Vucic, Victor D. Martinez, Raymond T. Ng, Wan L. Lam. Alterations in G2/M phase associated transcriptional networks highlight lung cancer predisposition in COPD patients [abstract]. In: Proceedings of the Fifth AACR-IASLC International Joint Conference: Lung Cancer Translational Science from the Bench to the Clinic; Jan 8-11, 2018; San Diego, CA. Philadelphia (PA): AACR; Clin Cancer Res 2018;24(17_Suppl):Abstract nr A07.
Journal of Thoracic Oncology | 2018
B. Minatel; E. Marshall; C. Anderson; K. Ng; K. Enfield; A. Sage; Zhaolin Xu; W. Lam; Victor D. Martinez
Journal of Thoracic Oncology | 2018
A. Sage; K. Ng; E. Marshall; K. Enfield; G. Stewart; S. Martin; B. Minatel; C. Brown; Ninan Abraham; W. Lam
Journal of Thoracic Oncology | 2018
E. Marshall; G. Stewart; A. Sage; W. Lam; C. Brown
Journal of Thoracic Oncology | 2018
A. Sage; G. Stewart; David A. Rowbotham; K. Enfield; E. Marshall; Victor D. Martinez; C. Anderson; W. Lam
Journal of Thoracic Oncology | 2018
B. Minatel; Victor D. Martinez; A. Sage; E. Marshall; Tomas Tokar; D. Becker-Santos; Wendy P. Robinson; Igor Jurisica; W. Lam
Journal of Thoracic Oncology | 2017
E. Marshall; K. Ng; K. Enfield; S. Martin; Katy Milne; Sonia Kung; Calum MacAulay; W. Lam
Journal of Thoracic Oncology | 2017
A. Sage; G. Stewart; K. Enfield; E. Marshall; Victor D. Martinez; W. Lam
Journal of Thoracic Oncology | 2017
K. Enfield; E. Marshall; K. Ng; C. Anderson; Sara Rahmati; Stephen Lam; Calum MacAulay; William W Lockwood; Aly Karsan; Igor Jurisica; W. Lam
Journal of Thoracic Oncology | 2017
B. Minatel; Victor D. Martinez; D. Becker-Santos; E. Marshall; K. Ng; A. Sage; C. Anderson; Wendy P. Robinson; Igor Jurisica; W. Lam