Return to search

The Role of Chronic Inflammation in the Development of Lung Cancer

Inflammation is believed to play a pivotal role in the development of cancer and in particular
lung cancer through both intrinsic and extrinsic pathways. This thesis aimed through 4
manuscripts to determine the role of lung-specific inflammation-related exposures as well as
genetic variants (Single Nucleotide Polymorphism (SNPs)) in genes related to inflammation
pathways in lung cancer risk. Risk factors of particular interest were lung diseases including
emphysema, chronic bronchitis, pneumonia and tuberculosis. Data were collected from a
Toronto-based case-control study and combined with data from the International Lung Cancer
Consortium (17 studies for the non-genetic analyses and 6 studies for the genetic analyses). For
non-genetic data, methods included, but were not limited to, unconditional logistic regression
within single studies, Cox proportional hazards regression, meta-analytic techniques and pooled
analyses techniques. For genetic data, additive models of association across 7,650 SNPs
(selected based on role in inflammation) were pooled across studies and hierarchical modeling
iv
(HM) was used to incorporate prior functional information from various sources concerning the
SNPs of interest. Within the Toronto study (manuscript 1) associations with increased lung
cancer risk were observed for occupational exposures, previous lung diseases and a family
history of cancer. The meta-analysis (manuscript 2) and pooled analysis (manuscript 3) showed
relatively consistent associations between previous lung diseases and lung cancer risk across
histology, gender and smoking categories. Results persisted when examining lung disease
diagnoses made >10 or >20 years before cancer diagnosis. Our pathway-based analysis of
inflammation-related variants and lung cancer risk using HM (manuscript 4) showed that HM is
applicable to SNP analysis using pooled designs where heterogeneity can be incorporated into
SNP priors. After HM a previously observed variant (rs2736100) and novel variant (rs2741354)
were observed to be associated with lung cancer risk at corrected levels and replicated in an
independent population. Taken together these results provide further evidence of both intrinsic
and extrinsic factors affecting risk of lung cancer through inflammation.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:OTU.1807/33939
Date10 December 2012
CreatorsBrenner, Darren
ContributorsHung, Rayjean
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
Languageen_ca
Detected LanguageEnglish
TypeThesis

Page generated in 0.0021 seconds