Research Areas

Cell Biology and Molecular Carcinogenesis Working Group


Research Working Group Lead: Simon Gayther, PhD
Team Members: Justyna Kanska, Kruttika Dabke, Norma Rodriguez-Malave

Research in the Gayther Laboratory is largely focused on understanding the underlying causes of ovarian cancer initiation and development. Simon Gayther, PhD, has a long-established track record in defining the heritable component of ovarian cancer and the functional role of both common and rare risk variants and their target susceptibility genes in the early-stage disease pathogenesis. The overall approach of research in the Gayther Lab is to integrate genomics and epigenomics analyses to identify molecular markers associated with disease, using cell biology modeling studies to validate the role of novel molecular markers in disease biology. The goal is to translate the findings from these studies into the clinical arena to improve risk prediction and prevention strategies, early-stage screening, and disease diagnosis and targeted therapeutics.

Genetic Epidemiology and Variant Discovery Working Group


Research Working Group Lead: Michelle Jones, PhD
Team Members: Alberto Reyes

The Gayther Laboratory uses next-generation sequencing methods to generate data to map genetic variation and apply population-based approaches to identify disease risk variants. Large population-based studies using genome-wide association study (GWAS) approaches have identified more than 30 germline risk loci for ovarian cancer. The Gayther Lab is now focused on understanding how these loci increase disease risk and how they direct disease initiation and progression.

Understanding How Ovarian Cancer Risk Loci Increase Disease Risk


Using genetic epidemiology tools to integrate genetic information with clinical, demographic, and environmental data will improve risk estimation by allowing clinicians to enhanced monitoring and disease prevention. The Gayther Lab applies statistical approaches to model how germline risk variants combine with environmental risk factors to contribute to heritable disease risk. Lab members also using novel statistical methods to investigate how noncoding variants in gene regulatory regions contribute to heritability.

Identifying How Ovarian Cancer Risk Loci Affect Disease Biology


Now that a number of ovarian cancer risk loci have been identified, it is critical that we understand how these variants lead to ovarian cancer. Our group works on functional annotation of risk loci with genomic datasets. In collaboration with Dennis Hazelett, PhD, and Simon Coetzee, and the Functional Genomics and GWAS working group, we are working to identify the functional role of credible causal variants that are identified by fine mapping.

Mapping Novel Variants for Ovarian Cancer


It is a major mission of the Gayther Laboratory to transition from single nucleotide polymorphism (SNP) array-based studies to next-generation sequencing (with a particular focus on whole genome sequencing) studies for variant discovery. This includes developing pipelines for sample handling and quality control, data generation, and informatics for data quality control and analysis.

Genetic epidemiology and variant discovery active projects include:

  • Identifying rare germline variants by exome sequencing in ovarian cancer.
  • Screening ovarian cancer cohorts for ovarian cancer risk variants.
  • Identifying drivers of chemo resistance in recurrent ovarian cancer.
  • Partitioning heritability of ovarian cancer risk loci by genomic function.
  • Developing pipelines for whole genome sequencing variant calling.
  • Identifying shared genetic risk between polycystic ovary syndrome and ovarian cancer.

Functional Genomics and GWAS Working Group


Research Working Group Lead: Jasmine Plummer, PhD
Team Members: Stephanie Chen, Brian Davis

The Functional Genomics Team is focused on the use of next-generation sequencing methods to identify candidate genes from genome-wide association studies (GWAS). Currently over 30 GWAS regions have been identified for ovarian cancer, and we are now focused on understanding how to link these GWAS loci with their most likely causal gene. Current projects include identifying various regions of the genome with functional effects on the transcriptome, with regard to ovarian cancer risk. Using epigenetic profiling methods, our plan is to provide a comprehensive landscape of the genetic determinants of gene expression in ovarian cancer in order to best prioritize genes and loci for further functional follow up.

Identification of Functional Variants in Ovarian GWAS Regions


GWAS studies have identified thousands of common variants associated with numerous diseases, but for the vast majority of genetic associations, the underlying functional mechanisms are unknown. Unlike Mendelian disorders, approximately 90 percent of trait- and risk-associated alleles lie outside of protein coding regions, suggesting that common variants lie in regulatory regions and cause disease by regulating target gene expression. In post-GWAS studies, the overall problem becomes identifying (i) the correct susceptibility gene(s) for each locus and their functional role in disease pathogenesis and (ii) the causal genetic variant(s) that drive disease development. Common variants that influence the activity of specific regulatory elements, such as enhancers, may affect target gene expression through direct, physical interactions. We use 3C/4C technologies to identify physical interactions between susceptibility cell lines. Using epigenetic profiling spanning all ovarian cancer histotypes, we are establishing histotype-specific enhancer profiles. Enhancer marks that overlap with positive 3C/4C SNP interaction are later validated in in vitro neoplastic models of ovarian cancer.

Identifying Candidate Susceptibility Genes Associated with Prostate, Breast and Ovarian Cancer Risk Loci


Prostrate, breast and ovarian cancer share common genetic and lifestyle/environmental etiologies, both epidemiological (hormonal risk factors) and genetic (BRCA1, BRCA2). This shared genetic background suggests similar biological mechanisms drive the development of these cancers. By determining the function of pleiotropic loci, we expect to identify similar mechanisms underlying these different cancer types. Using expression quantitative trait locus (eQTL) analysis, integrated with genetic fine mapping and regulatory profiling, we have identified candidate causal variants at 11 pleiotropic risk loci for prostate, ovarian and breast cancer. We use chromosome conformation capture techniques (3C and 4C) to identify physical interactions between these risk loci and target genes in experimental models of prostrate, breast and ovarian normal and tumor tissues. Positive interactions are then prioritized for further characterization in genome editing assays to confirm function of these plausible functional variants in regulatory regions.

Functional genomics and GWAS working group active projects include:

  • Identifying target genes of pleiotropic risk loci (breast, prostate and ovarian) using chromosome-capture technologies.
  • Epigenetic profiling of histotypes and cells of origin for ovarian cancer using various ChIPseq marks (including H3K27Ac, H3K4me, H3K4me3 and ovarian cancer-specific transcription factors).
  • Establishing TissueChIP seq techniques for epigenomic profiling of ovarian tumors.
  • Developing new chromatin technologies (HiC, ChIAPET) to identify histotype specific topologically associated domains (TADs) in ovarian cancer

Contact the Gayther Lab

8700 Beverly Blvd.
Steven Spielberg Building, Room 155
Los Angeles, CA 90048