The research group of Vessela N. Kristensen
Cancer Genome Variation
|”If it were not for the great variability
among individuals medicine might as
well be science and not an art”
Sir William Osler, 1892
The tumor initiation, progression and clinical presentation are directly dependent on its genetic and biochemical environment – the entire body. Our group is working on different projects related to how genetic variation affects occurrence of somatic alterations, gene expression patterns and genome wide copy number alterations in human breast and ovarian tumors. Understanding inherited genetic variability and how it affects crucial biological pathways is likely to lead to new successful prevention and treatment strategies.
The research in the group is focusing on constitutive variation such as single nucleotide polymorphisms (SNPs) and copy number variations (CNVs) in relation to:
- Clinical presentation
- Treatment response and adverse side effects of treatment
- Gene regulation and proximal phenotypes (RNA expression and metabolic profiles)
- Genomic instability, next gen sequencing and integrated pathway analysis in breast cancer.
- The epigenetic landscape of cancer.
- Functional studies in the post-omics era.
- Integrated molecular analysis of miRNAs in breast cancer with clinical outcome.
- Genetic and epigenetic mechanisms underlying treatment response.
- Germline biomarkers for clinical management of sporadic and familiar tumors.
- The immune system in breast carcinogenesis and treatment response.
- NorMa: Normal mammary tissue and cancer development.
- Sequencing the non-canonical genomes.
Oct 27, 2016
Oct 27, 2016
Jan 22, 2014
Vessela N. Kristensen
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Genome Biol, 17 (1), 250
A systematic comparison of copy number alterations in four types of female cancer
BMC Cancer, 16 (1), 913