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The Bladder Cancer Group
at MOMA
About Bladder Cancer
Bladder cancer is a common malignant disease, which basically presents
in two different forms:
superficial tumors (stage Ta and T1), where an attempt to local, organ-sparing
treatment may be made, and muscle invasive cancers (stage T2+), requiring
immediate radical treatment, if cure is intended.
Extensive research has been carried out to find reliable molecular markers
that predict the specific disease course a bladder cancer patient follows.
However, none of these markers have been accepted into clinical routine.
The overall purpose of our research activities is to utilize clinical
material with long-term follow-up information to identify new diagnostic
and prognostic markers for applying the optimal treatment regimens to
patients suffering from bladder cancer. Furthermore, our research aims
at acquiring a better understanding of the bladder cancer disease at the
molecular level.
Bladder Cancer Tissue Bank
Most of our research is based on our large bladder cancer tissue bank,
which now contains more than 40,000 samples of tumor tissue, blood and
urine from more that 1900 cancer patients, collected prospectively since
1994 in close collaboration with the Department
of Urology and the Department
of Oncology at Aarhus University Hospital. All information is organized
in a database, including pathology, treatment regimens followed, and sample
characteristics (size, growth pattern, multiplicity, concomitant carcinoma
in situ). We have full prospective clinical follow-up information for
all patients in the project and consequently it is possible for us to
make searches in the database for patients with specific disease courses.
Current research activities
Analysis of the variation in the genome in correlation to cancer progression
using SNP microarray technology.
Identification and description of the early molecular changes in premalignant
lesions of the bladder (stage Ta tumors and intraurothelial dysplasia)
in relation to bladder cancer development, using various molecular techniques
including gene expression microarrays, mapping SNP microarrays, target
SNP assays, mutation analysis, immunohistochemistry and functional genomics.
Characterization of diagnostic and prognostic markers in the urine and
urinary cells from patients with bladder cancer.
Identification of molecular gene expression signatures for predicting
disease outcome. We have previously identified signatures for disease
stage, recurrence rate, progression potential and for concomitant carcinoma
in situ.
Identification of molecular signatures for predicting disease outcome
in advanced bladder cancer. Including prediction of metastatic disease
in patients scheduled for cystectomy and prediction of response to various
forms of chemotherapy.
Prospective international multi-center validation study of identified
gene expression signatures.

Group Leader
Lars Dyrskjøt Andersen,
Associate Professor, MSc, PhD
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