Loss of heterozygosity (LOH) of chromosomal regions of tumors is of interest as it is suggestive of the presence of a tumor suppressor gene. Allelic losses on chromosomes 1p and 19q have been found frequently in oligodendrogliomas. Further, LOH on chromosomes 1p and 19q is of prognostic interest, as it has been shown to be highly associated with response to chemotherapy and long survival in patients with gliomas. Previous qualitative analyses of LOH in oligodendroglioma used three or four distally-located CA-repeat polymorphism markers to assess LOH. Loss at a marker was inferred if the ratio of the allele ratio in a normal sample to that in a tumor sample exceeded a fixed threshold. The tumor was then scored as LOH if LOH was observed at all informative markers. Recently, a """"""""medium throughput"""""""" quantitative method for assessing LOH at several markers was applied to gliomas by Dr. Bogler. This methodology raises the possibility of a refined LOH-based classification scheme for brain tumors that may be even more predictive of clinical outcomes than the qualitative, lower throughput LOH methodology. The primary goal of this proposal is to investigate optimal ways of using the multiple quantitative allele ratios to predict clinical outcomes, and thereby develop an LOH-based classification scheme. This goal coincides with priorities for the detection and diagnosis of brain tumors identified by the NCI/NINDS sponsored Brain Tumor Progress Review Group: """"""""to develop a molecular-based classification scheme for brain tumors that can be used to predict tumor behavior."""""""" The methodology developed here is not limited to LOH experiments, but could be applied also to array CGH experiments. A secondary goal of this proposal is to identify and apply unbiased tests for linkage between marker loci and a gene with functional significance.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Research Grants (R03)
Project #
1R03CA105956-01
Application #
6743040
Study Section
Special Emphasis Panel (ZCA1-SRRB-Q (O1))
Program Officer
Arena, Jose Fernando
Project Start
2003-09-30
Project End
2005-08-31
Budget Start
2003-09-30
Budget End
2004-08-31
Support Year
1
Fiscal Year
2003
Total Cost
$81,792
Indirect Cost
Name
Harvard University
Department
Biostatistics & Other Math Sci
Type
Schools of Public Health
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02115
Desantis, Stacia M; Houseman, E Andrés; Coull, Brent A et al. (2012) Supervised Bayesian latent class models for high-dimensional data. Stat Med 31:1342-60
Mandel, Micha; Betensky, Rebecca A (2007) Testing goodness of fit of a uniform truncation model. Biometrics 63:405-12
Houseman, E Andres; Coull, Brent A; Betensky, Rebecca A (2006) Feature-specific penalized latent class analysis for genomic data. Biometrics 62:1062-70