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Integration of somatic deletion analysis of prostate cancers and germline linkage analysis of prostate cancer families reveals two small consensus regions for prostate cancer genes at 8p.

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TLDR
Using high-resolution Affymetrix arrays, two small common deleted regions are identified among 55 prostate tumors at 8p23.1 and 8p21.3 and these smaller consensus regions may facilitate a more effective search for prostate cancer genes at 7p.
Abstract
The evidence for tumor suppressor genes at 8p is well supported by many somatic deletion studies and genetic linkage studies. However, it remains a challenge to pinpoint the tumor suppressor genes at 8p primarily because the implicated regions are broad. In this study, we attempted to narrow down the implicated regions by incorporating evidence from both somatic and germline studies. Using high-resolution Affymetrix arrays, we identified two small common deleted regions among 55 prostate tumors at 8p23.1 (9.8–11.5 Mb) and 8p21.3 (20.6–23.7 Mb). Interestingly, our fine mapping linkage analysis at 8p among 206 hereditary prostate cancer families also provided evidence for linkage at these two regions at 8p23.1 (5.8–11.2 Mb) and at 8p21.3 (19.6–23.9 Mb). More importantly, by combining the results from the somatic deletion analysis and genetic linkage analysis, we were able to further narrow the regions to ∼1.4 Mb at 8p23.1 and ∼3.1 Mb at 8p21.3. These smaller consensus regions may facilitate a more effective search for prostate cancer genes at 8p. [Cancer Res 2007;67(9):4098–103]

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DLC-1:a Rho GTPase-activating protein and tumour suppressor

TL;DR: The deleted in liver cancer family of RhoGAP domain proteins are connected to DLC‐1 as a metastasis suppressor gene and evidence for roles of DLC‐2 and DLC‐3 in neoplasia is found.
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Tumor suppressive miR-124 targets androgen receptor and inhibits proliferation of prostate cancer cells

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Homozygous Deletions and Recurrent Amplifications Implicate New Genes Involved in Prostate Cancer

TL;DR: The genomic alterations revealed in this study provide an important catalog of positional information relevant to efforts aimed at deciphering the molecular genetic basis of prostate cancer.
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Sox7 Is an Independent Checkpoint for β-Catenin Function in Prostate and Colon Epithelial Cells

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References
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Journal ArticleDOI

Mutation and Cancer: Statistical Study of Retinoblastoma

TL;DR: The hypothesis is developed that retinoblastoma is a cancer caused by two mutational events, in the dominantly inherited form, one mutation is inherited via the germinal cells and the second occurs in somatic cells.
Journal Article

Parametric and nonparametric linkage analysis: a unified multipoint approach.

TL;DR: It is shown that NPL is robust to uncertainty about mode of inheritance, is much more powerful than commonly used nonparametric methods, and loses little power relative to parametric linkage analysis, and appears to be the method of choice for pedigree studies of complex traits.
Journal ArticleDOI

Allele-sharing models: LOD scores and accurate linkage tests.

TL;DR: Starting with a test statistic for linkage analysis based on allele sharing, an associated one-parameter model is proposed that allows exact calculation of likelihood ratios and LOD scores and has been implemented by a simple modification of existing software.
Journal ArticleDOI

Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers.

TL;DR: A gene, MCC, which encodes an 829-amino acid protein with a short region of similarity to the G protein-coupled m3 muscarinic acetylcholine receptor is identified and is a candidate for the putative colorectal tumor suppressor gene located at chromosome region 5q21.
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