Human Molecular Genetics, 2001, Vol. 10, No. 20 2313-2318
© 2001 Oxford University Press
Heterogeneity of genetic alterations in prostate cancer: evidence of the complex nature of the disease
Department of Biology, North Carolina Central University, Durham, NC 27707, USA, 1National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA and 2DNA Sciences Laboratories, 3500 Paramount Parkway, Morrisville, NC 27560, USA
Prostate cancer is a complex, multifactorial disease with genetic and environmental factors involved in its etiology. The search for genetic determinants involved in the disease has proven to be challenging, in part because such complex diseases are often not amenable to characterization by linkage analysis and positional cloning as is the case for diseases with simple Mendelian genetic inheritance. Prostate cancer susceptibility loci that have been reported so far include HPC1 (1q24–q25), PCAP (1q42–q43), HPCX (Xq27–q28), CAPB (1p36), HPC20 (20q13), HPC2/ELAC2 (17p11) and 16q23. Prostate cancer aggressiveness loci have also been reported (5q31–q33, 7q32 and 19q12). Further complicating the process is the existence of polymorphisms in several genes associated with prostate cancer including, AR, PSA, SRD5A2, VDR and CYP isoforms. These polymorphisms, however, are not thought to be highly penetrant alleles in families at high risk for prostate cancer. It is clear that prostate cancer etiology involves several genetic loci with no major gene accounting for a large proportion of susceptibility to the disease.
+ To whom correspondence should be addressed. Tel: +1 301 435 5626; Fax: +1 301 435 5465; Email: jdc@nhgri.nih.gov
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