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- W2554843886 endingPage "91" @default.
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- W2554843886 abstract "Over the past decades, research has focussed on identifying the genetic underpinnings of prostate cancer. It has been recognized that a number of forms of genetic changes coupled with epigenetic and gene expression changes can increase the prediction to develop prostate cancer. This review outlines the role of somatic copy number alterations (SCNAs), structural rearrangements, point mutations, and single nucleotide polymorphisms (SNPs) as well as miRNAs. Identifying relevant genetic changes offers the ability to develop novel biomarkers to allow early and accurate detection of prostate cancer as well as provide risk stratification of patients following their diagnosis. The concept of personalized or individualized medicine has gained significant attention. Therefore, a better understanding of the genetic and metabolic pathways underlying prostate cancer development offers the opportunity to explore new therapeutic interventions with the possibility of offering patient-specific targeted therapy." @default.
- W2554843886 created "2016-11-30" @default.
- W2554843886 creator A5047781154 @default.
- W2554843886 creator A5090167552 @default.
- W2554843886 date "2015-03-01" @default.
- W2554843886 modified "2023-09-26" @default.
- W2554843886 title "Prostate Cancer Genetics: A Review." @default.
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- W2554843886 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4975354" @default.
- W2554843886 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27683484" @default.
- W2554843886 hasPublicationYear "2015" @default.
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