Abstract
Prostate cancer is a serious disease in terms of its high incidence and mortality rate in the USA and around the world. The prostate specific antigen (PSA) has been used for prostate cancer diagnosis and follow-up of treatment but a number of challenges remain. Epigenetic biomarkers, especially methylation and microRNA (miR) biomarkers provide an opportunity for diagnosis, prognosis, and recurrence of prostate cancer. Differential global methylation has shown some promising results. In this chapter, the emphasis is given on those biomarkers which can be assayed noninvasively in a prospective study and in a clinic. Challenges in the field, especially the validation of potential biomarkers, and their potential solutions are provided in this chapter.
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Abbreviations
- BPH:
-
Benign prostate hyperplasia
- EMR:
-
Electronic medical records
- HDM:
-
Histone demethylase
- HMT:
-
Histone methyltransferase
- MS-MLPA:
-
Methylation-specific multiplex ligation probe amplification
- PBMC:
-
Peripheral mononuclear blood cells
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Acknowledgments
We are thankful to Dr. L. Yan of EpigenDX Corporation (MA,USA). Portion of this work was supported by NIH-NIGMS grant# T34GM100831 and NIH-NCI grant# R01CA164318-03S1 to HNB.
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Banerjee, H.N., Kahan, W., Kumar, V., Verma, M. (2018). Methylation and MicroRNA Profiling to Understand Racial Disparities of Prostate Cancer. In: Dumitrescu, R., Verma, M. (eds) Cancer Epigenetics for Precision Medicine . Methods in Molecular Biology, vol 1856. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-8751-1_15
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DOI: https://doi.org/10.1007/978-1-4939-8751-1_15
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