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J Med Oncl Ther 2017 | Volume 2 Issue 4

Oncology and Biomarkers Summit

November 27-28, 2017 | Atlanta, USA

Annual Congress on

New biomarkers for prognosis of aggressive prostate cancer

Carlos S Moreno

Emory University, USA

A

large number of men are diagnosedwith prostate cancer each

year, but many will not experience morbidity or mortality as a

result of their cancers. Therefore, biomarkers for prostate cancer

are necessary to carefully select patients for initial diagnostic

biopsy or to facilitate care decisions for men who have already

been diagnosed with prostate cancer. RNA-based approaches to

biomarker discovery allow the investigation of non-coding RNAs,

gene fusion transcripts, splice variants and multi-gene expression

panels in tissue, urine or blood as opportunities to improve care

decisions. In an effort to identify biomarkers of recurrence, we

performed global RNA sequencing on 106 formalin-fixed, paraffin-

embedded (FFPE) prostatectomy samples from 100 patients

at three independent sites, defining a 24-gene signature panel

(Sig24). The 24 genes in this panel have functions in cell cycle

progression, angiogenesis, hypoxia, apoptosis, PI3K signaling,

steroid metabolism, translation, chromatin modification and

transcription. In our validation study, patients with high Sig24

scores had an increased risk of developing metastasis (HR: 3.78,

95% CI: 1.96-7.29, p<0.001) or experiencing prostate cancer

specificmortality (PCSM) (HR: 6.54, 95%CI: 2.16-19.83, p<0.001) in

an independent validation case cohort set of 235patients fromthe

MayoClinic. Thefindingsof this studydemonstratetheapplicability

of Sig24 for the prognosis of metastasis or PCSM following radical

prostatectomy. Future studies investigating the combination of

Sig24with available prognostic tests may provide new approaches

to improve risk stratification for patients with prostate cancer.

Speaker Biography

Carlos S Moreno is Associate Professor of Pathology and Laboratory Medicine and Biomedical

Informatics at Emory University, where he is a Member of the Winship Cancer Institute in

the Cancer Genetics and Epigenetics Program. He has obtained his BS and MS in Aeronautics

and Astronautics from MIT and worked for NASA before he earned his PhD in Genetics and

Molecular Biology from Emory University in 1998. He specializes in Cancer Bioinformatics and

Cancer Genomics and his laboratory has used whole genome expression analysis and next-

generation sequencing to identify biomarkers of aggressive disease in prostate cancer.

e:

cmoreno@emory.edu