Grant Details
Grant Number: |
5R01CA250018-04 Interpret this number |
Primary Investigator: |
Wang, Liang |
Organization: |
H. Lee Moffitt Cancer Ctr & Res Inst |
Project Title: |
Functional Characterization of Prostate Cancer Risk Loci By High Throughput Sequencing |
Fiscal Year: |
2023 |
Abstract
SUMMARY
Although the causes of human cancers are attributable to many factors, there is substantial evidence that
genetics likely plays a key role. Previous studies have used population-based approaches, such as genome-
wide association studies (GWASs), to identify cancer-associated genetic susceptibility variants (single nucleotide
polymorphisms or SNPs) in the human genome. Although GWASs have reported thousands of SNP loci
associated with an increased cancer risk, functional effects of these risk-SNPs remain largely unknown. Because
many of the risk-SNPs are located in genomic regions without known protein-coding genes and some reside
several hundred kilobases from any nearby gene, it is believed that many, if not most, of these SNPs have
regulatory effects on the genes that cause these cancers. To identify regulatory SNPs responsible for the disease
risk, we propose to apply two novel high-throughput sequencing technologies to screen thousands of candidate
SNPs at prostate cancer risk loci. Aim 1 is to determine SNP-dependent transcription factor (TF) binding
differences at prostate cancer risk loci through IP-SNPs-seq. Aim 2 is to determine biological significance of
SNP-dependent sequence variants at prostate cancer risk loci through CRISPRi-SNPs-seq. Aim 3 is to
functionally characterize a set of selected SNPs and their target genes. Successful completion of the proposed
study will gain further understanding of the functional role of GWAS-implicated SNPs. Characterization of the
functional effects of cancer risk loci will facilitate the translation of population-based discovery into biological
mechanisms and will eventually benefit clinical practice.
Publications
Extracellular microvesicle microRNAs, along with imaging metrics, improve detection of aggressive prostate cancer.
Authors: Avasthi K.K.
, Choi J.
, Glushko T.
, Manley B.J.
, Yu A.
, Pow-Sang J.
, Gatenby R.
, Wang L.
, Balagurunathan Y.
.
Source: Medrxiv : The Preprint Server For Health Sciences, 2024-08-23 00:00:00.0; , .
EPub date: 2024-08-23 00:00:00.0.
PMID: 39228742
Related Citations
Identify Regulatory eQTLs by Multiome Sequencing in Prostate Single Cells.
Authors: Tian Y.
, Wu L.
, Huang C.C.
, Wang L.
.
Source: Biorxiv : The Preprint Server For Biology, 2024-06-21 00:00:00.0; , .
EPub date: 2024-06-21 00:00:00.0.
PMID: 38948854
Related Citations
Combined SNPs sequencing and allele specific proteomics capture reveal functional causality underpinning the 2p25 prostate cancer susceptibility locus.
Authors: Wei G.H.
, Dong D.
, Zhang P.
, Liu M.
, Wei Y.
, Wang Z.
, Xu W.
, Zhang Q.
, Zhu Y.
, Zhang Q.
, et al.
.
Source: Research Square, 2024-04-04 00:00:00.0; , .
EPub date: 2024-04-04 00:00:00.0.
PMID: 38645058
Related Citations
5-hydroxymethylcytosine sequencing in plasma cell-free DNA identifies unique epigenomic features in prostate cancer patients resistant to androgen deprivation therapy.
Authors: Li Q.
, Huang C.C.
, Huang S.
, Tian Y.
, Huang J.
, Bitaraf A.
, Dong X.
, Nevalanen M.T.
, Zhang J.
, Manley B.J.
, et al.
.
Source: Medrxiv : The Preprint Server For Health Sciences, 2023-10-16 00:00:00.0; , .
EPub date: 2023-10-16 00:00:00.0.
PMID: 37904926
Related Citations
Combined CRISPRi and proteomics screening reveal a cohesin-CTCF-bound allele contributing to increased expression of RUVBL1 and prostate cancer progression.
Authors: Tian Y.
, Dong D.
, Wang Z.
, Wu L.
, Park J.Y.
, PRACTICAL consortium
, Wei G.H.
, Wang L.
.
Source: American Journal Of Human Genetics, 2023-08-03 00:00:00.0; 110(8), p. 1289-1303.
PMID: 37541187
Related Citations
Extensive germline-somatic interplay contributes to prostate cancer progression through HNF1B co-option of TMPRSS2-ERG.
Authors: Giannareas N.
, Zhang Q.
, Yang X.
, Na R.
, Tian Y.
, Yang Y.
, Ruan X.
, Huang D.
, Yang X.
, Wang C.
, et al.
.
Source: Nature Communications, 2022-11-28 00:00:00.0; 13(1), p. 7320.
EPub date: 2022-11-28 00:00:00.0.
PMID: 36443337
Related Citations
Novel role of prostate cancer risk variant rs7247241 on PPP1R14A isoform transition through allelic TF binding and CpG methylation.
Authors: Tian Y.
, Soupir A.
, Liu Q.
, Wu L.
, Huang C.C.
, Park J.Y.
, Wang L.
.
Source: Human Molecular Genetics, 2022-05-19 00:00:00.0; 31(10), p. 1610-1621.
PMID: 34849858
Related Citations
Clinical Applications of Liquid Biopsy in Prostate Cancer: From Screening to Predictive Biomarker.
Authors: Ionescu F.
, Zhang J.
, Wang L.
.
Source: Cancers, 2022-03-29 00:00:00.0; 14(7), .
EPub date: 2022-03-29 00:00:00.0.
PMID: 35406500
Related Citations
Cancer Detection and Classification by CpG Island Hypermethylation Signatures in Plasma Cell-Free DNA.
Authors: Huang J.
, Soupir A.C.
, Schlick B.D.
, Teng M.
, Sahin I.H.
, Permuth J.B.
, Siegel E.M.
, Manley B.J.
, Pellini B.
, Wang L.
.
Source: Cancers, 2021-11-09 00:00:00.0; 13(22), .
EPub date: 2021-11-09 00:00:00.0.
PMID: 34830765
Related Citations