TY - JOUR
T1 - Age and Tumor Differentiation-Associated Gene Expression Based Analysis of Non-Familial Prostate Cancers
AU - Sharad, Shashwat
AU - Allemang, Travis C.
AU - Li, Hua
AU - Nousome, Darryl
AU - Ku, Anson Tai
AU - Whitlock, Nichelle C.
AU - Sowalsky, Adam G.
AU - Cullen, Jennifer
AU - Sesterhenn, Isabell A.
AU - McLeod, David G.
AU - Srivastava, Shiv
AU - Dobi, Albert
N1 - Publisher Copyright:
© Copyright © 2021 Sharad, Allemang, Li, Nousome, Ku, Whitlock, Sowalsky, Cullen, Sesterhenn, McLeod, Srivastava and Dobi.
PY - 2021/1/26
Y1 - 2021/1/26
N2 - Prostate cancer incidence in young men has increased. Patients diagnosed at an earlier age are likely to have aggressive prostate cancer and treatment decisions are continuing to be weighted by patient age and life expectancy. Identification of age-associated gene-expression signatures hold great potential to augment current and future treatment modalities. To investigate age-specific tumor associated gene signatures and their potential biomarkers for disease aggressiveness, this study was designed and stratified into well and poorly differentiated tumor types of young (42–58 years) and old (66–73 years) prostate cancer patients. The differentially expressed genes related to tumor-normal differences between non-familial prostate cancer patients were identified and several genes uniquely associated with the age and tumor differentiation are markedly polarized. Overexpressed genes known to be associated with somatic genomic alterations was predominantly found in young men, such as TMPRESS2-ERG and c-MYC. On the other hand, old men have mostly down-regulated gene expressions indicating the loss of protective genes and reduced cell mediated immunity indicated by decreased HLA-A and HLA-B expression. The normalization for the benign signatures between the age groups indicates a significant age and tumor dependent heterogeneity exists among the patients with a great potential for age-specific and tumor differentiation-based therapeutic stratification of prostate cancer.
AB - Prostate cancer incidence in young men has increased. Patients diagnosed at an earlier age are likely to have aggressive prostate cancer and treatment decisions are continuing to be weighted by patient age and life expectancy. Identification of age-associated gene-expression signatures hold great potential to augment current and future treatment modalities. To investigate age-specific tumor associated gene signatures and their potential biomarkers for disease aggressiveness, this study was designed and stratified into well and poorly differentiated tumor types of young (42–58 years) and old (66–73 years) prostate cancer patients. The differentially expressed genes related to tumor-normal differences between non-familial prostate cancer patients were identified and several genes uniquely associated with the age and tumor differentiation are markedly polarized. Overexpressed genes known to be associated with somatic genomic alterations was predominantly found in young men, such as TMPRESS2-ERG and c-MYC. On the other hand, old men have mostly down-regulated gene expressions indicating the loss of protective genes and reduced cell mediated immunity indicated by decreased HLA-A and HLA-B expression. The normalization for the benign signatures between the age groups indicates a significant age and tumor dependent heterogeneity exists among the patients with a great potential for age-specific and tumor differentiation-based therapeutic stratification of prostate cancer.
KW - age-associated gene expression
KW - laser captured microdissection
KW - microarray
KW - prostate cancer
KW - tumor differentiation
KW - tumor-associate gene
UR - http://www.scopus.com/inward/record.url?scp=85100827922&partnerID=8YFLogxK
U2 - 10.3389/fonc.2020.584280
DO - 10.3389/fonc.2020.584280
M3 - Article
AN - SCOPUS:85100827922
SN - 2234-943X
VL - 10
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 584280
ER -