Expression of Sestrin Genes in Radiotherapy for Prostate Cancer and Its Association With Fatigue: A Proof-of-Concept Study

被引:9
作者
Gonzalez, Velda J. [1 ,2 ]
Abbas-Aghababazadeh, Farnoosh [3 ]
Fridley, Brooke L. [3 ]
Ghansah, Tomar [4 ]
Saligan, Leorey N. [5 ]
机构
[1] Univ S Florida, Coll Nursing, 12901 Bruce B Downs Blvd,MDC22, Tampa, FL 33612 USA
[2] UPR MDACC Partnership Excellence Canc Res, San Juan, PR USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Biostat & Bioinformat, Tampa, FL USA
[4] Univ S Florida, Dept Mol Med, Tampa, FL USA
[5] NINR, Symptoms Biol Unit, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
sestrins; SESN3; fatigue; Puerto Ricans; prostate cancer; radiotherapy; gene expression; MITOCHONDRIAL DYSFUNCTION; FUNCTIONAL ASSESSMENT; OXIDATIVE STRESS; METABOLISM; BREAST;
D O I
10.1177/1099800417749319
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Genetic factors that influence inflammation and energy production/expenditure in cells may affect patient outcomes following treatment with external beam radiation therapy (EBRT). Sestrins, stress-inducible genes with antioxidant properties, have recently been implicated in several behaviors including fatigue. This proof-of-concept study explored whether the sestrin family of genes (SESN1, SESN2, and SESN3) were differentially expressed from baseline to the midpoint of EBRT in a sample of 26 Puerto Rican men with nonmetastatic prostate cancer. We also examined whether changes in expression of these genes were associated with changes in fatigue scores during EBRT. Method: Participants completed the 13-item Functional Assessment of Cancer TherapyFatigue subscale, Spanish version. Whole blood samples were collected at baseline and at the midpoint of EBRT. Gene expression data were analyzed using the limma package in the R (version R 2.14.0.) statistical software. Linear models and empirical Bayes moderation, adjusted for radiation fraction (total number of days of prescribed radiation treatment), were used to examine potential associations between changes in gene expression and change in fatigue scores. Results: Expression of SESN3 (adjusted p < .01, log fold change -0.649) was significantly downregulated during EBRT, whereas the expressions of SESN1 and SESN2 remained unchanged. After adjustment for radiation fraction, change in SESN3 expression was associated with change in fatigue during EBRT (false discovery rate <.01). Conclusions: Downregulation of SESN3, a novel pharmacoactive stress response gene, was associated with fatigue intensification during EBRT. SESN3 may serve as an interventional target and a biomarker for the cellular and molecular events associated with EBRT-related fatigue.
引用
收藏
页码:218 / 226
页数:9
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