ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score

To investigate potential markers of the prostate cancer (PCa) Gleason score (GS), genetic arrays in 841 PCa patients were conducted followed by functional validation in PCa cell lines. A total of 841 PCa patients who received radical prostatectomy (RP) from November 2003 to July 2019 were enrolled....

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Main Authors: Jong Jin Oh, Jin-Nyoung Ho, Seok-Soo Byun
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/20/5209
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author Jong Jin Oh
Jin-Nyoung Ho
Seok-Soo Byun
author_facet Jong Jin Oh
Jin-Nyoung Ho
Seok-Soo Byun
author_sort Jong Jin Oh
collection DOAJ
description To investigate potential markers of the prostate cancer (PCa) Gleason score (GS), genetic arrays in 841 PCa patients were conducted followed by functional validation in PCa cell lines. A total of 841 PCa patients who received radical prostatectomy (RP) from November 2003 to July 2019 were enrolled. HumanExome BeadChip 12v1-1 (Illumina, Inc.; San Diego, CA, USA) exomic arrays were performed on RP tissue samples. Unconditional logistic regression was used to calculate odds ratios to generate estimates of the relative risk of pathologic GS (≥8); SNPs with the highest association were selected and validated using PCa cell lines (PC3, LNCaP, 22Rv1 and DU145). Following transfection with target-gene siRNA, assays for cell viability, wound healing, and transwell invasion were performed. Mean age of enrolled subjects was 66.34 years and median PSA was 8.43 ng/mL. After RP, 122 patients (14.5%) had pathological Gleason scores ≥8. The results from genotyping with 242,186 SNPs by exomic array revealed that 4 SNPs (rs200944490, rs117555780, rs34625170, and rs61754877) were significantly associated with high pathological GS (≥8) within cut-off level to <i>p</i> < 10<sup>−5</sup>. The most highly associated rs200944490 in ARRDC4 (<i>p</i> = 1.39 × 10<sup>−6</sup>) and rs117555780 in UBXN1 (<i>p</i> = 2.92 × 10<sup>−5</sup>) were selected for further validation. The knockdown of UBXN1 and ARRDC4 led to significantly reduced cell proliferation and suppressed migration and invasiveness in PCa cell lines. Epithelial mesenchymal transition (EMT) markers were significantly down-regulated in si-ARRDC4 and si-UBXN1-transfected cells. The expression levels of PI3K-phosphorylation and Akt phosphorylation and NF-κB were also suppressed following knockdown of UBXN1 and ARRDC4. The rs200944490 (ARRDC4) and rs117555780 (UBXN1) were identified as candidate markers predictive of PCa Gleason score which is strongly associated with cancer aggressiveness. Additional validation in future studies is warranted.
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spelling doaj.art-a99564d8fb284cad9f07f68e8a1730752023-11-22T17:42:03ZengMDPI AGCancers2072-66942021-10-011320520910.3390/cancers13205209ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason ScoreJong Jin Oh0Jin-Nyoung Ho1Seok-Soo Byun2Department of Urology, Seoul National University Bundang Hospital, Seongnam-si 463-707, KoreaDepartment of Urology, Seoul National University Bundang Hospital, Seongnam-si 463-707, KoreaDepartment of Urology, Seoul National University Bundang Hospital, Seongnam-si 463-707, KoreaTo investigate potential markers of the prostate cancer (PCa) Gleason score (GS), genetic arrays in 841 PCa patients were conducted followed by functional validation in PCa cell lines. A total of 841 PCa patients who received radical prostatectomy (RP) from November 2003 to July 2019 were enrolled. HumanExome BeadChip 12v1-1 (Illumina, Inc.; San Diego, CA, USA) exomic arrays were performed on RP tissue samples. Unconditional logistic regression was used to calculate odds ratios to generate estimates of the relative risk of pathologic GS (≥8); SNPs with the highest association were selected and validated using PCa cell lines (PC3, LNCaP, 22Rv1 and DU145). Following transfection with target-gene siRNA, assays for cell viability, wound healing, and transwell invasion were performed. Mean age of enrolled subjects was 66.34 years and median PSA was 8.43 ng/mL. After RP, 122 patients (14.5%) had pathological Gleason scores ≥8. The results from genotyping with 242,186 SNPs by exomic array revealed that 4 SNPs (rs200944490, rs117555780, rs34625170, and rs61754877) were significantly associated with high pathological GS (≥8) within cut-off level to <i>p</i> < 10<sup>−5</sup>. The most highly associated rs200944490 in ARRDC4 (<i>p</i> = 1.39 × 10<sup>−6</sup>) and rs117555780 in UBXN1 (<i>p</i> = 2.92 × 10<sup>−5</sup>) were selected for further validation. The knockdown of UBXN1 and ARRDC4 led to significantly reduced cell proliferation and suppressed migration and invasiveness in PCa cell lines. Epithelial mesenchymal transition (EMT) markers were significantly down-regulated in si-ARRDC4 and si-UBXN1-transfected cells. The expression levels of PI3K-phosphorylation and Akt phosphorylation and NF-κB were also suppressed following knockdown of UBXN1 and ARRDC4. The rs200944490 (ARRDC4) and rs117555780 (UBXN1) were identified as candidate markers predictive of PCa Gleason score which is strongly associated with cancer aggressiveness. Additional validation in future studies is warranted.https://www.mdpi.com/2072-6694/13/20/5209prostate cancerexome array
spellingShingle Jong Jin Oh
Jin-Nyoung Ho
Seok-Soo Byun
ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score
Cancers
prostate cancer
exome array
title ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score
title_full ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score
title_fullStr ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score
title_full_unstemmed ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score
title_short ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score
title_sort arrdc4 and ubxn1 novel target genes correlated with prostate cancer gleason score
topic prostate cancer
exome array
url https://www.mdpi.com/2072-6694/13/20/5209
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