Journals / Annals of Medical Research / 2019 / Cilt: 26 - Sayı: 6

Enzalutamide restores the testosterone effect on H19 expression in prostate cancer cells but not in exosomes

Pages
1056–1059
Publication Date
2022-10-12
DOI
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Cellular, and exosomalexpression of H19 was investigated using a quantitative polymerase chain reaction assay.Results: Our findings revealed that the mean cellular H19 expression decreased approximately 2.3 fold after androgen stimulationof PCa cells.

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Objective & Hypothesis:Aim: Cellular or exosomal expression of an oncofetal lncRNA gene H19, was evaluated during androgen stimulation viadihydrotestosterone (DHT) or androgen receptor (AR) blockage via enzalutamide in cultured hormone-sensitive prostate cancer(PCa) cells which overexpress the androgen receptor (LNCaP-AR+) in the present study.Material and Methods: Cells were treated using DHT (10 nM) and/or enzalutamide (10 uM) for 24 hours.
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Key Findings & Data:Cellular, and exosomalexpression of H19 was investigated using a quantitative polymerase chain reaction assay.Results: Our findings revealed that the mean cellular H19 expression decreased approximately 2.3 fold after androgen stimulationof PCa cells.
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Conclusion & Impact:Enzalutamide restored DHT effect with AR blockage, and we found increased H19 expression with the combined useof DHT, and enzalutamide compared with the levels in the control cells (p
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Aim: Cellular or exosomal expression of an oncofetal lncRNA gene H19, was evaluated during androgen stimulation viadihydrotestosterone (DHT) or androgen receptor (AR) blockage via enzalutamide in cultured hormone-sensitive prostate cancer(PCa) cells which overexpress the androgen receptor (LNCaP-AR+) in the present study.Material and Methods: Cells were treated using DHT (10 nM) and/or enzalutamide (10 uM) for 24 hours. Cellular, and exosomalexpression of H19 was investigated using a quantitative polymerase chain reaction assay.Results: Our findings revealed that the mean cellular H19 expression decreased approximately 2.3 fold after androgen stimulationof PCa cells. Enzalutamide restored DHT effect with AR blockage, and we found increased H19 expression with the combined useof DHT, and enzalutamide compared with the levels in the control cells (p

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Cite This Article

GEZER, U., OZGUR, E. (2022). Enzalutamide restores the testosterone effect on H19 expression in prostate cancer cells but not in exosomes. Annals of Medical Research, Cilt: 26 - Sayı: 6, 1056–1059. https://ajindex.com/articles/446896

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References (16)

  1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin 2018;68:7-30
  2. Filella X, Foj L. Prostate Cancer Detection and Prognosis: From Prostate Specific Antigen (PSA) to Exosomal Biomarkers. Int J Mol Sci 2016;17: pii: E1784 3. Beer TM, Armstrong AJ, Rathkopf DE, et al. Enzalutamide in metastatic prostate cancer before chemotherapy. N Engl J Med 2014;371:424-33. 4. de Bono JS, Logothetis CJ, Molina A, et al. COU-AA-301 Investigators. Abiraterone and increased survival in metastatic prostate cancer. N Engl J Med 2011;364:1995- 2005
  3. Tran C, Ouk S, Clegg NJ, et al. Development of a secondgeneration antiandrogen for treatment of advanced prostate cancer. Science 2009;324:787-90
  4. Hoffman RM. Clinical practice. Screening for prostate cancer. N Engl J Med 2011;365:2013-9
  5. Melo SA, Luecke LB, Kahlert C, et al. Glypican-1 identifies cancer exosomes and detects early pancreatic cancer. Nature 2015;523:177-82
  6. Tanaka Y, Kamohara H, Kinoshita K, et al. Clinical impact of serum exosomal microRNA-21 as a clinical biomarker in human esophageal squamous cell carcinoma. Cancer 2013;119:1159-67
  7. Gezer U, Özgür E, Cetinkaya M, et al. Long non-coding RNAs with low expression levels in cells are enriched in secreted exosomes. Cell Biol Int 2014;38:1076-9
  8. Yoshimoto R, Mayeda A, Yoshida M, et al. MALAT1 long noncoding RNA in cancer. Biochim Biophys Acta 2016;1859:192- 9
  9. Taheri M, Omrani MD, Ghafouri-Fard S. Long non-coding RNA expression in bladder cancer. Biophys Rev 2017;8:1205-13
  10. Yuan JH, Yang F, Wang F, et al. A long noncoding RNA activated by TGF-β promotes the invasion-metastasis cascade in hepatocellular carcinoma. Cancer Cell 2014;25:666-81
  11. Gupta RA, Shah N, Wang KC, et al. Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis. Nature 2010;464:1071–6
  12. Prensner JR, Iyer MK, Sahu A, et al. The long noncoding RNA SChLAP1 promotes aggressive prostate cancer and antagonizes the SWI/SNF complex. Nat Genet 2013;45:1392–8
  13. Hung CL, Wang LY, Yu YL, et al. A long noncoding RNA connects c-Myc to tumor metabolism. Proc Natl Acad Sci U S A 2014;111:18697–702
  14. Cheng W, Zhang Z, Wang J. Long noncoding RNAs: new players in prostate cancer. Cancer Lett 2013;339:8-14
  15. Brannan CI, Dees EC, Ingram RS, et al. The product of the H19 gene may function as an RNA. Mol Cell Biol 1990;10:28- 36
  16. Yoshimizu T, Miroglio A, Ripoche MA, et al. The H19 locus acts in vivo as a tumor suppressor. Proc