miR-141 and miR-375 induction and release are different from PSA mRNA and PCA3 upon androgen stimulation of LNCaP cells

被引:12
作者
Tiryakioglu, Duygu [1 ]
Bilgin, Elif [1 ]
Holdenrieder, Stefan [2 ]
Dalay, Nejat [1 ]
Gezer, Ugur [1 ]
机构
[1] Istanbul Univ, Inst Oncol, Dept Basic Oncol, TR-34390 Istanbul, Turkey
[2] Univ Bonn, Inst Clin Chem & Pharmacol, D-53105 Bonn, Germany
关键词
prostate cancer; androgens; microRNAs; molecule release;
D O I
10.3892/br.2013.135
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recent studies have demonstrated the differential expression of miR-141 and miR-375 in circulation of patients with advanced/metastatic prostate cancer (PCa). The aim of this study was to investigate the regulation of miR-141 and miR-375 by androgens and their release into the incubation medium in relation to prostate-specific antigen (PSA) mRNA and prostate cancer antigen 3 (PCA3). Plasma levels of these molecules were measured in a small cohort of patients with localized PCa. As an in vitro cell model we used androgen-sensitive LNCaP cells exposed to an androgen ablation of 48 h, and then treated with dihydrotestosterone (DHT) for 24 h. Expression of the four RNA molecules was measured by quantitative polymerase chain reaction (qPCR). miR-141 and miR-375 were induced in a dose-dependent manner where the median stimulation reached only 1.5-fold at maximum. The effect of DHT on PSA mRNA (up to 30-fold) and PCA3 (up to 195-fold) was much more evident. With regard to the release into the incubation medium, similar results were obtained with the exception of PCA3. At the highest DHT dose (100 nM), median miR-141 and miR-375 release was increased 1.7- and 1.4-fold (P= 0.07), respectively. DHT treatment led to a significant release of PSA mRNA (up to 12-fold) into the medium while PCA3 could not be amplified from the incubation medium. In plasma only PCA3 differed significantly between localized PCa patients and healthy subjects. In conclusion, our study provides evidence that miR-141 and miR-375 are increasingly released into incubation medium from androgen-stimulated cells. However, the extent of their induction was weaker than PSA mRNA or PCA3, suggesting differential regulation by androgens.
引用
收藏
页码:802 / 806
页数:5
相关论文
共 18 条
  • [1] Investigation of miR-21, miR-141, and miR-221 in blood circulation of patients with prostate cancer
    Agaoglu, Fulya Yaman
    Kovancilar, Muge
    Dizdar, Yavuz
    Darendeliler, Emin
    Holdenrieder, Stefan
    Dalay, Nejat
    Gezer, Ugur
    [J]. TUMOR BIOLOGY, 2011, 32 (03) : 583 - 588
  • [2] Circulating miRNAs are correlated with tumor progression in prostate cancer
    Brase, Jan C.
    Johannes, Marc
    Schlomm, Thorsten
    Faelth, Maria
    Haese, Alexander
    Steuber, Thomas
    Beissbarth, Tim
    Kuner, Ruprecht
    Sueltmann, Holger
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2011, 128 (03) : 608 - 616
  • [3] Changes in circulating microRNA levels associated with prostate cancer
    Bryant, R. J.
    Pawlowski, T.
    Catto, J. W. F.
    Marsden, G.
    Vessella, R. L.
    Rhees, B.
    Kuslich, C.
    Visakorpi, T.
    Hamdy, F. C.
    [J]. BRITISH JOURNAL OF CANCER, 2012, 106 (04) : 768 - 774
  • [4] PCA3 noncoding RNA is involved in the control of prostate-cancer cell survival and modulates androgen receptor signaling
    Ferreira, Luciana Bueno
    Palumbo, Antonio
    de Mello, Kivvi Duarte
    Sternberg, Cinthya
    Caetano, Mauricio S.
    de Oliveira, Felipe Leite
    Neves, Adriana Freitas
    Nasciutti, Luiz Eurico
    Goulart, Luiz Ricardo
    Pereira Gimba, Etel Rodrigues
    [J]. BMC CANCER, 2012, 12
  • [5] Comparison of Circulating MicroRNA 141 to Circulating Tumor Cells, Lactate Dehydrogenase, and Prostate-Specific Antigen for Determining Treatment Response in Patients With Metastatic Prostate Cancer
    Gonzales, Jason C.
    Fink, Louis M.
    Goodman, Oscar B., Jr.
    Symanowski, James T.
    Vogelzang, Nicholas J.
    Ward, David C.
    [J]. CLINICAL GENITOURINARY CANCER, 2011, 9 (01) : 39 - 45
  • [6] Cancer statistics, trends, and multiple primary cancer analyses from the surveillance, epidemiology, and end results (SEER) program
    Hayat, Matthew J.
    Howlader, Nadia
    Reichman, Marsha E.
    Edwards, Brenda K.
    [J]. ONCOLOGIST, 2007, 12 (01) : 20 - 37
  • [7] Circulating microRNA in body fluid: a new potential biomarker for cancer diagnosis and prognosis
    Kosaka, Nobuyoshi
    Iguchi, Haruhisa
    Ochiya, Takahiro
    [J]. CANCER SCIENCE, 2010, 101 (10): : 2087 - 2092
  • [8] microRNA biomarkers in body fluids of prostate cancer patients
    Kuner, Ruprecht
    Brase, Jan C.
    Sueltmann, Holger
    Wuttig, Daniela
    [J]. METHODS, 2013, 59 (01) : 132 - 137
  • [9] Castration-Resistant Prostate Cancer: Targeted Therapies
    Leo, S.
    Accettura, C.
    Lorusso, V.
    [J]. CHEMOTHERAPY, 2011, 57 (02) : 115 - 127
  • [10] Circulating microRNAs as stable blood-based markers for cancer detection
    Mitchell, Patrick S.
    Parkin, Rachael K.
    Kroh, Evan M.
    Fritz, Brian R.
    Wyman, Stacia K.
    Pogosova-Agadjanyan, Era L.
    Peterson, Amelia
    Noteboom, Jennifer
    O'Briant, Kathy C.
    Allen, April
    Lin, Daniel W.
    Urban, Nicole
    Drescher, Charles W.
    Knudsen, Beatrice S.
    Stirewalt, Derek L.
    Gentleman, Robert
    Vessella, Robert L.
    Nelson, Peter S.
    Martin, Daniel B.
    Tewari, Muneesh
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (30) : 10513 - 10518