Expression of tumour progression-associated genes in circulating tumour cells of patients at different stages of prostate cancer

被引:28
|
作者
Russo, Giorgio I. [1 ,2 ]
Bier, Simone [1 ]
Hennenlotter, Joerg [1 ]
Beger, Gunthild [1 ]
Pavlenco, Lucretia [1 ]
van de Flierdt, Jens [3 ]
Hauch, Siegfried [3 ]
Maas, Moritz [1 ]
Walz, Simon [1 ]
Rausch, Steffen [1 ]
Bedke, Jens [1 ]
Morgia, Giuseppe [2 ]
Stenzl, Arnulf [1 ]
Todenhoefer, Tilman [1 ]
机构
[1] Eberhard Karls Univ Tubingen, Dept Urol, Hoppe Seyler Str, D-72076 Tubingen, Germany
[2] Univ Catania, Urol Sect, Dept Surg, Catania, Italy
[3] Qiagen, Res & Dev, Hilden, Germany
关键词
AdnaTest((R)); circulating tumour cells; epithelial mesenchymal transition; prostate cancer; stem cell; #PCSM; #ProstateCancer; MESSENGER-RNA; WHOLE-BLOOD; C-KIT; ABIRATERONE; THERAPY; SYSTEM; AR-V7;
D O I
10.1111/bju.14200
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveTo evaluate the presence of circulating tumour cells (CTCs) at different stages of prostate cancer using the AdnaTest((R)) ProstateCancerDetect kit (Qiagen). Moreover, we aimed to assess the expression of transcripts that are specific for cancer stem cells (AdnaTest StemCell) and epithelial-mesenchymal transition (EMT) in CTCs (AdnaTest EMT), as well as additional genes that are known to promote prostate cancer progression. Patients and MethodsIn this prospective study, we included 81 patients who underwent treatment for prostate cancer between 07/2014 and 02/2015, including: Group A, 18 patients (22.2%) with low-risk clinically localised prostate cancer; Group B, 25 patients (30.9%) with high-risk clinically localised prostate cancer; Group C, 11 patients (13.6%) with metastatic castration-sensitive prostate cancer (mCSPC); and Group D, 27 patients (33.3%) with metastatic castration-resistant prostate cancer (mCRPC). AdnaTest ProstateCancer and AdnaTest StemCell/EMT were performed in all cases. In addition, expression of the androgen receptor (AR), c-met, c-kit and thymidylate synthase (TYMS) in CTCs was assessed using specific polymerase chain reaction assays. ResultsA positive AdnaTest ProstateCancer was present in three (16.7%), two (8.0%), six (54.5%) and 19 (70.5%) patients in groups A, B, C and D, respectively (P < 0.01, chi-squared test). The AdnaTest EMT and AdnaTest StemCell were positive in zero (0.0%), zero (0.0%), one (9.1%), and two (7.4%); and in five (27.8%), four (16.0%), three (27.3%), and 11 (40.7%) patients in groups A, B, C and D, respectively, with no significant differences noted between groups. CTCs expressing TYMS (44.4% and 50.0% vs 13.9%) or AR (18.2% and 25.9% vs 0.0%) were seen more commonly in patients in groups C and D vs patients with non-metastatic disease (all P < 0.05). Expression of c-kit and c-met were rare events, with only two patients positive for either marker. ConclusionsAdnaTest ProstateCancerDetect exhibits positive results mainly in patients with metastatic disease. Expression of AR and TYMS are frequent events in CTCs of patients with advanced disease, whereas c-met and c-kit gene expression is seen in only a small proportion of patients. The implications of these results for the use of CTC analysis as a decision factor for personalised treatment strategies in advanced prostate cancer remain to be determined.
引用
收藏
页码:152 / 159
页数:8
相关论文
共 50 条
  • [21] Detection of circulating tumor cells in different stages of prostate cancer
    Mark Thalgott
    Brigitte Rack
    Tobias Maurer
    Michael Souvatzoglou
    Matthias Eiber
    Veronika Kreß
    Matthias M. Heck
    Ulrich Andergassen
    Roman Nawroth
    Jürgen E. Gschwend
    Margitta Retz
    Journal of Cancer Research and Clinical Oncology, 2013, 139 : 755 - 763
  • [22] Circulating tumour cells in the central and the peripheral venous compartment in patients with metastatic breast cancer
    Peeters, D. J. E.
    Van den Eynden, G. G.
    van Dam, P-J
    Prove, A.
    Benoy, I. H.
    van Dam, P. A.
    Vermeulen, P. B.
    Pauwels, P.
    Peeters, M.
    Van Laere, S. J.
    Dirix, L. Y.
    BRITISH JOURNAL OF CANCER, 2011, 104 (09) : 1472 - 1477
  • [23] Circulating tumour DNA in patients with hepatocellular carcinoma across tumour stages and treatments
    Campani, Claudia
    Imbeaud, Sandrine
    Couchy, Gabrielle
    Ziol, Marianne
    Hirsch, Theo Z.
    Rebouissou, Sandra
    Noblet, Benedicte
    Nahon, Pierre
    Hormigos, Katia
    Sidali, Sabrina
    Seror, Olivier
    Taly, Valerie
    Carrie, Nathalie Ganne
    Laurent-Puig, Pierre
    Zucman-Rossi, Jessica
    Nault, Jean-Charles
    GUT, 2024, 73 (11) : 1870 - 1882
  • [24] Endothelial nitric oxide synthase gene polymorphisms and the shedding of circulating tumour cells in the blood of prostate cancer patients
    Medeiros, R
    Morais, A
    Vasconcelos, A
    Costa, S
    Carrilho, S
    Oliveira, J
    Lopes, C
    CANCER LETTERS, 2003, 189 (01) : 85 - 90
  • [25] Clinical relevance associated to the analysis of circulating tumour cells in patients with solid tumours
    Serrano Fernandez, Ma Jose
    Alvarez Merino, Juan Carlos
    Zubiaurre, Inigo Martinez
    Fernandez Garcia, Ana
    Sanchez Rovira, Pedro
    Lorente Acosta, Jose Antonio
    CLINICAL & TRANSLATIONAL ONCOLOGY, 2009, 11 (10) : 659 - 668
  • [26] Phenotypic diversity of circulating tumour cells in patients with metastatic castration-resistant prostate cancer
    McDaniel, Andrew S.
    Ferraldeschi, Roberta
    Krupa, Rachel
    Landers, Mark
    Graf, Ryon
    Louw, Jessica
    Jendrisak, Adam
    Bales, Natalee
    Marrinucci, Dena
    Zafeiriou, Zafeiris
    Flohr, Penelope
    Sideris, Spyridon
    Crespo, Mateus
    Figueiredo, Ines
    Mateo, Joaquin
    de Bono, Johann S.
    Dittamore, Ryan
    Tomlins, Scott A.
    Attard, Gerhardt
    BJU INTERNATIONAL, 2017, 120 (5B) : E30 - E44
  • [27] Perioperative detection of circulating tumour cells in patients with lung cancer
    Chudasama, Dimple
    Burnside, Nathan
    Beeson, Julie
    Karteris, Emmanouil
    Rice, Alexandra
    Anikin, Vladimir
    ONCOLOGY LETTERS, 2017, 14 (02) : 1281 - 1286
  • [28] Amplification and overexpression of vinculin are associated with increased tumour cell proliferation and progression in advanced prostate cancer
    Ruiz, Christian
    Holz, David R.
    Oeggerli, Martin
    Schneider, Sandra
    Gonzales, Irma M.
    Kiefer, Jeffrey M.
    Zellweger, Tobias
    Bachmann, Alexander
    Koivisto, Pasi A.
    Helin, Heikki J.
    Mousses, Spyro
    Barrett, Michael T.
    Azorsa, David O.
    Bubendorf, Lukas
    JOURNAL OF PATHOLOGY, 2011, 223 (04) : 543 - 552
  • [29] PrLZ Expression Is Associated With the Progression of Prostate Cancer LNCaP Cells
    Li, Lei
    Zhang, Dong
    Zhang, Linlin
    Zhu, Guodong
    Sun, Yi
    Wu, Kaijie
    Wang, Xinyang
    He, Dalin
    MOLECULAR CARCINOGENESIS, 2009, 48 (05) : 432 - 440
  • [30] Circulating tumour cells are associated with increased risk of venous thromboembolism in metastatic breast cancer patients
    M Mego
    U De Giorgi
    K Broglio
    S Dawood
    V Valero
    E Andreopoulou
    B Handy
    J M Reuben
    M Cristofanilli
    British Journal of Cancer, 2009, 101 : 1813 - 1816