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] Circulating tumour cells as biomarkers of prostate, bladder, and kidney cancer
    Michael A. Gorin
    James E. Verdone
    Emma van der Toom
    Trinity J. Bivalacqua
    Mohamad E. Allaf
    Kenneth J. Pienta
    Nature Reviews Urology, 2017, 14 : 90 - 97
  • [22] Circulating tumour cells as biomarkers of prostate, bladder, and kidney cancer
    Gorin, Michael A.
    Verdone, James E.
    van der Toom, Emma
    Bivalacqua, Trinity J.
    Allaf, Mohamad E.
    Pienta, Kenneth J.
    NATURE REVIEWS UROLOGY, 2017, 14 (02) : 90 - 97
  • [23] Circulating tumour cells—monitoring treatment response in prostate cancer
    David T. Miyamoto
    Lecia V. Sequist
    Richard J. Lee
    Nature Reviews Clinical Oncology, 2014, 11 : 401 - 412
  • [24] The prognosis value of circulating tumour cells for localised prostate cancer
    Lu, Y. J.
    Xu, L.
    Mao, X.
    Guo, T.
    Shaw, G.
    CLINICAL & EXPERIMENTAL METASTASIS, 2018, 35 (03) : 209 - 209
  • [25] Gene expression of breast cancer related genes in circulating tumour cells (CTCs) from patients with metastatic breast cancer
    Aaltonen, K. E.
    Graffman, C.
    Larsson, A. -M.
    Ryden, L.
    ANNALS OF ONCOLOGY, 2015, 26
  • [26] Circulating tumour cells: Quantitative gene expression analysis in patients with breast cancer
    Koliogiannis, D.
    Fersis, N.
    Sohn, S.
    Kaul, S.
    GEBURTSHILFE UND FRAUENHEILKUNDE, 2007, 67 (06) : 683 - 683
  • [27] Detection of circulating tumour DNA in localised prostate cancer is associated with more rapid progression to metastatic disease
    Corcoran, Niall
    McCoy, Patrick
    Lau, Edmund
    Reeves, Fairleigh
    Chow, Ken
    Clarkson, Michael
    Kwan, Edmond
    Packwood, Kate
    Northern, Helen
    He, Miao
    Kingsbury, Zoya
    Mangiola, Stefano
    Kerger, Michael
    Furrer, Marc
    Crowe, Helen
    Costello, Anthony
    McBride, David
    Ross, Mark
    Pope, Bernard
    Hovens, Chris
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2020, 16 : 37 - 38
  • [28] Molecular phenotyping of circulating tumour cells in patients with prostate cancer: prediction of distant metastases
    Giesing, Michael
    Driesel, Gerhard
    Molitor, Dietmar
    Suchy, Bernhard
    BJU INTERNATIONAL, 2012, 110 (11C) : E1202 - E1211
  • [29] Tumour suppressor genes in prostate cancer
    MacGrogan, D
    Bookstein, R
    SEMINARS IN CANCER BIOLOGY, 1997, 8 (01) : 11 - 19
  • [30] Circulating tumour cells and survival of patients with gastric cancer
    Pituch-Noworolska, Anna
    Kolodziejczyk, Piotr
    Kulig, Jan
    Drabik, Grazyna
    Szczepanik, Antoni
    Czupryna, Antoni
    Popiela, Tadeusz
    Zembala, Marek
    ANTICANCER RESEARCH, 2007, 27 (1B) : 635 - 640