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Sökning: id:"swepub:oai:lup.lub.lu.se:281ecb90-78e2-47d8-a4b2-142564c07d9a" > Preclinical evaluat...

Preclinical evaluation of PSMA expression in response to androgen receptor blockade for theranostics in prostate cancer

Lückerath, Katharina (författare)
University of California, Los Angeles
Wei, Liu (författare)
University of California, Los Angeles
Fendler, Wolfgang P. (författare)
University Hospital Essen
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Evans-Axelsson, Susan (författare)
Lund University,Lunds universitet,Urologisk cancerforskning, Malmö,Forskargrupper vid Lunds universitet,Urological cancer, Malmö,Lund University Research Groups
Stuparu, Andreea D. (författare)
University of California, Los Angeles
Slavik, Roger (författare)
University of California, Los Angeles
Mona, Christine E. (författare)
University of California, Los Angeles
Calais, Jeremie (författare)
University of California, Los Angeles
Rettig, Matthew (författare)
University of California, Los Angeles
Reiter, Robert E. (författare)
University of California, Los Angeles
Herrmann, Ken (författare)
University Hospital Essen
Radu, Caius G. (författare)
University of California, Los Angeles
Czernin, Johannes (författare)
University of California, Los Angeles
Eiber, Matthias (författare)
Klinikum rechts der Isar
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 (creator_code:org_t)
2018-10-29
2018
Engelska.
Ingår i: EJNMMI Research. - : Springer Science and Business Media LLC. - 2191-219X. ; 8
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Prostate-specific membrane antigen (PSMA)-directed radioligand therapy (RLT) is a promising yet not curative approach in castration-resistant (CR) prostate cancer (PC). Rational combination therapies may improve treatment efficacy. Here, we explored the effect of androgen receptor blockade (ARB) on PSMA expression visualized by PET and its potential additive effect when combined with 177Lu-PSMA RLT in a mouse model of prostate cancer. Methods: Mice bearing human CRPC (C4-2 cells) xenografts were treated with 10 mg/kg enzalutamide (ENZ), with 50 mg/kg bicalutamide (BIC), or vehicle (control) for 21 days. PSMA expression was evaluated by 68Ga-PSMA11 PET/CT and quantified by flow cytometry of tumor fine needle aspirations before treatment and on days 23, 29, 34, and 39 post-therapy induction. For the RLT combination approach, mice bearing C4-2 tumors were treated with 10 mg/kg ENZ or vehicle for 21 days before receiving either 15 MBq (84 GBq/μmol) 177Lu-PSMA617 or vehicle. DNA damage was assessed as phospho-γH2A.X foci in tumor biopsies. Reduction of tumor volume on CT and survival were used as study endpoints. Results: Tumor growth was delayed by ARB while 68Ga-PSMA11 uptake increased up to 2.3-fold over time when compared to controls. ABR-induced upregulation of PSMA expression was confirmed by flow cytometry. Phospho-γH2A.X levels increased 1.8- and 3.4-fold at 48 h in response to single treatment ENZ or RLT and ENZ+RLT, respectively. Despite significantly greater DNA damage and persistent increase of PSMA expression at the time of RLT, no additional tumor growth retardation was observed in the ENZ+RLT group (vs. RLT only, p = 0.372 at day 81). Median survival did not improve significantly when ENZ was combined with RLT. Conclusion: ARB-mediated increases in PSMA expression in PC xenografts were evident by 68Ga-PSMA11 PET imaging and flow cytometry. 177Lu-PSMA617 effectively decreased C4-2 tumor size. However, while pre-treatment with ARB increased DNA damage significantly, it did not result in synergistic effects when combined with RLT.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Ga-PSMA PET/CT
Androgen receptor blockade
Prostate cancer
PSMA
Radioligand therapy

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