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Search: onr:"swepub:oai:lup.lub.lu.se:31e604c6-4581-4747-8c45-1371ab11bc20" > Harnessing androgen...

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Harnessing androgen receptor pathway activation for targeted alpha particle radioimmunotherapy of breast cancer

Thorek, Daniel L.J. (author)
Washington University in St. Louis
Ku, Anson T. (author)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,Clinical Chemistry, Malmö,Lund University Research Groups
Mitsiades, Nicholas (author)
Baylor College of Medicine
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Veach, Darren (author)
Cornell University,Memorial Sloan-Kettering Cancer Center
Watson, Philip A. (author)
Memorial Sloan-Kettering Cancer Center
Metha, Dipti (author)
Memorial Sloan-Kettering Cancer Center
Strand, Sven Erik (author)
Lund University,Lunds universitet,Forskningsgruppen för Systemisk strålterapi,Forskargrupper vid Lunds universitet,Systemic Radiation Therapy Group,Lund University Research Groups,Skåne University Hospital
Sharma, Sai Kiran (author)
Memorial Sloan-Kettering Cancer Center
Lewis, Jason S. (author)
Cornell University,Memorial Sloan-Kettering Cancer Center
Abou, Diane S. (author)
Washington University in St. Louis
Lilja, Hans G. (author)
University of Oxford,Memorial Sloan-Kettering Cancer Center
Larson, Steven M. (author)
Memorial Sloan-Kettering Cancer Center
McDevitt, Michael R. (author)
Cornell University,Memorial Sloan-Kettering Cancer Center
Ulmert, David (author)
Lund University,Lunds universitet,Tumörmikromiljö,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Tumor microenvironment,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,University of California, Los Angeles,Jonsson Comprehensive Cancer Center,Memorial Sloan-Kettering Cancer Center
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Washington University in St Louis Klinisk kemi, Malmö (creator_code:org_t)
2019
2019
English 11 s.
In: Clinical Cancer Research. - 1078-0432. ; 25:2, s. 881-891
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose: The impact of androgen receptor (AR) activity Results: D-Norgestrel and DHT activated the AR pathway, in breast cancer biology is unclear. We characterized and while 17b-Estradiol did not. Competitive binding for AR tested a novel therapy to an AR-governed target in breast protein showed similar affinity between DHT and D-Norges-cancer. trel, indicating direct AR–ligand interaction. In vivo production Experimental Design: We evaluated the expression of of hK2 was sufficient to achieve site-specific delivery of ther-prototypical AR gene products human kallikrein 2 (hK2) apeutic radionuclide to tumor tissue at >20-fold over back- and PSA in breast cancer models. We screened 13 well-ground muscle uptake; effecting long-term local tumor characterized breast cancer cell lines for hK2 and PSA control. production upon in vitro hormone stimulation by testoster-Conclusions: [225Ac]hu11B6 targeted radiotherapy one [dihydrotestosterone (DHT)]. AR-positive lines were was potentiated by DHT and by D-Norgestrel in murine further evaluated by exposure to estrogen (17b-Estradiol) xenograft models of breast cancer. AR activity in and the synthetic progestin D-Norgestrel. We then evaluated breast cancer correlates with kallikrein-related peptidase-2 an anti-hK2–targeted radiotherapy platform (hu11B6), and can be activated by D-Norgestrel, a common con-labeled with alpha (a)-particle emitting Actinium-225, to traceptive, and AR induction can be harnessed for hK2-specifically treat AR-expressing breast cancer xenografts targeted breast cancer a-emitter radiotherapy. under hormone stimulation.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
NATURVETENSKAP  -- Fysik -- Annan fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Other Physics Topics (hsv//eng)

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