Androgen receptor expression in prostate cancer stem cells: is there a conundrum?
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作者:
Nima Sharifi
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机构:National Cancer Institute Frederick,Cancer Stem Cell Section, Laboratory of Cancer Prevention, National Cancer Institute at Frederick, Center for Cancer Research
Nima Sharifi
Elaine M. Hurt
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机构:National Cancer Institute Frederick,Cancer Stem Cell Section, Laboratory of Cancer Prevention, National Cancer Institute at Frederick, Center for Cancer Research
Elaine M. Hurt
William L. Farrar
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机构:National Cancer Institute Frederick,Cancer Stem Cell Section, Laboratory of Cancer Prevention, National Cancer Institute at Frederick, Center for Cancer Research
William L. Farrar
机构:
[1] National Cancer Institute Frederick,Cancer Stem Cell Section, Laboratory of Cancer Prevention, National Cancer Institute at Frederick, Center for Cancer Research
[2] National Cancer Institute,Medical Oncology Branch, Center for Cancer Research
来源:
Cancer Chemotherapy and Pharmacology
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2008年
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62卷
Androgen deprivation therapy (ADT) is standard frontline therapy for metastatic prostate cancer. However, prostate cancer progresses to a castrate-resistant state. The response of prostate cancer to androgen deprivation is mediated by the androgen receptor (AR). Castrate-resistant disease is marked by a gain-of-function in AR and AR reactivation. The stem cell hypothesis of cancer would therefore predict that AR should be expressed in the prostate cancer stem cell, since genetic selection for gain-of-function changes in AR, such as AR gene amplification, should occur at the level of the stem cell population. Initial reports characterizing prostate cancer stem cells suggest that AR is not expressed in this population, which is an apparent conundrum. Here, we examined the CD44+/24− LNCaP putative stem cell population by in-cell Western and show that AR is expressed at the protein level. Our findings suggest that at least a subset of prostate cancers express AR in the putative stem cell population.
机构:
Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Rajabi, Hasan
Joshi, Maya Datt
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Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Joshi, Maya Datt
Jin, Caining
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Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Jin, Caining
Ahmad, Rehan
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Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Ahmad, Rehan
Kufe, Donald
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机构:
Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USAHarvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
机构:
Univ Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, ItalyUniv Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, Italy
Bonaccorsi, L
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Muratori, M
Marchiani, S
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Univ Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, ItalyUniv Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, Italy
Marchiani, S
Forti, G
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Univ Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, ItalyUniv Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, Italy
Forti, G
Baldi, E
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Univ Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, ItalyUniv Florence, Ctr Res Transfer & High Educ DeNothe, Andol Unit, Dept Clin Physiopathol, I-50139 Florence, Italy