Androgen receptor expression in prostate cancer stem cells: is there a conundrum?

被引:0
|
作者
Nima Sharifi
Elaine M. Hurt
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
关键词
Prostate Cancer; Androgen Receptor; Androgen Deprivation Therapy; LNCaP Cell; Stem Cell Population;
D O I
暂无
中图分类号
学科分类号
摘要
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.
引用
收藏
页码:921 / 923
页数:2
相关论文
共 50 条
  • [31] Rapid signalling by androgen receptor in prostate cancer cells
    Peterziel, H
    Mink, S
    Schonert, A
    Becker, M
    Klocker, H
    Cato, ACB
    ONCOGENE, 1999, 18 (46) : 6322 - 6329
  • [32] Rapid signalling by androgen receptor in prostate cancer cells
    Heike Peterziel
    Sigrun Mink
    Annette Schonert
    Matthias Becker
    Helmut Klocker
    Andrew CB Cato
    Oncogene, 1999, 18 : 6322 - 6329
  • [33] Methylation of androgen receptor promoter in prostate cancer cells
    Fialova, B.
    Trtkova, K.
    Kolar, Z.
    HISTOPATHOLOGY, 2010, 57 : 252 - 253
  • [34] Differential transactivation by the androgen receptor in prostate cancer cells
    Snoek, R
    Bruchovsky, N
    Kasper, S
    Matusik, RJ
    Gleave, M
    Sato, N
    Mawji, NR
    Rennie, PS
    PROSTATE, 1998, 36 (04): : 256 - 263
  • [35] Mechanisms of the androgen receptor splicing in prostate cancer cells
    L L Liu
    N Xie
    S Sun
    S Plymate
    E Mostaghel
    X Dong
    Oncogene, 2014, 33 : 3140 - 3150
  • [36] Gene expression changes following androgen receptor elimination in LNCaP prostate cancer cells
    Eder, IE
    Haag, P
    Basik, M
    Mousses, S
    Bektic, J
    Bartsch, G
    Klocker, H
    MOLECULAR CARCINOGENESIS, 2003, 37 (04) : 181 - 191
  • [37] Complex regulation of human androgen receptor expression by Wnt signaling in prostate cancer cells
    Yang, X.
    Chen, M. -W.
    Terry, S.
    Vacherot, F.
    Bemis, D. L.
    Capodice, J.
    Kitajewski, J.
    de la Taille, A.
    Benson, M. C.
    Guo, Y.
    Buttyan, R.
    ONCOGENE, 2006, 25 (24) : 3436 - 3444
  • [38] Mechanisms of the androgen receptor splicing in prostate cancer cells
    Liu, L. L.
    Xie, N.
    Sun, S.
    Plymate, S.
    Mostaghel, E.
    Dong, X.
    ONCOGENE, 2014, 33 (24) : 3140 - 3150
  • [39] Modulation of androgen receptor activation in prostate cancer cells
    Brinkmann, AO
    de Ruiter, PE
    Doesburg, P
    Steketee, K
    Berrevoets, CA
    Trapman, J
    Biok, LJ
    JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (04): : B7 - B7
  • [40] Pharmacological inhibition of androgen receptor expression induces cell death in prostate cancer cells
    Song, In-Sung
    Jeong, Yu Jeong
    Kim, Jueun
    Seo, Kyoung-Hwa
    Baek, Nam-In
    Kim, Yunlim
    Kim, Choung-Soo
    Jang, Sung-Wuk
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2020, 77 (22) : 4663 - 4673