Signaling Inhibitors in the Treatment of Prostate Cancer

被引:0
|
作者
Gary R. Hudes
机构
[1] Fox Chase Cancer Center,Department of Medical Oncology
来源
Investigational New Drugs | 2002年 / 20卷
关键词
androgen receptor; growth factors; prostate cancer; signal transduction;
D O I
暂无
中图分类号
学科分类号
摘要
Inhibiting androgen receptor (AR) activation through medical or surgicalcastration and blockade of AR-androgen binding is the cornerstone oftreatment for advanced prostate cancer. However, in most cases tumorgrowth eventually becomes androgen independent. Alternative mechanisms ofAR activation, some of which involve growth factor receptor signaling,have been demonstrated in prostate cancer models, and it is likely that anumber of autocrine and paracrine growth factor ligand-receptorinteractions such as those of epidermal growth factors, fibroblast growthfactors, and insulin-like growth factors contribute to the androgenindependent phenotype by promoting cell proliferation and survival.Blocking activation through growth factor receptors and upstream signalingproteins has emerged as a credible approach to cancer treatment.Successful application of this approach in prostate cancer using a growingarray of small molecule kinase inhibitors, antibodies, and antisenseoligonucleotides will be greatly accelerated by elucidation of the keysignaling pathways that maintain the androgen independent phenotype.
引用
收藏
页码:159 / 172
页数:13
相关论文
共 50 条
  • [11] Combined Treatment with Ultrasound and Immune Checkpoint Inhibitors for Prostate Cancer
    Hayashi, Fuuka
    Shigemura, Katsumi
    Maeda, Koki
    Hiraoka, Aya
    Maeshige, Noriaki
    Ooya, Tooru
    Sung, Shian-Ying
    Yang, Yong-Ming
    Fujisawa, Masato
    JOURNAL OF CLINICAL MEDICINE, 2022, 11 (09)
  • [12] Comparison of the efficacy of different mTOR inhibitors for the treatment of prostate cancer
    D'Abronzo, Leandro Salati
    Beggs, Ryan
    Bose, Swagata
    Ghosh, Paramita
    CLINICAL CANCER RESEARCH, 2012, 18 (10)
  • [13] Role of 5α-Reductase Inhibitors in Prostate Cancer Prevention and Treatment
    Azzouni, Faris
    Mohler, James
    UROLOGY, 2012, 79 (06) : 1197 - 1205
  • [14] mTOR inhibitors for treatment of low-risk prostate cancer
    Liss, Michael A.
    Rickborn, Lanette
    DiGiovanni, John
    Bacich, Dean
    DeGraffenried, Linda A.
    Parihar, Manish
    Thompson, Ian M.
    Sharp, Zelton Dave
    MEDICAL HYPOTHESES, 2018, 117 : 63 - 68
  • [15] COMBINED TREATMENT WITH ULTRASOUND AND IMMUNE CHECKPOINT INHIBITORS FOR PROSTATE CANCER
    Hayashi, Fuuka
    Shigemura, Katsumi
    Kitagawa, Koichi
    Maeshige, Noriaki
    Maeda, Koki
    Fujisawa, Masato
    JOURNAL OF UROLOGY, 2022, 207 (05): : E791 - E791
  • [16] CYP17 inhibitors for prostate cancer treatment - An update
    Moreira, V. M.
    Salvador, J. A. R.
    Vasaitis, T. S.
    Njar, V. C. O.
    CURRENT MEDICINAL CHEMISTRY, 2008, 15 (09) : 868 - 899
  • [17] PD-L1 Inhibitors for the Treatment of Prostate Cancer
    Santoni, Matteo
    Massari, Francesco
    Cheng, Liang
    Cimadamore, Alessia
    Scarpelli, Marina
    Montironi, Rodolfo
    Lopez-Beltran, Antonio
    CURRENT DRUG TARGETS, 2020, 21 (15) : 1558 - 1565
  • [18] In silicodocking of phytocompounds to identify potent inhibitors of signaling pathways involved in prostate cancer
    Jonnalagadda, Bhavana
    Arockiasamy, Sumathy
    Vetrivel, Umashankar
    Abhinand, P. A.
    JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2021, 39 (14): : 5182 - 5208
  • [19] Combination treatment with docetaxel and histone deacetylase inhibitors downregulates androgen receptor signaling in castration-resistant prostate cancer
    Park, Sang Eun
    Kim, Ha-Gyeong
    Kim, Dong Eun
    Jung, Yoo
    Kim, Yunlim
    Jeong, Seong-Yun
    Choi, Eun Kyung
    Hwang, Jung Jin
    Kim, Choung-Soo
    INVESTIGATIONAL NEW DRUGS, 2018, 36 (02) : 195 - 205
  • [20] Combination treatment with docetaxel and histone deacetylase inhibitors downregulates androgen receptor signaling in castration-resistant prostate cancer
    Sang Eun Park
    Ha-Gyeong Kim
    Dong Eun Kim
    Yoo Jung Jung
    Yunlim Kim
    Seong-Yun Jeong
    Eun Kyung Choi
    Jung Jin Hwang
    Choung-Soo Kim
    Investigational New Drugs, 2018, 36 : 195 - 205