Clinical Trial Update and Novel Therapeutic Approaches for Metastatic Prostate Cancer.
(2011) In Current Medicinal Chemistry 18. p.4440-4453- Abstract
- Recurrent prostate cancer (PCa) remains a major clinical challenge. Invasive and metastatic PCa lesions often exhibit a partial and time-limited response to therapy before the cancer progresses and the patient succumbs to the disease. Despite recent advances in early diagnosis and treatment, approximately one-third of treated patients will relapse and become resistant to currently available treatments. In this review we evaluate current treatment practices and recent advances in therapy for localized prostate malignancy and advanced, metastatic prostate cancer. Some of the promising new drugs for PCa treatment include MDV3100, an androgen receptor (AR) antagonist that prevents androgens from binding to the AR and nuclear translocation and... (More)
- Recurrent prostate cancer (PCa) remains a major clinical challenge. Invasive and metastatic PCa lesions often exhibit a partial and time-limited response to therapy before the cancer progresses and the patient succumbs to the disease. Despite recent advances in early diagnosis and treatment, approximately one-third of treated patients will relapse and become resistant to currently available treatments. In this review we evaluate current treatment practices and recent advances in therapy for localized prostate malignancy and advanced, metastatic prostate cancer. Some of the promising new drugs for PCa treatment include MDV3100, an androgen receptor (AR) antagonist that prevents androgens from binding to the AR and nuclear translocation and co-activator recruitment of the ligand-receptor complex; abiraterone, an orally administered drug that irreversibly inhibits a rate-limiting enzyme in androgen biosynthesis, CYP17; and several newer cytotoxic drugs (epothilones, satraplatin). Key new insights are that cancer stem cells play a role in PCa and that PCa cells are dependent on the AR for proliferation, even in the hormone refractory state of the disease. We also discuss potential molecular targets for new drug candidates for the treatment of metastatic PCa. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2150730
- author
- Larsson, Rikard ; Mongan, Nigel ; Johansson, M C ; Shcherbina, Liliya LU ; Abrahamsson, Per-Anders LU ; Gudas, L ; Sterner, Olov and Persson, Jenny L LU
- organization
- publishing date
- 2011
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Current Medicinal Chemistry
- volume
- 18
- pages
- 4440 - 4453
- publisher
- Bentham Science Publishers
- external identifiers
-
- wos:000299011500002
- pmid:21864277
- scopus:80053042692
- ISSN
- 0929-8673
- language
- English
- LU publication?
- yes
- id
- a9e415ff-123a-4d02-abf9-f112fa25aae8 (old id 2150730)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/21864277?dopt=Abstract
- date added to LUP
- 2016-04-04 09:31:00
- date last changed
- 2022-01-29 18:16:19
@article{a9e415ff-123a-4d02-abf9-f112fa25aae8, abstract = {{Recurrent prostate cancer (PCa) remains a major clinical challenge. Invasive and metastatic PCa lesions often exhibit a partial and time-limited response to therapy before the cancer progresses and the patient succumbs to the disease. Despite recent advances in early diagnosis and treatment, approximately one-third of treated patients will relapse and become resistant to currently available treatments. In this review we evaluate current treatment practices and recent advances in therapy for localized prostate malignancy and advanced, metastatic prostate cancer. Some of the promising new drugs for PCa treatment include MDV3100, an androgen receptor (AR) antagonist that prevents androgens from binding to the AR and nuclear translocation and co-activator recruitment of the ligand-receptor complex; abiraterone, an orally administered drug that irreversibly inhibits a rate-limiting enzyme in androgen biosynthesis, CYP17; and several newer cytotoxic drugs (epothilones, satraplatin). Key new insights are that cancer stem cells play a role in PCa and that PCa cells are dependent on the AR for proliferation, even in the hormone refractory state of the disease. We also discuss potential molecular targets for new drug candidates for the treatment of metastatic PCa.}}, author = {{Larsson, Rikard and Mongan, Nigel and Johansson, M C and Shcherbina, Liliya and Abrahamsson, Per-Anders and Gudas, L and Sterner, Olov and Persson, Jenny L}}, issn = {{0929-8673}}, language = {{eng}}, pages = {{4440--4453}}, publisher = {{Bentham Science Publishers}}, series = {{Current Medicinal Chemistry}}, title = {{Clinical Trial Update and Novel Therapeutic Approaches for Metastatic Prostate Cancer.}}, url = {{http://www.ncbi.nlm.nih.gov/pubmed/21864277?dopt=Abstract}}, volume = {{18}}, year = {{2011}}, }