001     284766
005     20240229155055.0
024 7 _ |2 doi
|a 10.3390/ijms241914890
024 7 _ |2 pmid
|a pmid:37834336
024 7 _ |2 pmc
|a pmc:PMC10573523
024 7 _ |2 ISSN
|a 1422-0067
024 7 _ |2 ISSN
|a 1661-6596
037 _ _ |a DKFZ-2023-02077
041 _ _ |a English
082 _ _ |a 540
100 1 _ |a Koukourakis, Ioannis M
|b 0
245 _ _ |a Prostate Cancer Stem Cells: Biology and Treatment Implications.
260 _ _ |a Basel
|b Molecular Diversity Preservation International
|c 2023
336 7 _ |2 DRIVER
|a article
336 7 _ |2 DataCite
|a Output Types/Journal article
336 7 _ |0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
|a Journal Article
|b journal
|m journal
|s 1697525231_8574
|x Review Article
336 7 _ |2 BibTeX
|a ARTICLE
336 7 _ |2 ORCID
|a JOURNAL_ARTICLE
336 7 _ |0 0
|2 EndNote
|a Journal Article
520 _ _ |a Stem cells differentiate into mature organ/tissue-specific cells at a steady pace under normal conditions, but their growth can be accelerated during the process of tissue healing or in the context of certain diseases. It is postulated that the proliferation and growth of carcinomas are sustained by the presence of a vital cellular compartment resembling stem cells residing in normal tissues: 'stem-like cancer cells' or cancer stem cells (CSCs). Mutations in prostate stem cells can lead to the formation of prostate cancer. Prostate CSCs (PCSCs) have been identified and partially characterized. These express surface markers include CD44, CD133, integrin α2β1, and pluripotency factors like OCT4, NANOG, and SOX2. Several signaling pathways are also over-activated, including Notch, PTEN/Akt/PI3K, RAS-RAF-MEK-ERK and HH. Moreover, PCSCs appear to induce resistance to radiotherapy and chemotherapy, while their presence has been linked to aggressive cancer behavior and higher relapse rates. The development of treatment policies to target PCSCs in tumors is appealing as radiotherapy and chemotherapy, through cancer cell killing, trigger tumor repopulation via activated stem cells. Thus, blocking this reactive stem cell mobilization may facilitate a positive outcome through cytotoxic treatment.
536 _ _ |0 G:(DE-HGF)POF4-312
|a 312 - Funktionelle und strukturelle Genomforschung (POF4-312)
|c POF4-312
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |2 Other
|a chemotherapy
650 _ 7 |2 Other
|a prostate cancer
650 _ 7 |2 Other
|a radiotherapy
650 _ 7 |2 Other
|a stem cells
700 1 _ |0 0000-0003-2977-7895
|a Platoni, Kalliopi
|b 1
700 1 _ |a Kouloulias, Vassilis
|b 2
700 1 _ |0 P:(DE-He78)fa2079aae8ff5ea85fc4fc1504e5a730
|a Arelaki, Stella
|b 3
|u dkfz
700 1 _ |a Zygogianni, Anna
|b 4
773 _ _ |0 PERI:(DE-600)2019364-6
|a 10.3390/ijms241914890
|g Vol. 24, no. 19, p. 14890 -
|n 19
|p 14890
|t International journal of molecular sciences
|v 24
|x 1422-0067
|y 2023
909 C O |o oai:inrepo02.dkfz.de:284766
|p VDB
910 1 _ |0 I:(DE-588b)2036810-0
|6 P:(DE-He78)fa2079aae8ff5ea85fc4fc1504e5a730
|a Deutsches Krebsforschungszentrum
|b 3
|k DKFZ
913 1 _ |0 G:(DE-HGF)POF4-312
|1 G:(DE-HGF)POF4-310
|2 G:(DE-HGF)POF4-300
|3 G:(DE-HGF)POF4
|4 G:(DE-HGF)POF
|a DE-HGF
|b Gesundheit
|l Krebsforschung
|v Funktionelle und strukturelle Genomforschung
|x 0
914 1 _ |y 2023
915 _ _ |0 StatID:(DE-HGF)0100
|2 StatID
|a JCR
|b INT J MOL SCI : 2022
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0200
|2 StatID
|a DBCoverage
|b SCOPUS
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0300
|2 StatID
|a DBCoverage
|b Medline
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0320
|2 StatID
|a DBCoverage
|b PubMed Central
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0501
|2 StatID
|a DBCoverage
|b DOAJ Seal
|d 2023-07-07T16:31:47Z
915 _ _ |0 StatID:(DE-HGF)0500
|2 StatID
|a DBCoverage
|b DOAJ
|d 2023-07-07T16:31:47Z
915 _ _ |0 StatID:(DE-HGF)0030
|2 StatID
|a Peer Review
|b DOAJ : Anonymous peer review
|d 2023-07-07T16:31:47Z
915 _ _ |0 LIC:(DE-HGF)CCBYNV
|2 V:(DE-HGF)
|a Creative Commons Attribution CC BY (No Version)
|b DOAJ
|d 2023-07-07T16:31:47Z
915 _ _ |0 StatID:(DE-HGF)0199
|2 StatID
|a DBCoverage
|b Clarivate Analytics Master Journal List
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0113
|2 StatID
|a WoS
|b Science Citation Index Expanded
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0150
|2 StatID
|a DBCoverage
|b Web of Science Core Collection
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0160
|2 StatID
|a DBCoverage
|b Essential Science Indicators
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)1150
|2 StatID
|a DBCoverage
|b Current Contents - Physical, Chemical and Earth Sciences
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0600
|2 StatID
|a DBCoverage
|b Ebsco Academic Search
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0030
|2 StatID
|a Peer Review
|b ASC
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)9905
|2 StatID
|a IF >= 5
|b INT J MOL SCI : 2022
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0561
|2 StatID
|a Article Processing Charges
|d 2023-08-25
915 _ _ |0 StatID:(DE-HGF)0700
|2 StatID
|a Fees
|d 2023-08-25
920 1 _ |0 I:(DE-He78)B280-20160331
|k B280
|l B280 Translationale funktionelle Krebsgenomik
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)B280-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21