Positioning of proteasome inhibitors in therapy of solid malignancies
Targeting of the protein degradation pathway, in particular, the ubiquitin-proteasome system, has emerged as an attractive novel cancer chemotherapeutic modality. Although proteasome inhibitors have been most successfully applied in the treatment of hematological malignancies, they also received con...
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| Veröffentlicht in: | Cancer chemotherapy and pharmacology Jg. 81; H. 2; S. 227 - 243 |
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| Sprache: | Englisch |
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01.02.2018
Springer Nature B.V |
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| ISSN: | 0344-5704, 1432-0843, 1432-0843 |
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| Abstract | Targeting of the protein degradation pathway, in particular, the ubiquitin-proteasome system, has emerged as an attractive novel cancer chemotherapeutic modality. Although proteasome inhibitors have been most successfully applied in the treatment of hematological malignancies, they also received continuing interest for the treatment of solid tumors. In this review, we summarize the current positioning of proteasome inhibitors in the treatment of common solid malignancies (e.g., lung, colon, pancreas, breast, and head and neck cancer), addressing topics of their mechanism(s) of action, predictive factors and molecular mechanisms of resistance. |
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| AbstractList | Targeting of the protein degradation pathway, in particular, the ubiquitin-proteasome system, has emerged as an attractive novel cancer chemotherapeutic modality. Although proteasome inhibitors have been most successfully applied in the treatment of hematological malignancies, they also received continuing interest for the treatment of solid tumors. In this review, we summarize the current positioning of proteasome inhibitors in the treatment of common solid malignancies (e.g., lung, colon, pancreas, breast, and head and neck cancer), addressing topics of their mechanism(s) of action, predictive factors and molecular mechanisms of resistance.Targeting of the protein degradation pathway, in particular, the ubiquitin-proteasome system, has emerged as an attractive novel cancer chemotherapeutic modality. Although proteasome inhibitors have been most successfully applied in the treatment of hematological malignancies, they also received continuing interest for the treatment of solid tumors. In this review, we summarize the current positioning of proteasome inhibitors in the treatment of common solid malignancies (e.g., lung, colon, pancreas, breast, and head and neck cancer), addressing topics of their mechanism(s) of action, predictive factors and molecular mechanisms of resistance. Targeting of the protein degradation pathway, in particular, the ubiquitin-proteasome system, has emerged as an attractive novel cancer chemotherapeutic modality. Although proteasome inhibitors have been most successfully applied in the treatment of hematological malignancies, they also received continuing interest for the treatment of solid tumors. In this review, we summarize the current positioning of proteasome inhibitors in the treatment of common solid malignancies (e.g., lung, colon, pancreas, breast, and head and neck cancer), addressing topics of their mechanism(s) of action, predictive factors and molecular mechanisms of resistance. |
| Author | Roeten, Margot S. F. Cloos, Jacqueline Jansen, Gerrit |
| Author_xml | – sequence: 1 givenname: Margot S. F. surname: Roeten fullname: Roeten, Margot S. F. organization: Department of Hematology, VU University Medical Center – sequence: 2 givenname: Jacqueline orcidid: 0000-0001-9150-8026 surname: Cloos fullname: Cloos, Jacqueline email: j.cloos@vumc.nl organization: Department of Hematology, VU University Medical Center, Department of Pediatric Oncology/Hematology, VU University Medical Center – sequence: 3 givenname: Gerrit surname: Jansen fullname: Jansen, Gerrit organization: Amsterdam Rheumatology and Immunology Center, Location VUmc, VU University Medical Center |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29184971$$D View this record in MEDLINE/PubMed |
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| Keywords | Carfilzomib Bortezomib Solid tumors Drug resistance Proteasome inhibitors |
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| PublicationCentury | 2000 |
| PublicationDate | 2018-02-01 |
| PublicationDateYYYYMMDD | 2018-02-01 |
| PublicationDate_xml | – month: 02 year: 2018 text: 2018-02-01 day: 01 |
| PublicationDecade | 2010 |
| PublicationPlace | Berlin/Heidelberg |
| PublicationPlace_xml | – name: Berlin/Heidelberg – name: Germany – name: Heidelberg |
| PublicationTitle | Cancer chemotherapy and pharmacology |
| PublicationTitleAbbrev | Cancer Chemother Pharmacol |
| PublicationTitleAlternate | Cancer Chemother Pharmacol |
| PublicationYear | 2018 |
| Publisher | Springer Berlin Heidelberg Springer Nature B.V |
| Publisher_xml | – name: Springer Berlin Heidelberg – name: Springer Nature B.V |
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