Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer
The treatment of cancer patients has been mainly followed using chemotherapy and it is a gold standard in improving prognosis and survival rate of patients. Oxaliplatin (OXA) is a third-platinum anti-cancer agent that reduces DNA synthesis in cancer cells to interfere with their growth and cell cycl...
| Authors: | , , , , , , , , , , , , , , , |
|---|---|
| Format: | article |
| Publication Date: | 2024 |
| Country: | España |
| Institution: | Universitat Autònoma de Barcelona |
| Repository: | Dipòsit Digital de Documents de la UAB |
| Language: | English |
| OAI Identifier: | oai:ddd.uab.cat:311190 |
| Online Access: | https://ddd.uab.cat/record/311190 https://dx.doi.org/urn:doi:10.1016/j.tranon.2023.101846 |
| Access Level: | Open access |
| Keyword: | Oxaliplatin Cancer chemotherapy Drug resistance Molecular pathways Colorectal cancer |
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Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancerHashemi, MehrdadEsbati, NastaranRashidi, MohsenGholami, Sadaf|||0000-0002-4319-3346Raesi, RasoulBidoki, Seyed ShahabadinGoharrizi, Mohammad Ali Sheikh BeigMotlagh, Yasamin Sadat MousaviKhorrami, RaminTavakolpournegari, Alireza|||0000-0002-1555-7149Nabavi, NoushinZou, RongjunMohammadnahal, Leila|||0000-0002-0221-0381Entezari, MalihehTaheriazam, AfshinHushmandi, KiavashOxaliplatinCancer chemotherapyDrug resistanceMolecular pathwaysColorectal cancerThe treatment of cancer patients has been mainly followed using chemotherapy and it is a gold standard in improving prognosis and survival rate of patients. Oxaliplatin (OXA) is a third-platinum anti-cancer agent that reduces DNA synthesis in cancer cells to interfere with their growth and cell cycle progression. In spite of promising results of using OXA in cancer chemotherapy, the process of drug resistance has made some challenges. OXA is commonly applied in treatment of colorectal cancer (CRC) as a malignancy of gastrointestinal tract and when CRC cells increase their proliferation and metastasis, they can obtain resistance to OXA chemotherapy. A number of molecular factors such as CHK2, SIRT1, c-Myc, LATS2 and FOXC1 have been considered as regulators of OXA response in CRC cells. The non-coding RNAs are able to function as master regulator of other molecular pathways in modulating OXA resistance. There is a close association between molecular mechanisms such as apoptosis, autophagy, glycolysis and EMT with OXA resistance, so that apoptosis inhibition, pro-survival autophagy induction and stimulation of EMT and glycolysis can induce OXA resistance in CRC cells. A number of anti-tumor compounds including astragaloside IV, resveratrol and nobiletin are able to enhance OXA sensitivity in CRC cells. Nanoparticles for increasing potential of OXA in CRC suppression and reversing OXA resistance have been employed in cancer chemotherapy. These subjects are covered in this review article to shed light on molecular factors resulting in OXA resistance. 22024-01-0120242024-01-01Article de revisióhttp://purl.org/coar/resource_type/c_dcae04bcVoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/311190https://dx.doi.org/urn:doi:10.1016/j.tranon.2023.101846reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:3111902026-06-06T12:50:31Z |
| dc.title.none.fl_str_mv |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| title |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| spellingShingle |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer Hashemi, Mehrdad Oxaliplatin Cancer chemotherapy Drug resistance Molecular pathways Colorectal cancer |
| title_short |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| title_full |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| title_fullStr |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| title_full_unstemmed |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| title_sort |
Biological landscape and nanostructural view in development and reversal of oxaliplatin resistance in colorectal cancer |
| dc.creator.none.fl_str_mv |
Hashemi, Mehrdad Esbati, Nastaran Rashidi, Mohsen Gholami, Sadaf|||0000-0002-4319-3346 Raesi, Rasoul Bidoki, Seyed Shahabadin Goharrizi, Mohammad Ali Sheikh Beig Motlagh, Yasamin Sadat Mousavi Khorrami, Ramin Tavakolpournegari, Alireza|||0000-0002-1555-7149 Nabavi, Noushin Zou, Rongjun Mohammadnahal, Leila|||0000-0002-0221-0381 Entezari, Maliheh Taheriazam, Afshin Hushmandi, Kiavash |
| author |
Hashemi, Mehrdad |
| author_facet |
Hashemi, Mehrdad Esbati, Nastaran Rashidi, Mohsen Gholami, Sadaf|||0000-0002-4319-3346 Raesi, Rasoul Bidoki, Seyed Shahabadin Goharrizi, Mohammad Ali Sheikh Beig Motlagh, Yasamin Sadat Mousavi Khorrami, Ramin Tavakolpournegari, Alireza|||0000-0002-1555-7149 Nabavi, Noushin Zou, Rongjun Mohammadnahal, Leila|||0000-0002-0221-0381 Entezari, Maliheh Taheriazam, Afshin Hushmandi, Kiavash |
| author_role |
author |
| author2 |
Esbati, Nastaran Rashidi, Mohsen Gholami, Sadaf|||0000-0002-4319-3346 Raesi, Rasoul Bidoki, Seyed Shahabadin Goharrizi, Mohammad Ali Sheikh Beig Motlagh, Yasamin Sadat Mousavi Khorrami, Ramin Tavakolpournegari, Alireza|||0000-0002-1555-7149 Nabavi, Noushin Zou, Rongjun Mohammadnahal, Leila|||0000-0002-0221-0381 Entezari, Maliheh Taheriazam, Afshin Hushmandi, Kiavash |
| author2_role |
author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Oxaliplatin Cancer chemotherapy Drug resistance Molecular pathways Colorectal cancer |
| topic |
Oxaliplatin Cancer chemotherapy Drug resistance Molecular pathways Colorectal cancer |
| description |
The treatment of cancer patients has been mainly followed using chemotherapy and it is a gold standard in improving prognosis and survival rate of patients. Oxaliplatin (OXA) is a third-platinum anti-cancer agent that reduces DNA synthesis in cancer cells to interfere with their growth and cell cycle progression. In spite of promising results of using OXA in cancer chemotherapy, the process of drug resistance has made some challenges. OXA is commonly applied in treatment of colorectal cancer (CRC) as a malignancy of gastrointestinal tract and when CRC cells increase their proliferation and metastasis, they can obtain resistance to OXA chemotherapy. A number of molecular factors such as CHK2, SIRT1, c-Myc, LATS2 and FOXC1 have been considered as regulators of OXA response in CRC cells. The non-coding RNAs are able to function as master regulator of other molecular pathways in modulating OXA resistance. There is a close association between molecular mechanisms such as apoptosis, autophagy, glycolysis and EMT with OXA resistance, so that apoptosis inhibition, pro-survival autophagy induction and stimulation of EMT and glycolysis can induce OXA resistance in CRC cells. A number of anti-tumor compounds including astragaloside IV, resveratrol and nobiletin are able to enhance OXA sensitivity in CRC cells. Nanoparticles for increasing potential of OXA in CRC suppression and reversing OXA resistance have been employed in cancer chemotherapy. These subjects are covered in this review article to shed light on molecular factors resulting in OXA resistance. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2 2024-01-01 2024 2024-01-01 |
| dc.type.none.fl_str_mv |
Article de revisió http://purl.org/coar/resource_type/c_dcae04bc VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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article |
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https://ddd.uab.cat/record/311190 https://dx.doi.org/urn:doi:10.1016/j.tranon.2023.101846 |
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https://ddd.uab.cat/record/311190 https://dx.doi.org/urn:doi:10.1016/j.tranon.2023.101846 |
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Inglés eng |
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Inglés |
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eng |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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info:eu-repo/semantics/openAccess |
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