A perspective on tumor radiation resistance following high-LET radiation treatment
High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its ability to induce complex and clustered DNA lesions. However, the development of radiation resistance poses a significant barrier. The potential m...
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Published in: | Journal of cancer research and clinical oncology Vol. 150; no. 5; p. 226 |
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02-05-2024
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Abstract | High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its ability to induce complex and clustered DNA lesions. However, the development of radiation resistance poses a significant barrier. The potential molecular mechanisms that could confer resistance development are translesion synthesis (TLS), replication gap suppression (RGS) mechanisms, autophagy, epithelial-mesenchymal transition (EMT) activation, release of exosomes, and epigenetic changes. This article will discuss various types of complex clustered DNA damage, their repair mechanisms, mutagenic potential, and the development of radiation resistance strategies. Furthermore, it highlights the importance of careful consideration and patient selection when employing high-LET radiotherapy in clinical settings. |
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AbstractList | Abstract
High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its ability to induce complex and clustered DNA lesions. However, the development of radiation resistance poses a significant barrier. The potential molecular mechanisms that could confer resistance development are translesion synthesis (TLS), replication gap suppression (RGS) mechanisms, autophagy, epithelial-mesenchymal transition (EMT) activation, release of exosomes, and epigenetic changes. This article will discuss various types of complex clustered DNA damage, their repair mechanisms, mutagenic potential, and the development of radiation resistance strategies. Furthermore, it highlights the importance of careful consideration and patient selection when employing high-LET radiotherapy in clinical settings. High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its ability to induce complex and clustered DNA lesions. However, the development of radiation resistance poses a significant barrier. The potential molecular mechanisms that could confer resistance development are translesion synthesis (TLS), replication gap suppression (RGS) mechanisms, autophagy, epithelial-mesenchymal transition (EMT) activation, release of exosomes, and epigenetic changes. This article will discuss various types of complex clustered DNA damage, their repair mechanisms, mutagenic potential, and the development of radiation resistance strategies. Furthermore, it highlights the importance of careful consideration and patient selection when employing high-LET radiotherapy in clinical settings.High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its ability to induce complex and clustered DNA lesions. However, the development of radiation resistance poses a significant barrier. The potential molecular mechanisms that could confer resistance development are translesion synthesis (TLS), replication gap suppression (RGS) mechanisms, autophagy, epithelial-mesenchymal transition (EMT) activation, release of exosomes, and epigenetic changes. This article will discuss various types of complex clustered DNA damage, their repair mechanisms, mutagenic potential, and the development of radiation resistance strategies. Furthermore, it highlights the importance of careful consideration and patient selection when employing high-LET radiotherapy in clinical settings. High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its ability to induce complex and clustered DNA lesions. However, the development of radiation resistance poses a significant barrier. The potential molecular mechanisms that could confer resistance development are translesion synthesis (TLS), replication gap suppression (RGS) mechanisms, autophagy, epithelial-mesenchymal transition (EMT) activation, release of exosomes, and epigenetic changes. This article will discuss various types of complex clustered DNA damage, their repair mechanisms, mutagenic potential, and the development of radiation resistance strategies. Furthermore, it highlights the importance of careful consideration and patient selection when employing high-LET radiotherapy in clinical settings. |
ArticleNumber | 226 |
Author | Lal, Mitu Rajpurohit, Yogendra Singh Soni, Ishu Sharma, Dhirendra Kumar |
Author_xml | – sequence: 1 givenname: Yogendra Singh surname: Rajpurohit fullname: Rajpurohit, Yogendra Singh email: ysraj@barc.gov.in organization: Molecular Biology Division, Bhabha Atomic Research Centre, Homi Bhabha National Institute, DAE- Deemed University – sequence: 2 givenname: Dhirendra Kumar surname: Sharma fullname: Sharma, Dhirendra Kumar organization: Molecular Biology Division, Bhabha Atomic Research Centre – sequence: 3 givenname: Mitu surname: Lal fullname: Lal, Mitu organization: Molecular Biology Division, Bhabha Atomic Research Centre – sequence: 4 givenname: Ishu surname: Soni fullname: Soni, Ishu organization: Homi Bhabha National Institute, DAE- Deemed University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38696003$$D View this record in MEDLINE/PubMed |
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Keywords | Relative biological effectiveness (RBE) Photon therapy Linear energy transfer (LET) Clustered DNA lesions Translesion synthesis (TLS) |
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Snippet | High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to its... Abstract High-linear energy transfer (LET) radiation is a promising alternative to conventional low-LET radiation for therapeutic gain against cancer owing to... |
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SubjectTerms | Animals Autophagy Cancer Research DNA damage DNA Damage - radiation effects DNA repair DNA Repair - radiation effects Epigenetics Exosomes Hematology Humans Internal Medicine Linear Energy Transfer Matters Arising Medicine Medicine & Public Health Molecular modelling Neoplasms - pathology Neoplasms - radiotherapy Oncology Radiation therapy Radiation Tolerance |
Title | A perspective on tumor radiation resistance following high-LET radiation treatment |
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