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Long Non-Coding RNAs as Strategic Molecules to Augment the Radiation Therapy in Esophageal Squamous Cell Carcinoma.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2020 Sep 16; Vol. 21 (18). Date of Electronic Publication: 2020 Sep 16. - Publication Year :
- 2020
-
Abstract
- Intrinsic resistance to ionizing radiation is the major impediment in the treatment and clinical management of esophageal squamous cell carcinoma (ESCC), leading to tumor relapse and poor prognosis. Although several biological and molecular mechanisms are responsible for resistance to radiotherapy in ESCC, the molecule(s) involved in predicting radiotherapy response and prognosis are still lacking, thus requiring a detailed understanding. Recent studies have demonstrated an imperative correlation amongst several long non-coding RNAs and their involvement in complex cellular networks like DNA damage and repair, cell cycle, apoptosis, proliferation, and epithelial-mesenchymal transition. Additionally, accumulating evidence has suggested abnormal expression of lncRNAs in malignant tumor cells before and after radiotherapy effects in tumor cells' sensitivity. Thus, lncRNAs indeed represent unique molecules that can influence tumor cell susceptibility for various clinical interventions. On this note, herein, we have summarized the current status of lncRNAs in augmenting resistance/sensitivity in ESCC against radiotherapy. In addition, we have also discussed various strategies to increase the radiosensitivity in ESCC cells under clinical settings.
- Subjects :
- DNA Damage
Esophageal Squamous Cell Carcinoma genetics
Esophageal Squamous Cell Carcinoma therapy
Gene Expression Regulation, Neoplastic
Genetic Therapy
Humans
MicroRNAs genetics
Molecular Targeted Therapy
RNA, Antisense therapeutic use
RNA, Long Noncoding therapeutic use
Radiation Tolerance genetics
Esophageal Squamous Cell Carcinoma radiotherapy
RNA, Antisense genetics
RNA, Long Noncoding genetics
RNA, Neoplasm genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 21
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 32947897
- Full Text :
- https://doi.org/10.3390/ijms21186787