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EDITORIAL article
Front. Mol. Biosci.
Sec. Molecular Diagnostics and Therapeutics
Volume 11 - 2024 |
doi: 10.3389/fmolb.2024.1533057
This article is part of the Research Topic LncRNA and Their Role on Epigenome in Cancer View all 6 articles
Editorial: LncRNA and their role on epigenome in cancer
Provisionally accepted- 1 Shaanxi Normal University, Xi'an, China
- 2 University of Naples Parthenope, Naples, Campania, Italy
- 3 IRCCS SYNLAB SDN, Naples, Campania, Italy
In this research topic "LncRNA and their role on epigenome in cancer", a series of original comprehensive studies and reviews were collected, that describe the critical role of LncRNA (long non-coding RNA) in the regulation of cancer.LncRNAs refer to non-protein-coding RNA molecules with a length of more than 200 bp (Srinivas et al., 2024;Zhang, 2024). More studies have shown that LncRNAs play an important role in the regulation of gene expression at the epigenetic, transcriptional, and post-transcriptional levels (Luo et al., 2021;Yang et al., 2022), and are closely associated with the occurrence and development of cancer (Toden et al., 2021). Therefore, LncRNAs are likely to become a potential target for clinical treatment of cancer, and the establishment of LncRNA on the TCGA-COAD cohort, and identified that disulfidptosis responserelated LncRNA were a robust predictors of colon adenocarcinoma (COAD) (Chi et al., 2023). The model facilitated the precise classification of clinical COAD patients and identified specific subgroups that are more beneficial to immunotherapy and chemotherapy, providing favorable information for the development of personalized treatment strategies for COAD patients. In this study, these LncRNAs were evaluated as independent prognostic factors for COAD, and patients in the low-risk group showed higher overall survival, providing new insights into immunotherapy response and prognosis assessment in COAD. In conclusion, this study successfully identified specific LncRNAs that are closely associated with death by disulfide, revealing new prognostic biomarkers and potential therapeutic targets of COAD.In the next article, Moaveni et al. provide a comprehensive and critical analysis of recent advances and challenges in gene therapy for pediatric cancer (Moaveni et al., 2024). The challenges facing pediatric cancer are more unique and complex than those facing adult cancers. This review elucidates current innovative systems that promise to address pediatric tumors, such as Glutathione peroxidase 4 (GPX4) is a unique antioxidant enzyme that can protect cells from membrane lipid peroxidation and maintain redox homeostasis, and its role in patients with hepatitis B virus-associated acute-on-chronic liver failure (HBV-ACLF) was studied (Su et al., 2024). In 289 participants, GPX4 expression levels in serum and peripheral blood mononuclear cells (PBMCs) of HBV-ACLF patients were lower than in non-HBV ACLF patients, chronic hepatitis B (CHB) and healthy control (HC) individuals. At the same time, in HBV-ACLF patients, the methylation level of GPX4 promoter is higher, and it is related to oxidative stress and inflammation related molecules. The methylation level of the GPX4 promoter, as assessed by the ROC curve, was identified as a biomarker for predicting 90-day mortality in HBV-ACLF patients. This study shows the importance of GPX4 in HBV-ACLF, which provides new ideas for the clinical treatment and prognosis of HBV-ACLF, and the specific regulatory mechanism needs to be further explored.Finally, in this research topic, based on the correlation between the basement membrane and related LncRNA and the prognosis of head and neck squamous cell carcinoma (HNSCC), Bu et al. first used the Cancer Genome Atlas (TCGA) database to obtain HNSCC related data (Bu et al., 2024). In this study, differentially expressed LncRNAs were screened, and a basement membrane LncRNA-based prognostic model was successfully established and comprehensively analyzed from different perspectives. By establishing a risk model, 14 pairs of basement membrane LncRNA were evaluated comprehensively, indicating that risk assessment can be used as a reliable prognostic factor. If in vitro and in vivo studies can be combined at a later stage, it will be more helpful to explore new targets for head and neck squamous cell carcinoma (HNSCC) treatment, and provide clinical guidance for clinical research and drug development.The incidence and mortality of cancer are increasing year by year, and it has become the main cause threatening human life and health worldwide (He et al., 2023;Schwartz, 2024). In recent years, gene therapy approaches have become a new way of clinical treatment of cancer, such as CRISPR system has been widely used in cancer-related basic research (Schambach et al., 2024).Targeting gene mutations that drive tumor growth and spread provide new possibilities for the development of more effective and personalized cancer treatment (Chehelgerdi et al., 2024). With the application of gene editing technology, a large number of LncRNA have been found to play important regulatory roles in cancer, including participating in chromatin modification, genomic imprinting, and intranuclear transport (Kopp and Mendell, 2018;Liu et al., 2024). In addition, immunotherapy and other methods by regulating DNA levels are gradually being developed. In conclusion, this topic confirmed that the differential expression of LncRNA is closely related to the development of cancer, but the specific regulatory mechanism of LncRNA in cancer has been studied with further challenges. Therefore, as the potential mechanisms of LncRNA in the occurrence and development of cancer continue to be explored, future studies are expected to develop various cancer-related LncRNA, providing new targets for the early diagnosis and clinical treatment of cancer.
Keywords: lncRNA, Cancer, Gene Therapy, Gene editing technology, biomarkers, epigenetic
Received: 23 Nov 2024; Accepted: 26 Nov 2024.
Copyright: © 2024 Su, Orlandella, Smaldone and Qi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Yitao Qi, Shaanxi Normal University, Xi'an, China
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