LncRNAs and related molecular basis in malignant pleural mesothelioma: Challenges and potential
Critical Reviews in Oncology/Hematology, ISSN: 1040-8428, Vol: 186, Page: 104012
2023
- 3Citations
- 6Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Review Description
Malignant pleural mesothelioma (MPM) is a rare but invasive cancer, which mainly arises from mesothelial tissues of pleura, peritoneum and pericardium. Despite significant advances in treatments, the prognosis of MPM patients remains poor, and the 5-year survival rate is less than 10%. Therefore, it is urgent to explore novel therapeutic targets for the treatment of MPM. Growing evidence has indicated that long non-coding RNAs (lncRNAs) potentially could be promising therapeutic targets for numerous cancers. In this regard, lncRNAs might also potentially therapeutic targets for MPM. Recent advances have been made to investigate the molecular basis of MPM. This review first provides a comprehensive overview of roles of lncRNAs in MPM and then discusses the relationship between molecular basis of MPM and MPM-related lncRNAs to implement them as promising therapeutic targets for MPM.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1040842823001002; http://dx.doi.org/10.1016/j.critrevonc.2023.104012; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85153798883&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37116816; https://linkinghub.elsevier.com/retrieve/pii/S1040842823001002; https://dx.doi.org/10.1016/j.critrevonc.2023.104012
Elsevier BV
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