Circulating Long Non-Coding RNAs LINC00324 and LOC100507053 as Potential Liquid Biopsy Markers for Esophageal Squamous Cell Carcinoma: A Pilot Study

dc.contributor.authorSharma, Uttam
dc.contributor.authorBarwal, Tushar Singh
dc.contributor.authorKhandelwal, Akanksha
dc.contributor.authorRana, Manjit Kaur
dc.contributor.authorRana, Amrit Pal Singh
dc.contributor.authorSingh, Karuna
dc.contributor.authorJain, Aklank
dc.date.accessioned2024-01-21T10:44:38Z
dc.date.accessioned2024-08-13T13:21:43Z
dc.date.available2024-01-21T10:44:38Z
dc.date.available2024-08-13T13:21:43Z
dc.date.issued2022-02-14T00:00:00
dc.description.abstractBackground: Despite the availability of advanced technology to detect and treat esophageal squamous cell carcinoma (ESCC), the 5-year survival rate of ESCC patients is still meager. Recently, long non-coding RNAs (lncRNAs) have emerged as essential players in the diagnosis and prognosis of various cancers. Objective: This pilot study focused on identifying circulating lncRNAs as liquid biopsy markers for the ESCC. Methodology: We performed next-generation sequencing (NGS) to profile circulating lncRNAs in ESCC and healthy individuals� blood samples. The expression of the top five upregulated and top five downregulated lncRNAs were validated through quantitative real-time PCR (qRT-PCR), including samples used for the NGS. Later, we explored the diagnostic/prognostic potential of lncRNAs and their impact on the clinicopathological parameters of patients. To unravel the molecular target and pathways of identified lncRNAs, we utilized various bioinformatics tools such as lncRnome, RAID v2.0, Starbase, miRDB, TargetScan, Gene Ontology, and KEGG pathways. Results: Through NGS profiling, we obtained 159 upregulated, 137 downregulated, and 188 neutral lncRNAs in ESCC blood samples compared to healthy individuals. Among dysregulated lncRNAs, we observed LINC00324 significantly upregulated (2.11-fold; p-value = 0.0032) and LOC100507053 significantly downregulated (2.22-fold; p-value = 0.0001) in ESCC patients. Furthermore, we found LINC00324 and LOC100507053 could discriminate ESCC cancer patients� from non-cancer individuals with higher accuracy of Area Under the ROC Curve (AUC) = 0.627 and 0.668, respectively. The Kaplan-Meier and log-rank analysis revealed higher expression levels of LINC00324 and lower expression levels of LOC100507053 well correlated with the poor prognosis of ESCC patients with a Hazard ratio of LINC00324 = 2.48 (95% CI: 1.055 to 5.835) and Hazard ratio of LOC100507053 = 4.75 (95% CI: 2.098 to 10.76)]. Moreover, we also observed lncRNAs expression well correlated with the age (>50 years), gender (Female), alcohol, tobacco, and hot beverages consumers. Using bioinformatics tools, we saw miR-493-5p as the direct molecular target of LINC00324 and interacted with the MAPK signaling pathway in ESCC pathogenesis. Conclusion: This pilot study suggests that circulating LINC00324 and LOC100507053 can be used as a liquid biopsy marker of ESCC; however, multicentric studies are still warranted. Copyright � 2022 Sharma, Barwal, Khandelwal, Rana, Rana, Singh and Jain.en_US
dc.identifier.doi10.3389/fonc.2022.823953
dc.identifier.issn2234943X
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3816
dc.identifier.urlhttps://www.frontiersin.org/articles/10.3389/fonc.2022.823953/full
dc.language.isoen_USen_US
dc.publisherFrontiers Media S.A.en_US
dc.subjectbiomarkersen_US
dc.subjectESCCen_US
dc.subjectesophageal squamous cell carcinomaen_US
dc.subjectLncRNAen_US
dc.subjectlong non-coding RNAen_US
dc.subjectnext generation sequencingen_US
dc.titleCirculating Long Non-Coding RNAs LINC00324 and LOC100507053 as Potential Liquid Biopsy Markers for Esophageal Squamous Cell Carcinoma: A Pilot Studyen_US
dc.title.journalFrontiers in Oncologyen_US
dc.typeArticleen_US
dc.type.accesstypeOpen Accessen_US

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