Fahad Mansoor Samadi, Shaista Suhail, Manjari Sonam, Mohd Kaleem Ahmad, Vijay Kumar, Shaleen Chandra, Shadab Mohammad
{"title":"Comparing Length and Telomere Expression at Oral Precancerous and Cancerous Stages.","authors":"Fahad Mansoor Samadi, Shaista Suhail, Manjari Sonam, Mohd Kaleem Ahmad, Vijay Kumar, Shaleen Chandra, Shadab Mohammad","doi":"10.30699/IJP.2024.1996330.3081","DOIUrl":null,"url":null,"abstract":"<p><strong>Background & objective: </strong>Telomeres consist of repetitive G-rich nucleotides located at the end of each chromosome, acting as protein binding sites. The aim of this study was to examine the differences in telomere length in blood, saliva, and tissue samples at various stages of oral precancerous and cancerous lesions.</p><p><strong>Methods: </strong>Samples of blood, tissue, and saliva were collected from patients with oral precancerous and cancerous lesions. DNA extraction was performed. Then, a TRAP assay was conducted to assess and compare the telomere length and telomerase expression.</p><p><strong>Results: </strong>The levels of telomerase activity (TA) in the DNA samples ranged from 0.19 to 6.91 (2.05+1.37) among oral squamous cell carcinoma (OSCC) patients and from 0.17 to 4.5 (0.28+4.25) among precancerous patients. A significant difference was observed in TA levels between OSCC and precancerous samples (<i>t</i>=3.9691, <i>P</i>= 0.0000).</p><p><strong>Conclusion: </strong>Assessing the telomerase activity is crucial for studying the behavior of carcinoma in the clinical setting. The augmented telomerase expression and the length of telomere contribute to OSCC progression. Hence, this study adds a diagnostic tool that can serve as a biomarker for the early detection and prognosis of OSCC.</p>","PeriodicalId":38900,"journal":{"name":"Iranian Journal of Pathology","volume":"19 2","pages":"146-151"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11304464/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30699/IJP.2024.1996330.3081","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/15 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Background & objective: Telomeres consist of repetitive G-rich nucleotides located at the end of each chromosome, acting as protein binding sites. The aim of this study was to examine the differences in telomere length in blood, saliva, and tissue samples at various stages of oral precancerous and cancerous lesions.
Methods: Samples of blood, tissue, and saliva were collected from patients with oral precancerous and cancerous lesions. DNA extraction was performed. Then, a TRAP assay was conducted to assess and compare the telomere length and telomerase expression.
Results: The levels of telomerase activity (TA) in the DNA samples ranged from 0.19 to 6.91 (2.05+1.37) among oral squamous cell carcinoma (OSCC) patients and from 0.17 to 4.5 (0.28+4.25) among precancerous patients. A significant difference was observed in TA levels between OSCC and precancerous samples (t=3.9691, P= 0.0000).
Conclusion: Assessing the telomerase activity is crucial for studying the behavior of carcinoma in the clinical setting. The augmented telomerase expression and the length of telomere contribute to OSCC progression. Hence, this study adds a diagnostic tool that can serve as a biomarker for the early detection and prognosis of OSCC.
背景与目的:端粒由重复的富含G的核苷酸组成,位于每条染色体的末端,是蛋白质的结合位点。本研究旨在检测口腔癌前病变和癌症病变不同阶段的血液、唾液和组织样本中端粒长度的差异:方法:收集口腔癌前病变和癌症患者的血液、组织和唾液样本。进行 DNA 提取。结果:端粒酶活性(TRAP)、端粒长度(TRAP)和端粒长度(TRAP结果:在口腔鳞状细胞癌(OSCC)患者中,DNA样本中端粒酶活性(TA)的水平从0.19到6.91(2.05+1.37)不等;在癌前病变患者中,端粒酶活性(TA)的水平从0.17到4.5(0.28+4.25)不等。OSCC和癌前病变样本的端粒酶水平存在明显差异(t=3.9691,P=0.0000):评估端粒酶活性对于研究临床环境中的癌变行为至关重要。端粒酶表达的增强和端粒的长度有助于OSCC的进展。因此,这项研究为OSCC的早期检测和预后增加了一种可作为生物标志物的诊断工具。