نمایش مختصر رکورد

dc.contributor.authorThomas, Gigien_US
dc.contributor.authorTR, Santhoshkumaren_US
dc.contributor.authorGeorge S, Preethien_US
dc.contributor.authorSomanathan, Tharaen_US
dc.contributor.authorSarojam, Santhien_US
dc.contributor.authorKrishnankutti, Nandakumaren_US
dc.contributor.authorSreedharan, Hariharanen_US
dc.contributor.authorAnkathil, Ravindranen_US
dc.date.accessioned1399-07-08T17:52:05Zfa_IR
dc.date.accessioned2020-09-29T17:52:05Z
dc.date.available1399-07-08T17:52:05Zfa_IR
dc.date.available2020-09-29T17:52:05Z
dc.date.issued2020-02-01en_US
dc.date.issued1398-11-12fa_IR
dc.date.submitted2018-09-08en_US
dc.date.submitted1397-06-17fa_IR
dc.identifier.citationThomas, Gigi, TR, Santhoshkumar, George S, Preethi, Somanathan, Thara, Sarojam, Santhi, Krishnankutti, Nandakumar, Sreedharan, Hariharan, Ankathil, Ravindran. (2020). Prognostic Implications of DNA Repair, Ploidy and Telomerase in the Malignant Transformation Risk Assessment of Leukoplakia. Asian Pacific Journal of Cancer Prevention, 21(2), 309-316. doi: 10.31557/APJCP.2020.21.2.309en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttps://dx.doi.org/10.31557/APJCP.2020.21.2.309
dc.identifier.urihttp://journal.waocp.org/article_88928.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/30982
dc.description.abstractBackground: Although leukoplakia shows a higher risk for malignant transformation to oral cancer, currently there are no clinically relevant biomarker which can predict the potentially high risk leukoplakia. This study aimed to investigate the genetic alterations such as DNA ploidy, telomerase expression and DNA repair capacity as predictive markers of malignant transformation risk of leukoplakia. Methods: The study was initiated in September 2005 and patients were followed up to March 2014. Two hundred patients with oral leukoplakia, 100 patients with oral cancer and 100 healthy, age and sex matched adults with normal oral mucosa as controls were recruited. The DNA ploidy content was measured by high resolution flow cytometry, level of telomerase expression was identified by TRAP assay and intrinsic DNA repair capacity was measured by mutagen induced chromosome sensitivity assay of cultured peripheral blood lymphocytes. The Chi-square test or Fisher's Exact test was used for comparison of categorical variables between biomarkers. A p value less than or equal to 0.05 was considered as statistically significant. Analysis was performed with SPSS software version 16. Logistic regression was used to find the association between the dependent and three independent variables. Results: There was significant difference in the distribution of ploidy status, telomerase activity and DNA repair capacity among control, leukoplakia and oral cancer group (p<0.001). When the molecular markers were compared with histological grading of leukoplakia, both DNA ploidy analysis and telomerase activity showed statistical significance (p<0.001). Both aneuploidy and telomerase positivity was found to coincide with high-risk sites of leukoplakia and were statistically significant (pen_US
dc.format.extent1022
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.relation.isversionofhttps://dx.doi.org/10.31557/APJCP.2020.21.2.309
dc.subjectleukoplakiaen_US
dc.subjectAneuploiden_US
dc.subjectDiploiden_US
dc.subjectDNA repair Capacityen_US
dc.subjectTelomeraseen_US
dc.subjectMolecular and cellularen_US
dc.titlePrognostic Implications of DNA Repair, Ploidy and Telomerase in the Malignant Transformation Risk Assessment of Leukoplakiaen_US
dc.typeTexten_US
dc.typeResearch Articlesen_US
dc.contributor.departmentDivision of Community Oncology, Regional Cancer Centre, Medical College Campus, Thiruvananthapuram, Kerala, India.en_US
dc.contributor.departmentDivision of Cancer Research, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.en_US
dc.contributor.departmentDivision of Cancer Epidemiology and Biostatistics, Regional Cancer Centre, Medical College Campus, Thiruvananthapuram, Kerala, India.en_US
dc.contributor.departmentDivision of Cytopathology, Regional Cancer Centre, Medical College Campus, Thiruvananthapuram, Kerala, India.en_US
dc.contributor.departmentResearch Associate, Child Development Centre, Medical College Campus,Thiruvananthapuram, Kerala,India.en_US
dc.contributor.departmentDean, Azeezia Dental College, Meyannoor, Kollam, Kerala, India.en_US
dc.contributor.departmentDivision of Cancer Research, Regional Cancer Centre, Medical College Campus, Thiruvananthapuram, Kerala, India.en_US
dc.contributor.departmentHuman Genome Centre, School of Medical Sciences, Health Campus, University Sains Malaysia, 16150, KubangKerian, Kelantan, Malaysia.en_US
dc.citation.volume21
dc.citation.issue2
dc.citation.spage309
dc.citation.epage316
nlai.contributor.orcid0000-0003-2769-0083


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