2015
DOI: 10.1016/j.humpath.2015.05.013
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Gain of hTERC: a genetic marker of malignancy in oral potentially malignant lesions

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Cited by 25 publications
(13 citation statements)
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“…Furthermore, our study results are not only in accordance with those of several other groups who have identified telomerase activity in the majority of malignant tumors, but also in line with those who have identified telomerase activity in proliferative diseases, predisposing the development of malignant tumors [28][29][30][31][32] .…”
Section: Discussionsupporting
confidence: 92%
See 1 more Smart Citation
“…Furthermore, our study results are not only in accordance with those of several other groups who have identified telomerase activity in the majority of malignant tumors, but also in line with those who have identified telomerase activity in proliferative diseases, predisposing the development of malignant tumors [28][29][30][31][32] .…”
Section: Discussionsupporting
confidence: 92%
“…Studies reporting a positive correlation between telomerase activity and pathologic degree of tumor [29][30] suggest that the cells with higher telomerase activity…”
Section: Discussionmentioning
confidence: 99%
“…While the majority of human tumors maintain telomeres by overexpressing the reverse transcriptase TERT, single nucleotide polymorphisms at the TERC locus are associated with telomere lengthening and an increased risk of developing high-grade glioma (Walsh et al, 2014). Furthermore, TERC copy number gain strongly predicts the progression of premalignant oral cavity neoplasms to invasive cancer (Dorji et al, 2015). Meanwhile, Marek’s disease virus efficiently induces T cell lymphomas in chickens by expressing a viral telomerase RNA to promote telomere lengthening (Trapp et al, 2006).…”
Section: Lncrna Drivers Of Cancer Phenotypesmentioning
confidence: 99%
“…Human telomerase reverse transcriptase (hTERT) and human telomerase RNA component (hTERC) are essential components of telomerase and have been suggested to play a critical role in tumor progression of several types of cancer. 69,70 Although the number of studies related to oral carcinogenesis are limited, Kim et al 71 demonstrated hTERT expression by using in situ reverse transcriptase-polymerase chain reaction in moderate and severe dysplasia and invasive OSCC, whereas no expression was observed in the normal epithelium and in mild dysplasia. In addition, progression to OSCC was observed in 90% of PPOELs harboring human telomerase RNA component (hTERC) gene gain, but only in 5% of cases with a normal copy number of the hTERC gene.…”
Section: Immortalizationmentioning
confidence: 99%