2016
DOI: 10.1590/1678-775720160156
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Immunoexpression of cleaved caspase-3 shows lower apoptotic area indices in lip carcinomas than in intraoral cancer

Abstract: Objective This study aimed to evaluate apoptosis by assessing cleaved caspase-3 immunoexpression in hyperplastic, potentially malignant disorder (PMD), and malignant tumors in intraoral and lower lip sites.Material and Methods A retrospective study using paraffin blocks with tissues from patients with inflammatory fibrous hyperplasia (IFH), actinic cheilitis, oral leukoplakia, lower lip and intraoral squamous cell carcinoma (SCC) was performed. The tissues were evaluated by immunohistochemical analysis with an… Show more

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Cited by 10 publications
(14 citation statements)
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“…Moreover, Fu et al, (2016) confirmed our results and added that the high expression of caspase-3 was associated especially with advanced stage in OSCC and was dependent on the site of cancer. Also, Hague et al, (2004) and Leite et al, (2016) result revealed that OSCC had a higher apoptotic area index compared to other types of lesions. Hence, apoptosis plays a dual role in cancer development and malignancy.…”
Section: Discussionmentioning
confidence: 89%
“…Moreover, Fu et al, (2016) confirmed our results and added that the high expression of caspase-3 was associated especially with advanced stage in OSCC and was dependent on the site of cancer. Also, Hague et al, (2004) and Leite et al, (2016) result revealed that OSCC had a higher apoptotic area index compared to other types of lesions. Hence, apoptosis plays a dual role in cancer development and malignancy.…”
Section: Discussionmentioning
confidence: 89%
“…Cleaved caspase 3 functions as a kind of control tower of apoptosis: it cleaves poly (ADP-ribose) polymerase (PARP), cytokeratin 18, vimentin, actin and other intracytoplasmic proteins. Cleaved caspase 3 has been applied to detecting apoptotic neoplastic cells in paraffin sections [ 24 - 26 ].…”
Section: Discussionmentioning
confidence: 99%
“…The slides were evaluated under a light microscope, and labelling index was calculated as the ratio of caspase-3-positive cells to the total number of cells. The number of labelled cells in immunostained sections was counted relative to 2000 cells [ 24 , 25 ].…”
Section: Methodsmentioning
confidence: 99%