川地34
间质细胞
类胰蛋白酶
肥大细胞
血管生成
化学
病理
川地163
免疫组织化学
淋巴管
淋巴管新生
癌症研究
医学
免疫学
内科学
生物
细胞生物学
癌症
生物化学
表型
转移
基因
干细胞
作者
Ernesto Santos Sousa‐Neto,Maria Cristina Teixeira Cangussú,Clarissa Araújo Silva Gurgel,Vanessa Sousa Nazaré Guimarães,Eduardo Antônio Gonçalves Ramos,Flávia Caló de Aquino Xavier,Patrícia Ramos Cury,Bráulio Carneiro Júnior,Rosalia Leonardi,Jean Nunes dos Santos
摘要
Little is known about the interaction of stromal components in odontogenic tumors. Thus, the aim of this study was to investigate mast cells (MCs), myofibroblasts, macrophages, and their possible association with angiogenesis and lymphangiogenesis in keratocystic odontogenic tumors (KCOTs).Thirty cases of KCOTs were included and analyzed by immunohistochemistry for mast cell tryptase, α-SMA, CD34, CD163, and D240. For comparative purpose, 15 radicular cysts (CRs) and 7 pericoronal follicles (PFs) were included.There was an increase in MCs for RCs and this difference was significant when they were compared to KCOTS and PFs. A significant increase in the density of MFs was observed for KCOTs when compared to RCs and PFs (P = 0.00). No significant difference in CD163-positive macrophages (P = 0.084) and CD34-positive vessels (P = 0.244) densities was observed between KCOTs, RCs, and PFs, although KCOTs showed a higher density of all proteins. Significant difference in lymphatic vessel density was observed for KCOTs when compared to RCs and PFs (P = 0.00). Positive correlation was observed between mast cell tryptase and CD34 in KCOTs (P = 0.025).A significant interaction between the MC population and CD34-positive vessels in KCOTs supported the hypothesis that MCs and blood vessels contribute to the stromal scaffold of KCOT.
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