Oliveira-Neto Helenisa Helena, Leite Angélica Ferreira, Costa Nádia Lago, Alencar Rita Cássia, Lara Vanessa Soares, Silva Tarcília Aparecida, Leles Claudio Rodrigues, Mendonça Francisco Elismauro, Batista Aline Carvalho
Dental School, Federal University of Goiás, Department of Stomatology (Oral Pathology), 74810-230 Goiânia, Goiás, Brazil.
Oral Oncol. 2007 May;43(5):484-90. doi: 10.1016/j.oraloncology.2006.05.004. Epub 2006 Sep 18.
It is becoming accepted that multiple cell types in stromal microenvironment are involved in tumorigenesis. In this setting, mast cells (MC) display a diversity of roles that may contribute to the defense against tumors or tumor progression. Thus, the aim of this study was to evaluate density and migration of MCs in OSCC (oral squamous cell carcinoma) and pre-malignant oral hyperkeratosis (leukoplakia) as well as their relationship with clinical and microscopic parameters. The tryptase and c-kit expression was analyzed in 38 cases of OSCC, 26 cases of leukoplakia, and 12 cases of clinically healthy oral mucosa (control) by means of immunohistochemistry. The tryptase(+) cell numbers were decreased in OSCC (P=0.0003) and leukoplakia (P=0.03) compared with control. Similar numbers of tryptase(+) cells were observed in leukoplakia and OSCC (P=0.31). The density of c-kit(+) MCs was also significantly lower in OSCC and leukoplakia in relation to control resulting in a reduced c-kit(+)/tryptase(+) relationship in OSCC (19%) in comparison with leukoplakia (59%) and control (63%). No correlation was observed between MC populations with clinical and microscopic characteristics of OSCC. Our findings suggest that the decrease in MC numbers in pre-malignant and malignant oral lesions may be related to the migration failure of these cells, possibly reflecting an important modification in the microenvironment during tumor initiation and progression.
越来越多的人认为,基质微环境中的多种细胞类型参与了肿瘤的发生。在这种情况下,肥大细胞(MC)发挥着多种作用,可能有助于抵御肿瘤或促进肿瘤进展。因此,本研究的目的是评估MC在口腔鳞状细胞癌(OSCC)和癌前口腔角化过度(白斑)中的密度和迁移情况,以及它们与临床和微观参数的关系。通过免疫组织化学分析了38例OSCC、26例白斑和12例临床健康口腔黏膜(对照)中类胰蛋白酶和c-kit的表达。与对照相比,OSCC(P=0.0003)和白斑(P=0.03)中类胰蛋白酶(+)细胞数量减少。在白斑和OSCC中观察到的类胰蛋白酶(+)细胞数量相似(P=0.31)。与对照相比,OSCC和白斑中c-kit(+)MC的密度也显著降低,导致OSCC中c-kit(+)/类胰蛋白酶(+)的比例(19%)低于白斑(59%)和对照(63%)。未观察到MC群体与OSCC的临床和微观特征之间存在相关性。我们的研究结果表明,癌前和恶性口腔病变中MC数量的减少可能与这些细胞的迁移失败有关,这可能反映了肿瘤发生和进展过程中微环境的重要变化。