Department of Oral Pathology, Dentistry School, Federal University of Rio Grande do Norte, Natal/RN, Brazil.
Am J Otolaryngol. 2010 Jul-Aug;31(4):266-71. doi: 10.1016/j.amjoto.2009.03.002. Epub 2009 Jun 3.
The study aimed to analyze the expression of bone morphogenetic protein-2/4 (BMP-2/4) and its receptor BMPR-IA (BMP receptor type IA) in metastatic and nonmetastatic oral squamous cell carcinoma (OSCC) and its implications for disease prognosis.
The experimental group included 16 cases of OSCC without metastasis and 7 cases of OSCC with metastasis. The presence or absence of nodal metastasis was used as a parameter for the evaluation of disease prognosis. Ten cases of oral fibroepithelial hyperplasia were selected as the control group. The expression of BMP-2/4 and BMPR-IA was analyzed by immunohistochemistry.
In the experimental group with metastasis, strong expression of BMP-2/4 was observed in most cases (71.4%), whereas BMPR-IA exhibited weak expression (85.7%). In the experimental group without metastasis, there was strong expression of BMP-2/4 (62.5%) and BMPR-IA (100%). A significant association was observed between the prognosis of OSCC and the intensity of BMP-2/4 staining (P = .002). Weak immunoreactivity to BMP-2/4 and BMPR-IA was observed in all control specimens.
The results suggest that strong expression of BMP-2/4, associated with low expression of BMPR-IA, observed in metastatic OSCC has a prognostic value, with the loss of responsiveness to BMPs through the loss of expression of their receptors being indicative of the development of metastasis.
本研究旨在分析骨形态发生蛋白-2/4(BMP-2/4)及其受体 BMP 受体 IA(BMPR-IA)在转移性和非转移性口腔鳞状细胞癌(OSCC)中的表达及其对疾病预后的影响。
实验组包括 16 例无转移的 OSCC 病例和 7 例有转移的 OSCC 病例。淋巴结转移的存在与否被用作评估疾病预后的参数。选择 10 例口腔纤维上皮增生病例作为对照组。采用免疫组织化学法分析 BMP-2/4 和 BMPR-IA 的表达。
在有转移的实验组中,大多数病例(71.4%)表现出强烈的 BMP-2/4 表达,而 BMPR-IA 表达较弱(85.7%)。在无转移的实验组中,BMP-2/4(62.5%)和 BMPR-IA(100%)表达均较强。OSCC 的预后与 BMP-2/4 染色强度之间存在显著相关性(P=0.002)。所有对照组标本均表现出 BMP-2/4 和 BMPR-IA 的弱免疫反应性。
结果表明,转移性 OSCC 中观察到的 BMP-2/4 强表达与 BMPR-IA 低表达相关,具有预后价值,BMP 受体表达缺失导致对 BMPs 的反应性丧失,提示转移的发生。