Sato Hirotaka, Takeda Yasunori
Department of Oral Pathology, School of Dentistry, Iwate Medical University, Morioka, Iwate, Japan.
J Oral Sci. 2009 Dec;51(4):551-7. doi: 10.2334/josnusd.51.551.
Neovascularization in the stroma of a tumor plays an important role in tumor growth and the establishment of metastases. The present study examined the immunohistochemical expression of vascular endothelial growth factor receptor 2 (VEGFR2) in 34 cases of oral squamous cell carcinoma (OSCC). Moreover, the relationships between parameters of tumor neovascularization (count of VEGFR2-positive [+] cells and total size of vessel lumen [TSVL]) and those of histology (differentiation type and mode of invasion) were analyzed statistically. Immunohistochemical expression of VEGFR2 was localized in stromal cells at the tumor invasive front. The VEGFR2+ cell count around poorly differentiated tumors was significantly higher than that around well differentiated tumors (P = 0.032, one-way ANOVA). The TSVL around the well differentiated type was found to be significantly larger than that around the poorly or moderately differentiated type (P < 0.001, respectively; one-way ANOVA). With regard to the mode of invasion, the TSVL was significantly larger for lower-grade (Grades 1+2) than for higher-grade (Grades 3+4) tumors (P < 0.001, unpaired t-test). On the basis of our results, we suggest that vascular development at the invasive front of OSCC is governed by the following factors: the tumor cells themselves may induce hemangiogenesis in the adjoining stromal tissue; hemangiogenic activity is higher when parenchymal intercellular adhesion is looser and when the parenchymal area exposed to the stroma is greater; and the rate of blood flow is higher when parenchymal intercellular adhesion is tighter and parenchymal nests are larger.
肿瘤基质中的新生血管形成在肿瘤生长和转移的建立中起着重要作用。本研究检测了34例口腔鳞状细胞癌(OSCC)中血管内皮生长因子受体2(VEGFR2)的免疫组化表达。此外,还对肿瘤新生血管形成参数(VEGFR2阳性[+]细胞计数和血管腔总大小[TSVL])与组织学参数(分化类型和侵袭方式)之间的关系进行了统计学分析。VEGFR2的免疫组化表达定位于肿瘤侵袭前沿的基质细胞中。低分化肿瘤周围的VEGFR2+细胞计数显著高于高分化肿瘤周围(P = 0.032,单因素方差分析)。发现高分化类型周围的TSVL显著大于低分化或中分化类型周围(分别为P < 0.001;单因素方差分析)。关于侵袭方式,低级别(1+2级)肿瘤的TSVL显著大于高级别(3+4级)肿瘤(P < 0.001,非配对t检验)。根据我们的结果,我们认为OSCC侵袭前沿的血管发育受以下因素支配:肿瘤细胞本身可能诱导相邻基质组织中的血管生成;当实质细胞间粘附较松散且暴露于基质的实质面积较大时,血管生成活性较高;当实质细胞间粘附较紧密且实质巢较大时,血流速度较高。