Baer Susan, Casaubon Luis, Schwartz Mary R, Marcogliese Andrea, Younes Mamoun
Department of Pathology, Baylor College of Medicine and Methodist Hospital, Houston, Texas 77030, USA.
Laryngoscope. 2002 Feb;112(2):393-6. doi: 10.1097/00005537-200202000-00034.
OBJECTIVES/HYPOTHESIS: The aim of the study was to determine the clinical significance of the expression of Glut1 and Glut3 proteins in biopsy specimens of squamous cell carcinoma (SCC) of the larynx.
A retrospective study.
Using immunohistochemistry, we immunostained sections of formalin-fixed, paraffin-embedded tissues from 48 biopsies of invasive SCC of the larynx for Glut1 and Glut3. The percentages of positive cells were recorded, then correlated with overall patient survival using the Kaplan-Meier method and the Breslow-Gehan-Wilcoxon test for statistical significance.
All cases were positive for Glut1, and Glut1 expression was not associated with survival difference at any cut-off value. Eighteen (38%) of the cases were Glut3-negative and 30 (62%) were Glut3-positive. Glut3-positive cases were associated with poorer survival than Glut3-negative cases (P =.0336). No significant difference was found between Glut3-negative and Glut3-positive groups in respect to sex, tumor site (glottic vs. supraglottic), nodal or distant metastasis, or treatment modality. However, there were significantly more poorly differentiated tumors in the Glut3-positive group than in the Glut3-negative group (27% vs. 0%, respectively; P =.0182, Fisher's Exact Test). After poorly differentiated tumors were excluded from the survival analysis, Glut3 immunoreactivity remained a significant marker of poor prognosis (P =.0385).
Immunohistochemical detection of Glut3 in biopsy specimens of SCC of the larynx is a marker of poorer prognosis.
目的/假设:本研究旨在确定喉鳞状细胞癌(SCC)活检标本中Glut1和Glut3蛋白表达的临床意义。
一项回顾性研究。
我们采用免疫组织化学方法,对48例喉浸润性SCC活检标本的福尔马林固定、石蜡包埋组织切片进行Glut1和Glut3免疫染色。记录阳性细胞百分比,然后使用Kaplan-Meier法和Breslow-Gehan-Wilcoxon检验将其与患者总生存期进行相关性分析,以确定统计学意义。
所有病例Glut1均呈阳性,且在任何临界值下Glut1表达均与生存差异无关。18例(38%)病例Glut3呈阴性,30例(62%)呈阳性。Glut3阳性病例的生存期比Glut3阴性病例差(P = 0.0336)。在性别、肿瘤部位(声门型与声门上型)、淋巴结或远处转移或治疗方式方面,Glut3阴性和阳性组之间未发现显著差异。然而,Glut3阳性组中低分化肿瘤明显多于Glut3阴性组(分别为27%和0%;P = 0.0182,Fisher精确检验)。在生存分析中排除低分化肿瘤后,Glut3免疫反应性仍然是预后不良的重要标志物(P = 0.0385)。
喉SCC活检标本中Glut3的免疫组织化学检测是预后较差的标志物。