Kanke M, Fujii M, Kameyama K, Kanzaki J, Tokumaru Y, Imanishi Y, Tomita T, Matsumura Y
Department of Otolaryngology-Head and Neck Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Arch Otolaryngol Head Neck Surg. 2000 Oct;126(10):1217-23. doi: 10.1001/archotol.126.10.1217.
To determine the correlation between the expression of CD44 variant exon 6 (v6) and the clinicopathological features of head and neck squamous cell carcinomas (HNSCCs), and to study the role of CD44v6 in cell invasion using a human HNSCC cell line (HSC-2).
The expression of CD44v6 was evaluated using immunohistochemical analysis in paraffin-embedded tissue specimens from 89 primary lesions. The concentration of CD44v6 protein in 37 cryopreserved tumor specimens was evaluated using the enzyme-linked immunosorbent assay. The HSC-2 cells were treated with 2F10, a monoclonal antibody against CD44v6. The effects of 2F10 on HSC-2 cell proliferation, migration, and invasion potential were evaluated.
The down-regulation of CD44v6 expression or the concentration of cancer tissue significantly correlated with a lower degree of pathohistological differentiation and a higher rate of cervical metastasis. The invasion of HSC-2 cells into type I collagen gel and the expression of CD44v6 were decreased in invading cells released from the upper layer. Furthermore, the treatment of HSC-2 cells with 2F10 significantly enhanced cell invasion. However, 2F10 did not affect either the proliferation or migration properties of HSC-2 cells.
The down-regulation of CD44v6 expression may be useful as a biological marker for the degree of malignancy in HNSCCs. We assume that the loss or dysfunction of CD44v6 is involved in the acquisition of invasion ability in HSC-2 cells. In addition, the potential existence of a CD44v6-mediated signal transduction pathway may play a role in inhibiting the invasion in HNSCCs.
确定CD44变异外显子6(v6)的表达与头颈部鳞状细胞癌(HNSCC)临床病理特征之间的相关性,并使用人HNSCC细胞系(HSC-2)研究CD44v6在细胞侵袭中的作用。
采用免疫组织化学分析评估89例原发灶石蜡包埋组织标本中CD44v6的表达。使用酶联免疫吸附测定法评估37例冷冻保存肿瘤标本中CD44v6蛋白的浓度。用抗CD44v6单克隆抗体2F10处理HSC-2细胞。评估2F10对HSC-2细胞增殖、迁移和侵袭潜能的影响。
CD44v6表达下调或癌组织浓度与病理组织学分化程度较低和颈部转移率较高显著相关。从上层释放的侵袭性HSC-2细胞对I型胶原凝胶的侵袭以及CD44v6的表达降低。此外,用2F10处理HSC-2细胞显著增强了细胞侵袭。然而,2F10对HSC-2细胞的增殖或迁移特性均无影响。
CD44v6表达下调可能作为HNSCC恶性程度的生物学标志物。我们推测CD44v6的缺失或功能障碍与HSC-2细胞侵袭能力的获得有关。此外,CD44v6介导的信号转导途径的潜在存在可能在抑制HNSCC侵袭中起作用。