The involvement of Kv3.4 voltage-gated potassium channel in the growth of an oral squamous cell carcinoma cell line

被引:17
作者
Lew, TS
Chang, CS
Fang, KP
Chen, CY
Chen, CH
Lin, SC
机构
[1] Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Inst Physiol, Taipei 112, Taiwan
[3] Vet Gen Hosp Taipei, Dept Dent, Taipei, Taiwan
关键词
K(v)3.4; mouth; neoplasm; oral carcinoma; potassium channel;
D O I
10.1111/j.1600-0714.2004.00236.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BACKGROUND: In our previous study, an A-type voltage-gated K+ channel, K(v)3.4, was found more frequently expressed in oral squamous cell carcinoma (OSCC) when compared with non-cancerous matched oral tissue. An OSCC cell line, OECM-1, was found to have moderate level of K(v)3.4 expression. METHODS: To further elucidate the roles of K(v)3.4 for the involvement of neoplastic process, we amplified K(v)3.4 coding sequence by reverse transcriptase polymerase chain reaction (RT-PCR), constructed an expression vector carrying this sequence and then stably transfected into OECM-! OSCC cells. RESULTS: We demonstrated the integration and constitutive expression of K(v)3.4 in the cell. A unique A-type current elicited by such expression in OECM-! cells was defined by patch clamp analysis. This current pattern can be reversibly blocked by an A-type K+ channel blocker 2 mM 4-aminopyridine (4-AP). The acquisition of K(v)3.4 activity in OECM-! cells bestowed growth advantage. However, in 3T3 cell, transfected K(v)3.4 caused only limited increase of growth without forming transformation foci. CONCLUSION: The present study established a stable keratinocyte system carrying functional K(v)3.4 and increase of growth, by which the anti-K(v)3.4 modalities for potential OSCC control can be further investigated.
引用
收藏
页码:543 / 549
页数:7
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