Kuniyasu H, Oue N, Tsutsumi M, Tahara E, Yasui W
Department of Oncological Pathology, Cancer Center, Nara Medical University, 840 Shijo-cho, Kashihara 634-8521, Japan.
Clin Cancer Res. 2001 Dec;7(12):4067-72.
CD44 variant exon (CD44v) 3 is a heparan sulfate-binding isoform of CD44. The role of CD44v3 in invasion and metastasis associated with heparan sulfate in colon cancer cell lines and cases of colon cancer was examined. Expression of CD44v3 mRNA and protein was observed in five of six human colorectal cancer cell lines. Colo320 and WiDr cells expressed CD44v3 at high levels. Heparan sulfate treatment increased the invasive activity of Colo320 and WiDr cells to rates 14.3 and 12.6 times higher, respectively, than that of untreated cells. However, heparan sulfate treatment did not affect cell growth. Repression of CD44v3 protein production by antisense S-oligodeoxynucleotide treatment reduced the binding affinities and capacities for heparan sulfate by Colo320 and WiDr cells in comparison with that of control cells, and it also reduced the invasiveness of both cell lines to one-fifth that of control cells. In heparan sulfate-treated Colo320 cells, the levels of CD44v3 protein in the Triton X-100-insoluble fraction and moesin-precipitated fraction were increased, suggesting that heparan sulfate treatment facilitates association of CD44 molecules with the cytoskeleton. Immunohistochemical analysis showed CD44v3 to be expressed in 21 of 37 (57%) colorectal cancer cases. Positive CD44v3 expression was associated with more advanced pathological stage and poorer prognosis than negative CD44v3 expression. These data support a role for CD44v3 in invasion and metastasis by colorectal carcinoma cells.
CD44变异外显子(CD44v)3是CD44的一种硫酸乙酰肝素结合异构体。研究了CD44v3在结肠癌细胞系及结肠癌病例中与硫酸乙酰肝素相关的侵袭和转移中的作用。在6种人结肠癌细胞系中的5种中观察到了CD44v3 mRNA和蛋白的表达。Colo320和WiDr细胞高水平表达CD44v3。硫酸乙酰肝素处理使Colo320和WiDr细胞的侵袭活性分别提高到未处理细胞的14.3倍和12.6倍。然而,硫酸乙酰肝素处理不影响细胞生长。与对照细胞相比,反义S - 寡脱氧核苷酸处理抑制CD44v3蛋白产生降低了Colo320和WiDr细胞对硫酸乙酰肝素的结合亲和力和结合能力,并且也将两种细胞系的侵袭性降低到对照细胞的五分之一。在硫酸乙酰肝素处理的Colo320细胞中,Triton X - 100不溶性组分和埃兹蛋白沉淀组分中的CD44v3蛋白水平升高,表明硫酸乙酰肝素处理促进CD44分子与细胞骨架的结合。免疫组织化学分析显示,在37例结肠癌病例中的21例(57%)中表达CD44v3。与CD44v3阴性表达相比,CD44v3阳性表达与更晚期的病理分期和更差的预后相关。这些数据支持CD44v3在结肠癌细胞侵袭和转移中的作用。