激活的Vav2通过Rac1和Cdc42调节口腔鳞状细胞癌的细胞侵袭。
Activated Vav2 modulates cellular invasion through Rac1 and Cdc42 in oral squamous cell carcinoma.
作者信息
Lai Stephen Y, Ziober Amy F, Lee Megan N, Cohen Noam A, Falls Erica M, Ziober Barry L
机构信息
Molecular Tumor Biology Laboratory, Department of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania Health System, 3400 Spruce Street, Philadelphia, PA 19104, USA.
出版信息
Oral Oncol. 2008 Jul;44(7):683-8. doi: 10.1016/j.oraloncology.2007.08.017. Epub 2007 Nov 9.
The Rho family of GTPases regulates cellular adhesion and motility. Guanine nucleotide exchange factors (GEFs) in turn regulate GTPases by promoting nucleotide exchange from GDP to GTP. We have determined that GTP-bound Rac1 is elevated in invasive oral squamous cell carcinoma (OSCC) cell lines. Because of the critical role of invasion in the progression and metastasis of OSCC, we investigated if the GEF Vav2 modulated Rac1 and Cdc42 activation and thus influenced OSCC invasion. Expression levels of Vav2 did not correlate with invasion but phosphorylated or activated Vav2 was associated with the more invasive cell lines. Transfection of activated Vav2 into the immortalized keratinocyte cell line HaCat and a low-level expressing Vav2 invasive OSCC cell line resulted in increased GTP-bound Rac1 and Cdc42 and increased invasion. Thus, activation of Vav2 appears to modulate cellular invasion through specific regulation of Rac1 and Cdc42 activity in OSCC.
Rho家族的GTP酶调节细胞黏附和运动。鸟嘌呤核苷酸交换因子(GEFs)通过促进核苷酸从GDP交换为GTP来调节GTP酶。我们已经确定,在侵袭性口腔鳞状细胞癌(OSCC)细胞系中,结合GTP的Rac1水平升高。由于侵袭在OSCC进展和转移中起关键作用,我们研究了GEF Vav2是否调节Rac1和Cdc42的激活,从而影响OSCC的侵袭。Vav2的表达水平与侵袭无关,但磷酸化或激活的Vav2与侵袭性更强的细胞系相关。将激活的Vav2转染到永生化角质形成细胞系HaCat和低水平表达Vav2的侵袭性OSCC细胞系中,导致结合GTP的Rac1和Cdc42增加,侵袭增加。因此,Vav2的激活似乎通过特异性调节OSCC中Rac1和Cdc42的活性来调节细胞侵袭。