Sossey-Alaoui Khalid, Safina Alfiya, Li Xiurong, Vaughan Mary M, Hicks David G, Bakin Andrei V, Cowell John K
Roswell Park Cancer Institute, Department of Cancer Genetics, Elm and Carlton Streets, Buffalo, NY 14263, USA.
Am J Pathol. 2007 Jun;170(6):2112-21. doi: 10.2353/ajpath.2007.060975.
The expression of WAVE3, an actin-cytoskeleton and reorganization protein, is elevated in malignant human breast cancer, yet the role of WAVE3 in promoting tumor progression remains undefined. We have recently shown that knockdown of WAVE3 expression in human breast adenocarcinoma MDA-MB-231 cells using small interfering RNA resulted in a significant reduction of cell motility, migration, and invasion, which correlated with a reduction in the levels of active p38 mitogen-activated protein kinase. Here, we investigated the effect of stable suppression of WAVE3 by short hairpin RNA on tumor growth and metastasis in xenograft models. Breast cancer MDA-MB-231 cells expressing short hairpin RNA to WAVE3 (shWAVE3) showed a significant reduction in Matrigel invasion and formation of lung colonies after tail-vein injection in SCID mice. In the orthotopic model, we observed a reduction in growth rate of the primary tumors, as well as in the metastases to the lungs. We also show that suppression of p38 mitogen-activated protein kinase activity by dominant-negative p38 results in comparable phenotypes to the knockdown of WAVE3. These studies provide direct evidence that the WAVE3-p38 pathway contributes to breast cancer progression and metastasis.
肌动蛋白细胞骨架重组蛋白WAVE3在人类恶性乳腺癌中表达上调,但其在促进肿瘤进展中的作用仍不明确。我们最近发现,使用小干扰RNA敲低人乳腺腺癌MDA-MB-231细胞中WAVE3的表达,会导致细胞运动性、迁移和侵袭显著降低,这与活性p38丝裂原活化蛋白激酶水平的降低相关。在此,我们研究了短发夹RNA稳定抑制WAVE3对异种移植模型中肿瘤生长和转移的影响。在SCID小鼠尾静脉注射后,表达针对WAVE3的短发夹RNA(shWAVE3)的乳腺癌MDA-MB-231细胞在基质胶侵袭和肺集落形成方面显著减少。在原位模型中,我们观察到原发性肿瘤的生长速度以及肺转移均有所降低。我们还表明,显性负性p38抑制p38丝裂原活化蛋白激酶活性会导致与敲低WAVE3相当的表型。这些研究提供了直接证据,表明WAVE3-p38通路有助于乳腺癌的进展和转移。