https://ror.org/042aqky30 Institute for Physiological Chemistry, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
https://ror.org/042aqky30 Cluster of Excellence Physics of Life, Technische Universität Dresden, Dresden, Germany.
Life Sci Alliance. 2024 May 17;7(8). doi: 10.26508/lsa.202302307. Print 2024 Aug.
Dynamic rearrangements of the F-actin cytoskeleton are a hallmark of tumor metastasis. Thus, proteins that govern F-actin rearrangements are of major interest for understanding metastasis and potential therapies. We hypothesized that the unique F-actin binding and bundling protein SWAP-70 contributes importantly to metastasis. Orthotopic, ectopic, and short-term tail vein injection mouse breast and lung cancer models revealed a strong positive dependence of lung and bone metastasis on SWAP-70. Breast cancer cell growth, migration, adhesion, and invasion assays revealed SWAP-70's key role in these metastasis-related cell features and the requirement for SWAP-70 to bind F-actin. Biophysical experiments showed that tumor cell stiffness and deformability are negatively modulated by SWAP-70. Together, we present a hitherto undescribed, unique F-actin modulator as an important contributor to tumor metastasis.
细胞骨架的动态重排是肿瘤转移的一个标志。因此,调控 F-actin 重排的蛋白质对于理解转移和潜在的治疗方法具有重要意义。我们假设独特的 F-actin 结合和束集蛋白 SWAP-70 对转移有重要贡献。在原位、异位和短期尾静脉注射的小鼠乳腺癌和肺癌模型中,SWAP-70 对肺和骨转移有很强的正依赖性。乳腺癌细胞生长、迁移、黏附和侵袭实验揭示了 SWAP-70 在这些与转移相关的细胞特征中的关键作用,以及 SWAP-70 结合 F-actin 的必要性。生物物理实验表明,肿瘤细胞的刚性和变形性被 SWAP-70 负调节。总之,我们提出了一个迄今为止尚未描述的独特的 F-actin 调节剂,作为肿瘤转移的一个重要贡献者。