Department of Pharmacology, Penn State College of Medicine, The Pennsylvania State University, Hershey, PA, 17033, USA.
Department of Chemical Engineering, The Pennsylvania State University, University Park, PA, 16802, USA.
Adv Sci (Weinh). 2023 Nov;10(31):e2302229. doi: 10.1002/advs.202302229. Epub 2023 Sep 19.
The principal cause of death in cancer patients is metastasis, which remains an unresolved problem. Conventionally, metastatic dissemination is linked to actomyosin-driven cell locomotion. However, the locomotion of cancer cells often does not strictly line up with the measured actomyosin forces. Here, a complementary mechanism of metastatic locomotion powered by dynein-generated forces is identified. These forces arise within a non-stretchable microtubule network and drive persistent contact guidance of migrating cancer cells along the biomimetic collagen fibers. It is also shown that the dynein-powered locomotion becomes indispensable during invasive 3D migration within a tissue-like luminal network formed by spatially confining granular hydrogel scaffolds (GHS) made up of microscale hydrogel particles (microgels). These results indicate that the complementary motricity mediated by dynein is always necessary and, in certain instances, sufficient for disseminating metastatic breast cancer cells. These findings advance the fundamental understanding of cell locomotion mechanisms and expand the spectrum of clinical targets against metastasis.
癌症患者死亡的主要原因是转移,这仍然是一个未解决的问题。传统上,转移性扩散与肌动球蛋白驱动的细胞运动有关。然而,癌细胞的运动通常与测量到的肌动球蛋白力并不严格一致。在这里,确定了一种由动力蛋白产生的力驱动的转移性运动的补充机制。这些力出现在不可拉伸的微管网络内,并沿仿生胶原蛋白纤维驱动迁移癌细胞的持续接触引导。还表明,在由空间限制的颗粒水凝胶支架(GHS)形成的组织状腔网络内进行侵入性 3D 迁移期间,动力蛋白驱动的运动变得不可或缺,GHS 由微尺度水凝胶颗粒(微凝胶)组成。这些结果表明,由动力蛋白介导的互补运动总是必要的,并且在某些情况下,足以传播转移性乳腺癌细胞。这些发现推进了对细胞运动机制的基本理解,并扩大了针对转移的临床目标范围。