Department of Neurosurgery, University Hospital Frankfurt, Goethe University Frankfurt, Frankfurt, Germany.
Frankfurt Cancer Institute (FCI), Goethe University Frankfurt, Frankfurt, Germany.
Clin Exp Metastasis. 2024 Dec;41(6):817-828. doi: 10.1007/s10585-024-10308-z. Epub 2024 Sep 2.
Cells constantly reshape there plasma membrane and cytoskeleton during physiological and pathological processes (Hagmann et al. in J Cell Biochem 73:488-499, 1999). Cell blebbing, the formation of bulges or protrusions on the cell membrane, is related to mechanical stress, changes in intracellular pressure, chemical signals, or genetic anomalies. These membrane bulges interfere with the force balance of actin filaments, microtubules, and intermediate filaments, the basic components of the cytoskeleton (Charras in J Microsc 231:466-478, 2008). In the past, these blebs with circular structures were considered apoptotic markers (Blaser et al. in Dev Cell 11:613-627, 2006). Cell blebbing activates phagocytes and promotes the rapid removal of intrinsic compartments. However, recent studies have revealed that blebbing is associated with dynamic cell reorganization and alters the movement of cells in-vivo and in-vitro (Charras and Paluch in Nat Rev Mol Cell Biol 9:730-736, 2008). During tumor progression, blebbing promotes invasion of cancer cells into blood, and lymphatic vessels, facilitating tumor progression and metastasis (Weems et al. in Nature 615:517-525, 2023). Blebbing is a dominant feature of tumor cells generally absent in normal cells. Restricting tumor blebbing reduces anoikis resistance (survival in suspension) (Weems et al. in Nature 615:517-525, 2023). Hence, therapeutic intervention with targeting blebbing could be highly selective for proliferating pro-metastatic tumor cells, providing a novel therapeutic pathway for tumor metastasis with minimal side effects. Here, we review the association between cell blebbing and tumor cells, to uncover new research directions and strategies for metastatic cancer therapy. Finaly, we aim to identify the druggable targets of metastatic cancer in relation to cell blebbing.
细胞在生理和病理过程中不断重塑质膜和细胞骨架(Hagmann 等人,《细胞生化学杂志》73:488-499, 1999)。细胞膜起泡,即细胞膜上形成的隆起或突起,与机械应力、细胞内压力变化、化学信号或遗传异常有关。这些膜泡干扰了肌动蛋白丝、微管和中间丝的力平衡,这些都是细胞骨架的基本组成部分(Charras,《显微镜学杂志》231:466-478, 2008)。过去,这些具有圆形结构的泡被认为是细胞凋亡的标志物(Blaser 等人,《发育细胞》11:613-627, 2006)。细胞起泡激活吞噬细胞,并促进固有隔室的快速清除。然而,最近的研究表明,起泡与细胞的动态重组有关,并改变了细胞在体内和体外的运动(Charras 和 Paluch,《自然评论分子细胞生物学》9:730-736, 2008)。在肿瘤进展过程中,起泡促进癌细胞侵入血液和淋巴管,促进肿瘤进展和转移(Weems 等人,《自然》615:517-525, 2023)。起泡是肿瘤细胞的一个主要特征,在正常细胞中通常不存在。限制肿瘤起泡可降低失巢凋亡抗性(悬浮生存)(Weems 等人,《自然》615:517-525, 2023)。因此,针对起泡的治疗干预可能对增殖性促转移肿瘤细胞具有高度选择性,为肿瘤转移提供了一种新的治疗途径,副作用最小。在这里,我们综述了细胞起泡与肿瘤细胞之间的关联,以揭示转移性癌症治疗的新研究方向和策略。最后,我们旨在确定与细胞起泡相关的转移性癌症的可药物靶点。