The Rab25-ADAMTS5 axis as a previously undescribed mechanism for sensing tumor microenvironment complexity.

François Tyckaert, Francesco Baschieri
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引用次数: 0

Abstract

The tumor microenvironment (TME), particularly the extracellular matrix (ECM), plays a critical role in cancer progression. Focusing on ovarian cancer, Yuan et al. reveal an ECM-dependent signaling axis where cancer-associated fibroblasts (CAFs) enhance the invasiveness of cancer cells via Rab25-driven upregulation of the protease ADAMTS5. This process is only triggered in the presence of native ECM. In turn, stimulated cancer cells favor CAF invasiveness through a mechanism that remains to be identified. These findings uncover a bidirectional crosstalk between cancer cells and CAFs and highlight the importance of context-specific in vitro models to decipher ECM-mediated tumor dynamics.

Rab25-ADAMTS5轴是先前描述的感知肿瘤微环境复杂性的机制。
肿瘤微环境(TME),特别是细胞外基质(ECM),在癌症进展中起着关键作用。Yuan等人在卵巢癌研究中揭示了一个依赖于ecm的信号轴,其中癌症相关成纤维细胞(CAFs)通过rab25驱动的蛋白酶ADAMTS5上调来增强癌细胞的侵袭性。此过程仅在本机ECM存在时触发。反过来,受刺激的癌细胞通过一种尚待确定的机制支持CAF侵袭。这些发现揭示了癌细胞和CAFs之间的双向串扰,并强调了上下文特异性体外模型对破译ecm介导的肿瘤动力学的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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