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Compression-induced dedifferentiation of adipocytes promotes tumor progression

机译:压缩诱导的脂肪细胞的去细胞促进肿瘤进展

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摘要

Dysregulated physical stresses are generated during tumorigenesis that affect the surrounding compliant tissues including adipocytes. However, the effect of physical stressors on the behavior of adipocytes and their cross-talk with tumor cells remain elusive. Here, we demonstrate that compression of cells, resulting from various types of physical stresses, can induce dedifferentiation of adipocytes via mechanically activating Wnt/β-catenin signaling. The compression-induced dedifferentiated adipocytes (CiDAs) have a distinct transcriptome profile, long-term self-renewal, and serial clonogenicity, but do not form teratomas. We then show that CiDAs notably enhance human mammary adenocarcinoma proliferation both in vitro and in a xenograft model, owing to myofibrogenesis of CiDAs in the tumor-conditioned environment. Collectively, our results highlight unique physical interplay in the tumor ecosystem; tumor-induced physical stresses stimulate de novo generation of CiDAs, which feedback to tumor growth.
机译:在肿瘤发生期间产生具有吸引力的物理应力,其影响包括脂肪细胞在内的周围兼容组织。然而,物理压力源对脂肪细胞的行为的影响及其与肿瘤细胞的串扰仍然难以捉摸。这里,我们证明了由各种类型的物理应力产生的细胞的压缩可以通过机械激活Wnt /β-catenin信号传导来诱导脂肪细胞的消退。压缩诱导的去脱脂脂肪细胞(CIDA)具有不同的转录组型材,长期自我更新和串行克隆性,但不形成畸胎瘤。然后,我们认为CIDAS在肿瘤条件环境中,由于CIDA的肌波发生,因此在体外和异种移植模型中尤其增强人类乳腺癌腺癌增殖。集体,我们的结果突出了肿瘤生态系统中的独特物理相互作用;肿瘤诱导的物理应力刺激De Novo生成CIDA,反馈肿瘤生长。

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