Life Sciences and Radiation Research, Graduate School of Biomedical Sciences Nagasaki University, Nagasaki, Japan.
Department of Radiation Medical Sciences, Nagasaki University Atomic Bomb Disease Institute, Nagasaki, Japan.
PLoS One. 2021 Apr 1;16(4):e0249059. doi: 10.1371/journal.pone.0249059. eCollection 2021.
The microenvironment of an early-stage tumor, in which a small number of cancer cells is surrounded by a normal counterpart milieu, plays a crucial role in determining the fate of initiated cells. Here, we examined cell competition between anaplastic thyroid cancer cells and normal thyroid follicular cells using co-culture method. Cancer cells were grown until they formed small clusters, to which normal cells were added to create high-density co-culture condition. We found that co-culture with normal cells significantly suppressed the growth of cancer cell clusters through the activation of Akt-Skp2 pathway. In turn, cancer cells triggered apoptosis in the neighboring normal cells through local activation of ERK1/2. A bi-directional cell competition provides a suppressive mechanism of anaplastic thyroid cancer progression. Since the competitive effect was negated by terminal growth arrest caused by radiation exposure to normal cells, modulation of reciprocal stress response in vivo could be an intrinsic mechanism associated with tumor initiation, propagation, and metastasis.
早期肿瘤的微环境中,少数癌细胞被正常细胞环境所包围,在决定起始细胞的命运方面起着至关重要的作用。在这里,我们使用共培养方法研究了间变性甲状腺癌细胞与正常甲状腺滤泡细胞之间的细胞竞争。将癌细胞培养至形成小簇,然后加入正常细胞以创建高密度共培养条件。我们发现,与正常细胞共培养通过激活 Akt-Skp2 途径显著抑制了癌细胞簇的生长。反过来,癌细胞通过局部激活 ERK1/2 诱导相邻正常细胞凋亡。双向细胞竞争提供了一种抑制间变性甲状腺癌进展的机制。由于正常细胞受到辐射导致的末端生长停滞否定了竞争效应,因此体内调节相互的应激反应可能是与肿瘤起始、传播和转移相关的内在机制。