Molina Paola, Daniel Mikiyas, Wang Jason, Macara Ian G
bioRxiv. 2025 May 17:2025.05.16.654585. doi: 10.1101/2025.05.16.654585.
Individual epithelial cells that acutely express oncogenes such as Ras or Src are extruded apically from monolayers of wildtype cells. Multiple signaling networks have been implicated but the extrusion mechanism is still not fully understood. We examined extrusion of mammary epithelial cells caused by acute induction of oncogenic Ras(Q61L). As reported by others, Ras-dependent extrusion requires downstream activation of ERK but not AKT. Unexpectedly, however, extrusion was completely blocked by Erlotinib, which inhibits Epidermal growth factor receptor (EGFR) activity, or by deletion of the receptor. In pancreatic and lung cancers, EGFR is required for full activation of Ras and consequent ERK activation. However, inhibition or deletion of EGFR had no impact in our system on Ras(Q61L)-GTP levels or ERK phosphorylation. Importantly, receptor function was cell autonomous, because EGFR expression was not required in surrounding WT cells but was essential in the Ras(Q61L) cells, yet did not act through the canonical ERK signaling pathway. Deletion of Ras exchange factors Sos1/2 did not block cell extrusion. Moreover, expression of a constitutively active MEK mutant, instead of Ras, was sufficient to drive extrusion, and EGFR inhibition or knockout in these cells blocked extrusion, with no change in phospho-ERK levels. Notably, acute expression of Ras triggered internalization of E-cadherin, which was partially blocked by inhibition of EGFR. Knockout of E-cadherin was alone sufficient to promote extrusion. Together, these data demonstrate an unanticipated requirement for noncanonical EGFR signaling in cancer cell extrusion, which may act in part through the promotion of E-cadherin endocytosis.
急性表达致癌基因(如Ras或Src)的单个上皮细胞会从野生型细胞单层中顶端挤出。多个信号网络已被牵连其中,但挤出机制仍未完全理解。我们研究了致癌性Ras(Q61L)急性诱导引起的乳腺上皮细胞挤出。正如其他人所报道的,Ras依赖性挤出需要ERK的下游激活,但不需要AKT。然而,出乎意料的是,厄洛替尼(抑制表皮生长因子受体(EGFR)活性)或受体缺失完全阻断了挤出。在胰腺癌和肺癌中,EGFR是Ras完全激活和随后ERK激活所必需的。然而,EGFR的抑制或缺失在我们的系统中对Ras(Q61L)-GTP水平或ERK磷酸化没有影响。重要的是,受体功能是细胞自主的,因为周围野生型细胞中不需要EGFR表达,但在Ras(Q61L)细胞中是必不可少的,且不通过经典的ERK信号通路起作用。Ras交换因子Sos1/2的缺失不会阻断细胞挤出。此外,组成型活性MEK突变体的表达而非Ras的表达足以驱动挤出,并且这些细胞中EGFR的抑制或敲除会阻断挤出,而磷酸化ERK水平没有变化。值得注意的是,Ras的急性表达触发了E-钙黏蛋白的内化,这被EGFR抑制部分阻断。E-钙黏蛋白的敲除单独就足以促进挤出。总之,这些数据表明癌细胞挤出中对非经典EGFR信号有意外需求,这可能部分通过促进E-钙黏蛋白内吞作用起作用。