Project for Cellular Senescence, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Department of Maxillofacial Orthognathics, Tokyo Medical and Dental University, Tokyo, Japan.
Nat Commun. 2022 Jul 18;13(1):4157. doi: 10.1038/s41467-022-31642-4.
Cellular senescence and cell competition are important tumor suppression mechanisms that restrain cells with oncogenic mutations at the initial stage of cancer development. However, the link between cellular senescence and cell competition remains unclear. Senescent cells accumulated during the in vivo aging process contribute toward age-related cancers via the development of senescence-associated secretory phenotype (SASP). Here, we report that hepatocyte growth factor (HGF), a SASP factor, inhibits apical extrusion and promotes basal protrusion of Ras-mutated cells in the cell competition assay. Additionally, cellular senescence induced by a high-fat diet promotes the survival of cells with oncogenic mutations, whereas crizotinib, an inhibitor of HGF signaling, provokes the removal of mutated cells from mouse livers and intestines. Our study provides evidence that cellular senescence inhibits cell competition-mediated elimination of oncogenic cells through HGF signaling, suggesting that it may lead to cancer incidence during aging.
细胞衰老和细胞竞争是重要的肿瘤抑制机制,可在癌症发展的初始阶段抑制携带致癌突变的细胞。然而,细胞衰老与细胞竞争之间的联系尚不清楚。在体内衰老过程中积累的衰老细胞通过衰老相关分泌表型 (SASP) 的发展促进与年龄相关的癌症。在这里,我们报告称,HGF(SASP 因子之一)可抑制 Ras 突变细胞的顶端挤出,并促进其基底突出,从而在细胞竞争测定中发挥作用。此外,高脂肪饮食诱导的细胞衰老促进了致癌突变细胞的存活,而 HGF 信号抑制剂克唑替尼可促使突变细胞从小鼠肝脏和肠道中清除。我们的研究提供了证据表明,细胞衰老通过 HGF 信号抑制细胞竞争介导的致癌细胞消除,这表明它可能导致衰老过程中的癌症发病率。