a Department of Molecular Cell Biology , Institute for Cancer Research, Oslo University Hospital , Montebello , Oslo , Norway.
b Centre for Cancer Biomedicine , Institute of Clinical Medicine, Faculty of Medicine, University of Oslo , Norway.
Autophagy. 2017 Jul 3;13(7):1241-1243. doi: 10.1080/15548627.2017.1310361.
When exposed to adverse environmental conditions, cells degrade their own content to recycle cellular building blocks through a process called autophagy. A large body of literature has connected autophagy to cancer, but most studies up until now focused on its function in transformed cells. In her thesis, Nadja Katheder dissected the role of autophagy in a well-characterized neoplastic in vivo tumor model in Drosophila and demonstrates a novel non-cell-autonomous requirement of this process for tumor growth. Neighboring epithelial cells and distal tissues increase autophagy in the presence of a malignant tumor. Pharmacological autophagy inhibition reduces tumor growth and genetic ablation of autophagy in the microenvironment reveals a tumor-supportive role of this process in this specific cell population. Tumor cells are metabolically stressed and induce autophagy in their neighbors through a TNFα-JNK-IL-6 signaling cascade. Moreover, they are dependent on amino acid import to sustain their proliferation, which indicates a coupling of metabolism between these two cell populations. Finally, allografted growth-impaired tumors from autophagy-deficient donor animals resume growth in an autophagy-competent host. Together, the results described in this thesis highlight the tumor-promoting role of autophagy the microenvironment and show that cancer cells engage their epithelial neighbors as essential contributors aiding their own growth.
当暴露于不利的环境条件时,细胞通过自噬过程降解自身内容物以回收细胞构建块。大量文献将自噬与癌症联系起来,但直到现在,大多数研究都集中在其在转化细胞中的功能上。在她的论文中,Nadja Katheder 剖析了自噬在果蝇中一种特征明确的肿瘤体内模型中的作用,并证明了该过程对肿瘤生长的一种新的非细胞自主需求。在存在恶性肿瘤的情况下,相邻的上皮细胞和远端组织会增加自噬。药理学自噬抑制可减少肿瘤生长,而微环境中自噬的遗传消融则揭示了该过程在该特定细胞群中的肿瘤支持作用。肿瘤细胞代谢应激,并通过 TNFα-JNK-IL6 信号级联诱导其邻居中的自噬。此外,它们依赖于氨基酸输入来维持增殖,这表明这两个细胞群体之间存在代谢偶联。最后,来自自噬缺陷供体动物的同种异体移植生长受损的肿瘤在自噬功能正常的宿主中恢复生长。总之,本论文中描述的结果强调了自噬在微环境中的促肿瘤作用,并表明癌细胞将其上皮邻居作为重要的贡献者,帮助自身生长。