It remains unknown for decades how some of the therapeutic fusion proteins positive in a small percentage of cancer cells account for patient outcome. Here, we report that osteosarcoma Rab22a-NeoF1 fusion protein, together with its binding partner PYK2, is sorted into exosomes by HSP90 via its KFERQ-like motif (RVLFLN(142)). The exosomal Rab22a-NeoF1 fusion protein facilitates the pulmonary pre-metastatic niche formation by recruiting bone marrow-derived macrophages. The exosomal PYK2 activates RhoA in its negative recipient osteosarcoma cells and induces signal transducer and activator of transcription 3 activation in its recipient macrophages to increase M2 phenotype. Consequently, lung metastases of its recipient osteosarcoma cells are promoted by this exosomal Rab22a-NeoF1 fusion protein, and this event can be targeted by disrupting its interaction with PYK2 using a designed internalizing RGD peptide.
Rab22a-NeoF1 fusion protein promotes osteosarcoma lung metastasis through its secretion into exosomes.
Rab22a-NeoF1融合蛋白通过分泌到外泌体中促进骨肉瘤肺转移
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作者:Zhong Li, Liao Dan, Li Jingjing, Liu Wenqiang, Wang Jingxuan, Zeng Cuiling, Wang Xin, Cao Zhiliang, Zhang Ruhua, Li Miao, Jiang Kuntai, Zeng Yi-Xin, Sui Jianhua, Kang Tiebang
| 期刊: | Signal Transduction and Targeted Therapy | 影响因子: | 52.700 |
| 时间: | 2021 | 起止号: | 2021 Feb 11; 6(1):59 |
| doi: | 10.1038/s41392-020-00414-1 | 研究方向: | 免疫/内分泌 |
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