Chioureas Dimitrios, Beck Janina, Baltatzis George, Vardaki Ioulia, Fonseca Pedro, Tsesmetzis Nikolaos, Vega Francisco, Leventaki Vasiliki, Eliopoulos Aristides G, Drakos Elias, Rassidakis George Z, Panaretakis Theocharis
Department of Oncology and Pathology, Karolinska Institutet, SE-17176 Stockholm, Sweden.
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Cancers (Basel). 2022 Jun 14;14(12):2939. doi: 10.3390/cancers14122939.
The oncogenic pathways activated by the NPM-ALK chimeric kinase of ALK+ anaplastic large cell lymphoma (ALCL) are well characterized; however, the potential interactions of ALK signaling with the microenvironment are not yet known. Here we report that ALK+ ALCL-derived exosomes contain critical components of ALK signaling as well as CD30, and that exosome uptake by lymphoid cells led to increased proliferation and expression of critical antiapoptotic proteins by the recipient cells. The bone marrow fibroblasts highly uptake ALK+ ALCL-derived exosomes and acquire a cancer-associated fibroblast (CAF) phenotype. Moreover, exosome-mediated activation of stromal cells altered the cytokine profile of the microenvironment. These interactions may contribute to tumor aggressiveness and possibly resistance to treatment.
ALK阳性间变性大细胞淋巴瘤(ALCL)的NPM-ALK嵌合激酶激活的致癌途径已得到充分表征;然而,ALK信号与微环境之间的潜在相互作用尚不清楚。在此,我们报告ALK阳性ALCL来源的外泌体含有ALK信号的关键成分以及CD30,并且淋巴细胞对外泌体的摄取导致受体细胞增殖增加和关键抗凋亡蛋白的表达增加。骨髓成纤维细胞高度摄取ALK阳性ALCL来源的外泌体并获得癌症相关成纤维细胞(CAF)表型。此外,外泌体介导的基质细胞激活改变了微环境的细胞因子谱。这些相互作用可能导致肿瘤侵袭性增加,并可能导致治疗耐药。