V-ATPase as an effective therapeutic target for sarcomas

被引:51
作者
Perut, Francesca [1 ]
Avnet, Sofia [1 ]
Fotia, Caterina [1 ]
Baglio, Serena Rubina [1 ]
Salerno, Manuela [1 ]
Hosogi, Shigekuni [1 ,2 ]
Kusuzaki, Katsuyuki [2 ]
Baldini, Nicola [1 ,3 ]
机构
[1] Ist Ortoped Rizzoli, Lab Orthopaed Pathophysiol & Regenerat Med, I-40136 Bologna, Italy
[2] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Mol Cell Physiol, Kyoto, Japan
[3] Univ Bologna, Dept Biomed & Neuromotor Sci, Bologna, Italy
关键词
Osteosarcoma; Rhabdomyosarcoma; Chondrosarcoma; V-ATPase; Lysosomes; PROTON PUMP INHIBITORS; CARBONIC-ANHYDRASE-IX; HUMAN-MELANOMA CELLS; BREAST-CANCER CELLS; PH; TUMORS; OMEPRAZOLE; STRATEGY; INVASION; HYPOXIA;
D O I
10.1016/j.yexcr.2013.10.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant tumors show intense glycolysis and, as a consequence, high lactate production and proton efflux activity. We investigated proton dynamics in osteosarcoma, rhabdomyosarcoma, and chondrosarcoma, and evaluated the effects of esomeprazole as a therapeutic agent interfering with tumor acidic microenvironment All sarcomas were able to survive in an acidic microenvironment (up to 5.9-6.0 pH) and abundant acidic lysosomes were found in all sarcoma subtypes. V-ATPase, a proton pump that acidifies intracellular compartments and transports protons across the plasma membrane, was detected in all cell types with a histotype-specific expression pattern. Esomeprazole administration interfered with proton compartmentalization in acidic organelles and induced a significant dose-dependent toxicity. Among the different histotypes, rhabdomyosarcoma, expressing the highest levels of V-ATPase and whose lysosomes are most acidic, was mostly susceptible to ESOM treatment. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 32
页数:12
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