Erler Janine T, Giaccia Amato J
Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California 94305, USA.
Cancer Res. 2006 Nov 1;66(21):10238-41. doi: 10.1158/0008-5472.CAN-06-3197.
Hypoxic cancer cells pose a great challenge to the oncologist because they are especially aggressive, metastatic, and resistant to therapy. Recently, we showed that elevation of the extracellular matrix protein lysyl oxidase (LOX) correlates with metastatic disease and is essential for hypoxia-induced metastasis. In an orthotopic rodent model of breast cancer, a small-molecule or antibody inhibitor of LOX abolished metastasis, offering preclinical validation of this enzyme as a therapeutic target.
缺氧癌细胞给肿瘤学家带来了巨大挑战,因为它们极具侵袭性、转移性且对治疗有抗性。最近,我们发现细胞外基质蛋白赖氨酰氧化酶(LOX)水平升高与转移性疾病相关,并且是缺氧诱导转移所必需的。在乳腺癌原位啮齿动物模型中,LOX的小分子抑制剂或抗体抑制剂可消除转移,为将该酶作为治疗靶点提供了临床前验证。
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