Mayorca-Guiliani Alejandro, Erler Janine T
Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Onco Targets Ther. 2013 Nov 25;6:1729-35. doi: 10.2147/OTT.S38110.
The extracellular matrix (ECM) is the physical scaffold where cells are organized into tissues and organs. The ECM may be modified during cancer to allow and promote proliferation, invasion, and metastasis. The family of lysyl oxidase (LOX) enzymes cross-links collagens and elastin and, therefore, is a central player in ECM deposition and maturation. Extensive research has revealed how the LOX proteins participate in every stage of cancer progression, and two family members, LOX and LOX-like 2, have been linked to metastasis, the final stage of cancer responsible for over 90% of cancer patient deaths. However, LOX biosynthesis results in by-product with antiproliferative properties in certain cancers, and LOX enzymes may have different effects depending on the molecular network in which they are active. Therefore, the design of therapies targeting the LOX family needs to be guided by the molecular makeup of the individual disease and will probably require other agents to act on both the LOX enzymes and their associated network.
细胞外基质(ECM)是一种物理支架,细胞在其中被组织成组织和器官。在癌症发生过程中,ECM可能会发生改变,以允许并促进癌细胞的增殖、侵袭和转移。赖氨酰氧化酶(LOX)家族的酶可使胶原蛋白和弹性蛋白交联,因此是ECM沉积和成熟过程中的关键因子。大量研究揭示了LOX蛋白如何参与癌症进展的各个阶段,其中两个家族成员,即LOX和类LOX 2,与转移相关,转移是癌症的最后阶段,超过90%的癌症患者死亡都与之有关。然而,在某些癌症中,LOX的生物合成会产生具有抗增殖特性的副产物,并且LOX酶可能会因其所处的分子网络不同而产生不同的作用。因此,针对LOX家族的治疗方案设计需要以个体疾病的分子构成作为指导,可能还需要其他药物作用于LOX酶及其相关网络。