Makale Milan
Moores UCSD Cancer Center, University of California, San Diego, La Jolla, California 92093-0819, USA.
Birth Defects Res C Embryo Today. 2007 Dec;81(4):329-43. doi: 10.1002/bdrc.20110.
The primary cause of cancer treatment failure is invasion and metastasis, and invading tumor cells utilize many of the motility patterns that have been documented for normal morphogenesis. Recently, the role of mechanical forces in guiding various tissue and cell movements in embryonic development has been systematically analyzed with new experimental and computational methods. The tissue and cellular mechanobiology approach also holds promise for increasing the understanding of tumor invasion. In fact, the mechanical stiffness of tumors has correlated with invasiveness, and manipulation of extracellular matrix (ECM) stiffness in vitro has suppressed the cancer phenotype. Several important signaling molecules reside on the cytoskeleton, which is affected by external stress imparted by the ECM, and deformation of the nucleus can trigger the activation of certain genes. All these observations suggest that a synthesis of the biology of cancer cell invasion and cellular mechanobiology may offer new targets for the treatment of malignant disease. Accordingly, sensitive and relevant in vivo models and methods to study cancer mechanobiology are needed.
癌症治疗失败的主要原因是侵袭和转移,侵袭性肿瘤细胞利用了许多已被记录用于正常形态发生的运动模式。最近,通过新的实验和计算方法,对机械力在胚胎发育中引导各种组织和细胞运动的作用进行了系统分析。组织和细胞力学生物学方法也有望增进对肿瘤侵袭的理解。事实上,肿瘤的机械硬度与侵袭性相关,体外对细胞外基质(ECM)硬度的操控已抑制了癌症表型。几种重要的信号分子存在于细胞骨架上,细胞骨架会受到ECM施加的外部应力影响,而细胞核的变形可触发某些基因的激活。所有这些观察结果表明,将癌细胞侵袭生物学与细胞力学生物学相结合可能为恶性疾病的治疗提供新靶点。因此,需要灵敏且相关的体内模型和方法来研究癌症力学生物学。