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Lowering of Tumor Interstitial Fluid Pressure Reduces Tumor Cell Proliferation in a Xenograft Tumor Model

机译:降低肿瘤间质液压力降低异种移植肿瘤模型中的肿瘤细胞增殖

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摘要

High tumor interstitial fluid pressure (TIFP) is a characteristic of most solid tumors. TIFP may hamper adequate uptake of macromolecular therapeutics in tumor tissue. In addition, TIFP generates mechanical forces affecting the tumor cortex, which might influence the growth parameters of tumor cells. This seems likely as, in other tissues (namely, blood vessels or the skin), mechanical stretch is known to trigger proliferation. Therefore, we hypothesize that TIFP-induced stretch modulates proliferation-associated parameters. Solid epithelial tumors (A431 and A549) were grown in Naval Medical Research Institute nude mice, generating a TIFP of about 10 mm Hg (A431) or 5 mm Hg (A549). Tumor drainage of the central cystic area led to a rapid decline of TIFP, together with visible relaxation of the tumor cortex. It was found by sodium dodecyl sulfate polyacrylamide gel electrophoresis and Western blot analysis that TIFP lowering yields a decreased phosphorylation of proliferation-associated p44/42 mitogen-activated protein kinase and tumor relaxation. In confirmation, immunohistochemical staining showed a decrease of tumor-associated proliferation marker Ki-67 after TIFP lowering. These data suggest that the mechanical stretch induced by TIFP is a positive modulator of tumor proliferation.
机译:高肿瘤间质液压力(TIFP)是大多数实体瘤的特征。 TIFP可能会妨碍肿瘤组织中大分子治疗剂的充分摄取。另外,TIFP产生影响肿瘤皮层的机械力,这可能会影响肿瘤细胞的生长参数。这似乎是因为,在其他组织(即血管或皮肤)中,已知机械拉伸会触发增殖。因此,我们假设TIFP诱导的拉伸调节增殖相关的参数。实体上皮肿瘤(A431和A549)在海军医学研究所裸鼠中生长,产生约10 mm Hg(A431)或5 mm Hg(A549)的TIFP。中央囊性区域的肿瘤引流导致TIFP迅速下降,同时肿瘤皮层可见松弛。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳和蛋白质印迹分析发现,TIFP降低会降低与增殖相关的p44 / 42丝裂原激活的蛋白激酶的磷酸化和肿瘤松弛。为了证实这一点,免疫组织化学染色显示,TIFP降低后,肿瘤相关增殖标志物Ki-67降低。这些数据表明,TIFP诱导的机械拉伸是肿瘤增殖的正调节剂。

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