Rofstad Einar K, Tunheim Siv H, Mathiesen Berit, Graff Bjørn A, Halsør Ellen F, Nilsen Kristin, Galappathi Kanthi
Group of Radiation Biology and Tumor Physiology, Department of Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, N-0310 Oslo, Norway.
Cancer Res. 2002 Feb 1;62(3):661-4.
Interstitial fluid pressure (IFP) is elevated in many experimental and human tumors, and high IFP is associated with poor prognosis in human cancer. The significance of elevated IFP in the development of metastatic disease was investigated in the present work by using A-07 human melanoma xenografts as models of cancer in humans. IFP was measured with the micropipette technique (tumor periphery) and the wick-in-needle technique (tumor center). Tumor hypoxia was studied by immunohistochemistry using pimonidazole as a hypoxia marker and by using a radiobiological assay. High central tumor IFP was found to be associated with the development of pulmonary (P = 0.000085) and lymph node (P = 0.000036) metastases in small (150-200 mm(3)) A-07 tumors. Hypoxic cells could not be detected in these tumors. Our study suggests that interstitial hypertension may facilitate tumor cell intravasation and, hence, promote metastasis by mechanisms independent of tumor hypoxia.
在许多实验性肿瘤和人类肿瘤中,组织间液压力(IFP)会升高,而高IFP与人类癌症的不良预后相关。在本研究中,通过使用A-07人黑色素瘤异种移植模型作为人类癌症模型,研究了升高的IFP在转移性疾病发展中的意义。IFP采用微量移液器技术(肿瘤周边)和针芯技术(肿瘤中心)进行测量。通过使用匹莫硝唑作为缺氧标志物的免疫组织化学和放射生物学测定法研究肿瘤缺氧情况。发现在小(150 - 200 mm³)A-07肿瘤中,高肿瘤中心IFP与肺转移(P = 0.000085)和淋巴结转移(P = 0.000036)的发生相关。在这些肿瘤中未检测到缺氧细胞。我们的研究表明,组织间高压可能促进肿瘤细胞进入血管,从而通过独立于肿瘤缺氧的机制促进转移。