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©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Feb 14, 2006; 12(6): 858-867
Published online Feb 14, 2006. doi: 10.3748/wjg.v12.i6.858
Published online Feb 14, 2006. doi: 10.3748/wjg.v12.i6.858
Figure 1 Intravital fluorescence microscopy at d 7 after tumor cell implantation.
A: Displays the normal liver microvasculature; B: shows the microvasculature of the tumor of a non-resected control animal (Con); C: displays a 7-day tumor and its microvasculature of an animal which underwent hepatectomy (PHx); D: shows the tumor microvasculature after additional anti-MIP-2 treatment (PHx+mAB). Quantitative analysis of tumor area (E) and tumor volume (F) showed that hepatectomy (PHx) markedly accelerated tumor growth when compared with controls (Con), and that additional anti-MIP-2 treatment (PHx+mAB) was capable of significantly reducing this liver resection-induced tumor growth. Mean ± SE; aP < 0.05 vs Con; cP < 0.05 vs PHx. Magnifications (A-D) ×16.
- Citation: Kollmar O, Menger MD, Schilling MK. Macrophage inflammatory protein-2 contributes to liver resection-induced acceleration of hepatic metastatic tumor growth. World J Gastroenterol 2006; 12(6): 858-867
- URL: https://www.wjgnet.com/1007-9327/full/v12/i6/858.htm
- DOI: https://dx.doi.org/10.3748/wjg.v12.i6.858