Copyright
©The Author(s) 2018.
World J Gastroenterol. Jul 7, 2018; 24(25): 2710-2721
Published online Jul 7, 2018. doi: 10.3748/wjg.v24.i25.2710
Published online Jul 7, 2018. doi: 10.3748/wjg.v24.i25.2710
Figure 4 Changes of semiquantitative dynamic contrast-enhanced parameter of primary hepatocellular carcinomas and implanted liver R1-tumors and quantification of combretastatin-A4-phosphate-induced tumoral necrosis.
A: Representative contrast enhancement-time curves of a primary HCC and a secondary liver R1-tumor before, and 1 h and 12 h after CA4P treatment, for calculating tumor AUC30 at different time points; B: Quantitative changes of tumor blood supply between HCCs and R1-tumors at baseline and 1 h and 12 h after CA4P treatment indicated by AUC30; C: Bar chart comparing the percentile tumoral necrosis between primary HCCs and implanted liver R1 at 12 h after CA4P therapy, which was estimated by postmortem HE staining. aP < 0.05, bP < 0.01. AUC30: Area under the time signal intensity curve; HCC: Hepatocellular carcinoma.
- Citation: Liu YW, De Keyzer F, Feng YB, Chen F, Song SL, Swinnen J, Bormans G, Oyen R, Huang G, Ni YC. Intra-individual comparison of therapeutic responses to vascular disrupting agent CA4P between rodent primary and secondary liver cancers. World J Gastroenterol 2018; 24(25): 2710-2721
- URL: https://www.wjgnet.com/1007-9327/full/v24/i25/2710.htm
- DOI: https://dx.doi.org/10.3748/wjg.v24.i25.2710