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©The Author(s) 2023.
World J Gastroenterol. Oct 21, 2023; 29(39): 5452-5470
Published online Oct 21, 2023. doi: 10.3748/wjg.v29.i39.5452
Published online Oct 21, 2023. doi: 10.3748/wjg.v29.i39.5452
Figure 5 Prostaglandin F2α synthase knockdown improves oxaliplatin efficiency in vivo.
A: Morphologies of collected tumors in subcutaneous HCT8-OxR xenografts in nude mice; B: Curves of tumor growth in each group; C: Tumor weights were measured after collection; D: Hematoxylin-eosin (upper panel; magnification, × 200) and immunohistochemical staining for proliferating cell nuclear antigen (bottom panel; magnification, × 200) using xenograft tumor samples from each group. aP < 0.05, bP < 0.01. PCNA: Proliferating cell nuclear antigen; PGFS: Prostaglandin F2α synthase; HE: Hematoxylin and eosin; Oxa: Oxaliplatin.
- Citation: Wang YJ, Xie XL, Liu HQ, Tian H, Jiang XY, Zhang JN, Chen SX, Liu T, Wang SL, Zhou X, Jin XX, Liu SM, Jiang HQ. Prostaglandin F2α synthase promotes oxaliplatin resistance in colorectal cancer through prostaglandin F2α-dependent and F2α-independent mechanism. World J Gastroenterol 2023; 29(39): 5452-5470
- URL: https://www.wjgnet.com/1007-9327/full/v29/i39/5452.htm
- DOI: https://dx.doi.org/10.3748/wjg.v29.i39.5452