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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 1 Prostaglandin F2α synthase is upregulation in patients with colorectal cancer.
A: Prostaglandin F2α synthase (PGFS) protein expression was verified using western blot in 37 pairs of colorectal cancer (CRC) and adjacent normal tissues; B: Real-time polymerase chain reaction analysis of PGFS mRNA expression in 37 pairs of CRC and adjacent normal tissues; C: Hematoxylin and eosin staining and immunohistochemistry for PGFS expression (scale bar, 50 μm); D: PGFS expression in non-response and response patients analyzed by the Cancer Treatment Response gene signature DataBase (http://ctrdb.ncpsb.org.cn/). aP < 0.05, bP < 0.01. T: Tumor; N: Adjacent normal tissues; PGFS: Prostaglandin F2α synthase; HE: Hematoxylin and eosin.
- 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