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©The Author(s) 2025.
World J Gastrointest Oncol. Apr 15, 2025; 17(4): 102619
Published online Apr 15, 2025. doi: 10.4251/wjgo.v17.i4.102619
Published online Apr 15, 2025. doi: 10.4251/wjgo.v17.i4.102619
Figure 6 O6-methylguanine DNA methyltransferase inhibited rectal cancer progression by reducing protein tyrosine phosphatase nonreceptor type 4 expression.
A and B: Protein tyrosine phosphatase nonreceptor type 4 (PTPN4) protein levels in SW837 cells were assessed through Western blot analysis; C: SW837 cell proliferation detected using Cell Counting kit-8 assay; D and E: Transwell assay performed used to assess SW837 cell invasion; F and G: SW837 cell apoptosis was examined using flow cytometry; H and I: E-cadherin, N-cadherin and vimentin levels in SW837 cells were measured using Western blot analysis. Data are presented as mean ± SE. aP < 0.05; bP < 0.01; GAPDH: Glyceraldehyde-3-phosphate dehydrogenase; MGMT: O6-methylguanine DNA methyltransferase; PTPN4: Protein tyrosine phosphatase nonreceptor type 4; sh-MGMT: Short hairpin RNAs targeting O6-methylguanine DNA methyltransferase; sh-PTPN4: Short hairpin RNAs targeting protein tyrosine phosphatase nonreceptor type 4.
- Citation: Xin MJ, Yuan Y. Centromere protein A knockdown inhibits rectal cancer through O6-methylguanine DNA methyltransferase/protein tyrosine phosphatase nonreceptor type 4 axis. World J Gastrointest Oncol 2025; 17(4): 102619
- URL: https://www.wjgnet.com/1948-5204/full/v17/i4/102619.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v17.i4.102619