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©The Author(s) 2024.
World J Gastrointest Oncol. Dec 15, 2024; 16(12): 4716-4727
Published online Dec 15, 2024. doi: 10.4251/wjgo.v16.i12.4716
Published online Dec 15, 2024. doi: 10.4251/wjgo.v16.i12.4716
Figure 5 Knocking down spermine synthase enhances radiosensitivity of HCT116 cells by suppressing the mammalian target of rapamy cin pathway.
Western blot analysis for detecting the protein expression levels of mammalian target of rapamycin (mTOR), p-mTOR, S6K1, p-S6K1, S6, and p-S6 in HCT116 cells under the following conditions: Negative control shRNA (ShNC), shNC + IR, spermine synthase shRNA (sh-SMS), and sh-SMS + IR. bP < 0.01 vs shNC, dP < 0.01 vs shNC + IR, fP < 0.01 vs sh-SMS; SMS: Spermine synthase; sh-SMS: Spermine synthase shRNA; shNC: Negative control shRNA; OE-SMS: Spermine synthase over-expression vector; OE-NC: Negative control over-expression vector; mTOR: Mammalian target of rapamycin.
- Citation: Guo YB, Wu YM, Lin ZZ. Enhancing the radiosensitivity of colorectal cancer cells by reducing spermine synthase through promoting autophagy and DNA damage. World J Gastrointest Oncol 2024; 16(12): 4716-4727
- URL: https://www.wjgnet.com/1948-5204/full/v16/i12/4716.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v16.i12.4716