Copyright: ©Author(s) 2026.
World J Gastroenterol. Dec 28, 2026; 32(48): 123033
Published online Dec 28, 2026. doi: 10.3748/wjg.123033
Published online Dec 28, 2026. doi: 10.3748/wjg.123033
Figure 10 Validation of Lmod3 knockdown by small interfering RNA in AML12 cells (n = 3).
A: Lmod3 protein expression level; B: Intracellular triglycerides content; C: Malondialdehyde level; D: Α-smooth muscle actin protein expression level; E: Cell viability. aP < 0.01 vs AML12 group; bP < 0.01 vs AML12 + free fatty acids + negative control small interfering RNA (siRNA) group; cP < 0.01 vs AML12 + free fatty acids + siRNA targeting mouse Lmod3 + control group. MDA: Malondialdehyde; TG: Triglycerides; si-NC: Negative control small interfering RNA; si-Lmod3: Small interfering RNA targeting mouse Lmod3; Con: Control; JQF: Jiangtang Qingre formula; FFA: Free fatty acids; α-SMA: Α-smooth muscle actin.
- Citation: Zhou LJ, Wu JL, Wang H, Han R, Tang C, Fang F, Zhu DP. Integrating proteomics, metabolomics, and molecular docking to elucidate the mechanism of Jiangtang Qingre formula against metabolic dysfunction-associated steatohepatitis. World J Gastroenterol 2026; 32(48): 123033
- URL: https://www.wjgnet.com/1007-9327/full/v32/i48/123033.htm
- DOI: https://dx.doi.org/10.3748/wjg.123033