Sulforaphane Suppresses the Nicotine-Induced Expression of the Matrix Metalloproteinase-9 via Inhibiting ROS-Mediated AP-1 and NF-κB Signaling in Human Gastric Cancer Cells.
Shinan LiPham Ngoc KhoiHong YinDhiraj Kumar SahNam-Ho KimSen LianYoung Do JungPublished in: International journal of molecular sciences (2022)
Sulforaphane, a natural phytochemical compound found in various cruciferous vegetables, has been discovered to present anti-cancer properties. Matrix metalloproteinase-9 (MMP-9) plays a crucial role in gastric cancer metastasis. However, the role of sulforaphane in MMP-9 expression in gastric cancer is not yet defined. Nicotine, a psychoactive alkaloid found in tobacco, is associated with the development of gastric cancer. Here, we found that sulforaphane suppresses the nicotine-mediated induction of MMP-9 in human gastric cancer cells. We discovered that reactive oxygen species (ROS) and MAPKs (p38 MAPK, Erk1/2) are involved in nicotine-induced MMP-9 expression. AP-1 and NF-κB are the critical transcription factors in MMP-9 expression. ROS/MAPK (p38 MAPK, Erk1/2) and ROS functioned as upstream signaling of AP-1 and NF-κB, respectively. Sulforaphane suppresses the nicotine-induced MMP-9 by inhibiting ROS-mediated MAPK (p38 MAPK, Erk1/2)/AP-1 and ROS-mediated NF-κB signaling axes, which in turn inhibit cell invasion in human gastric cancer AGS cells. Therefore, the current study provides valuable evidence for developing sulforaphane as a new anti-invasion strategy for human gastric cancer therapy.
Keyphrases
- signaling pathway
- reactive oxygen species
- pi k akt
- induced apoptosis
- endothelial cells
- transcription factor
- poor prognosis
- high glucose
- dna damage
- cell migration
- cell death
- smoking cessation
- cell cycle arrest
- oxidative stress
- induced pluripotent stem cells
- cancer therapy
- diabetic rats
- cell proliferation
- pluripotent stem cells
- lps induced
- risk assessment
- immune response
- living cells
- sensitive detection
- dna binding