du Plessis Julianne, Deroubaix Aurelie, Omar Aadilah, Penny Clement
Department of Internal Medicine, Oncology Division, Faculty of Health Sciences, University of the Witwatersrand, 7 York Road, Parktown, Johannesburg 2193, South Africa.
Life Sciences Imaging Facility, Faculty of Health Sciences, University of the Witwatersrand, 7 York Road, Parktown, Johannesburg 2193, South Africa.
Curr Issues Mol Biol. 2024 Aug 5;46(8):8600-8610. doi: 10.3390/cimb46080506.
Colorectal cancer (CRC), found in the intestinal tract, is initiated and progresses through various mechanisms, including the dysregulation of signaling pathways. Several signaling pathways, such as EGFR and MAPK, involved in cell proliferation, migration, and apoptosis, are often dysregulated in CRC. Although cannabidiol (CBD) has previously induced apoptosis and cell cycle arrest in vitro in CRC cell lines, its effects on signaling pathways have not yet been determined. An in silico analysis was used here to assess partner proteins that can bind to CBD, and docking simulations were used to predict precisely where CBD would bind to these selected proteins. A survey of the current literature was used to hypothesize the effect of CBD binding on such proteins. The results predict that CBD could interact with EGFR, RAS/RAF isoforms, MEK1/2, and ERK1/2. The predicted CBD-induced inhibition might be due to CBD binding to the ATP binding site of the target proteins. This prevents the required phosphoryl transfer to activate substrate proteins and/or CBD binding to the DFG motif from taking place, thus reducing catalytic activity.
结直肠癌(CRC)发生于肠道,其起始和进展涉及多种机制,包括信号通路失调。一些参与细胞增殖、迁移和凋亡的信号通路,如表皮生长因子受体(EGFR)和丝裂原活化蛋白激酶(MAPK),在结直肠癌中常常失调。尽管大麻二酚(CBD)此前已在体外诱导结直肠癌细胞系发生凋亡和细胞周期停滞,但其对信号通路的影响尚未确定。本文采用计算机模拟分析来评估可与CBD结合的伴侣蛋白,并通过对接模拟精确预测CBD与这些选定蛋白的结合位置。通过对当前文献的调研,推测CBD与这些蛋白结合的作用。结果预测,CBD可能与EGFR、RAS/RAF亚型、MEK1/2和ERK1/2相互作用。预测CBD诱导的抑制作用可能是由于CBD与靶蛋白的ATP结合位点结合。这会阻止所需的磷酸转移以激活底物蛋白和/或阻止CBD与DFG模体结合,从而降低催化活性。