Notaro Antonietta, Lauricella Marianna, Di Liberto Diana, Emanuele Sonia, Giuliano Michela, Attanzio Alessandro, Tesoriere Luisa, Carlisi Daniela, Allegra Mario, De Blasio Anna, Calvaruso Giuseppe, D'Anneo Antonella
Laboratory of Biochemistry, Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, 90127 Palermo, Italy.
Section of Biochemistry, Department of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), University of Palermo, 90127 Palermo, Italy.
Antioxidants (Basel). 2023 Jun 16;12(6):1292. doi: 10.3390/antiox12061292.
Methyl gallate (MG), which is a gallotannin widely found in plants, is a polyphenol used in traditional Chinese phytotherapy to alleviate several cancer symptoms. Our studies provided evidence that MG is capable of reducing the viability of HCT116 colon cancer cells, while it was found to be ineffective on differentiated Caco-2 cells, which is a model of polarized colon cells. In the first phase of treatment, MG promoted both early ROS generation and endoplasmic reticulum (ER) stress, sustained by elevated PERK, Grp78 and CHOP expression levels, as well as an upregulation in intracellular calcium content. Such events were accompanied by an autophagic process (16-24 h), where prolonging the time (48 h) of MG exposure led to cellular homeostasis collapse and apoptotic cell death with DNA fragmentation and p53 and γH2Ax activation. Our data demonstrated that a crucial role in the MG-induced mechanism is played by p53. Its level, which increased precociously (4 h) in MG-treated cells, was tightly intertwined with oxidative injury. Indeed, the addition of N-acetylcysteine (NAC), which is a ROS scavenger, counteracted the p53 increase, as well as the MG effect on cell viability. Moreover, MG promoted p53 accumulation into the nucleus and its inhibition by pifithrin-α (PFT-α), which is a negative modulator of p53 transcriptional activity, enhanced autophagy, increased the LC3-II level and inhibited apoptotic cell death. These findings provide new clues to the potential action of MG as a possible anti-tumor phytomolecule for colon cancer treatment.
没食子酸甲酯(MG)是一种广泛存在于植物中的没食子鞣质,是一种用于传统中医植物疗法以缓解多种癌症症状的多酚。我们的研究表明,MG能够降低HCT116结肠癌细胞的活力,而在分化的Caco-2细胞(一种极化结肠细胞模型)上却无效。在治疗的第一阶段,MG促进了早期活性氧(ROS)的产生和内质网(ER)应激,这是由PERK、Grp78和CHOP表达水平升高以及细胞内钙含量上调所维持的。这些事件伴随着自噬过程(16 - 24小时),延长MG暴露时间(48小时)会导致细胞稳态崩溃和凋亡性细胞死亡,伴有DNA片段化以及p53和γH2Ax激活。我们的数据表明,p53在MG诱导的机制中起着关键作用。其水平在MG处理的细胞中早熟增加(4小时),与氧化损伤紧密相关。事实上,添加作为ROS清除剂的N - 乙酰半胱氨酸(NAC)可抵消p53的增加以及MG对细胞活力的影响。此外,MG促进p53积累到细胞核中,而p53转录活性的负调节剂pifithrin-α(PFT-α)对其的抑制增强了自噬,增加了LC3-II水平并抑制了凋亡性细胞死亡。这些发现为MG作为结肠癌治疗的潜在抗肿瘤植物分子的潜在作用提供了新线索。