Biomaterial and Tissue Engineering Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati (IITG), Guwahati, 781039, Assam, India.
Biomaterial and Tissue Engineering Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati (IITG), Guwahati, 781039, Assam, India.
Food Chem Toxicol. 2019 Jan;123:275-287. doi: 10.1016/j.fct.2018.10.063. Epub 2018 Oct 31.
Pro-oxidative stress induced by dietary polyphenols elevates reactive oxygen species (ROS) production in cancer cells, which subsequently leads to oxidative stress-mediated apoptosis. Sericin, a principal component of silk is associated with a mixture of polyphenols and flavonoids, possesses various biomedical attributes including anticancer activity. In the present study, we have evaluated the pro-oxidative effect of Bombyx mori sericin (BMS), Antheraea assamensis sericin (AAS), and Philosamia ricini sericin (PRS) against different cancer cells. Cytotoxicity of silk sericin (SS) evaluated using A431, SAS, and MCF-7 cells showed ≥50% reduction in their viability at 4 mg/mL. Intracellular ROS levels, cell cycle arrest, and apoptosis assessed using flow cytometry corroborated that SS treatment elevated the intracellular ROS levels, caused cell cycle arrest at the sub-G1 phase and resulted in apoptotic cell death. SS treated A431 and SAS cells showed upregulation of p53 and dysregulation of Bax and Bcl-2 gene expression. Whereas, AAS treated MCF-7 cells showed upregulation of Bax and downregulation of Bcl-2 gene expression. AAS treated MCF-7 and SAS cells showed downregulation of Bcl-2 protein expression in comparison to their control cells. Thus, the present study demonstrates that the pro-oxidative effect induced by SS suppresses the cancer growth indicating its potential anticancer activity.
膳食多酚引起的促氧化应激会增加癌细胞中活性氧(ROS)的产生,从而导致氧化应激介导的细胞凋亡。丝素是丝的主要成分,与多酚和类黄酮的混合物有关,具有多种生物医学特性,包括抗癌活性。在本研究中,我们评估了家蚕丝素(BMS)、阿萨姆野蚕丝素(AAS)和蓖麻蚕丝素(PRS)对不同癌细胞的促氧化作用。使用 A431、SAS 和 MCF-7 细胞评估丝素(SS)的细胞毒性,结果表明在 4mg/mL 时其活力降低≥50%。使用流式细胞术评估细胞内 ROS 水平、细胞周期停滞和细胞凋亡,结果表明 SS 处理可提高细胞内 ROS 水平,导致细胞周期停滞在 sub-G1 期,并导致细胞凋亡。SS 处理的 A431 和 SAS 细胞显示 p53 上调和 Bax 和 Bcl-2 基因表达失调。然而,AAS 处理的 MCF-7 细胞显示 Bax 上调和 Bcl-2 基因表达下调。与对照细胞相比,AAS 处理的 MCF-7 和 SAS 细胞中 Bcl-2 蛋白表达下调。因此,本研究表明 SS 诱导的促氧化作用抑制了癌细胞的生长,表明其具有潜在的抗癌活性。