Mishra Sudha, Vinayak Manjula
a Biochemistry & Molecular Biology Unit , Centre of Advanced Study in Zoology, Banaras Hindu University , Varanasi , India.
Nutr Cancer. 2014;66(4):675-81. doi: 10.1080/01635581.2013.878735. Epub 2014 Feb 26.
Antioxidant ellagic acid is a herbal polyphenolic compound shown to possess growth-inhibiting and apoptotic activities in cancer. Protein kinase C (PKC) plays an important role in cell proliferation, apoptosis, and differentiation. Apoptosis of tumor cells is induced by inactivation of glycolytic enzyme of anaerobic metabolism, lactate dehydrogenase (LDH)-A, and by activating apoptotic protein caspase-3 via PKCδ. The present study aims to analyze the role of ellagic acid on regulation of novel and atypical isozymes of PKC to modulate apoptosis and anaerobic metabolism to prevent lymphoma growth as its role on classical PKCs is reported earlier. Expression of novel and atypical isozymes of PKC, activity of PKCδ, expression and activity of caspase-3, and LDH-A have been analyzed. Expression is measured by RT-PCR, activities of PKCδ as level of its catalytic fragment, caspase-3 as level of its p17 fragment, and LDH-A by specific staining. Lymphoma bearing mice were treated with 3 different doses of ellagic acid. The treatment enhanced expression of all novel and atypical PKCs, activity and expression of caspase-3, and activity of PKCδ but decreased activity and expression of LDH-A. Our results suggest that ellagic acid induces apoptosis via novel and atypical PKCs in association with caspase-3 and induces cancer cell death by blocking the energy metabolism.
抗氧化剂鞣花酸是一种草本多酚化合物,已证明其在癌症中具有生长抑制和凋亡活性。蛋白激酶C(PKC)在细胞增殖、凋亡和分化中起重要作用。肿瘤细胞的凋亡是通过使无氧代谢的糖酵解酶乳酸脱氢酶(LDH)-A失活,并通过PKCδ激活凋亡蛋白半胱天冬酶-3来诱导的。本研究旨在分析鞣花酸在调节PKC新的和非典型同工酶以调节凋亡和无氧代谢以预防淋巴瘤生长中的作用,因为此前已报道其对经典PKC的作用。分析了PKC新的和非典型同工酶的表达、PKCδ的活性、半胱天冬酶-3的表达和活性以及LDH-A。通过RT-PCR测量表达,通过其催化片段水平测量PKCδ的活性,通过其p17片段水平测量半胱天冬酶-3的活性,通过特异性染色测量LDH-A的活性。用3种不同剂量的鞣花酸处理荷瘤小鼠。该处理增强了所有新的和非典型PKC的表达、半胱天冬酶-3的活性和表达以及PKCδ的活性,但降低了LDH-A的活性和表达。我们的结果表明,鞣花酸通过与半胱天冬酶-3相关的新的和非典型PKC诱导凋亡,并通过阻断能量代谢诱导癌细胞死亡。