Effect of Oversulfation on the Composition, Structure, and In Vitro Anti-Lung Cancer Activity of Fucoidans Extracted from Sargassum aquifolium.

作者: Chia-Hung Kuo , Yong-Han Hong , Yung-Hsiang Tsai , Chun-Yung Huang , Ren-Han Huang

DOI: 10.3390/MD19040215

关键词: Propidium iodideSulfationCancerBiochemistryPI3K/AKT/mTOR pathwayFucoidanApoptosisAnnexinChemistryCytotoxicity

摘要: Intensive efforts have been undertaken in the fields of prevention, diagnosis, and therapy lung cancer. Fucoidans exhibit a wide range biological activities, which are dependent on degree sulfation, sulfation pattern, glycosidic branches, molecular weight fucoidan. The determination oversulfation fucoidan its effect anti-lung cancer activity related signaling cascades is challenging. In this investigation, we used previously developed (SCA), served as native fucoidan, to generate two oversulfated derivatives (SCA-S1 SCA-S2). SCA, SCA-S1, SCA-S2 showed differences compositions had characteristic structural features by Fourier transform infrared (FTIR) nuclear magnetic resonance (NMR) analyses. anticancer properties against human carcinoma A-549 cells were analyzed terms cytotoxicity, cell cycle, Bcl-2 expression, mitochondrial membrane potential (MMP), expression caspase-3, cytochrome c release, Annexin V/propidium iodide (PI) staining, DNA fragmentation, underlying cascades. Our findings indicate that promotes apoptosis mechanism may involve Akt/mTOR/S6 pathway. Further vivo research needed establish precise whereby mitigates progression

参考文章(48)
Cheng-Yuan Wang, Tien-Chou Wu, Shu-Ling Hsieh, Yung-Hsiang Tsai, Chia-Wen Yeh, Chun-Yung Huang, Antioxidant activity and growth inhibition of human colon cancer cells by crude and purified fucoidan preparations extracted from Sargassum cristaefolium. Journal of Food and Drug Analysis. ,vol. 23, pp. 766- 777 ,(2015) , 10.1016/J.JFDA.2015.07.002
M.S. Patankar, S Oehninger, T Barnett, R.L. Williams, G.F. Clark, A revised structure for fucoidan may explain some of its biological activities Journal of Biological Chemistry. ,vol. 268, pp. 21770- 21776 ,(1993) , 10.1016/S0021-9258(20)80609-7
Tatiana I. Imbs, Svetlana P. Ermakova, Olesya S. Malyarenko (Vishchuk), Vladimir V. Isakov, Tatiana N. Zvyagintseva, Structural elucidation of polysaccharide fractions from the brown alga Coccophora langsdorfii and in vitro investigation of their anticancer activity. Carbohydrate Polymers. ,vol. 135, pp. 162- 168 ,(2016) , 10.1016/J.CARBPOL.2015.08.062
Yahima Frión-Herrera, Alexis Díaz-García, Jenny Ruiz-Fuentes, Hermis Rodríguez-Sánchez, José Maurício Sforcin, Brazilian green propolis induced apoptosis in human lung cancer A549 cells through mitochondrial-mediated pathway. Journal of Pharmacy and Pharmacology. ,vol. 67, pp. 1448- 1456 ,(2015) , 10.1111/JPHP.12449
Masato Enari, Hideki Sakahira, Hideki Yokoyama, Katsuya Okawa, Akihiro Iwamatsu, Shigekazu Nagata, A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD Nature. ,vol. 391, pp. 43- 50 ,(1998) , 10.1038/34112
Manon van Engeland, Luc J.W. Nieland, Frans C.S. Ramaekers, Bert Schutte, Chris P.M. Reutelingsperger, Annexin V‐Affinity assay: A review on an apoptosis detection system based on phosphatidylserine exposure Cytometry. ,vol. 31, pp. 1- 9 ,(1998) , 10.1002/(SICI)1097-0320(19980101)31:1<1::AID-CYTO1>3.0.CO;2-R
John D. Robertson, Sten Orrenius, Boris Zhivotovsky, Review: Nuclear Events in Apoptosis Journal of Structural Biology. ,vol. 129, pp. 346- 358 ,(2000) , 10.1006/JSBI.2000.4254
Vladimir Gogvadze, Sten Orrenius, Boris Zhivotovsky, Multiple pathways of cytochrome c release from mitochondria in apoptosis. Biochimica et Biophysica Acta. ,vol. 1757, pp. 639- 647 ,(2006) , 10.1016/J.BBABIO.2006.03.016
Camille Jégou, Nelly Kervarec, Stéphane Cérantola, Isabelle Bihannic, Valérie Stiger-Pouvreau, NMR use to quantify phlorotannins: the case of Cystoseira tamariscifolia, a phloroglucinol-producing brown macroalga in Brittany (France). Talanta. ,vol. 135, pp. 1- 6 ,(2015) , 10.1016/J.TALANTA.2014.11.059