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2013
DOI: 10.1016/j.foodchem.2013.01.030
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Anti-inflammatory and anticancer activities of extracts and compounds from the mushroom Inonotus obliquus

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Cited by 227 publications
(151 citation statements)
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References 25 publications
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“…polysaccharides (Dore, et al, 2007;Lu, et al, 2008;Lavi, Levinson, Peri, Hadar, & Schwartz, 2010;Adebayo, Oloke, Majolagbe, Ajani, & Bora, 2012;Ruthes, et al, 2013aRuthes, et al, , 2013bRuthes, et al, , 2013cChang, Lur, Lu, & Cheng, 2013;Castro et al, 2014;Silveira et al, 2014;Silveira et al, 2015), terpenes (Kamo, Asanoma, Shibata, & Hirota, 2003;Yoshikawa et al, 2005;Dudhgaonkar, Thyagarajan, & Sliva, 2009;Ma, Chen, Dong, & Lu, 2013;Tung et al, 2013;Xu, Yan, Bi, Han, Chen, & Wu, 2013;Choi, et al, 2014a), phenolic compounds (Quang, Harinantenaina, Nishizawa, Hashimoto, Kohchi, Soma, & Asakawa, 2006a;Quang et al, 2006bKohno et al, 2008Stanikunaite, Khan, Trappe, & Ross, 2009;Hsieh et al, 2010;Lee, & Huang et al, 2011b;Chen et al, 2013;Taofiq et al, 2015), sterols (Huang, et al, 2010;Ma, Chen, Dong, & Lu, 2013 anti-inflammatory activity of extracts prepared from mushrooms after undergoing some food processing procedures. The results showed reduced activity compared to fresh samples, which implies that anti-inflammatory compounds present in these mushrooms were degraded, e.g due to suseptibility to heating.…”
Section: The Anti-inflammatory Potential Of Mushroom Extractsmentioning
confidence: 99%
See 1 more Smart Citation
“…polysaccharides (Dore, et al, 2007;Lu, et al, 2008;Lavi, Levinson, Peri, Hadar, & Schwartz, 2010;Adebayo, Oloke, Majolagbe, Ajani, & Bora, 2012;Ruthes, et al, 2013aRuthes, et al, , 2013bRuthes, et al, , 2013cChang, Lur, Lu, & Cheng, 2013;Castro et al, 2014;Silveira et al, 2014;Silveira et al, 2015), terpenes (Kamo, Asanoma, Shibata, & Hirota, 2003;Yoshikawa et al, 2005;Dudhgaonkar, Thyagarajan, & Sliva, 2009;Ma, Chen, Dong, & Lu, 2013;Tung et al, 2013;Xu, Yan, Bi, Han, Chen, & Wu, 2013;Choi, et al, 2014a), phenolic compounds (Quang, Harinantenaina, Nishizawa, Hashimoto, Kohchi, Soma, & Asakawa, 2006a;Quang et al, 2006bKohno et al, 2008Stanikunaite, Khan, Trappe, & Ross, 2009;Hsieh et al, 2010;Lee, & Huang et al, 2011b;Chen et al, 2013;Taofiq et al, 2015), sterols (Huang, et al, 2010;Ma, Chen, Dong, & Lu, 2013 anti-inflammatory activity of extracts prepared from mushrooms after undergoing some food processing procedures. The results showed reduced activity compared to fresh samples, which implies that anti-inflammatory compounds present in these mushrooms were degraded, e.g due to suseptibility to heating.…”
Section: The Anti-inflammatory Potential Of Mushroom Extractsmentioning
confidence: 99%
“…It is usually associated with the pathogenesis of diseases such as diabetes, arthritis, obesity, metabolic syndrome, cancer and several cardiovascular diseases (Bellik et al, 2012;Moro et al, 2012;Ma, Chen, Dong, & Lu, 2013). …”
Section: Introductionmentioning
confidence: 99%
“…The discovery of new molecules from natural origin is a global trend currently for the less toxicity of natural products (Wang et al., 2012). A number of bioactive compounds from natural resources had been investigated, identified, and isolated as inhibitor to various cancer cell lines (Ma, Chen, Dong, & Lu, 2013). In this study, the anticancer activity of water extracts of selected mushrooms was subjected to in vitro cytotoxicity assay in certain cancer cell lines including HT‐29 colon and H‐1299 lungs carcinoma cell lines.…”
Section: Resultsmentioning
confidence: 99%
“…Активные концентрации этих экстрактов составляли в отношении клеток карциномы простаты РС3 29,57±12,18 мкг/мл и 19,22±0,46 мкг/мл, соответственно, а в отношении карциномы молочной железы MDA-MB-231 57,39±14,46 мкг/мл и 46,49±13,21 мкг/мл [36]. Активность петролейного экстракта в отношении обеих линий раковых клеток и активность этилацетатного экстракта против клеток MDA-MB-231 находятся на уровне известного цитостатика -доксорубицина, а против клеток РС3 -в 3 раза ниже по сравнению с доксорубицином [36].…”
Section: Introductionunclassified
“…Например, А, А2, А7, А15 оказали in vitro выраженный гепатопротекторный эффект: 74,8, 81,2, 75,0 и 71,9% соответственно по отношению к контролю -гепатопротектору бициклолу [26]. А1 и А5 проявляют гипогликемические свойства in vitro [55,59], А2, А5 и А24 -противогрибковые свойства in vitro, A1, А2,A5, Б, Б3 -противовоспалительные свойства in vitro [35], А1, А5, А23 -антиоксидантные свойства [36]. А1 и А5 обладают антимутагенным действием, снижают уровень мутагенов MNNG, 4NQO, в Salmonella typhimurium TA98 и TA100 [63].…”
Section: Introductionunclassified