{"title":"从一种可食用毒蘑菇 Sarcosphaera crassa 中分离出的新代谢物的抗癌评估。","authors":"Zain Ullah , Mehmet Öztürk","doi":"10.1016/j.steroids.2024.109523","DOIUrl":null,"url":null,"abstract":"<div><div>The growing demand for wild mushrooms as functional foods has increased due to their pharmacological significance. <em>Sarcosphaera crassa</em> is a deadly poisonous mushroom consumed by people living in northern and eastern Europe after being cooked adequately due to its significant properties. Herein, the baked <em>Sarcosphaera crassa</em> was studied for its ingredients. The cytotoxicity of hexane, acetone, and methanol extracts of baked <em>Sarcosphaera crassa</em> was investigated against MCF-7, HT-29, and HeLa cancer cell lines while toxicity against PDF fibroblast healthy cell lines using MTT assay. Acetone and methanol extracts of the baked mushroom exhibited significant cytotoxic activity. Further investigation of cytotoxic extracts afforded three new secondary metabolites, namely, (3<em>β,</em> 22<em>E</em>) ergosta-5, 22-dienyl 3-<em>O</em>-<em>α</em>-yl decanoate (Brassicasteryl decanoate) (<strong>1</strong>), bis (2- ethylpentadecyl) benzene-1,2-dicarboxylate (<strong>2</strong>), and (2<em>S</em>)-4-(aziridine-1-yl)-4-oxobutan-2-yl hexadecanoate (<strong>3</strong>), and six known compounds including ᴅ-sorbitol (<strong>4</strong>), 3<em>β</em>-ergosta-5,22-dien (<strong>5</strong>), two ergosterol-endoperoxides (<strong>6</strong> and <strong>7</strong>), nigerasterol A (<strong>8</strong>) and 5<em>α</em>,9<em>α</em>-epoksiergosta-7,22-dien, 3<em>β</em>,6<em>α</em>-diol (<strong>9</strong>). Among them, <strong>2</strong> exhibited effective cytotoxic activity against MCF-7 (IC<sub>50</sub>: 33.45 ± 2.9 μg/mL) and HT-29 (IC<sub>50</sub>: 45.53 ± 0.8 μg/mL) cancer cell lines. Compound <strong>3</strong> demonstrated high activity against HeLa (IC<sub>50</sub>: 30.45 ± 0.35 μg/mL) and MCF-7 (IC<sub>50</sub>: 33.55 ± 0.49 μg/mL) cancer cell lines, respectively. On the other hand, compound <strong>1</strong> demonstrated moderate cytotoxic activity against MCF-7 and HT-29 cancer cell lines. Besides, against PDF healthy cell lines, all extracts demonstrated lower toxicity. This discovery highlights the significance of <em>Sarcosphaera crassa</em> as a natural functional food reservoir.</div></div>","PeriodicalId":21997,"journal":{"name":"Steroids","volume":"212 ","pages":"Article 109523"},"PeriodicalIF":2.1000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Assessment of anti-cancer evaluation of new metabolites isolated from baked Sarcosphaera crassa: An edible poisonous mushroom\",\"authors\":\"Zain Ullah , Mehmet Öztürk\",\"doi\":\"10.1016/j.steroids.2024.109523\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The growing demand for wild mushrooms as functional foods has increased due to their pharmacological significance. <em>Sarcosphaera crassa</em> is a deadly poisonous mushroom consumed by people living in northern and eastern Europe after being cooked adequately due to its significant properties. Herein, the baked <em>Sarcosphaera crassa</em> was studied for its ingredients. The cytotoxicity of hexane, acetone, and methanol extracts of baked <em>Sarcosphaera crassa</em> was investigated against MCF-7, HT-29, and HeLa cancer cell lines while toxicity against PDF fibroblast healthy cell lines using MTT assay. Acetone and methanol extracts of the baked mushroom exhibited significant cytotoxic activity. Further investigation of cytotoxic extracts afforded three new secondary metabolites, namely, (3<em>β,</em> 22<em>E</em>) ergosta-5, 22-dienyl 3-<em>O</em>-<em>α</em>-yl decanoate (Brassicasteryl decanoate) (<strong>1</strong>), bis (2- ethylpentadecyl) benzene-1,2-dicarboxylate (<strong>2</strong>), and (2<em>S</em>)-4-(aziridine-1-yl)-4-oxobutan-2-yl hexadecanoate (<strong>3</strong>), and six known compounds including ᴅ-sorbitol (<strong>4</strong>), 3<em>β</em>-ergosta-5,22-dien (<strong>5</strong>), two ergosterol-endoperoxides (<strong>6</strong> and <strong>7</strong>), nigerasterol A (<strong>8</strong>) and 5<em>α</em>,9<em>α</em>-epoksiergosta-7,22-dien, 3<em>β</em>,6<em>α</em>-diol (<strong>9</strong>). Among them, <strong>2</strong> exhibited effective cytotoxic activity against MCF-7 (IC<sub>50</sub>: 33.45 ± 2.9 μg/mL) and HT-29 (IC<sub>50</sub>: 45.53 ± 0.8 μg/mL) cancer cell lines. Compound <strong>3</strong> demonstrated high activity against HeLa (IC<sub>50</sub>: 30.45 ± 0.35 μg/mL) and MCF-7 (IC<sub>50</sub>: 33.55 ± 0.49 μg/mL) cancer cell lines, respectively. On the other hand, compound <strong>1</strong> demonstrated moderate cytotoxic activity against MCF-7 and HT-29 cancer cell lines. Besides, against PDF healthy cell lines, all extracts demonstrated lower toxicity. This discovery highlights the significance of <em>Sarcosphaera crassa</em> as a natural functional food reservoir.</div></div>\",\"PeriodicalId\":21997,\"journal\":{\"name\":\"Steroids\",\"volume\":\"212 \",\"pages\":\"Article 109523\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Steroids\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0039128X24001612\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Steroids","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0039128X24001612","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Assessment of anti-cancer evaluation of new metabolites isolated from baked Sarcosphaera crassa: An edible poisonous mushroom
The growing demand for wild mushrooms as functional foods has increased due to their pharmacological significance. Sarcosphaera crassa is a deadly poisonous mushroom consumed by people living in northern and eastern Europe after being cooked adequately due to its significant properties. Herein, the baked Sarcosphaera crassa was studied for its ingredients. The cytotoxicity of hexane, acetone, and methanol extracts of baked Sarcosphaera crassa was investigated against MCF-7, HT-29, and HeLa cancer cell lines while toxicity against PDF fibroblast healthy cell lines using MTT assay. Acetone and methanol extracts of the baked mushroom exhibited significant cytotoxic activity. Further investigation of cytotoxic extracts afforded three new secondary metabolites, namely, (3β, 22E) ergosta-5, 22-dienyl 3-O-α-yl decanoate (Brassicasteryl decanoate) (1), bis (2- ethylpentadecyl) benzene-1,2-dicarboxylate (2), and (2S)-4-(aziridine-1-yl)-4-oxobutan-2-yl hexadecanoate (3), and six known compounds including ᴅ-sorbitol (4), 3β-ergosta-5,22-dien (5), two ergosterol-endoperoxides (6 and 7), nigerasterol A (8) and 5α,9α-epoksiergosta-7,22-dien, 3β,6α-diol (9). Among them, 2 exhibited effective cytotoxic activity against MCF-7 (IC50: 33.45 ± 2.9 μg/mL) and HT-29 (IC50: 45.53 ± 0.8 μg/mL) cancer cell lines. Compound 3 demonstrated high activity against HeLa (IC50: 30.45 ± 0.35 μg/mL) and MCF-7 (IC50: 33.55 ± 0.49 μg/mL) cancer cell lines, respectively. On the other hand, compound 1 demonstrated moderate cytotoxic activity against MCF-7 and HT-29 cancer cell lines. Besides, against PDF healthy cell lines, all extracts demonstrated lower toxicity. This discovery highlights the significance of Sarcosphaera crassa as a natural functional food reservoir.
期刊介绍:
STEROIDS is an international research journal devoted to studies on all chemical and biological aspects of steroidal moieties. The journal focuses on both experimental and theoretical studies on the biology, chemistry, biosynthesis, metabolism, molecular biology, physiology and pharmacology of steroids and other molecules that target or regulate steroid receptors. Manuscripts presenting clinical research related to steroids, steroid drug development, comparative endocrinology of steroid hormones, investigations on the mechanism of steroid action and steroid chemistry are all appropriate for submission for peer review. STEROIDS publishes both original research and timely reviews. For details concerning the preparation of manuscripts see Instructions to Authors, which is published in each issue of the journal.