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Pharmacological basis and new insights of deguelin concerning its anticancer effects
Deguelin is a rotenoid of the flavonoid family, which can be extracted from Lonchocarpus, Derris, or Tephrosia. It possesses the inhibition of cancer cell proliferation by inducing apoptosis through regulating the phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) signaling pathway, the NF-κB sig...
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Published in: | Pharmacological research 2021-12, Vol.174, p.105935-105935, Article 105935 |
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description | Deguelin is a rotenoid of the flavonoid family, which can be extracted from Lonchocarpus, Derris, or Tephrosia. It possesses the inhibition of cancer cell proliferation by inducing apoptosis through regulating the phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) signaling pathway, the NF-κB signaling pathway, the Wnt signaling pathway, the adenosine 5‘-monophosphate (AMP)-activated protein kinase (AMPK) signaling pathway and epidermal growth factor receptor (EGFR) signaling, activating the p38 mitogen-activated protein kinase (MAPK) pathway, repression of Bmi1, targeting cyclooxygenase-2 (COX-2), targeting galectin-1, promotion of glycogen synthase kinase-3β (GSK3β)/FBW7-mediated Mcl-1 destabilization and targeting mitochondria via down-regulating Hexokinases II-mediated glycolysis, PUMA-mediation, which are some crucial molecules which modulate closely cancer cell growth and metastasis. Deguelin inhibits tumor cell propagation and malignant transformation through targeting angiogenesis, targeting lymphangiogenesis, targeting focal adhesion kinase (FAK), inhibiting the CtsZ/FAK signaling pathway, targeting epithelial–mesenchymal transition (EMT), the NF-κB signaling pathway, regulating NIMA-related kinase 2 (NEK2). In addition, deguelin possesses other biological activities, such as targeting cell cycle arrest, modulation of autophagy, inhibition of hedgehog pathway, inducing differentiation of mutated NPM1 acute myeloid leukemia etc. Therefore, deguelin is a promising chemopreventive agent for cancer therapy.
Anticancer activity of deguelin and its derivatives: recent advances in mechanisms of action (AMPK: Adenosine 5‘-monophosphate (AMP)-activated protein kinase; COX-2: Cyclooxygenase; EGFR: Epidermal growth factor receptor; EMT: Epithelial–mesenchymal transition; FAK: Focal adhesion kinase; GSK3β: Glycogen synthase kinase-3; Hh: Hedgehog; MAPK: p38 mitogen-activated protein kinase; NF-κB: Nuclear factor κB; PI3K/Akt: Phosphoinositide 3-kinase/protein kinase B). [Display omitted] |
doi_str_mv | 10.1016/j.phrs.2021.105935 |
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Anticancer activity of deguelin and its derivatives: recent advances in mechanisms of action (AMPK: Adenosine 5‘-monophosphate (AMP)-activated protein kinase; COX-2: Cyclooxygenase; EGFR: Epidermal growth factor receptor; EMT: Epithelial–mesenchymal transition; FAK: Focal adhesion kinase; GSK3β: Glycogen synthase kinase-3; Hh: Hedgehog; MAPK: p38 mitogen-activated protein kinase; NF-κB: Nuclear factor κB; PI3K/Akt: Phosphoinositide 3-kinase/protein kinase B). [Display omitted]</description><identifier>ISSN: 1043-6618</identifier><identifier>EISSN: 1096-1186</identifier><identifier>DOI: 10.1016/j.phrs.2021.105935</identifier><identifier>PMID: 34644595</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Animals ; Anticancer ; Antineoplastic Agents, Phytogenic - pharmacology ; Antineoplastic Agents, Phytogenic - therapeutic use ; Apoptosis ; Apoptosis - drug effects ; Autophagy - drug effects ; Cell Cycle - drug effects ; Deguelin ; Humans ; Neoplasm Metastasis ; Neoplasms - drug therapy ; Neoplasms - genetics ; Neoplasms - metabolism ; Neoplasms - pathology ; NF-κB signaling pathway ; Nucleophosmin - genetics ; PI3K/Akt signaling pathway ; Rotenone - analogs & derivatives ; Rotenone - pharmacology ; Rotenone - therapeutic use ; Wnt signaling pathway</subject><ispartof>Pharmacological research, 2021-12, Vol.174, p.105935-105935, Article 105935</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-82230d019199e6915b50fa459b2a6259b004c0b8c2fb658b9d12110a9d7df3e3</citedby><cites>FETCH-LOGICAL-c356t-82230d019199e6915b50fa459b2a6259b004c0b8c2fb658b9d12110a9d7df3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1043661821005193$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27901,27902,45756</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34644595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Zhu Yue</creatorcontrib><creatorcontrib>Yun, Qu Zhen</creatorcontrib><creatorcontrib>Wu, Liu</creatorcontrib><creatorcontrib>Zhang, Tian Wen</creatorcontrib><creatorcontrib>Yao, Tang Ze</creatorcontrib><title>Pharmacological basis and new insights of deguelin concerning its anticancer effects</title><title>Pharmacological research</title><addtitle>Pharmacol Res</addtitle><description>Deguelin is a rotenoid of the flavonoid family, which can be extracted from Lonchocarpus, Derris, or Tephrosia. It possesses the inhibition of cancer cell proliferation by inducing apoptosis through regulating the phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) signaling pathway, the NF-κB signaling pathway, the Wnt signaling pathway, the adenosine 5‘-monophosphate (AMP)-activated protein kinase (AMPK) signaling pathway and epidermal growth factor receptor (EGFR) signaling, activating the p38 mitogen-activated protein kinase (MAPK) pathway, repression of Bmi1, targeting cyclooxygenase-2 (COX-2), targeting galectin-1, promotion of glycogen synthase kinase-3β (GSK3β)/FBW7-mediated Mcl-1 destabilization and targeting mitochondria via down-regulating Hexokinases II-mediated glycolysis, PUMA-mediation, which are some crucial molecules which modulate closely cancer cell growth and metastasis. Deguelin inhibits tumor cell propagation and malignant transformation through targeting angiogenesis, targeting lymphangiogenesis, targeting focal adhesion kinase (FAK), inhibiting the CtsZ/FAK signaling pathway, targeting epithelial–mesenchymal transition (EMT), the NF-κB signaling pathway, regulating NIMA-related kinase 2 (NEK2). In addition, deguelin possesses other biological activities, such as targeting cell cycle arrest, modulation of autophagy, inhibition of hedgehog pathway, inducing differentiation of mutated NPM1 acute myeloid leukemia etc. Therefore, deguelin is a promising chemopreventive agent for cancer therapy.
Anticancer activity of deguelin and its derivatives: recent advances in mechanisms of action (AMPK: Adenosine 5‘-monophosphate (AMP)-activated protein kinase; COX-2: Cyclooxygenase; EGFR: Epidermal growth factor receptor; EMT: Epithelial–mesenchymal transition; FAK: Focal adhesion kinase; GSK3β: Glycogen synthase kinase-3; Hh: Hedgehog; MAPK: p38 mitogen-activated protein kinase; NF-κB: Nuclear factor κB; PI3K/Akt: Phosphoinositide 3-kinase/protein kinase B). [Display omitted]</description><subject>Animals</subject><subject>Anticancer</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Antineoplastic Agents, Phytogenic - therapeutic use</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Autophagy - drug effects</subject><subject>Cell Cycle - drug effects</subject><subject>Deguelin</subject><subject>Humans</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>NF-κB signaling pathway</subject><subject>Nucleophosmin - genetics</subject><subject>PI3K/Akt signaling pathway</subject><subject>Rotenone - analogs & derivatives</subject><subject>Rotenone - pharmacology</subject><subject>Rotenone - therapeutic use</subject><subject>Wnt signaling pathway</subject><issn>1043-6618</issn><issn>1096-1186</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EoqXwAyyQl2xSbCd2YokNqnhJlWDRveXYk9RVHsVOQPw9jlpYshprdO6V5yB0TcmSEirudsv91oclI4zGBZcpP0FzSqRIKC3E6fTO0kQIWszQRQg7QojMKDlHszQTWcYln6PN-1b7Vpu-6WtndINLHVzAurO4gy_suuDq7RBwX2EL9QiN67DpOwO-c12N3TCxQ0xOKwxVBWYIl-is0k2Aq-NcoM3T42b1kqzfnl9XD-vEpFwMScFYSiyhkkoJQlJeclLp-K-SacHiICQzpCwMq0rBi1JayiglWtrcVimkC3R7qN37_mOEMKjWBQNNozvox6AYL1jUked5RNkBNb4PwUOl9t612n8rStQkU-3UJFNNMtVBZgzdHPvHsgX7F_m1F4H7AwDxyE8HXgXjIJqwzkcPyvbuv_4fX0CFhg</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>Lin, Zhu Yue</creator><creator>Yun, Qu Zhen</creator><creator>Wu, Liu</creator><creator>Zhang, Tian Wen</creator><creator>Yao, Tang Ze</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202112</creationdate><title>Pharmacological basis and new insights of deguelin concerning its anticancer effects</title><author>Lin, Zhu Yue ; Yun, Qu Zhen ; Wu, Liu ; Zhang, Tian Wen ; Yao, Tang Ze</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-82230d019199e6915b50fa459b2a6259b004c0b8c2fb658b9d12110a9d7df3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Anticancer</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Antineoplastic Agents, Phytogenic - therapeutic use</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Autophagy - drug effects</topic><topic>Cell Cycle - drug effects</topic><topic>Deguelin</topic><topic>Humans</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - genetics</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>NF-κB signaling pathway</topic><topic>Nucleophosmin - genetics</topic><topic>PI3K/Akt signaling pathway</topic><topic>Rotenone - analogs & derivatives</topic><topic>Rotenone - pharmacology</topic><topic>Rotenone - therapeutic use</topic><topic>Wnt signaling pathway</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Zhu Yue</creatorcontrib><creatorcontrib>Yun, Qu Zhen</creatorcontrib><creatorcontrib>Wu, Liu</creatorcontrib><creatorcontrib>Zhang, Tian Wen</creatorcontrib><creatorcontrib>Yao, Tang Ze</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Zhu Yue</au><au>Yun, Qu Zhen</au><au>Wu, Liu</au><au>Zhang, Tian Wen</au><au>Yao, Tang Ze</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacological basis and new insights of deguelin concerning its anticancer effects</atitle><jtitle>Pharmacological research</jtitle><addtitle>Pharmacol Res</addtitle><date>2021-12</date><risdate>2021</risdate><volume>174</volume><spage>105935</spage><epage>105935</epage><pages>105935-105935</pages><artnum>105935</artnum><issn>1043-6618</issn><eissn>1096-1186</eissn><abstract>Deguelin is a rotenoid of the flavonoid family, which can be extracted from Lonchocarpus, Derris, or Tephrosia. It possesses the inhibition of cancer cell proliferation by inducing apoptosis through regulating the phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) signaling pathway, the NF-κB signaling pathway, the Wnt signaling pathway, the adenosine 5‘-monophosphate (AMP)-activated protein kinase (AMPK) signaling pathway and epidermal growth factor receptor (EGFR) signaling, activating the p38 mitogen-activated protein kinase (MAPK) pathway, repression of Bmi1, targeting cyclooxygenase-2 (COX-2), targeting galectin-1, promotion of glycogen synthase kinase-3β (GSK3β)/FBW7-mediated Mcl-1 destabilization and targeting mitochondria via down-regulating Hexokinases II-mediated glycolysis, PUMA-mediation, which are some crucial molecules which modulate closely cancer cell growth and metastasis. Deguelin inhibits tumor cell propagation and malignant transformation through targeting angiogenesis, targeting lymphangiogenesis, targeting focal adhesion kinase (FAK), inhibiting the CtsZ/FAK signaling pathway, targeting epithelial–mesenchymal transition (EMT), the NF-κB signaling pathway, regulating NIMA-related kinase 2 (NEK2). In addition, deguelin possesses other biological activities, such as targeting cell cycle arrest, modulation of autophagy, inhibition of hedgehog pathway, inducing differentiation of mutated NPM1 acute myeloid leukemia etc. Therefore, deguelin is a promising chemopreventive agent for cancer therapy.
Anticancer activity of deguelin and its derivatives: recent advances in mechanisms of action (AMPK: Adenosine 5‘-monophosphate (AMP)-activated protein kinase; COX-2: Cyclooxygenase; EGFR: Epidermal growth factor receptor; EMT: Epithelial–mesenchymal transition; FAK: Focal adhesion kinase; GSK3β: Glycogen synthase kinase-3; Hh: Hedgehog; MAPK: p38 mitogen-activated protein kinase; NF-κB: Nuclear factor κB; PI3K/Akt: Phosphoinositide 3-kinase/protein kinase B). [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>34644595</pmid><doi>10.1016/j.phrs.2021.105935</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Anticancer Antineoplastic Agents, Phytogenic - pharmacology Antineoplastic Agents, Phytogenic - therapeutic use Apoptosis Apoptosis - drug effects Autophagy - drug effects Cell Cycle - drug effects Deguelin Humans Neoplasm Metastasis Neoplasms - drug therapy Neoplasms - genetics Neoplasms - metabolism Neoplasms - pathology NF-κB signaling pathway Nucleophosmin - genetics PI3K/Akt signaling pathway Rotenone - analogs & derivatives Rotenone - pharmacology Rotenone - therapeutic use Wnt signaling pathway |
title | Pharmacological basis and new insights of deguelin concerning its anticancer effects |
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