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The Marine Natural Product Manzamine A Inhibits Cervical Cancer by Targeting the SIX1 Protein
Natural products remain an important source of drug leads covering unique chemical space and providing significant therapeutic value for the control of cancer and infectious diseases resistant to current drugs. Here, we determined the antiproliferative activity of a natural product manzamine A (1) f...
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Published in: | Journal of natural products (Washington, D.C.) D.C.), 2020-02, Vol.83 (2), p.286-295 |
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container_title | Journal of natural products (Washington, D.C.) |
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creator | Karan, Dev Dubey, Seema Pirisi, Lucia Nagel, Alexis Pina, Ivett Choo, Yeun-Mun Hamann, Mark T |
description | Natural products remain an important source of drug leads covering unique chemical space and providing significant therapeutic value for the control of cancer and infectious diseases resistant to current drugs. Here, we determined the antiproliferative activity of a natural product manzamine A (1) from an Indo-Pacific sponge following various in vitro cellular assays targeting cervical cancer (C33A, HeLa, SiHa, and CaSki). Our data demonstrated the antiproliferative effects of 1 at relatively low and non-cytotoxic concentrations (up to 4 μM). Mechanistic investigations confirmed that 1 blocked cell cycle progression in SiHa and CaSki cells at G1/S phase and regulated cell cycle-related genes, including restoration of p21 and p53 expression. In apoptotic assays, HeLa cells showed the highest sensitivity to 1 as compared to other cell types (C33A, SiHa, and CaSki). Interestingly, 1 decreased the levels of the oncoprotein SIX1, which is associated with oncogenesis in cervical cancer. To further investigate the structure–activity relationship among manzamine A (1) class with potential antiproliferative activity, molecular networking facilitated the efficient identification, dereplication, and assignment of structures from the manzamine class and revealed the significant potential in the design of optimized molecules for the treatment of cervical cancer. These data suggest that this sponge-derived natural product class warrants further attention regarding the design and development of novel manzamine analogues, which may be efficacious for preventive and therapeutic treatment of cancer. Additionally, this study reveals the significance of protecting fragile marine ecosystems from climate change-induced loss of species diversity. |
doi_str_mv | 10.1021/acs.jnatprod.9b00577 |
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Here, we determined the antiproliferative activity of a natural product manzamine A (1) from an Indo-Pacific sponge following various in vitro cellular assays targeting cervical cancer (C33A, HeLa, SiHa, and CaSki). Our data demonstrated the antiproliferative effects of 1 at relatively low and non-cytotoxic concentrations (up to 4 μM). Mechanistic investigations confirmed that 1 blocked cell cycle progression in SiHa and CaSki cells at G1/S phase and regulated cell cycle-related genes, including restoration of p21 and p53 expression. In apoptotic assays, HeLa cells showed the highest sensitivity to 1 as compared to other cell types (C33A, SiHa, and CaSki). Interestingly, 1 decreased the levels of the oncoprotein SIX1, which is associated with oncogenesis in cervical cancer. To further investigate the structure–activity relationship among manzamine A (1) class with potential antiproliferative activity, molecular networking facilitated the efficient identification, dereplication, and assignment of structures from the manzamine class and revealed the significant potential in the design of optimized molecules for the treatment of cervical cancer. These data suggest that this sponge-derived natural product class warrants further attention regarding the design and development of novel manzamine analogues, which may be efficacious for preventive and therapeutic treatment of cancer. Additionally, this study reveals the significance of protecting fragile marine ecosystems from climate change-induced loss of species diversity.</description><identifier>ISSN: 0163-3864</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/acs.jnatprod.9b00577</identifier><identifier>PMID: 32022559</identifier><language>eng</language><publisher>United States: American Chemical Society and American Society of Pharmacognosy</publisher><subject>Apoptosis - drug effects ; Biological Products - chemistry ; Biological Products - pharmacology ; Carbazoles - chemistry ; Carbazoles - pharmacology ; Cell Line, Tumor ; Ecosystem ; Female ; HeLa Cells ; Homeodomain Proteins - chemistry ; Homeodomain Proteins - metabolism ; Humans ; Structure-Activity Relationship ; Uterine Cervical Neoplasms - chemistry ; Uterine Cervical Neoplasms - drug therapy</subject><ispartof>Journal of natural products (Washington, D.C.), 2020-02, Vol.83 (2), p.286-295</ispartof><rights>Copyright © 2020 American Chemical Society and American Society of Pharmacognosy 2020 American Chemical Society and American Society of Pharmacognosy</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a515t-f5470cbc35a777a2628d211ab1dc7b0e96254f4b75c7dbcc04996e87327298593</citedby><cites>FETCH-LOGICAL-a515t-f5470cbc35a777a2628d211ab1dc7b0e96254f4b75c7dbcc04996e87327298593</cites><orcidid>0000-0002-0905-0886 ; 0000-0002-3798-4002</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32022559$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karan, Dev</creatorcontrib><creatorcontrib>Dubey, Seema</creatorcontrib><creatorcontrib>Pirisi, Lucia</creatorcontrib><creatorcontrib>Nagel, Alexis</creatorcontrib><creatorcontrib>Pina, Ivett</creatorcontrib><creatorcontrib>Choo, Yeun-Mun</creatorcontrib><creatorcontrib>Hamann, Mark T</creatorcontrib><title>The Marine Natural Product Manzamine A Inhibits Cervical Cancer by Targeting the SIX1 Protein</title><title>Journal of natural products (Washington, D.C.)</title><addtitle>J. Nat. Prod</addtitle><description>Natural products remain an important source of drug leads covering unique chemical space and providing significant therapeutic value for the control of cancer and infectious diseases resistant to current drugs. Here, we determined the antiproliferative activity of a natural product manzamine A (1) from an Indo-Pacific sponge following various in vitro cellular assays targeting cervical cancer (C33A, HeLa, SiHa, and CaSki). Our data demonstrated the antiproliferative effects of 1 at relatively low and non-cytotoxic concentrations (up to 4 μM). Mechanistic investigations confirmed that 1 blocked cell cycle progression in SiHa and CaSki cells at G1/S phase and regulated cell cycle-related genes, including restoration of p21 and p53 expression. In apoptotic assays, HeLa cells showed the highest sensitivity to 1 as compared to other cell types (C33A, SiHa, and CaSki). Interestingly, 1 decreased the levels of the oncoprotein SIX1, which is associated with oncogenesis in cervical cancer. To further investigate the structure–activity relationship among manzamine A (1) class with potential antiproliferative activity, molecular networking facilitated the efficient identification, dereplication, and assignment of structures from the manzamine class and revealed the significant potential in the design of optimized molecules for the treatment of cervical cancer. These data suggest that this sponge-derived natural product class warrants further attention regarding the design and development of novel manzamine analogues, which may be efficacious for preventive and therapeutic treatment of cancer. Additionally, this study reveals the significance of protecting fragile marine ecosystems from climate change-induced loss of species diversity.</description><subject>Apoptosis - drug effects</subject><subject>Biological Products - chemistry</subject><subject>Biological Products - pharmacology</subject><subject>Carbazoles - chemistry</subject><subject>Carbazoles - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Ecosystem</subject><subject>Female</subject><subject>HeLa Cells</subject><subject>Homeodomain Proteins - chemistry</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Humans</subject><subject>Structure-Activity Relationship</subject><subject>Uterine Cervical Neoplasms - chemistry</subject><subject>Uterine Cervical Neoplasms - drug therapy</subject><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kF1LwzAUhoMobk7_gUj_QOdJ2jTtjSDDj8H8ACd4IyFJ0y1jS0eaDuavN3Mf6I1XB3Le9znkQegSQx8DwddCNf2ZFX7p6rJfSADK2BHqYkogzoDQY9QFnCVxkmdpB501zQwAEijoKeokBAihtOiiz_FUR0_CGaujZ-FbJ-bRayC2yodn-yUWm81tNLRTI41vooF2K6NCaiCs0i6S62gs3ER7YyeRD7C34QfeILw29hydVGLe6Ivd7KH3-7vx4DEevTwMB7ejWFBMfVzRlIGSKqGCMSZIRvKSYCwkLhWToIuM0LRKJaOKlVIpSIsi0zlLCCNFToukh2623GUrF7pU2vrwEb50ZiHcmtfC8L8ba6Z8Uq84wxmmLA-AdAtQrm4ap6tDFwPf6OZBN9_r5jvdoXb1--6htPcbArAN_NTr1tmg4X_mNwgokHE</recordid><startdate>20200228</startdate><enddate>20200228</enddate><creator>Karan, Dev</creator><creator>Dubey, Seema</creator><creator>Pirisi, Lucia</creator><creator>Nagel, Alexis</creator><creator>Pina, Ivett</creator><creator>Choo, Yeun-Mun</creator><creator>Hamann, Mark T</creator><general>American Chemical Society and American Society of Pharmacognosy</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>5PM</scope><orcidid>https://orcid.org/0000-0002-0905-0886</orcidid><orcidid>https://orcid.org/0000-0002-3798-4002</orcidid></search><sort><creationdate>20200228</creationdate><title>The Marine Natural Product Manzamine A Inhibits Cervical Cancer by Targeting the SIX1 Protein</title><author>Karan, Dev ; Dubey, Seema ; Pirisi, Lucia ; Nagel, Alexis ; Pina, Ivett ; Choo, Yeun-Mun ; Hamann, Mark T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a515t-f5470cbc35a777a2628d211ab1dc7b0e96254f4b75c7dbcc04996e87327298593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Apoptosis - drug effects</topic><topic>Biological Products - chemistry</topic><topic>Biological Products - pharmacology</topic><topic>Carbazoles - chemistry</topic><topic>Carbazoles - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>Ecosystem</topic><topic>Female</topic><topic>HeLa Cells</topic><topic>Homeodomain Proteins - chemistry</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Humans</topic><topic>Structure-Activity Relationship</topic><topic>Uterine Cervical Neoplasms - chemistry</topic><topic>Uterine Cervical Neoplasms - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karan, Dev</creatorcontrib><creatorcontrib>Dubey, Seema</creatorcontrib><creatorcontrib>Pirisi, Lucia</creatorcontrib><creatorcontrib>Nagel, Alexis</creatorcontrib><creatorcontrib>Pina, Ivett</creatorcontrib><creatorcontrib>Choo, Yeun-Mun</creatorcontrib><creatorcontrib>Hamann, Mark T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karan, Dev</au><au>Dubey, Seema</au><au>Pirisi, Lucia</au><au>Nagel, Alexis</au><au>Pina, Ivett</au><au>Choo, Yeun-Mun</au><au>Hamann, Mark T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Marine Natural Product Manzamine A Inhibits Cervical Cancer by Targeting the SIX1 Protein</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><addtitle>J. Nat. Prod</addtitle><date>2020-02-28</date><risdate>2020</risdate><volume>83</volume><issue>2</issue><spage>286</spage><epage>295</epage><pages>286-295</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>Natural products remain an important source of drug leads covering unique chemical space and providing significant therapeutic value for the control of cancer and infectious diseases resistant to current drugs. Here, we determined the antiproliferative activity of a natural product manzamine A (1) from an Indo-Pacific sponge following various in vitro cellular assays targeting cervical cancer (C33A, HeLa, SiHa, and CaSki). Our data demonstrated the antiproliferative effects of 1 at relatively low and non-cytotoxic concentrations (up to 4 μM). Mechanistic investigations confirmed that 1 blocked cell cycle progression in SiHa and CaSki cells at G1/S phase and regulated cell cycle-related genes, including restoration of p21 and p53 expression. In apoptotic assays, HeLa cells showed the highest sensitivity to 1 as compared to other cell types (C33A, SiHa, and CaSki). Interestingly, 1 decreased the levels of the oncoprotein SIX1, which is associated with oncogenesis in cervical cancer. To further investigate the structure–activity relationship among manzamine A (1) class with potential antiproliferative activity, molecular networking facilitated the efficient identification, dereplication, and assignment of structures from the manzamine class and revealed the significant potential in the design of optimized molecules for the treatment of cervical cancer. These data suggest that this sponge-derived natural product class warrants further attention regarding the design and development of novel manzamine analogues, which may be efficacious for preventive and therapeutic treatment of cancer. 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subjects | Apoptosis - drug effects Biological Products - chemistry Biological Products - pharmacology Carbazoles - chemistry Carbazoles - pharmacology Cell Line, Tumor Ecosystem Female HeLa Cells Homeodomain Proteins - chemistry Homeodomain Proteins - metabolism Humans Structure-Activity Relationship Uterine Cervical Neoplasms - chemistry Uterine Cervical Neoplasms - drug therapy |
title | The Marine Natural Product Manzamine A Inhibits Cervical Cancer by Targeting the SIX1 Protein |
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