Loading…

Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement

Breast cancer is the most frequent cancer in women worldwide, and drug resistance is common in all breast cancer types. The combination of natural products with chemotherapies has attracted attention, as it was found that natural compounds enhance the effects of standard cancer chemotherapeutic drug...

Full description

Saved in:
Bibliographic Details
Published in:Fundamental & clinical pharmacology 2020-12, Vol.34 (6), p.671-686
Main Authors: Rosas‐González, Vida Celeste, Téllez‐Bañuelos, Martha Cecilia, Hernández‐Flores, Georgina, Bravo‐Cuellar, Alejandro, Aguilar-Lemarroy, Adriana, Jave‐Suárez, Luis Felipe, Haramati, Jesse, Solorzano‐Ibarra, Fabiola, Ortiz‐Lazareno, Pablo Cesar
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53
cites cdi_FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53
container_end_page 686
container_issue 6
container_start_page 671
container_title Fundamental & clinical pharmacology
container_volume 34
creator Rosas‐González, Vida Celeste
Téllez‐Bañuelos, Martha Cecilia
Hernández‐Flores, Georgina
Bravo‐Cuellar, Alejandro
Aguilar-Lemarroy, Adriana
Jave‐Suárez, Luis Felipe
Haramati, Jesse
Solorzano‐Ibarra, Fabiola
Ortiz‐Lazareno, Pablo Cesar
description Breast cancer is the most frequent cancer in women worldwide, and drug resistance is common in all breast cancer types. The combination of natural products with chemotherapies has attracted attention, as it was found that natural compounds enhance the effects of standard cancer chemotherapeutic drugs and protect from side effects. Into the different natural products, garlic has been recognized for its antitumor properties. It is suggested that its anticancer effects are associated with its organo‐sulfur compounds, especially alliin and allicin. Here, we evaluated the effects of both molecules on cell death, senescence, and their senolytic potential in luminal A and triple‐negative breast cancer cells. MCF‐7 (luminal A) and HCC‐70 (triple‐negative) cells were cultured and treated with different concentrations of alliin or allicin. Then, cell viability was determined using the WST‐1 reagent. Apoptosis and caspase activity were evaluated by flow cytometry; ΔΨm was assessed using a JC‐10 fluorometric assay kit. Apoptosis‐related genes were evaluated by RT‐PCR. Proliferation was measured using bromodeoxyuridine incorporation. We also evaluated clonogenicity, senescence (β‐Galactosidase Staining), and the senolytic effect of the compounds. Our results showed that allicin has antiproliferative, anticlonogenic, and senolytic effects. In addition, allicin decreased cell viability and induced apoptosis by loss of ΔΨm, caspase‐3, caspase‐8, and caspase‐9 activation, upregulation of NOXA, P21, and BAK, as well as downregulation of BCL‐XL expression. Contrary to allicin, alliin promoted clonogenicity, induced senescence, and did not exhibit pro‐apoptotic effects in breast cancer cells.
doi_str_mv 10.1111/fcp.12559
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2389693902</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2389693902</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53</originalsourceid><addsrcrecordid>eNp1kU9u1TAQxi0Eoo_CggsgS2xAalrbcRybXfVoAakSLGAdOX7jypXzBzt5qDuOwIJDsOlVeghOwpAUFkh44xnNb74Z-yPkKWfHHM-Jd-MxF1Vl7pENl7UotGDqPtmwWtVFaTQ_II9yvmKM14yrh-SgFEKrmokNuXkdvIcE_RRspICxmzIdPLUxhtBT2--W0GE8YDoO4zTkkJdChh6yg94BxXKcu9CjyOlSm1IYI_z8-q2HSzuFPdA2gc0TdRb59IpubR5thiN6-_32R3e0NI1pwI51yBQcvcQBKL0f4h463PExeeBtzPDk7j4kn87PPm7fFhfv37zbnl4UTihtilobzyyzTskdl1VrtJdcl06BYkYwoyqQXJVcs7ZShkvPai1KqFrm29bYqjwkL1ZdXOjzDHlquoAPjdH2MMy5EaU2ypSGCUSf_4NeDXPCf0BKKqkrJUWN1MuVcmnIOYFvxhQ6m64bzprfHjboYbN4iOyzO8W57WD3l_xjGgInK_AlRLj-v1Jzvv2wSv4Cb0Sp7w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2464856427</pqid></control><display><type>article</type><title>Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement</title><source>Wiley Online Library</source><creator>Rosas‐González, Vida Celeste ; Téllez‐Bañuelos, Martha Cecilia ; Hernández‐Flores, Georgina ; Bravo‐Cuellar, Alejandro ; Aguilar-Lemarroy, Adriana ; Jave‐Suárez, Luis Felipe ; Haramati, Jesse ; Solorzano‐Ibarra, Fabiola ; Ortiz‐Lazareno, Pablo Cesar</creator><creatorcontrib>Rosas‐González, Vida Celeste ; Téllez‐Bañuelos, Martha Cecilia ; Hernández‐Flores, Georgina ; Bravo‐Cuellar, Alejandro ; Aguilar-Lemarroy, Adriana ; Jave‐Suárez, Luis Felipe ; Haramati, Jesse ; Solorzano‐Ibarra, Fabiola ; Ortiz‐Lazareno, Pablo Cesar</creatorcontrib><description>Breast cancer is the most frequent cancer in women worldwide, and drug resistance is common in all breast cancer types. The combination of natural products with chemotherapies has attracted attention, as it was found that natural compounds enhance the effects of standard cancer chemotherapeutic drugs and protect from side effects. Into the different natural products, garlic has been recognized for its antitumor properties. It is suggested that its anticancer effects are associated with its organo‐sulfur compounds, especially alliin and allicin. Here, we evaluated the effects of both molecules on cell death, senescence, and their senolytic potential in luminal A and triple‐negative breast cancer cells. MCF‐7 (luminal A) and HCC‐70 (triple‐negative) cells were cultured and treated with different concentrations of alliin or allicin. Then, cell viability was determined using the WST‐1 reagent. Apoptosis and caspase activity were evaluated by flow cytometry; ΔΨm was assessed using a JC‐10 fluorometric assay kit. Apoptosis‐related genes were evaluated by RT‐PCR. Proliferation was measured using bromodeoxyuridine incorporation. We also evaluated clonogenicity, senescence (β‐Galactosidase Staining), and the senolytic effect of the compounds. Our results showed that allicin has antiproliferative, anticlonogenic, and senolytic effects. In addition, allicin decreased cell viability and induced apoptosis by loss of ΔΨm, caspase‐3, caspase‐8, and caspase‐9 activation, upregulation of NOXA, P21, and BAK, as well as downregulation of BCL‐XL expression. Contrary to allicin, alliin promoted clonogenicity, induced senescence, and did not exhibit pro‐apoptotic effects in breast cancer cells.</description><identifier>ISSN: 0767-3981</identifier><identifier>EISSN: 1472-8206</identifier><identifier>DOI: 10.1111/fcp.12559</identifier><identifier>PMID: 32286702</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>allicin ; alliin ; Anticancer properties ; Apoptosis ; Breast cancer ; Bromodeoxyuridine ; Caspase ; Cell death ; Cell viability ; clonogenic ; Drug resistance ; Evaluation ; Flow cytometry ; Garlic ; Natural products ; Pharmacology ; Reagents ; Senescence ; senolytic ; Side effects ; Sulfur ; Sulfur compounds ; β-Galactosidase</subject><ispartof>Fundamental &amp; clinical pharmacology, 2020-12, Vol.34 (6), p.671-686</ispartof><rights>2020 Société Française de Pharmacologie et de Thérapeutique</rights><rights>2020 Société Française de Pharmacologie et de Thérapeutique.</rights><rights>Copyright © 2020 Société Française de Pharmacologie et de Thérapeutique</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53</citedby><cites>FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53</cites><orcidid>0000-0001-9045-7052 ; 0000-0003-1952-1431 ; 0000-0001-5663-852X ; 0000-0002-4861-0065 ; 0000-0002-4675-2203 ; 0000-0002-9057-1397 ; 0000-0002-2945-4503 ; 0000-0001-9288-4824 ; 0000-0001-6209-5031</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ffcp.12559$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ffcp.12559$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,786,790,27957,27958,50923,51032</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32286702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosas‐González, Vida Celeste</creatorcontrib><creatorcontrib>Téllez‐Bañuelos, Martha Cecilia</creatorcontrib><creatorcontrib>Hernández‐Flores, Georgina</creatorcontrib><creatorcontrib>Bravo‐Cuellar, Alejandro</creatorcontrib><creatorcontrib>Aguilar-Lemarroy, Adriana</creatorcontrib><creatorcontrib>Jave‐Suárez, Luis Felipe</creatorcontrib><creatorcontrib>Haramati, Jesse</creatorcontrib><creatorcontrib>Solorzano‐Ibarra, Fabiola</creatorcontrib><creatorcontrib>Ortiz‐Lazareno, Pablo Cesar</creatorcontrib><title>Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement</title><title>Fundamental &amp; clinical pharmacology</title><addtitle>Fundam Clin Pharmacol</addtitle><description>Breast cancer is the most frequent cancer in women worldwide, and drug resistance is common in all breast cancer types. The combination of natural products with chemotherapies has attracted attention, as it was found that natural compounds enhance the effects of standard cancer chemotherapeutic drugs and protect from side effects. Into the different natural products, garlic has been recognized for its antitumor properties. It is suggested that its anticancer effects are associated with its organo‐sulfur compounds, especially alliin and allicin. Here, we evaluated the effects of both molecules on cell death, senescence, and their senolytic potential in luminal A and triple‐negative breast cancer cells. MCF‐7 (luminal A) and HCC‐70 (triple‐negative) cells were cultured and treated with different concentrations of alliin or allicin. Then, cell viability was determined using the WST‐1 reagent. Apoptosis and caspase activity were evaluated by flow cytometry; ΔΨm was assessed using a JC‐10 fluorometric assay kit. Apoptosis‐related genes were evaluated by RT‐PCR. Proliferation was measured using bromodeoxyuridine incorporation. We also evaluated clonogenicity, senescence (β‐Galactosidase Staining), and the senolytic effect of the compounds. Our results showed that allicin has antiproliferative, anticlonogenic, and senolytic effects. In addition, allicin decreased cell viability and induced apoptosis by loss of ΔΨm, caspase‐3, caspase‐8, and caspase‐9 activation, upregulation of NOXA, P21, and BAK, as well as downregulation of BCL‐XL expression. Contrary to allicin, alliin promoted clonogenicity, induced senescence, and did not exhibit pro‐apoptotic effects in breast cancer cells.</description><subject>allicin</subject><subject>alliin</subject><subject>Anticancer properties</subject><subject>Apoptosis</subject><subject>Breast cancer</subject><subject>Bromodeoxyuridine</subject><subject>Caspase</subject><subject>Cell death</subject><subject>Cell viability</subject><subject>clonogenic</subject><subject>Drug resistance</subject><subject>Evaluation</subject><subject>Flow cytometry</subject><subject>Garlic</subject><subject>Natural products</subject><subject>Pharmacology</subject><subject>Reagents</subject><subject>Senescence</subject><subject>senolytic</subject><subject>Side effects</subject><subject>Sulfur</subject><subject>Sulfur compounds</subject><subject>β-Galactosidase</subject><issn>0767-3981</issn><issn>1472-8206</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kU9u1TAQxi0Eoo_CggsgS2xAalrbcRybXfVoAakSLGAdOX7jypXzBzt5qDuOwIJDsOlVeghOwpAUFkh44xnNb74Z-yPkKWfHHM-Jd-MxF1Vl7pENl7UotGDqPtmwWtVFaTQ_II9yvmKM14yrh-SgFEKrmokNuXkdvIcE_RRspICxmzIdPLUxhtBT2--W0GE8YDoO4zTkkJdChh6yg94BxXKcu9CjyOlSm1IYI_z8-q2HSzuFPdA2gc0TdRb59IpubR5thiN6-_32R3e0NI1pwI51yBQcvcQBKL0f4h463PExeeBtzPDk7j4kn87PPm7fFhfv37zbnl4UTihtilobzyyzTskdl1VrtJdcl06BYkYwoyqQXJVcs7ZShkvPai1KqFrm29bYqjwkL1ZdXOjzDHlquoAPjdH2MMy5EaU2ypSGCUSf_4NeDXPCf0BKKqkrJUWN1MuVcmnIOYFvxhQ6m64bzprfHjboYbN4iOyzO8W57WD3l_xjGgInK_AlRLj-v1Jzvv2wSv4Cb0Sp7w</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Rosas‐González, Vida Celeste</creator><creator>Téllez‐Bañuelos, Martha Cecilia</creator><creator>Hernández‐Flores, Georgina</creator><creator>Bravo‐Cuellar, Alejandro</creator><creator>Aguilar-Lemarroy, Adriana</creator><creator>Jave‐Suárez, Luis Felipe</creator><creator>Haramati, Jesse</creator><creator>Solorzano‐Ibarra, Fabiola</creator><creator>Ortiz‐Lazareno, Pablo Cesar</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9045-7052</orcidid><orcidid>https://orcid.org/0000-0003-1952-1431</orcidid><orcidid>https://orcid.org/0000-0001-5663-852X</orcidid><orcidid>https://orcid.org/0000-0002-4861-0065</orcidid><orcidid>https://orcid.org/0000-0002-4675-2203</orcidid><orcidid>https://orcid.org/0000-0002-9057-1397</orcidid><orcidid>https://orcid.org/0000-0002-2945-4503</orcidid><orcidid>https://orcid.org/0000-0001-9288-4824</orcidid><orcidid>https://orcid.org/0000-0001-6209-5031</orcidid></search><sort><creationdate>202012</creationdate><title>Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement</title><author>Rosas‐González, Vida Celeste ; Téllez‐Bañuelos, Martha Cecilia ; Hernández‐Flores, Georgina ; Bravo‐Cuellar, Alejandro ; Aguilar-Lemarroy, Adriana ; Jave‐Suárez, Luis Felipe ; Haramati, Jesse ; Solorzano‐Ibarra, Fabiola ; Ortiz‐Lazareno, Pablo Cesar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>allicin</topic><topic>alliin</topic><topic>Anticancer properties</topic><topic>Apoptosis</topic><topic>Breast cancer</topic><topic>Bromodeoxyuridine</topic><topic>Caspase</topic><topic>Cell death</topic><topic>Cell viability</topic><topic>clonogenic</topic><topic>Drug resistance</topic><topic>Evaluation</topic><topic>Flow cytometry</topic><topic>Garlic</topic><topic>Natural products</topic><topic>Pharmacology</topic><topic>Reagents</topic><topic>Senescence</topic><topic>senolytic</topic><topic>Side effects</topic><topic>Sulfur</topic><topic>Sulfur compounds</topic><topic>β-Galactosidase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosas‐González, Vida Celeste</creatorcontrib><creatorcontrib>Téllez‐Bañuelos, Martha Cecilia</creatorcontrib><creatorcontrib>Hernández‐Flores, Georgina</creatorcontrib><creatorcontrib>Bravo‐Cuellar, Alejandro</creatorcontrib><creatorcontrib>Aguilar-Lemarroy, Adriana</creatorcontrib><creatorcontrib>Jave‐Suárez, Luis Felipe</creatorcontrib><creatorcontrib>Haramati, Jesse</creatorcontrib><creatorcontrib>Solorzano‐Ibarra, Fabiola</creatorcontrib><creatorcontrib>Ortiz‐Lazareno, Pablo Cesar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Fundamental &amp; clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosas‐González, Vida Celeste</au><au>Téllez‐Bañuelos, Martha Cecilia</au><au>Hernández‐Flores, Georgina</au><au>Bravo‐Cuellar, Alejandro</au><au>Aguilar-Lemarroy, Adriana</au><au>Jave‐Suárez, Luis Felipe</au><au>Haramati, Jesse</au><au>Solorzano‐Ibarra, Fabiola</au><au>Ortiz‐Lazareno, Pablo Cesar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement</atitle><jtitle>Fundamental &amp; clinical pharmacology</jtitle><addtitle>Fundam Clin Pharmacol</addtitle><date>2020-12</date><risdate>2020</risdate><volume>34</volume><issue>6</issue><spage>671</spage><epage>686</epage><pages>671-686</pages><issn>0767-3981</issn><eissn>1472-8206</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>Breast cancer is the most frequent cancer in women worldwide, and drug resistance is common in all breast cancer types. The combination of natural products with chemotherapies has attracted attention, as it was found that natural compounds enhance the effects of standard cancer chemotherapeutic drugs and protect from side effects. Into the different natural products, garlic has been recognized for its antitumor properties. It is suggested that its anticancer effects are associated with its organo‐sulfur compounds, especially alliin and allicin. Here, we evaluated the effects of both molecules on cell death, senescence, and their senolytic potential in luminal A and triple‐negative breast cancer cells. MCF‐7 (luminal A) and HCC‐70 (triple‐negative) cells were cultured and treated with different concentrations of alliin or allicin. Then, cell viability was determined using the WST‐1 reagent. Apoptosis and caspase activity were evaluated by flow cytometry; ΔΨm was assessed using a JC‐10 fluorometric assay kit. Apoptosis‐related genes were evaluated by RT‐PCR. Proliferation was measured using bromodeoxyuridine incorporation. We also evaluated clonogenicity, senescence (β‐Galactosidase Staining), and the senolytic effect of the compounds. Our results showed that allicin has antiproliferative, anticlonogenic, and senolytic effects. In addition, allicin decreased cell viability and induced apoptosis by loss of ΔΨm, caspase‐3, caspase‐8, and caspase‐9 activation, upregulation of NOXA, P21, and BAK, as well as downregulation of BCL‐XL expression. Contrary to allicin, alliin promoted clonogenicity, induced senescence, and did not exhibit pro‐apoptotic effects in breast cancer cells.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32286702</pmid><doi>10.1111/fcp.12559</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0001-9045-7052</orcidid><orcidid>https://orcid.org/0000-0003-1952-1431</orcidid><orcidid>https://orcid.org/0000-0001-5663-852X</orcidid><orcidid>https://orcid.org/0000-0002-4861-0065</orcidid><orcidid>https://orcid.org/0000-0002-4675-2203</orcidid><orcidid>https://orcid.org/0000-0002-9057-1397</orcidid><orcidid>https://orcid.org/0000-0002-2945-4503</orcidid><orcidid>https://orcid.org/0000-0001-9288-4824</orcidid><orcidid>https://orcid.org/0000-0001-6209-5031</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0767-3981
ispartof Fundamental & clinical pharmacology, 2020-12, Vol.34 (6), p.671-686
issn 0767-3981
1472-8206
language eng
recordid cdi_proquest_miscellaneous_2389693902
source Wiley Online Library
subjects allicin
alliin
Anticancer properties
Apoptosis
Breast cancer
Bromodeoxyuridine
Caspase
Cell death
Cell viability
clonogenic
Drug resistance
Evaluation
Flow cytometry
Garlic
Natural products
Pharmacology
Reagents
Senescence
senolytic
Side effects
Sulfur
Sulfur compounds
β-Galactosidase
title Differential effects of alliin and allicin on apoptosis and senescence in luminal A and triple‐negative breast cancer: Caspase, ΔΨm, and pro‐apoptotic gene involvement
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-09-21T17%3A57%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differential%20effects%20of%20alliin%20and%20allicin%20on%20apoptosis%20and%20senescence%20in%20luminal%20A%20and%20triple%E2%80%90negative%20breast%20cancer:%20Caspase,%20%CE%94%CE%A8m,%20and%20pro%E2%80%90apoptotic%20gene%20involvement&rft.jtitle=Fundamental%20&%20clinical%20pharmacology&rft.au=Rosas%E2%80%90Gonz%C3%A1lez,%20Vida%20Celeste&rft.date=2020-12&rft.volume=34&rft.issue=6&rft.spage=671&rft.epage=686&rft.pages=671-686&rft.issn=0767-3981&rft.eissn=1472-8206&rft_id=info:doi/10.1111/fcp.12559&rft_dat=%3Cproquest_cross%3E2389693902%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2689-789f0a0ac64d145b98f4183c6e60920965e4163180b56914f07823e5b0fbb9a53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2464856427&rft_id=info:pmid/32286702&rfr_iscdi=true