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Pleurotus highking mushrooms potentiate antiproliferative and antimigratory activity against triple-negative breast cancer cells by suppressing Akt signaling
In this study, we evaluated the antiproliferative and antimetastatic effects of the Pleurotus highking mushroom on the human triple-negative breast cancer cell lines MDA-MB-231 and HCC-1937 and attempted to elucidate the underlying molecular mechanisms. The antiproliferative effects of P. highking p...
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Published in: | Integrative cancer therapies 2020, Vol.19, p.1534735420969809-1534735420969809 |
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description | In this study, we evaluated the antiproliferative and antimetastatic effects of the Pleurotus highking mushroom on the human triple-negative breast cancer cell lines MDA-MB-231 and HCC-1937 and attempted to elucidate the underlying molecular mechanisms. The antiproliferative effects of P. highking purified fraction-III (PEF-III) were investigated using colony formation and MTS assays. The antimigratory effects of PEF-III were determined by wound healing, transwell migration, and matrigel cell invasion assays. The protein expression levels were evaluated using Western blot analysis. The effect of PEF-III on tumor-sphere formation was examined in a 3D sphere-forming medium, and the mRNA expressions of proliferation- and migration-related genes in the cells from the tumor spheres were determined using RT-qPCR. PEF-III treatment caused a potent and concentration-dependent decrease in the numbers of colonies and viable cells. It also remarkably suppressed the migratory ability of the cells. Mechanistically, PEF-III treatment reduced the expression of pAkt, matrix metallopeptidase-9 (MMP-9), and vimentin. Furthermore, PEF-III reduced the number and size of the tumor spheres in the 3D culture system. It also significantly reduced the mRNA expression of Ki-67, MMP-9, and vimentin in the PEF-III-treated tumor-sphere cells. PEF-III exerted promising antiproliferative and antimigratory effects in triple-negative breast cancer cell lines by suppressing Akt signaling. Therefore, P. highking mushrooms may be considered a potential source for the development of potent anticancer drug(s) for the treatment of breast cancer. |
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Anwarul ; Reza, A. S. M. Ali ; Nasrin, Mst. Samima ; Rahman, Md. Atiar</creator><creatorcontrib>Haque, Md. Anwarul ; Reza, A. S. M. Ali ; Nasrin, Mst. Samima ; Rahman, Md. Atiar</creatorcontrib><description>In this study, we evaluated the antiproliferative and antimetastatic effects of the Pleurotus highking mushroom on the human triple-negative breast cancer cell lines MDA-MB-231 and HCC-1937 and attempted to elucidate the underlying molecular mechanisms. The antiproliferative effects of P. highking purified fraction-III (PEF-III) were investigated using colony formation and MTS assays. The antimigratory effects of PEF-III were determined by wound healing, transwell migration, and matrigel cell invasion assays. The protein expression levels were evaluated using Western blot analysis. The effect of PEF-III on tumor-sphere formation was examined in a 3D sphere-forming medium, and the mRNA expressions of proliferation- and migration-related genes in the cells from the tumor spheres were determined using RT-qPCR. PEF-III treatment caused a potent and concentration-dependent decrease in the numbers of colonies and viable cells. It also remarkably suppressed the migratory ability of the cells. Mechanistically, PEF-III treatment reduced the expression of pAkt, matrix metallopeptidase-9 (MMP-9), and vimentin. Furthermore, PEF-III reduced the number and size of the tumor spheres in the 3D culture system. It also significantly reduced the mRNA expression of Ki-67, MMP-9, and vimentin in the PEF-III-treated tumor-sphere cells. PEF-III exerted promising antiproliferative and antimigratory effects in triple-negative breast cancer cell lines by suppressing Akt signaling. Therefore, P. highking mushrooms may be considered a potential source for the development of potent anticancer drug(s) for the treatment of breast cancer.</description><identifier>ISSN: 1534-7354</identifier><identifier>EISSN: 1552-695X</identifier><identifier>DOI: 10.1177/1534735420969809</identifier><identifier>PMID: 33176517</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>AKT protein ; Breast cancer ; Cell culture ; Cell migration ; Cell proliferation ; Colonies ; Gelatinase B ; Gene expression ; Metalloproteinase ; Molecular modelling ; Pleurotus ; Tumor cell lines ; Vimentin ; Wound healing</subject><ispartof>Integrative cancer therapies, 2020, Vol.19, p.1534735420969809-1534735420969809</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). 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Anwarul</creatorcontrib><creatorcontrib>Reza, A. S. M. Ali</creatorcontrib><creatorcontrib>Nasrin, Mst. Samima</creatorcontrib><creatorcontrib>Rahman, Md. Atiar</creatorcontrib><title>Pleurotus highking mushrooms potentiate antiproliferative and antimigratory activity against triple-negative breast cancer cells by suppressing Akt signaling</title><title>Integrative cancer therapies</title><addtitle>Integr Cancer Ther</addtitle><description>In this study, we evaluated the antiproliferative and antimetastatic effects of the Pleurotus highking mushroom on the human triple-negative breast cancer cell lines MDA-MB-231 and HCC-1937 and attempted to elucidate the underlying molecular mechanisms. The antiproliferative effects of P. highking purified fraction-III (PEF-III) were investigated using colony formation and MTS assays. The antimigratory effects of PEF-III were determined by wound healing, transwell migration, and matrigel cell invasion assays. The protein expression levels were evaluated using Western blot analysis. The effect of PEF-III on tumor-sphere formation was examined in a 3D sphere-forming medium, and the mRNA expressions of proliferation- and migration-related genes in the cells from the tumor spheres were determined using RT-qPCR. PEF-III treatment caused a potent and concentration-dependent decrease in the numbers of colonies and viable cells. It also remarkably suppressed the migratory ability of the cells. Mechanistically, PEF-III treatment reduced the expression of pAkt, matrix metallopeptidase-9 (MMP-9), and vimentin. Furthermore, PEF-III reduced the number and size of the tumor spheres in the 3D culture system. It also significantly reduced the mRNA expression of Ki-67, MMP-9, and vimentin in the PEF-III-treated tumor-sphere cells. PEF-III exerted promising antiproliferative and antimigratory effects in triple-negative breast cancer cell lines by suppressing Akt signaling. Therefore, P. highking mushrooms may be considered a potential source for the development of potent anticancer drug(s) for the treatment of breast cancer.</description><subject>AKT protein</subject><subject>Breast cancer</subject><subject>Cell culture</subject><subject>Cell migration</subject><subject>Cell proliferation</subject><subject>Colonies</subject><subject>Gelatinase B</subject><subject>Gene expression</subject><subject>Metalloproteinase</subject><subject>Molecular modelling</subject><subject>Pleurotus</subject><subject>Tumor cell lines</subject><subject>Vimentin</subject><subject>Wound healing</subject><issn>1534-7354</issn><issn>1552-695X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1kUFvFSEQx4nR2Fq9ezIkXryswrLAcjFpmlZNmtRDm3gjs8DbR7u7rMA2eR_G71rWV6tt4olh5jf_4c8g9JaSj5RK-Yly1kjGm5oooVqinqFDynldCcV_PF9j1lRr_QC9SumakJoSwV-iA8aoFJzKQ_Tr--CWGPKS8Nb32xs_9Xhc0jaGMCY8h-ym7CE7DOWcYxj8xkXI_nbN2N_Z0fclE-IOgykFn0vQg59Sxjn6eXDV5Pp9SxcdlLSBybiIjRuGhLsdTss8R5fSOvz4JuPk-wmGcnuNXmxgSO7N_XmErs5OL0--VucXX76dHJ9XphF1rrqWdq0gVoIBaIiBxtiu3VhmpbVWdOVruJKkay21xbclTLFW2QIpWXjBjtDnve68dKOzppiOMOg5-hHiTgfw-nFl8lvdh1sthWSEsyLw4V4ghp-LS1mPPq3-YHJhSbpuBCEtpbwt6Psn6HVYYvG7UpJJqhoiC0X2lIkhpeg2D4-hRK-71093X1re_WvioeHPsgtQ7YEEvfs79b-Cd69YvV4</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Haque, Md. Anwarul</creator><creator>Reza, A. S. M. Ali</creator><creator>Nasrin, Mst. Samima</creator><creator>Rahman, Md. 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Anwarul ; Reza, A. S. M. Ali ; Nasrin, Mst. Samima ; Rahman, Md. Atiar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-b81b860d7acaa40ca4cdb8fd3d7ddd6b9805970b8d1d765d039389dcdb97a4063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>AKT protein</topic><topic>Breast cancer</topic><topic>Cell culture</topic><topic>Cell migration</topic><topic>Cell proliferation</topic><topic>Colonies</topic><topic>Gelatinase B</topic><topic>Gene expression</topic><topic>Metalloproteinase</topic><topic>Molecular modelling</topic><topic>Pleurotus</topic><topic>Tumor cell lines</topic><topic>Vimentin</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haque, Md. Anwarul</creatorcontrib><creatorcontrib>Reza, A. S. M. Ali</creatorcontrib><creatorcontrib>Nasrin, Mst. Samima</creatorcontrib><creatorcontrib>Rahman, Md. 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Anwarul</au><au>Reza, A. S. M. Ali</au><au>Nasrin, Mst. Samima</au><au>Rahman, Md. Atiar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pleurotus highking mushrooms potentiate antiproliferative and antimigratory activity against triple-negative breast cancer cells by suppressing Akt signaling</atitle><jtitle>Integrative cancer therapies</jtitle><addtitle>Integr Cancer Ther</addtitle><date>2020</date><risdate>2020</risdate><volume>19</volume><spage>1534735420969809</spage><epage>1534735420969809</epage><pages>1534735420969809-1534735420969809</pages><issn>1534-7354</issn><eissn>1552-695X</eissn><abstract>In this study, we evaluated the antiproliferative and antimetastatic effects of the Pleurotus highking mushroom on the human triple-negative breast cancer cell lines MDA-MB-231 and HCC-1937 and attempted to elucidate the underlying molecular mechanisms. The antiproliferative effects of P. highking purified fraction-III (PEF-III) were investigated using colony formation and MTS assays. The antimigratory effects of PEF-III were determined by wound healing, transwell migration, and matrigel cell invasion assays. The protein expression levels were evaluated using Western blot analysis. The effect of PEF-III on tumor-sphere formation was examined in a 3D sphere-forming medium, and the mRNA expressions of proliferation- and migration-related genes in the cells from the tumor spheres were determined using RT-qPCR. PEF-III treatment caused a potent and concentration-dependent decrease in the numbers of colonies and viable cells. It also remarkably suppressed the migratory ability of the cells. Mechanistically, PEF-III treatment reduced the expression of pAkt, matrix metallopeptidase-9 (MMP-9), and vimentin. Furthermore, PEF-III reduced the number and size of the tumor spheres in the 3D culture system. It also significantly reduced the mRNA expression of Ki-67, MMP-9, and vimentin in the PEF-III-treated tumor-sphere cells. PEF-III exerted promising antiproliferative and antimigratory effects in triple-negative breast cancer cell lines by suppressing Akt signaling. Therefore, P. highking mushrooms may be considered a potential source for the development of potent anticancer drug(s) for the treatment of breast cancer.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>33176517</pmid><doi>10.1177/1534735420969809</doi><orcidid>https://orcid.org/0000-0002-4902-8923</orcidid><orcidid>https://orcid.org/0000-0002-1457-0245</orcidid><orcidid>https://orcid.org/0000-0001-6785-4121</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | AKT protein Breast cancer Cell culture Cell migration Cell proliferation Colonies Gelatinase B Gene expression Metalloproteinase Molecular modelling Pleurotus Tumor cell lines Vimentin Wound healing |
title | Pleurotus highking mushrooms potentiate antiproliferative and antimigratory activity against triple-negative breast cancer cells by suppressing Akt signaling |
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