Synthesize of Bi 2 O 3 /Gln-TSC nanoparticles and evaluation of their toxicity on prostate cancer cells and expression of CASP8, BAX, and Bcl-2 genes
Due to the high prevalence and considerable increase of prostate cancer, finding novel therapeutic compounds for the treatment of prostatic cancer has been the goal of many researches. In this study, we aimed to fabricate the Bismuth oxide (Bi O ) NPs, functionalized with glutamine (Gln) and conjuga...
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| Veröffentlicht in: | Scientific reports 2022-12, Vol.12 (1), p.21245 |
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| creator | Moradi, Asal Abdihaji, Mohammadreza Kouchaksaraie, Sara Barari Alkinani, Tabarek Abdulrazaq Mahmoudi, Aida Davoudi, Arash Dashtmiani, William Ghezeljeh, Somayeh Mikaeili Aghajani, Shahrzad Ghasemian, Reza Taramsari, Somayeh Maghsoomi Majlesi, Amitis Niyaki, Zahra Mahdavi Salehzadeh, Ali |
| description | Due to the high prevalence and considerable increase of prostate cancer, finding novel therapeutic compounds for the treatment of prostatic cancer has been the goal of many researches. In this study, we aimed to fabricate the Bismuth oxide (Bi
O
) NPs, functionalized with glutamine (Gln) and conjugated with Thiosemicarbazide (TSC). Then, the anticancer mechanism of the synthesized NPs was investigated using the cellular and molecular tests including MTT assay, Flow cytometry, Caspase-3 activity assay, Hoechst staining and Real Time PCR. The FT-IR and XRD assays confirmed the identity of the synthesized Bi
O
/Gln-TSC NPs. The size range of the synthesized spherical particles was 10-60 nm and the zeta potential was - 23.8 mV. The purity of the NPs was confirmed by EDX-mapping analysis. The Bi
O
/Gln-TSC was considerably more toxic for prostate cancer cells than normal human cells and the IC
was calculated 35.4 and 305 µg/mL, respectively. The exposure to the NPs significantly increased the frequency of apoptotic cells from 4.7 to 75.3%. Moreover, the expression of the CASP8, BAX, and Bcl-2 genes after exposure to the NPs increased by 2.8, 2.3, and 1.39 folds. Treating the cancer cells with Bi
O
/Gln-TSC increased the activity of the Caspase-3 protein and apoptotic morphological features were observed by Hoechst staining in the treated cells. This work showed that Bi
O
/Gln-TSC has considerable cytotoxicity for prostate cancer cells and could inducing both intrinsic and extrinsic pathways of apoptosis. |
| format | Article |
| fullrecord | <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_36482061</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>36482061</sourcerecordid><originalsourceid>FETCH-pubmed_primary_364820613</originalsourceid><addsrcrecordid>eNqFj8FuwjAQRC2kqqCWX0D7AUQEJyA4kqiFW5GSQ29oa5ZiZGzLayrS_-j_klbh3LmMNDPvMD0xkGk-S2QmZV8MmU9pq5lc5tPlo-hn83wh0_l0IH6qxsYjsf4mcAcoNEh4gwwma2OTuirBonUeQ9TKEAPaPdAXmgtG7ewv0cI6QHRXrXRsoA19cBwxEii0igIoMqYjrz4Qc0eWq2q7GEOxeh__tYUyiYRPssTP4uGAhmnY-ZMYvb7U5Sbxl48z7Xc-6DOGZnf_kf07uAHftVLe</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesize of Bi 2 O 3 /Gln-TSC nanoparticles and evaluation of their toxicity on prostate cancer cells and expression of CASP8, BAX, and Bcl-2 genes</title><source>SpringerOpen</source><source>MEDLINE</source><source>Nature Free</source><source>DOAJ Directory of Open Access Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>EZB Electronic Journals Library</source><creator>Moradi, Asal ; Abdihaji, Mohammadreza ; Kouchaksaraie, Sara Barari ; Alkinani, Tabarek Abdulrazaq ; Mahmoudi, Aida ; Davoudi, Arash ; Dashtmiani, William ; Ghezeljeh, Somayeh Mikaeili ; Aghajani, Shahrzad ; Ghasemian, Reza ; Taramsari, Somayeh Maghsoomi ; Majlesi, Amitis ; Niyaki, Zahra Mahdavi ; Salehzadeh, Ali</creator><creatorcontrib>Moradi, Asal ; Abdihaji, Mohammadreza ; Kouchaksaraie, Sara Barari ; Alkinani, Tabarek Abdulrazaq ; Mahmoudi, Aida ; Davoudi, Arash ; Dashtmiani, William ; Ghezeljeh, Somayeh Mikaeili ; Aghajani, Shahrzad ; Ghasemian, Reza ; Taramsari, Somayeh Maghsoomi ; Majlesi, Amitis ; Niyaki, Zahra Mahdavi ; Salehzadeh, Ali</creatorcontrib><description>Due to the high prevalence and considerable increase of prostate cancer, finding novel therapeutic compounds for the treatment of prostatic cancer has been the goal of many researches. In this study, we aimed to fabricate the Bismuth oxide (Bi
O
) NPs, functionalized with glutamine (Gln) and conjugated with Thiosemicarbazide (TSC). Then, the anticancer mechanism of the synthesized NPs was investigated using the cellular and molecular tests including MTT assay, Flow cytometry, Caspase-3 activity assay, Hoechst staining and Real Time PCR. The FT-IR and XRD assays confirmed the identity of the synthesized Bi
O
/Gln-TSC NPs. The size range of the synthesized spherical particles was 10-60 nm and the zeta potential was - 23.8 mV. The purity of the NPs was confirmed by EDX-mapping analysis. The Bi
O
/Gln-TSC was considerably more toxic for prostate cancer cells than normal human cells and the IC
was calculated 35.4 and 305 µg/mL, respectively. The exposure to the NPs significantly increased the frequency of apoptotic cells from 4.7 to 75.3%. Moreover, the expression of the CASP8, BAX, and Bcl-2 genes after exposure to the NPs increased by 2.8, 2.3, and 1.39 folds. Treating the cancer cells with Bi
O
/Gln-TSC increased the activity of the Caspase-3 protein and apoptotic morphological features were observed by Hoechst staining in the treated cells. This work showed that Bi
O
/Gln-TSC has considerable cytotoxicity for prostate cancer cells and could inducing both intrinsic and extrinsic pathways of apoptosis.</description><identifier>EISSN: 2045-2322</identifier><identifier>PMID: 36482061</identifier><language>eng</language><publisher>England</publisher><subject>Caspase 3 - genetics ; Caspase 8 ; Genes, bcl-2 ; Glutamine ; Humans ; Male ; Prostatic Neoplasms - genetics ; Spectroscopy, Fourier Transform Infrared</subject><ispartof>Scientific reports, 2022-12, Vol.12 (1), p.21245</ispartof><rights>2022. The Author(s).</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36482061$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moradi, Asal</creatorcontrib><creatorcontrib>Abdihaji, Mohammadreza</creatorcontrib><creatorcontrib>Kouchaksaraie, Sara Barari</creatorcontrib><creatorcontrib>Alkinani, Tabarek Abdulrazaq</creatorcontrib><creatorcontrib>Mahmoudi, Aida</creatorcontrib><creatorcontrib>Davoudi, Arash</creatorcontrib><creatorcontrib>Dashtmiani, William</creatorcontrib><creatorcontrib>Ghezeljeh, Somayeh Mikaeili</creatorcontrib><creatorcontrib>Aghajani, Shahrzad</creatorcontrib><creatorcontrib>Ghasemian, Reza</creatorcontrib><creatorcontrib>Taramsari, Somayeh Maghsoomi</creatorcontrib><creatorcontrib>Majlesi, Amitis</creatorcontrib><creatorcontrib>Niyaki, Zahra Mahdavi</creatorcontrib><creatorcontrib>Salehzadeh, Ali</creatorcontrib><title>Synthesize of Bi 2 O 3 /Gln-TSC nanoparticles and evaluation of their toxicity on prostate cancer cells and expression of CASP8, BAX, and Bcl-2 genes</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><description>Due to the high prevalence and considerable increase of prostate cancer, finding novel therapeutic compounds for the treatment of prostatic cancer has been the goal of many researches. In this study, we aimed to fabricate the Bismuth oxide (Bi
O
) NPs, functionalized with glutamine (Gln) and conjugated with Thiosemicarbazide (TSC). Then, the anticancer mechanism of the synthesized NPs was investigated using the cellular and molecular tests including MTT assay, Flow cytometry, Caspase-3 activity assay, Hoechst staining and Real Time PCR. The FT-IR and XRD assays confirmed the identity of the synthesized Bi
O
/Gln-TSC NPs. The size range of the synthesized spherical particles was 10-60 nm and the zeta potential was - 23.8 mV. The purity of the NPs was confirmed by EDX-mapping analysis. The Bi
O
/Gln-TSC was considerably more toxic for prostate cancer cells than normal human cells and the IC
was calculated 35.4 and 305 µg/mL, respectively. The exposure to the NPs significantly increased the frequency of apoptotic cells from 4.7 to 75.3%. Moreover, the expression of the CASP8, BAX, and Bcl-2 genes after exposure to the NPs increased by 2.8, 2.3, and 1.39 folds. Treating the cancer cells with Bi
O
/Gln-TSC increased the activity of the Caspase-3 protein and apoptotic morphological features were observed by Hoechst staining in the treated cells. This work showed that Bi
O
/Gln-TSC has considerable cytotoxicity for prostate cancer cells and could inducing both intrinsic and extrinsic pathways of apoptosis.</description><subject>Caspase 3 - genetics</subject><subject>Caspase 8</subject><subject>Genes, bcl-2</subject><subject>Glutamine</subject><subject>Humans</subject><subject>Male</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFj8FuwjAQRC2kqqCWX0D7AUQEJyA4kqiFW5GSQ29oa5ZiZGzLayrS_-j_klbh3LmMNDPvMD0xkGk-S2QmZV8MmU9pq5lc5tPlo-hn83wh0_l0IH6qxsYjsf4mcAcoNEh4gwwma2OTuirBonUeQ9TKEAPaPdAXmgtG7ewv0cI6QHRXrXRsoA19cBwxEii0igIoMqYjrz4Qc0eWq2q7GEOxeh__tYUyiYRPssTP4uGAhmnY-ZMYvb7U5Sbxl48z7Xc-6DOGZnf_kf07uAHftVLe</recordid><startdate>20221208</startdate><enddate>20221208</enddate><creator>Moradi, Asal</creator><creator>Abdihaji, Mohammadreza</creator><creator>Kouchaksaraie, Sara Barari</creator><creator>Alkinani, Tabarek Abdulrazaq</creator><creator>Mahmoudi, Aida</creator><creator>Davoudi, Arash</creator><creator>Dashtmiani, William</creator><creator>Ghezeljeh, Somayeh Mikaeili</creator><creator>Aghajani, Shahrzad</creator><creator>Ghasemian, Reza</creator><creator>Taramsari, Somayeh Maghsoomi</creator><creator>Majlesi, Amitis</creator><creator>Niyaki, Zahra Mahdavi</creator><creator>Salehzadeh, Ali</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20221208</creationdate><title>Synthesize of Bi 2 O 3 /Gln-TSC nanoparticles and evaluation of their toxicity on prostate cancer cells and expression of CASP8, BAX, and Bcl-2 genes</title><author>Moradi, Asal ; Abdihaji, Mohammadreza ; Kouchaksaraie, Sara Barari ; Alkinani, Tabarek Abdulrazaq ; Mahmoudi, Aida ; Davoudi, Arash ; Dashtmiani, William ; Ghezeljeh, Somayeh Mikaeili ; Aghajani, Shahrzad ; Ghasemian, Reza ; Taramsari, Somayeh Maghsoomi ; Majlesi, Amitis ; Niyaki, Zahra Mahdavi ; Salehzadeh, Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_364820613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Caspase 3 - genetics</topic><topic>Caspase 8</topic><topic>Genes, bcl-2</topic><topic>Glutamine</topic><topic>Humans</topic><topic>Male</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moradi, Asal</creatorcontrib><creatorcontrib>Abdihaji, Mohammadreza</creatorcontrib><creatorcontrib>Kouchaksaraie, Sara Barari</creatorcontrib><creatorcontrib>Alkinani, Tabarek Abdulrazaq</creatorcontrib><creatorcontrib>Mahmoudi, Aida</creatorcontrib><creatorcontrib>Davoudi, Arash</creatorcontrib><creatorcontrib>Dashtmiani, William</creatorcontrib><creatorcontrib>Ghezeljeh, Somayeh Mikaeili</creatorcontrib><creatorcontrib>Aghajani, Shahrzad</creatorcontrib><creatorcontrib>Ghasemian, Reza</creatorcontrib><creatorcontrib>Taramsari, Somayeh Maghsoomi</creatorcontrib><creatorcontrib>Majlesi, Amitis</creatorcontrib><creatorcontrib>Niyaki, Zahra Mahdavi</creatorcontrib><creatorcontrib>Salehzadeh, Ali</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moradi, Asal</au><au>Abdihaji, Mohammadreza</au><au>Kouchaksaraie, Sara Barari</au><au>Alkinani, Tabarek Abdulrazaq</au><au>Mahmoudi, Aida</au><au>Davoudi, Arash</au><au>Dashtmiani, William</au><au>Ghezeljeh, Somayeh Mikaeili</au><au>Aghajani, Shahrzad</au><au>Ghasemian, Reza</au><au>Taramsari, Somayeh Maghsoomi</au><au>Majlesi, Amitis</au><au>Niyaki, Zahra Mahdavi</au><au>Salehzadeh, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesize of Bi 2 O 3 /Gln-TSC nanoparticles and evaluation of their toxicity on prostate cancer cells and expression of CASP8, BAX, and Bcl-2 genes</atitle><jtitle>Scientific reports</jtitle><addtitle>Sci Rep</addtitle><date>2022-12-08</date><risdate>2022</risdate><volume>12</volume><issue>1</issue><spage>21245</spage><pages>21245-</pages><eissn>2045-2322</eissn><abstract>Due to the high prevalence and considerable increase of prostate cancer, finding novel therapeutic compounds for the treatment of prostatic cancer has been the goal of many researches. In this study, we aimed to fabricate the Bismuth oxide (Bi
O
) NPs, functionalized with glutamine (Gln) and conjugated with Thiosemicarbazide (TSC). Then, the anticancer mechanism of the synthesized NPs was investigated using the cellular and molecular tests including MTT assay, Flow cytometry, Caspase-3 activity assay, Hoechst staining and Real Time PCR. The FT-IR and XRD assays confirmed the identity of the synthesized Bi
O
/Gln-TSC NPs. The size range of the synthesized spherical particles was 10-60 nm and the zeta potential was - 23.8 mV. The purity of the NPs was confirmed by EDX-mapping analysis. The Bi
O
/Gln-TSC was considerably more toxic for prostate cancer cells than normal human cells and the IC
was calculated 35.4 and 305 µg/mL, respectively. The exposure to the NPs significantly increased the frequency of apoptotic cells from 4.7 to 75.3%. Moreover, the expression of the CASP8, BAX, and Bcl-2 genes after exposure to the NPs increased by 2.8, 2.3, and 1.39 folds. Treating the cancer cells with Bi
O
/Gln-TSC increased the activity of the Caspase-3 protein and apoptotic morphological features were observed by Hoechst staining in the treated cells. This work showed that Bi
O
/Gln-TSC has considerable cytotoxicity for prostate cancer cells and could inducing both intrinsic and extrinsic pathways of apoptosis.</abstract><cop>England</cop><pmid>36482061</pmid></addata></record> |
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| ispartof | Scientific reports, 2022-12, Vol.12 (1), p.21245 |
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| source | SpringerOpen; MEDLINE; Nature Free; DOAJ Directory of Open Access Journals; PubMed Central; Free Full-Text Journals in Chemistry; EZB Electronic Journals Library |
| subjects | Caspase 3 - genetics Caspase 8 Genes, bcl-2 Glutamine Humans Male Prostatic Neoplasms - genetics Spectroscopy, Fourier Transform Infrared |
| title | Synthesize of Bi 2 O 3 /Gln-TSC nanoparticles and evaluation of their toxicity on prostate cancer cells and expression of CASP8, BAX, and Bcl-2 genes |
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