The Antitumour Effect of Prunella vulgaris Extract on Thyroid Cancer Cells In Vitro and In Vivo
Prunella vulgaris, a traditional Chinese medicine, has been used to treat various benign and malignant tumours for centuries in China. In our previous studies, Prunella vulgaris extract (PVE) was shown to promote apoptosis in differentiated thyroid cancer (DTC) cells. However, whether other mechanis...
Gespeichert in:
Veröffentlicht in: | Evidence-based complementary and alternative medicine 2021, Vol.2021, p.8869323-12 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 12 |
---|---|
container_issue | |
container_start_page | 8869323 |
container_title | Evidence-based complementary and alternative medicine |
container_volume | 2021 |
creator | Yu, Fangqin Zhang, Lele Ma, Runsheng Liu, Chenguang Wang, Qingduan Yin, Detao |
description | Prunella vulgaris, a traditional Chinese medicine, has been used to treat various benign and malignant tumours for centuries in China. In our previous studies, Prunella vulgaris extract (PVE) was shown to promote apoptosis in differentiated thyroid cancer (DTC) cells. However, whether other mechanisms are involved in the antitumour effect of PVE in thyroid cancer (TC) cells remains unclear. The present study aimed to investigate the antiproliferative and antimigratory effects of PVE on TC cell lines both in vitro and in vivo. First, the TPC-1 and SW579 human TC cell lines were screened by MTT assay for their high level of sensitivity to PVE. Then, the results of cell growth curve and colony formation assay and cell cycle analyses, wound healing, and migration assays demonstrated that PVE inhibited the proliferation and migration of TPC-1 and SW579 cells. Moreover, the antitumour effect of PVE was verified in a subcutaneous xenotransplanted tumour model. Next, MKI67, PCNA, CTNNB1, and CDH1 were screened by qRT-PCR for their significantly differential expression levels in xenograft tissue with and without PVE treatment, and expression of MKI67, PCNA, and CDH1 was verified by Western blot. Finally, an integrated bioinformatics analysis containing protein-protein interaction network, KEGG pathway, and GO analysis was conducted to explore more potential antitumour mechanisms of PVE. In summary, PVE could inhibit the proliferation and migration of TC cells both in vitro and in vivo, which may have been achieved by modulation of the expression of MKI67, PCNA, and CDH1. These data suggest that PVE has the potential to be developed into a new anticancer drug for the treatment of TC. |
doi_str_mv | 10.1155/2021/8869323 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7811421</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2478359413</sourcerecordid><originalsourceid>FETCH-LOGICAL-c448t-7dd6714deda61c213b7d6c223ea334145d79bbf9c6efcc0c0e89010602f619dd3</originalsourceid><addsrcrecordid>eNp9kU1vEzEQhi0EoiVw44ws9VIJQj221_ZeKlVRgEqV4BCq3izH9jauNnZr76btv8dRQgQcOM2M5tE7Hy9C74F8BmiaM0oonCklWkbZC3QMksOUU6VeHnJ5c4TelHJHCG2llK_REWMNaRqAY6QXK48v4hCGcZ3GjOdd5-2AU4d_5DH6vjd4M_a3JoeC509DNttmxIvVc07B4ZmJ1mc8q2DBlxFfhyEnbKLbFZv0Fr3qTF_8u32coJ9f5ovZt-nV96-Xs4urqeVcDVPpnJDAnXdGgKXAltIJSynzhjEOvHGyXS671grfWUss8aolQAShnYDWOTZB5zvd-3G59s76WHft9X0Oa5OfdTJB_92JYaVv00ZLBcDrwAk63Qvk9DD6Muh1KHb7gOjTWDTligpJGyoqevIPeldfF-t5lZKKNS0HVqlPO8rmVEr23WEZIHrrnN46p_fOVfzDnwcc4N9WVeDjDliF6Mxj-L_cL0JqoGY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2478359413</pqid></control><display><type>article</type><title>The Antitumour Effect of Prunella vulgaris Extract on Thyroid Cancer Cells In Vitro and In Vivo</title><source>Wiley-Blackwell Open Access Collection</source><source>NCBI_PubMed Central(免费)</source><source>Free E-Journal (出版社公開部分のみ)</source><source>Alma/SFX Local Collection</source><source>PubMed Central Open Access</source><creator>Yu, Fangqin ; Zhang, Lele ; Ma, Runsheng ; Liu, Chenguang ; Wang, Qingduan ; Yin, Detao</creator><contributor>Shi, San Jun ; San Jun Shi</contributor><creatorcontrib>Yu, Fangqin ; Zhang, Lele ; Ma, Runsheng ; Liu, Chenguang ; Wang, Qingduan ; Yin, Detao ; Shi, San Jun ; San Jun Shi</creatorcontrib><description>Prunella vulgaris, a traditional Chinese medicine, has been used to treat various benign and malignant tumours for centuries in China. In our previous studies, Prunella vulgaris extract (PVE) was shown to promote apoptosis in differentiated thyroid cancer (DTC) cells. However, whether other mechanisms are involved in the antitumour effect of PVE in thyroid cancer (TC) cells remains unclear. The present study aimed to investigate the antiproliferative and antimigratory effects of PVE on TC cell lines both in vitro and in vivo. First, the TPC-1 and SW579 human TC cell lines were screened by MTT assay for their high level of sensitivity to PVE. Then, the results of cell growth curve and colony formation assay and cell cycle analyses, wound healing, and migration assays demonstrated that PVE inhibited the proliferation and migration of TPC-1 and SW579 cells. Moreover, the antitumour effect of PVE was verified in a subcutaneous xenotransplanted tumour model. Next, MKI67, PCNA, CTNNB1, and CDH1 were screened by qRT-PCR for their significantly differential expression levels in xenograft tissue with and without PVE treatment, and expression of MKI67, PCNA, and CDH1 was verified by Western blot. Finally, an integrated bioinformatics analysis containing protein-protein interaction network, KEGG pathway, and GO analysis was conducted to explore more potential antitumour mechanisms of PVE. In summary, PVE could inhibit the proliferation and migration of TC cells both in vitro and in vivo, which may have been achieved by modulation of the expression of MKI67, PCNA, and CDH1. These data suggest that PVE has the potential to be developed into a new anticancer drug for the treatment of TC.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2021/8869323</identifier><identifier>PMID: 33505511</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Alternative medicine ; Apoptosis ; Bioinformatics ; Cancer therapies ; Cell culture ; Cell cycle ; Cell differentiation ; Cell growth ; Cell migration ; Cell proliferation ; Computer programs ; E-cadherin ; Experiments ; Flow cytometry ; Herbal medicine ; Iodine ; Medical research ; Pharmaceuticals ; Proliferating cell nuclear antigen ; Protein interaction ; Prunella vulgaris ; Software ; Thyroid cancer ; Traditional Chinese medicine ; Tumors ; Wound healing ; Xenografts</subject><ispartof>Evidence-based complementary and alternative medicine, 2021, Vol.2021, p.8869323-12</ispartof><rights>Copyright © 2021 Fangqin Yu et al.</rights><rights>Copyright © 2021 Fangqin Yu et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2021 Fangqin Yu et al. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-7dd6714deda61c213b7d6c223ea334145d79bbf9c6efcc0c0e89010602f619dd3</citedby><cites>FETCH-LOGICAL-c448t-7dd6714deda61c213b7d6c223ea334145d79bbf9c6efcc0c0e89010602f619dd3</cites><orcidid>0000-0002-4349-6857 ; 0000-0002-8400-5188</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811421/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811421/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33505511$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Shi, San Jun</contributor><contributor>San Jun Shi</contributor><creatorcontrib>Yu, Fangqin</creatorcontrib><creatorcontrib>Zhang, Lele</creatorcontrib><creatorcontrib>Ma, Runsheng</creatorcontrib><creatorcontrib>Liu, Chenguang</creatorcontrib><creatorcontrib>Wang, Qingduan</creatorcontrib><creatorcontrib>Yin, Detao</creatorcontrib><title>The Antitumour Effect of Prunella vulgaris Extract on Thyroid Cancer Cells In Vitro and In Vivo</title><title>Evidence-based complementary and alternative medicine</title><addtitle>Evid Based Complement Alternat Med</addtitle><description>Prunella vulgaris, a traditional Chinese medicine, has been used to treat various benign and malignant tumours for centuries in China. In our previous studies, Prunella vulgaris extract (PVE) was shown to promote apoptosis in differentiated thyroid cancer (DTC) cells. However, whether other mechanisms are involved in the antitumour effect of PVE in thyroid cancer (TC) cells remains unclear. The present study aimed to investigate the antiproliferative and antimigratory effects of PVE on TC cell lines both in vitro and in vivo. First, the TPC-1 and SW579 human TC cell lines were screened by MTT assay for their high level of sensitivity to PVE. Then, the results of cell growth curve and colony formation assay and cell cycle analyses, wound healing, and migration assays demonstrated that PVE inhibited the proliferation and migration of TPC-1 and SW579 cells. Moreover, the antitumour effect of PVE was verified in a subcutaneous xenotransplanted tumour model. Next, MKI67, PCNA, CTNNB1, and CDH1 were screened by qRT-PCR for their significantly differential expression levels in xenograft tissue with and without PVE treatment, and expression of MKI67, PCNA, and CDH1 was verified by Western blot. Finally, an integrated bioinformatics analysis containing protein-protein interaction network, KEGG pathway, and GO analysis was conducted to explore more potential antitumour mechanisms of PVE. In summary, PVE could inhibit the proliferation and migration of TC cells both in vitro and in vivo, which may have been achieved by modulation of the expression of MKI67, PCNA, and CDH1. These data suggest that PVE has the potential to be developed into a new anticancer drug for the treatment of TC.</description><subject>Alternative medicine</subject><subject>Apoptosis</subject><subject>Bioinformatics</subject><subject>Cancer therapies</subject><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Cell differentiation</subject><subject>Cell growth</subject><subject>Cell migration</subject><subject>Cell proliferation</subject><subject>Computer programs</subject><subject>E-cadherin</subject><subject>Experiments</subject><subject>Flow cytometry</subject><subject>Herbal medicine</subject><subject>Iodine</subject><subject>Medical research</subject><subject>Pharmaceuticals</subject><subject>Proliferating cell nuclear antigen</subject><subject>Protein interaction</subject><subject>Prunella vulgaris</subject><subject>Software</subject><subject>Thyroid cancer</subject><subject>Traditional Chinese medicine</subject><subject>Tumors</subject><subject>Wound healing</subject><subject>Xenografts</subject><issn>1741-427X</issn><issn>1741-4288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU1vEzEQhi0EoiVw44ws9VIJQj221_ZeKlVRgEqV4BCq3izH9jauNnZr76btv8dRQgQcOM2M5tE7Hy9C74F8BmiaM0oonCklWkbZC3QMksOUU6VeHnJ5c4TelHJHCG2llK_REWMNaRqAY6QXK48v4hCGcZ3GjOdd5-2AU4d_5DH6vjd4M_a3JoeC509DNttmxIvVc07B4ZmJ1mc8q2DBlxFfhyEnbKLbFZv0Fr3qTF_8u32coJ9f5ovZt-nV96-Xs4urqeVcDVPpnJDAnXdGgKXAltIJSynzhjEOvHGyXS671grfWUss8aolQAShnYDWOTZB5zvd-3G59s76WHft9X0Oa5OfdTJB_92JYaVv00ZLBcDrwAk63Qvk9DD6Muh1KHb7gOjTWDTligpJGyoqevIPeldfF-t5lZKKNS0HVqlPO8rmVEr23WEZIHrrnN46p_fOVfzDnwcc4N9WVeDjDliF6Mxj-L_cL0JqoGY</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Yu, Fangqin</creator><creator>Zhang, Lele</creator><creator>Ma, Runsheng</creator><creator>Liu, Chenguang</creator><creator>Wang, Qingduan</creator><creator>Yin, Detao</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4349-6857</orcidid><orcidid>https://orcid.org/0000-0002-8400-5188</orcidid></search><sort><creationdate>2021</creationdate><title>The Antitumour Effect of Prunella vulgaris Extract on Thyroid Cancer Cells In Vitro and In Vivo</title><author>Yu, Fangqin ; Zhang, Lele ; Ma, Runsheng ; Liu, Chenguang ; Wang, Qingduan ; Yin, Detao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-7dd6714deda61c213b7d6c223ea334145d79bbf9c6efcc0c0e89010602f619dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alternative medicine</topic><topic>Apoptosis</topic><topic>Bioinformatics</topic><topic>Cancer therapies</topic><topic>Cell culture</topic><topic>Cell cycle</topic><topic>Cell differentiation</topic><topic>Cell growth</topic><topic>Cell migration</topic><topic>Cell proliferation</topic><topic>Computer programs</topic><topic>E-cadherin</topic><topic>Experiments</topic><topic>Flow cytometry</topic><topic>Herbal medicine</topic><topic>Iodine</topic><topic>Medical research</topic><topic>Pharmaceuticals</topic><topic>Proliferating cell nuclear antigen</topic><topic>Protein interaction</topic><topic>Prunella vulgaris</topic><topic>Software</topic><topic>Thyroid cancer</topic><topic>Traditional Chinese medicine</topic><topic>Tumors</topic><topic>Wound healing</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Fangqin</creatorcontrib><creatorcontrib>Zhang, Lele</creatorcontrib><creatorcontrib>Ma, Runsheng</creatorcontrib><creatorcontrib>Liu, Chenguang</creatorcontrib><creatorcontrib>Wang, Qingduan</creatorcontrib><creatorcontrib>Yin, Detao</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Psychology Database</collection><collection>ProQuest_Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Fangqin</au><au>Zhang, Lele</au><au>Ma, Runsheng</au><au>Liu, Chenguang</au><au>Wang, Qingduan</au><au>Yin, Detao</au><au>Shi, San Jun</au><au>San Jun Shi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Antitumour Effect of Prunella vulgaris Extract on Thyroid Cancer Cells In Vitro and In Vivo</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2021</date><risdate>2021</risdate><volume>2021</volume><spage>8869323</spage><epage>12</epage><pages>8869323-12</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Prunella vulgaris, a traditional Chinese medicine, has been used to treat various benign and malignant tumours for centuries in China. In our previous studies, Prunella vulgaris extract (PVE) was shown to promote apoptosis in differentiated thyroid cancer (DTC) cells. However, whether other mechanisms are involved in the antitumour effect of PVE in thyroid cancer (TC) cells remains unclear. The present study aimed to investigate the antiproliferative and antimigratory effects of PVE on TC cell lines both in vitro and in vivo. First, the TPC-1 and SW579 human TC cell lines were screened by MTT assay for their high level of sensitivity to PVE. Then, the results of cell growth curve and colony formation assay and cell cycle analyses, wound healing, and migration assays demonstrated that PVE inhibited the proliferation and migration of TPC-1 and SW579 cells. Moreover, the antitumour effect of PVE was verified in a subcutaneous xenotransplanted tumour model. Next, MKI67, PCNA, CTNNB1, and CDH1 were screened by qRT-PCR for their significantly differential expression levels in xenograft tissue with and without PVE treatment, and expression of MKI67, PCNA, and CDH1 was verified by Western blot. Finally, an integrated bioinformatics analysis containing protein-protein interaction network, KEGG pathway, and GO analysis was conducted to explore more potential antitumour mechanisms of PVE. In summary, PVE could inhibit the proliferation and migration of TC cells both in vitro and in vivo, which may have been achieved by modulation of the expression of MKI67, PCNA, and CDH1. These data suggest that PVE has the potential to be developed into a new anticancer drug for the treatment of TC.</abstract><cop>United States</cop><pub>Hindawi</pub><pmid>33505511</pmid><doi>10.1155/2021/8869323</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-4349-6857</orcidid><orcidid>https://orcid.org/0000-0002-8400-5188</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1741-427X |
ispartof | Evidence-based complementary and alternative medicine, 2021, Vol.2021, p.8869323-12 |
issn | 1741-427X 1741-4288 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7811421 |
source | Wiley-Blackwell Open Access Collection; NCBI_PubMed Central(免费); Free E-Journal (出版社公開部分のみ); Alma/SFX Local Collection; PubMed Central Open Access |
subjects | Alternative medicine Apoptosis Bioinformatics Cancer therapies Cell culture Cell cycle Cell differentiation Cell growth Cell migration Cell proliferation Computer programs E-cadherin Experiments Flow cytometry Herbal medicine Iodine Medical research Pharmaceuticals Proliferating cell nuclear antigen Protein interaction Prunella vulgaris Software Thyroid cancer Traditional Chinese medicine Tumors Wound healing Xenografts |
title | The Antitumour Effect of Prunella vulgaris Extract on Thyroid Cancer Cells In Vitro and In Vivo |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T07%3A13%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Antitumour%20Effect%20of%20Prunella%20vulgaris%20Extract%20on%20Thyroid%20Cancer%20Cells%20In%20Vitro%20and%20In%20Vivo&rft.jtitle=Evidence-based%20complementary%20and%20alternative%20medicine&rft.au=Yu,%20Fangqin&rft.date=2021&rft.volume=2021&rft.spage=8869323&rft.epage=12&rft.pages=8869323-12&rft.issn=1741-427X&rft.eissn=1741-4288&rft_id=info:doi/10.1155/2021/8869323&rft_dat=%3Cproquest_pubme%3E2478359413%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2478359413&rft_id=info:pmid/33505511&rfr_iscdi=true |