Application of cell growth analysis to the quality assessment of human cell-processed therapeutic products as a testing method for immortalized cellular impurities
In human cell-processed therapeutic products (hCTPs) for clinical application, tumorigenic cellular impurities in the manufacturing process are a major concern. Because cellular immortalization is one of the prerequisite steps in tumorigenesis, we tested whether cell growth analysis can be employed...
Gespeichert in:
Veröffentlicht in: | Regenerative therapy 2016-12, Vol.5, p.49-54 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 54 |
---|---|
container_issue | |
container_start_page | 49 |
container_title | Regenerative therapy |
container_volume | 5 |
creator | Hasebe-Takada, Nozomi Kono, Ken Yasuda, Satoshi Sawada, Rumi Matsuyama, Akifumi Sato, Yoji |
description | In human cell-processed therapeutic products (hCTPs) for clinical application, tumorigenic cellular impurities in the manufacturing process are a major concern. Because cellular immortalization is one of the prerequisite steps in tumorigenesis, we tested whether cell growth analysis can be employed to check for immortalized (and potentially tumorigenic) cellular impurities in hCTPs. We monitored the growth of human bone marrow-derived mesenchymal stem cells (BMSCs) mixed with HeLa cells at a ratio of 1/106 or more and compared their growth rates with that of BMSCs alone. The cell growth analysis detected a significant increase in the growth rate of the BMSCs spiked with 0.0001% HeLa within 30 days at a probability of 47%. When human adipose-derived stem cells (ADSCs) were spiked with ASC52telo cells, a human telomerase reverse transcriptase (hTERT)-immortalized adipose-derived mesenchymal stem cell line, at a ratio of 0.001% or more, their growth rates were significantly increased within 15 passages, compared with that of ADSCs alone. These results indicate that cell growth analysis for the detection of immortalized cellular impurities in human somatic stem cells is simple and can be useful for the quality assessment of hCTPs in the manufacturing process.
•The performance of cell growth analysis was evaluated.•Cell growth analysis detected 0.0001% HeLa contamination in BMSCs at 47% probability.•Growth rates of ADSCs spiked with 0.001% ASC52telo was increased within 15 passages. |
doi_str_mv | 10.1016/j.reth.2016.06.005 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6581850</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2352320416300293</els_id><sourcerecordid>2248380828</sourcerecordid><originalsourceid>FETCH-LOGICAL-c545t-60f33f1fa217eb074a4538cf9fe3733b089d9121d36daeb815b16c333d0454923</originalsourceid><addsrcrecordid>eNp9UU1r3DAQNaWhCUn-QA9Fx1681YfllaEUQmjaQqCX9ixkabTWYluOPlI2f6d_NHI3DemlMKBh5r2nmXlV9ZbgDcGk_bDfBEjDhpZ8g0tg_qo6o4zTmlHcvH6Rn1aXMe4xxkRwQjvxpjplhDacY3JW_b5altFplZyfkbdIwziiXfC_0oDUrMZDdBElj9IA6C6r0aUDUjFCjBPMaWUMeVLzH169BK9LB8wKD2qBnJxGpWqyTrHwkEIJYnLzDk1lem-Q9QG5afIhFe2HwlyF8qjW6pKDSw7iRXVi1Rjh8uk9r37efP5x_bW-_f7l2_XVba15w1PdYsuYJVZRsoUebxvVcCa07SywLWM9Fp3pCCWGtUZBLwjvSasZYwY3vOkoO68-HXWX3E9gdFkwqFEuwU0qHKRXTv7bmd0gd_5etlyU2-Ii8P5JIPi7XBaVk4vrQmoGn6OktBFMYEFFgdIjVAcfYwD7_A3BcjVY7uVqsFwNlrgE5oX07uWAz5S_dhbAxyMAypnuHQQZtYNZg3EBdJLGu__pPwIBfLyN</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2248380828</pqid></control><display><type>article</type><title>Application of cell growth analysis to the quality assessment of human cell-processed therapeutic products as a testing method for immortalized cellular impurities</title><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Hasebe-Takada, Nozomi ; Kono, Ken ; Yasuda, Satoshi ; Sawada, Rumi ; Matsuyama, Akifumi ; Sato, Yoji</creator><creatorcontrib>Hasebe-Takada, Nozomi ; Kono, Ken ; Yasuda, Satoshi ; Sawada, Rumi ; Matsuyama, Akifumi ; Sato, Yoji</creatorcontrib><description>In human cell-processed therapeutic products (hCTPs) for clinical application, tumorigenic cellular impurities in the manufacturing process are a major concern. Because cellular immortalization is one of the prerequisite steps in tumorigenesis, we tested whether cell growth analysis can be employed to check for immortalized (and potentially tumorigenic) cellular impurities in hCTPs. We monitored the growth of human bone marrow-derived mesenchymal stem cells (BMSCs) mixed with HeLa cells at a ratio of 1/106 or more and compared their growth rates with that of BMSCs alone. The cell growth analysis detected a significant increase in the growth rate of the BMSCs spiked with 0.0001% HeLa within 30 days at a probability of 47%. When human adipose-derived stem cells (ADSCs) were spiked with ASC52telo cells, a human telomerase reverse transcriptase (hTERT)-immortalized adipose-derived mesenchymal stem cell line, at a ratio of 0.001% or more, their growth rates were significantly increased within 15 passages, compared with that of ADSCs alone. These results indicate that cell growth analysis for the detection of immortalized cellular impurities in human somatic stem cells is simple and can be useful for the quality assessment of hCTPs in the manufacturing process.
•The performance of cell growth analysis was evaluated.•Cell growth analysis detected 0.0001% HeLa contamination in BMSCs at 47% probability.•Growth rates of ADSCs spiked with 0.001% ASC52telo was increased within 15 passages.</description><identifier>ISSN: 2352-3204</identifier><identifier>EISSN: 2352-3204</identifier><identifier>DOI: 10.1016/j.reth.2016.06.005</identifier><identifier>PMID: 31245501</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adipose-derived stem cell ; Bone marrow-derived mesenchymal stem cell ; Cellular therapy ; Original ; Quality assessment ; Regenerative medicine ; Tumorigenicity</subject><ispartof>Regenerative therapy, 2016-12, Vol.5, p.49-54</ispartof><rights>2016 The Japanese Society for Regenerative Medicine</rights><rights>2016, The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. 2016 The Japanese Society for Regenerative Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c545t-60f33f1fa217eb074a4538cf9fe3733b089d9121d36daeb815b16c333d0454923</citedby><cites>FETCH-LOGICAL-c545t-60f33f1fa217eb074a4538cf9fe3733b089d9121d36daeb815b16c333d0454923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581850/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581850/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31245501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hasebe-Takada, Nozomi</creatorcontrib><creatorcontrib>Kono, Ken</creatorcontrib><creatorcontrib>Yasuda, Satoshi</creatorcontrib><creatorcontrib>Sawada, Rumi</creatorcontrib><creatorcontrib>Matsuyama, Akifumi</creatorcontrib><creatorcontrib>Sato, Yoji</creatorcontrib><title>Application of cell growth analysis to the quality assessment of human cell-processed therapeutic products as a testing method for immortalized cellular impurities</title><title>Regenerative therapy</title><addtitle>Regen Ther</addtitle><description>In human cell-processed therapeutic products (hCTPs) for clinical application, tumorigenic cellular impurities in the manufacturing process are a major concern. Because cellular immortalization is one of the prerequisite steps in tumorigenesis, we tested whether cell growth analysis can be employed to check for immortalized (and potentially tumorigenic) cellular impurities in hCTPs. We monitored the growth of human bone marrow-derived mesenchymal stem cells (BMSCs) mixed with HeLa cells at a ratio of 1/106 or more and compared their growth rates with that of BMSCs alone. The cell growth analysis detected a significant increase in the growth rate of the BMSCs spiked with 0.0001% HeLa within 30 days at a probability of 47%. When human adipose-derived stem cells (ADSCs) were spiked with ASC52telo cells, a human telomerase reverse transcriptase (hTERT)-immortalized adipose-derived mesenchymal stem cell line, at a ratio of 0.001% or more, their growth rates were significantly increased within 15 passages, compared with that of ADSCs alone. These results indicate that cell growth analysis for the detection of immortalized cellular impurities in human somatic stem cells is simple and can be useful for the quality assessment of hCTPs in the manufacturing process.
•The performance of cell growth analysis was evaluated.•Cell growth analysis detected 0.0001% HeLa contamination in BMSCs at 47% probability.•Growth rates of ADSCs spiked with 0.001% ASC52telo was increased within 15 passages.</description><subject>Adipose-derived stem cell</subject><subject>Bone marrow-derived mesenchymal stem cell</subject><subject>Cellular therapy</subject><subject>Original</subject><subject>Quality assessment</subject><subject>Regenerative medicine</subject><subject>Tumorigenicity</subject><issn>2352-3204</issn><issn>2352-3204</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9UU1r3DAQNaWhCUn-QA9Fx1681YfllaEUQmjaQqCX9ixkabTWYluOPlI2f6d_NHI3DemlMKBh5r2nmXlV9ZbgDcGk_bDfBEjDhpZ8g0tg_qo6o4zTmlHcvH6Rn1aXMe4xxkRwQjvxpjplhDacY3JW_b5altFplZyfkbdIwziiXfC_0oDUrMZDdBElj9IA6C6r0aUDUjFCjBPMaWUMeVLzH169BK9LB8wKD2qBnJxGpWqyTrHwkEIJYnLzDk1lem-Q9QG5afIhFe2HwlyF8qjW6pKDSw7iRXVi1Rjh8uk9r37efP5x_bW-_f7l2_XVba15w1PdYsuYJVZRsoUebxvVcCa07SywLWM9Fp3pCCWGtUZBLwjvSasZYwY3vOkoO68-HXWX3E9gdFkwqFEuwU0qHKRXTv7bmd0gd_5etlyU2-Ii8P5JIPi7XBaVk4vrQmoGn6OktBFMYEFFgdIjVAcfYwD7_A3BcjVY7uVqsFwNlrgE5oX07uWAz5S_dhbAxyMAypnuHQQZtYNZg3EBdJLGu__pPwIBfLyN</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Hasebe-Takada, Nozomi</creator><creator>Kono, Ken</creator><creator>Yasuda, Satoshi</creator><creator>Sawada, Rumi</creator><creator>Matsuyama, Akifumi</creator><creator>Sato, Yoji</creator><general>Elsevier B.V</general><general>Japanese Society for Regenerative Medicine</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161201</creationdate><title>Application of cell growth analysis to the quality assessment of human cell-processed therapeutic products as a testing method for immortalized cellular impurities</title><author>Hasebe-Takada, Nozomi ; Kono, Ken ; Yasuda, Satoshi ; Sawada, Rumi ; Matsuyama, Akifumi ; Sato, Yoji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c545t-60f33f1fa217eb074a4538cf9fe3733b089d9121d36daeb815b16c333d0454923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adipose-derived stem cell</topic><topic>Bone marrow-derived mesenchymal stem cell</topic><topic>Cellular therapy</topic><topic>Original</topic><topic>Quality assessment</topic><topic>Regenerative medicine</topic><topic>Tumorigenicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hasebe-Takada, Nozomi</creatorcontrib><creatorcontrib>Kono, Ken</creatorcontrib><creatorcontrib>Yasuda, Satoshi</creatorcontrib><creatorcontrib>Sawada, Rumi</creatorcontrib><creatorcontrib>Matsuyama, Akifumi</creatorcontrib><creatorcontrib>Sato, Yoji</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Regenerative therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hasebe-Takada, Nozomi</au><au>Kono, Ken</au><au>Yasuda, Satoshi</au><au>Sawada, Rumi</au><au>Matsuyama, Akifumi</au><au>Sato, Yoji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of cell growth analysis to the quality assessment of human cell-processed therapeutic products as a testing method for immortalized cellular impurities</atitle><jtitle>Regenerative therapy</jtitle><addtitle>Regen Ther</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>5</volume><spage>49</spage><epage>54</epage><pages>49-54</pages><issn>2352-3204</issn><eissn>2352-3204</eissn><abstract>In human cell-processed therapeutic products (hCTPs) for clinical application, tumorigenic cellular impurities in the manufacturing process are a major concern. Because cellular immortalization is one of the prerequisite steps in tumorigenesis, we tested whether cell growth analysis can be employed to check for immortalized (and potentially tumorigenic) cellular impurities in hCTPs. We monitored the growth of human bone marrow-derived mesenchymal stem cells (BMSCs) mixed with HeLa cells at a ratio of 1/106 or more and compared their growth rates with that of BMSCs alone. The cell growth analysis detected a significant increase in the growth rate of the BMSCs spiked with 0.0001% HeLa within 30 days at a probability of 47%. When human adipose-derived stem cells (ADSCs) were spiked with ASC52telo cells, a human telomerase reverse transcriptase (hTERT)-immortalized adipose-derived mesenchymal stem cell line, at a ratio of 0.001% or more, their growth rates were significantly increased within 15 passages, compared with that of ADSCs alone. These results indicate that cell growth analysis for the detection of immortalized cellular impurities in human somatic stem cells is simple and can be useful for the quality assessment of hCTPs in the manufacturing process.
•The performance of cell growth analysis was evaluated.•Cell growth analysis detected 0.0001% HeLa contamination in BMSCs at 47% probability.•Growth rates of ADSCs spiked with 0.001% ASC52telo was increased within 15 passages.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31245501</pmid><doi>10.1016/j.reth.2016.06.005</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2352-3204 |
ispartof | Regenerative therapy, 2016-12, Vol.5, p.49-54 |
issn | 2352-3204 2352-3204 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6581850 |
source | DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Adipose-derived stem cell Bone marrow-derived mesenchymal stem cell Cellular therapy Original Quality assessment Regenerative medicine Tumorigenicity |
title | Application of cell growth analysis to the quality assessment of human cell-processed therapeutic products as a testing method for immortalized cellular impurities |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T11%3A39%3A30IST&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=Application%20of%20cell%20growth%20analysis%20to%20the%20quality%20assessment%20of%20human%20cell-processed%20therapeutic%20products%20as%20a%20testing%20method%20for%20immortalized%20cellular%20impurities&rft.jtitle=Regenerative%20therapy&rft.au=Hasebe-Takada,%20Nozomi&rft.date=2016-12-01&rft.volume=5&rft.spage=49&rft.epage=54&rft.pages=49-54&rft.issn=2352-3204&rft.eissn=2352-3204&rft_id=info:doi/10.1016/j.reth.2016.06.005&rft_dat=%3Cproquest_pubme%3E2248380828%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=2248380828&rft_id=info:pmid/31245501&rft_els_id=S2352320416300293&rfr_iscdi=true |