Platelet-Rich and Platelet-Poor Plasma Might Play Supportive Roles in Cancer Cell Culture: A Replacement for Fetal Bovine Serum?


Journal

Anti-cancer agents in medicinal chemistry
ISSN: 1875-5992
Titre abrégé: Anticancer Agents Med Chem
Pays: Netherlands
ID NLM: 101265649

Informations de publication

Date de publication:
28 10 2021
Historique:
received: 22 07 2020
revised: 17 10 2020
accepted: 26 10 2020
pubmed: 6 1 2021
medline: 21 1 2022
entrez: 5 1 2021
Statut: ppublish

Résumé

Platelet-Rich (PRP) and Platelet-Poor plasma (PPP) are widely used in research and clinical platforms mainly due to their capacities to enhance cell growth. Although the short half-life (5 days) and the high price of platelet products pose challenges regarding their usage, they maintain the growth regulatory functions for weeks. Thus, we aimed to assess the supplementary values of these products in human CCRF- CEM cancer cells. Mechanistically, we also checked if the PRP/PPP treatment enhances YKL-40 expression as a known protein regulating cell growth. The PRP/PPP was prepared from healthy donors using manual stepwise centrifugation and phase separation. The viability of the cells treated with gradient PRP/PPP concentrations (2, 5, 10, and 15%) was measured by the MTT assay. The YKL-40 mRNA and protein levels were assessed using qRT-PCR and western blotting. The data were compared to FBS-treated cells. Our findings revealed that the cells treated by PRP/PPP not only were morphologically comparable to those treated by FBS but also showed greater viability at the concentrations of 10 and 15%. Moreover, it was shown that PRP/PPP induce cell culture support, at least in part, via inducing YKL-40 expression at both mRNA and protein levels in a time- and dose-dependent manner. Collectively, by showing cell culture support comparable to FBS, the PRP/PPP might be used as good candidates to supplement the cancer cell culture and overcome concerns regarding the use of FBS as a non-human source in human cancer research.

Sections du résumé

BACKGROUND
Platelet-Rich (PRP) and Platelet-Poor plasma (PPP) are widely used in research and clinical platforms mainly due to their capacities to enhance cell growth. Although the short half-life (5 days) and the high price of platelet products pose challenges regarding their usage, they maintain the growth regulatory functions for weeks. Thus, we aimed to assess the supplementary values of these products in human CCRF- CEM cancer cells. Mechanistically, we also checked if the PRP/PPP treatment enhances YKL-40 expression as a known protein regulating cell growth.
METHODS
The PRP/PPP was prepared from healthy donors using manual stepwise centrifugation and phase separation. The viability of the cells treated with gradient PRP/PPP concentrations (2, 5, 10, and 15%) was measured by the MTT assay. The YKL-40 mRNA and protein levels were assessed using qRT-PCR and western blotting. The data were compared to FBS-treated cells.
RESULTS
Our findings revealed that the cells treated by PRP/PPP not only were morphologically comparable to those treated by FBS but also showed greater viability at the concentrations of 10 and 15%. Moreover, it was shown that PRP/PPP induce cell culture support, at least in part, via inducing YKL-40 expression at both mRNA and protein levels in a time- and dose-dependent manner.
CONCLUSION
Collectively, by showing cell culture support comparable to FBS, the PRP/PPP might be used as good candidates to supplement the cancer cell culture and overcome concerns regarding the use of FBS as a non-human source in human cancer research.

Identifiants

pubmed: 33397262
pii: ACAMC-EPUB-112972
doi: 10.2174/1871520621999210101225912
doi:

Substances chimiques

Serum Albumin, Bovine 27432CM55Q

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2236-2242

Subventions

Organisme : Tabriz University of Medical Sciences
ID : 94/74

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Mehdi Talebi (M)

Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Mousa Vatanmakanian (M)

Department of Biochemistry and Molecular Biology, LSUHSC, School of Medicine, New Orleans, LA, United States.

Ali Mirzaei (A)

Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

Yaghoub Barfar (Y)

Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

Maryam Hemmatzadeh (M)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Milad A Nahayati (MA)

Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Kobra Velaei (K)

Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Asghar Hosseinzadeh (A)

Department of Biology, Tabriz Branch, Islamic Azad. University, Tabriz, Iran.

Behruz Yazdanpanah (B)

Department of Laboratory Sciences, School Paramedics, Yasuj University of Medical Sciences, Yasuj, Iran.

Yahya Yahyavi (Y)

Department of Immunology, Tabriz University of Medical Sciences, Tabriz, Iran.

Ako Azimi (A)

Department of Basic Sciences, Maragheh University of Medical Sciences, Maragheh, Iran.

Mina Rahmani (M)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Milad Z Heydarabad (MZ)

Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

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Classifications MeSH