TY - JOUR
T1 - Patient-derived oral mucosa organoids as an in vitro model for methotrexate induced toxicity in pediatric acute lymphoblastic leukemia
AU - Driehuis, E
AU - Oosterom, N
AU - Heil, S G
AU - Muller, I B
AU - Lin, M
AU - Kolders, S
AU - Jansen, G
AU - de Jonge, R
AU - Pieters, R
AU - Clevers, H
AU - van den Heuvel-Eibrink, M M
N1 - Funding Information:
Funded by the Oncode Institute (partly financed by the Dutch Cancer Society), by the gravitation program CancerGenomiCs.nl from the Netherlands Organization for Scientific Research (NWO) and by a Stand Up to Cancer International Translational Cancer Research Grant, a program of the Entertainment Industry Foundation administered by the AACR (SU2C-AACR-DT1213) and a ZonMw grant (116.006.103)
Publisher Copyright:
© 2020 Driehuis et al.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/5/18
Y1 - 2020/5/18
N2 - We have recently established a protocol to grow wildtype human oral mucosa organoids. These three-dimensional structures can be maintained in culture long-term, do not require immortalization, and recapitulate the multilayered composition of the epithelial lining of the oral mucosa. Here, we validate the use of this model to study the effect of Leucovorin (LV) on Methotrexate (MTX)-induced toxicity. MTX is a chemotherapeutic agent used in the treatment of pediatric acute lymphoblastic leukemia. Although effective, the use of MTX often results in severe side-effects, including oral mucositis, which is characterized by epithelial cell death. Here, we show that organoids are sensitive to MTX, and that the addition of LV reduces MTX toxicity, in both a concentration- and timing-dependent manner. Additionally, we show that a 24 hour 'pretreatment' with LV reduces MTX-induced cell death, suggesting that such a pretreatment could decrease mucositis in patients. Taken together, we provide the first in vitro model to study the effect of MTX on wildtype oral mucosa cells. Our findings underscore the relevance of the clinically applied LV regimen and highlight the potential of this model to further optimize modifications in dosing and timing of Leucovorin on oral mucosa cells.
AB - We have recently established a protocol to grow wildtype human oral mucosa organoids. These three-dimensional structures can be maintained in culture long-term, do not require immortalization, and recapitulate the multilayered composition of the epithelial lining of the oral mucosa. Here, we validate the use of this model to study the effect of Leucovorin (LV) on Methotrexate (MTX)-induced toxicity. MTX is a chemotherapeutic agent used in the treatment of pediatric acute lymphoblastic leukemia. Although effective, the use of MTX often results in severe side-effects, including oral mucositis, which is characterized by epithelial cell death. Here, we show that organoids are sensitive to MTX, and that the addition of LV reduces MTX toxicity, in both a concentration- and timing-dependent manner. Additionally, we show that a 24 hour 'pretreatment' with LV reduces MTX-induced cell death, suggesting that such a pretreatment could decrease mucositis in patients. Taken together, we provide the first in vitro model to study the effect of MTX on wildtype oral mucosa cells. Our findings underscore the relevance of the clinically applied LV regimen and highlight the potential of this model to further optimize modifications in dosing and timing of Leucovorin on oral mucosa cells.
KW - Adolescent
KW - Antineoplastic Combined Chemotherapy Protocols/adverse effects
KW - Apoptosis/drug effects
KW - Child
KW - Humans
KW - In Vitro Techniques
KW - Leucovorin/administration & dosage
KW - Methotrexate/administration & dosage
KW - Mouth Mucosa/drug effects
KW - Organ Culture Techniques
KW - Organoids/drug effects
KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy
KW - Stomatitis/chemically induced
UR - http://www.scopus.com/inward/record.url?scp=85084901724&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0231588
DO - 10.1371/journal.pone.0231588
M3 - Article
C2 - 32421698
SN - 1932-6203
VL - 15
JO - PLoS ONE
JF - PLoS ONE
IS - 5
M1 - e0231588
ER -