TY - JOUR
T1 - Phenotypic screening system using three-dimensional (3D) culture models for natural product screening
AU - Suenaga, Hikaru
AU - Kagaya, Noritaka
AU - Kawada, Manabu
AU - Tatsuda, Daisuke
AU - Sato, Toshiro
AU - Shin-ya, Kazuo
N1 - Funding Information:
Acknowledgements This work was supported by Technology Research Association for Next Generation Natural Products Chemistry.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to the Japan Antibiotics Research Association.
PY - 2021/10
Y1 - 2021/10
N2 - Recent progress in three-dimensional (3D) cell culture systems has attracted much attention in the fields of basic life science and drug development. Newly established methods include 3D co-culture, spheroid culture, and organoid culture; these methods enable more human tissue-like culture and have largely replaced traditional two-dimensional (2D) monolayer culture. By combining 3D culture methods with high-content imaging analysis, it is possible to obtain diverse and convincing data even during initial screening (which requires rapid and easy operating procedures). Until recently, 3D culture methods were considered expensive, time-consuming, complex, and unstable. However, by exploiting the self-assembling nature of cells and adding several technical improvements, we have developed several phenotypic screenings aimed at discovering anticancer compounds.
AB - Recent progress in three-dimensional (3D) cell culture systems has attracted much attention in the fields of basic life science and drug development. Newly established methods include 3D co-culture, spheroid culture, and organoid culture; these methods enable more human tissue-like culture and have largely replaced traditional two-dimensional (2D) monolayer culture. By combining 3D culture methods with high-content imaging analysis, it is possible to obtain diverse and convincing data even during initial screening (which requires rapid and easy operating procedures). Until recently, 3D culture methods were considered expensive, time-consuming, complex, and unstable. However, by exploiting the self-assembling nature of cells and adding several technical improvements, we have developed several phenotypic screenings aimed at discovering anticancer compounds.
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U2 - 10.1038/s41429-021-00457-8
DO - 10.1038/s41429-021-00457-8
M3 - Review article
C2 - 34326483
AN - SCOPUS:85111685677
SN - 0021-8820
VL - 74
SP - 660
EP - 666
JO - Journal of Antibiotics
JF - Journal of Antibiotics
IS - 10
ER -