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Establishment of Coala: a novel 3D and 2D cancer cell line derived from colorectal cancer liver metastasis

Sandra Mersakova; Juraj Marcinek; Dusan Brany; Olga Chodelkova; Martin Vorcak; Martin Cermak; Martina Poturnajova; Zuzana Kozovska; Henrieta Skovierova; Slavomira Novakova; Barbora Mitruskova; Dusan Loderer; Marian Grendar; Veronika Holubekova; Andrea Hornakova; Jana Melegova; Mariana Brozmanova; Blazej Palkoci; Martin Vojtko; Roman Kycina; Miroslav Pindura; Jan Janik; Peter Mikolajcik; Eva Gabonova; Ludovit Laca; Andreas Nicodemou; Lubos Danisovic; Lukas Plank; Erika Halasova; Marek Mraz; Miroslava Matuskova; Zora Lasabova; Michal Kalman; Jan Strnadel
Human Cell · Vol. 38, Issue 5 · 2025

Abstract

Metastatic colorectal cancer is one of the most critical causes of cancer-related dead in patients suffering this type of malignancy. As the liver metastases are found in almost 25–50% of all colorectal cancer patients, there is an urgent need for suitable in vitro and in vivo models. To the best of our knowledge, only a limited number of well-described 2D or 3D organoid/spheroid cell lines originated from human liver metastases was reported for this type of malignancy and submitted to ATCC and other repository centers for general use. Here, we present a novel, well-characterized cell line Coala that was derived directly from liver metastasis of patient with colorectal cancer. Coala cancer cell line was derived by 2D and 3D culture technology and can be, therefore, cultured as standard 2D cell line or as 3D spheroid culture. When transplanted into athymic mice, Coala cell line forms fast growing tumors with histological features similar to original tumor and expressed CDX2, SATB2, and CK20 . Whole exome sequencing analysis of Coala cell line showed the presence of pathogenic mutations in C8B , PRKCQ , IRGM , FGFR4 , POLR1C , APC and TP53 genes. As verified by antibody array chip analysis, Coala cells express Snail , Pdx-1 , FoxA2, and E-cadherin . Our cell line represents a new, well characterized in vitro research tool for cancer research and will be available to researchers in the field via biorepository centers.

Bibliographic Information

JournalHuman Cell
PublisherSpringer
Publication Date2025-08-04
Publication Year2025
Volume38
Issue5
Document TypeJournal Article
eISSN1749-0774
DOI10.1007/s13577-025-01256-1

Access Information

NARA Access Coverage2002-01-01~Current
Journal Homepagehttps://www.springer.com/journal/13577
Publisher PageOpen Publisher Page
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