A high-sensitivity ELISA for detection of human FGF18 in culture supernatants from tumor cell lines

Tsuchiya, Y.; Komazawa-Sakon, S.; Tanaka, M.; Kanakogi, T.; Moriwaki, K.; Akiba, H.; Yagita, H.; Okumura, K.; Entzminger, K.; Okumura, C.; Maruyama, T.; Nakano, H.

doi:10.1101/2023.06.16.545249

bioRxiv · 10.1101/2023.06.16.545249

A high-sensitivity ELISA for detection of human FGF18 in culture supernatants from tumor cell lines

Tsuchiya, Y.·Komazawa-Sakon, S.·Tanaka, M.·Kanakogi, T.·Moriwaki, K.·Akiba, H.·Yagita, H.·Okumura, K.·Entzminger, K.·Okumura, C.·Maruyama, T.·Nakano, H.

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Abstract

Fibroblast growth factor 18 (FGF18) is elevated in several human cancers, such as gastrointestinal and ovarian cancers, and stimulates the proliferation of tumor cells. This suggests that FGF18 may be a promising candidate biomarker in cancer patients. However, the lack of a high-sensitivity enzyme-linked immunosorbent assay (ELISA) does not permit testing of this possibility. In this study, we generated monoclonal antibodies against human FGF18 and developed a high-sensitivity ELISA to measure human FGF18 at concentrations as low as 10 pg/mL. Of the eight tumor cell lines investigated, we detected human FGF18 in culture supernatants from four tumor cell lines, including HeLa, OVCAR-3, BxPC-3, and SW620 cells, albeit the production levels were relatively low in the latter two cell lines. Moreover, the in-house ELISA could detect murine FGF18 in sera from mice overexpressing murine Fgf18 in hepatocytes, although the sensitivity in detecting murine FGF18 was relatively low. This FGF18 ELISA could be a valuable tool to validate FGF18 as a potential biomarker for cancer patients and to test the contribution of FGF18 for various disease models in vivo and in vitro.

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Tsuchiya, Y., Komazawa-Sakon, S., Tanaka, M., Kanakogi, T., Moriwaki, K., Akiba, H., Yagita, H., Okumura, K., Entzminger, K., Okumura, C., Maruyama, T., Nakano, H.. 2023-06-19. A high-sensitivity ELISA for detection of human FGF18 in culture supernatants from tumor cell lines. https://doi.org/10.1101/2023.06.16.545249

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