# Anti-CD44 Variant 10 Monoclonal Antibody Exerts Antitumor Activity in Mouse Xenograft Models of Oral Squamous Cell Carcinomas

**Authors:** Kenichiro Ishikawa, Hiroyuki Suzuki, Tomokazu Ohishi, Guanjie Li, Tomohiro Tanaka, Manabu Kawada, Akira Ohkoshi, Mika K. Kaneko, Yukio Katori, Yukinari Kato

PMC · DOI: 10.3390/ijms25179190 · International Journal of Molecular Sciences · 2024-08-24

## TL;DR

A new monoclonal antibody targeting CD44v10 shows strong antitumor effects in mouse models of oral cancer.

## Contribution

Development and evaluation of a novel anti-CD44v10 monoclonal antibody with superior antitumor activity.

## Key findings

- C44Mab-18-mG2a showed higher reactivity and ADCC against CD44v3–10-expressing cells.
- Both C44Mab-18-mG2a and C44Mab-46-mG2a significantly suppressed tumor growth in xenograft models.
- C44Mab-18-mG2a is a promising therapeutic option for CD44v10-positive tumors.

## Abstract

CD44 regulates cell adhesion, proliferation, survival, and stemness and has been considered a tumor therapy target. CD44 possesses the shortest CD44 standard (CD44s) and a variety of CD44 variant (CD44v) isoforms. Since the expression of CD44v is restricted in epithelial cells and carcinomas compared to CD44s, CD44v has been considered a promising target for monoclonal antibody (mAb) therapy. We previously developed an anti-CD44v10 mAb, C44Mab-18 (IgM, kappa), to recognize the variant exon 10-encoded region. In the present study, a mouse IgG2a version of C44Mab-18 (C44Mab-18-mG2a) was generated to evaluate the antitumor activities against CD44-positive cells compared with the previously established anti-pan CD44 mAb, C44Mab-46-mG2a. C44Mab-18-mG2a exhibited higher reactivity compared with C44Mab-46-mG2a to CD44v3–10-overexpressed CHO-K1 (CHO/CD44v3–10) and oral squamous cell carcinoma cell lines (HSC-2 and SAS) in flow cytometry. C44Mab-18-mG2a exerted a superior antibody-dependent cellular cytotoxicity (ADCC) against CHO/CD44v3–10. In contrast, C44Mab-46-mG2a showed a superior complement-dependent cytotoxicity (CDC) against CHO/CD44v3–10. A similar tendency was observed in ADCC and CDC against HSC-2 and SAS. Furthermore, administering C44Mab-18-mG2a or C44Mab-46-mG2a significantly suppressed CHO/CD44v3–10, HSC-2, and SAS xenograft tumor growth compared with the control mouse IgG2a. These results indicate that C44Mab-18-mG2a could be a promising therapeutic regimen for CD44v10-positive tumors.

## Linked entities

- **Genes:** CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960]
- **Proteins:** CD44 (CD44 molecule (IN blood group)), cd44.S (CD44 molecule (IN blood group) S homeolog)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Ighv1-9 (immunoglobulin heavy variable 1-9) [NCBI Gene 668478] {aka Gm16697, Igg2a}, Cd44 (CD44 antigen) [NCBI Gene 12505] {aka HERMES, Ly-24, Pgp-1}, LOC641025 (Ig heavy chain Mem5-like) [NCBI Gene 641025] {aka CRP55H, IGHV, IgVH, Igh, Igm}
- **Diseases:** complement (MESH:D007153), carcinomas (MESH:D009369), Oral Squamous Cell Carcinomas (MESH:D000077195), cytotoxicity (MESH:D064420)
- **Chemicals:** C44Mab-18 (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** HSC-2 — Homo sapiens (Human), Oral cavity squamous cell carcinoma, Cancer cell line (CVCL_1287), SAS — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_1675), CHO-K1 — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0214), CHO — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0213)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11395228/full.md

## References

80 references — full list in the complete paper: https://tomesphere.com/paper/PMC11395228/full.md

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Source: https://tomesphere.com/paper/PMC11395228