Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan.
Department of Otolaryngology, Head and Neck Surgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan.
Int J Mol Sci. 2024 Aug 24;25(17):9190. doi: 10.3390/ijms25179190.
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, CMab-18 (IgM, kappa), to recognize the variant exon 10-encoded region. In the present study, a mouse IgG version of CMab-18 (CMab-18-mG) was generated to evaluate the antitumor activities against CD44-positive cells compared with the previously established anti-pan CD44 mAb, CMab-46-mG. CMab-18-mG exhibited higher reactivity compared with CMab-46-mG to CD44v3-10-overexpressed CHO-K1 (CHO/CD44v3-10) and oral squamous cell carcinoma cell lines (HSC-2 and SAS) in flow cytometry. CMab-18-mG exerted a superior antibody-dependent cellular cytotoxicity (ADCC) against CHO/CD44v3-10. In contrast, CMab-46-mG 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 CMab-18-mG or CMab-46-mG significantly suppressed CHO/CD44v3-10, HSC-2, and SAS xenograft tumor growth compared with the control mouse IgG. These results indicate that CMab-18-mG could be a promising therapeutic regimen for CD44v10-positive tumors.
CD44 调节细胞黏附、增殖、存活和干细胞特性,被认为是肿瘤治疗的靶点。CD44 具有最短的 CD44 标准型(CD44s)和多种 CD44 变体(CD44v)同工型。由于与 CD44s 相比,CD44v 的表达仅限于上皮细胞和癌,因此 CD44v 已被认为是单克隆抗体(mAb)治疗的有前途的靶点。我们之前开发了一种抗 CD44v10 mAb,CMab-18(IgM,kappa),以识别变体外显子 10 编码区域。在本研究中,生成了 CMab-18 的小鼠 IgG 版本(CMab-18-mG),以评估其与先前建立的抗泛 CD44 mAb,CMab-46-mG 相比,对 CD44 阳性细胞的抗肿瘤活性。与 CMab-46-mG 相比,CMab-18-mG 在流式细胞术上对过表达 CD44v3-10 的 CHO-K1(CHO/CD44v3-10)和口腔鳞状细胞癌细胞系(HSC-2 和 SAS)具有更高的反应性。CMab-18-mG 对 CHO/CD44v3-10 发挥了更好的抗体依赖性细胞毒性(ADCC)作用。相比之下,CMab-46-mG 对 CHO/CD44v3-10 表现出更好的补体依赖性细胞毒性(CDC)。在对 HSC-2 和 SAS 的 ADCC 和 CDC 中也观察到类似的趋势。此外,与对照小鼠 IgG 相比,给予 CMab-18-mG 或 CMab-46-mG 可显著抑制 CHO/CD44v3-10、HSC-2 和 SAS 异种移植肿瘤的生长。这些结果表明,CMab-18-mG 可能是 CD44v10 阳性肿瘤的一种有前途的治疗方案。