Multimeric Anti-DR5 IgM Agonist Antibody IGM-8444 Is a Potent Inducer of Cancer Cell Apoptosis and Synergizes with Chemotherapy and BCL-2 Inhibitor ABT-199.
Beatrice T WangTasnim KothambawalaLing WangThomas J MatthewSusan E CalhounAvneesh K SainiMaya F KotturiGenevive HernandezEric W HumkeMarvin S PetersonAngus M SinclairBruce A KeytPublished in: Molecular cancer therapeutics (2021)
Death receptor 5 (DR5) is an attractive target for cancer therapy due to its broad upregulated expression in multiple cancers and ability to directly induce apoptosis. Though anti-DR5 IgG antibodies have been evaluated in clinical trials, limited efficacy has been attributed to insufficient receptor crosslinking. IGM-8444 is an engineered, multivalent agonistic IgM antibody with 10 binding sites to DR5 that induces cancer cell apoptosis through efficient DR5 multimerization. IGM-8444 bound to DR5 with high avidity and was substantially more potent than an IgG with the same binding domains. IGM-8444 induced cytotoxicity in a broad panel of solid and hematologic cancer cell lines but did not kill primary human hepatocytes in vitro, a potential toxicity of DR5 agonists. In multiple xenograft tumor models, IGM-8444 monotherapy inhibited tumor growth, with strong and sustained tumor regression observed in a gastric PDX model. When combined with chemotherapy or the BCL-2 inhibitor ABT-199, IGM-8444 exhibited synergistic in vitro tumor cytotoxicity and enhanced in vivo efficacy, without augmenting in vitro hepatotoxicity. These results support the clinical development of IGM-8444 in solid and hematologic malignancies as a monotherapy and in combination with chemotherapy or BCL-2 inhibition.
Keyphrases
- editorial comment
- cancer therapy
- papillary thyroid
- clinical trial
- oxidative stress
- cell proliferation
- squamous cell
- locally advanced
- poor prognosis
- endothelial cells
- endoplasmic reticulum stress
- randomized controlled trial
- binding protein
- cell death
- combination therapy
- drug induced
- radiation therapy
- drug delivery
- open label
- rectal cancer
- transcription factor
- risk assessment
- long non coding rna
- young adults
- cell cycle arrest
- anti inflammatory
- pi k akt