Bladder cancer therapy using a conformationally fluid tumoricidal peptide complex.
Antonín BrisudaJames C S HoPancham S KandiyalJustin T-Y NgMurphy Lam Yim WanDaniel S C ButlerJaromir HáčekMurphy Lam Yim WanThi Hien TranAftab NadeemTuan Hiep TranAnna HastingsPetter StormDaniel L FortunatiParisa EsmaeiliHana NovotnaJakub HorňákYuguang MuK H MokMarek BabjukCatharina SvanborgPublished in: Nature communications (2021)
Partially unfolded alpha-lactalbumin forms the oleic acid complex HAMLET, with potent tumoricidal activity. Here we define a peptide-based molecular approach for targeting and killing tumor cells, and evidence of its clinical potential (ClinicalTrials.gov NCT03560479). A 39-residue alpha-helical peptide from alpha-lactalbumin is shown to gain lethality for tumor cells by forming oleic acid complexes (alpha1-oleate). Nuclear magnetic resonance measurements and computational simulations reveal a lipid core surrounded by conformationally fluid, alpha-helical peptide motifs. In a single center, placebo controlled, double blinded Phase I/II interventional clinical trial of non-muscle invasive bladder cancer, all primary end points of safety and efficacy of alpha1-oleate treatment are reached, as evaluated in an interim analysis. Intra-vesical instillations of alpha1-oleate triggers massive shedding of tumor cells and the tumor size is reduced but no drug-related side effects are detected (primary endpoints). Shed cells contain alpha1-oleate, treated tumors show evidence of apoptosis and the expression of cancer-related genes is inhibited (secondary endpoints). The results are especially encouraging for bladder cancer, where therapeutic failures and high recurrence rates create a great, unmet medical need.
Keyphrases
- magnetic resonance
- clinical trial
- healthcare
- oxidative stress
- muscle invasive bladder cancer
- randomized controlled trial
- cell cycle arrest
- poor prognosis
- cell death
- computed tomography
- radiation therapy
- magnetic resonance imaging
- cell proliferation
- molecular dynamics
- double blind
- induced apoptosis
- papillary thyroid
- dna methylation
- pi k akt
- phase iii
- cell therapy
- endoplasmic reticulum