Gold Nanorods Exhibit Intrinsic Therapeutic Activity via Controlling <i>N</i>6-Methyladenosine-Based Epitranscriptomics in Acute Myeloid Leukemia.

Abstract

Reprograming the <i>N</i>6-methyladenosine (m⁶A) landscape is a promising therapeutic strategy against recalcitrant leukemia. In this study, we synthesized gold nanorods (GNRs) of different aspect ratios using a binary surfactant mixture of hexadecyltrimethylammonium bromide and sodium oleate. Following surface functionalization with chitosan and a 12-mer peptide, GNRa-CSP12 measuring 130 × 21 nm² was selectively taken up by leukemia cells via targeted endocytosis. Low doses of GNRa-CSP12 inhibited the growth of leukemia cells by disrupting the redox balance and inducing ferroptosis. Mechanistically, GNRa-CSP12 abrogated endogenous Fe²⁺-dependent m⁶A demethylase activity, which led to global m⁶A hypomethylation and post-transcriptional regulation of downstream genes that are involved in glycolysis, hypoxia, and immune checkpoint pathways. In addition, combination treatment with GNRa-CSP12 and tyrosine kinases inhibitors (TKIs) synergistically obviated the m⁶A-mediated TKI resistance phenotype. Finally, GNRa-CSP12 as a potential immunotherapeutic agent could enhance immunotherapy outcome in leukemia. Our preclinical findings provide the proof-of-concept for targeting m⁶A-methylation-based epitranscriptomics using nanoparticle as an "epigenetic drug" for cancer therapy.