Selective inhibition of ALDH1A3 impedes breast cancer growth and metastasis by blocking ALDH1A3-driven transcriptional programs
Maya R. MacLean, Bianca Laura Bernardoni, Wasundara Fernando, Giovanni Petrarolo, Ilaria D’Agostino, Cheryl A. Dean, Jaganathan Venkatesh, Christopher S. Hughes, Kerry B. Goralski, Geetha Subramanian, Raj Pranap Arun, Hannah F. Cahill, Olivia L. Walker, Lynn N. Thomas

TL;DR
A new drug called CLM296 selectively blocks ALDH1A3, a protein linked to breast cancer growth and spread, showing promise in preclinical models.
Contribution
Development of CLM296, a first-in-class selective ALDH1A3 inhibitor with demonstrated anti-cancer effects in triple-negative breast cancer.
Findings
CLM296 inhibits ALDH1A3 with high potency (2 nM) and no off-target effects on ALDH1A1.
CLM296 reduces ALDH1A3-driven tumor growth and metastasis in TNBC xenografts.
Pharmacokinetic studies show CLM296 has favorable oral bioavailability and tissue distribution.
Abstract
Aldehyde dehydrogenase 1A3 (ALDH1A3) promotes tumor growth, metastasis, and chemoresistance in multiple cancers, including triple-negative breast cancer (TNBC), yet no clinically approved, isoform-selective inhibitors exist. Here, we present CLM296, a novel, rationally designed, highly potent ALDH1A3 inhibitor. CLM296 exhibits nanomolar inhibition of ALDH1A3 in TNBC cells (half-maximal inhibitory concentration = 2 nM) with no off-target effects on ALDH1A1. Transcriptomic analysis shows that CLM296 selectively suppresses ALDH1A3-driven gene expression, confirming on-target activity. Functionally, CLM296 impedes ALDH1A3-mediated cell invasion in vitro and, with daily dosing in vivo, significantly reduces only ALDH1A3-dependent tumor growth and lung metastasis in TNBC xenografts. These effects are accompanied by selective inhibition of ALDH1A3 target genes in tumors, while pharmacokinetic…
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Taxonomy
TopicsHistone Deacetylase Inhibitors Research · Alcohol Consumption and Health Effects · Sphingolipid Metabolism and Signaling
