A groundbreaking study recently published in the prestigious journal Acta Pharmaceutica Sinica B has unveiled a promising new therapeutic candidate, DHL-11, a novel prieurianin-type limonoid isolated from the plant Munronia henryi, which shows potent efficacy against triple-negative breast cancer (TNBC). TNBC remains one of the most challenging and aggressive subtypes of breast cancer, noted for its poor prognosis due to the lack of targeted therapies and resistance to conventional treatments. This discovery holds significant promise in addressing this urgent medical need.
TNBC accounts for approximately 15-20% of breast cancer cases and is defined by the absence of estrogen receptor (ER), progesterone receptor (PR), and HER2 receptor expression, which severely limits treatment options. The newly identified compound DHL-11 emerges as a targeted agent exhibiting robust antitumor activity, selectively striking at a molecular vulnerability in TNBC cells. This compound represents a novel class of naturally derived prieurianin-type limonoids, a group of triterpenoids known for diverse biological activities, yet unexplored in this oncological context until now.
The research delves into the biochemical underpinnings of how DHL-11 exerts its anticancer effects. Experimental evidence demonstrates that DHL-11 effectively curtails TNBC cell proliferation and impairs their migratory capabilities, crucial factors in tumor growth and metastasis. The compound induces arrest of TNBC cells in the G2/M phase of the cell cycle, a checkpoint that ensures DNA integrity before mitosis, thereby halting cellular division. Further, DHL-11 promotes apoptotic cell death, amplifying cytotoxic effects against cancerous cells.
A particularly compelling feature of DHL-11 is its ability to elevate intracellular reactive oxygen species (ROS) levels. ROS are chemically reactive molecules that, in excess, induce oxidative stress, damaging DNA and other cellular components. The study observes that DHL-11 triggers a surge in ROS accumulation within TNBC cells, precipitating DNA damage that undermines cellular survival and replication processes. This mechanistic insight places oxidative stress induction at the center of DHL-11’s anticancer activity.
At the molecular level, DHL-11 targets inosine monophosphate dehydrogenase 2 (IMPDH2), an essential enzyme involved in guanine nucleotide biosynthesis. IMPDH2 catalyzes the rate-limiting step of converting inosine monophosphate (IMP) to xanthosine monophosphate (XMP), ultimately leading to guanine nucleotide triphosphate (GTP) production, critical for DNA and RNA synthesis. The study reveals that DHL-11 binds specifically to a non-catalytic pocket on IMPDH2, a novel binding site distinct from the enzyme’s active center.
Intriguingly, this binding disrupts the interaction between IMPDH2 and another protein, FANCI (Fanconi anemia complementary group I), which is known for its role in DNA repair. The dissociation destabilizes IMPDH2, triggering its degradation via the cellular protein degradation machinery. Loss of IMPDH2 function drastically reduces guanine synthesis, depleting nucleotide pools required for tumor cell proliferation and increasing susceptibility to DNA replication stress.
The degradation of IMPDH2 caused by DHL-11 culminates in a cascade of cellular disturbances. Guanine scarcity contributes to impediments in DNA replication fidelity, while concurrent ROS accumulation exacerbates DNA damage. This dual assault on cancer cell genomic maintenance mechanisms leads to replication stress and ultimately to apoptosis of TNBC cells. The therapeutic implications of these findings highlight a multifaceted approach leveraging metabolic disruption and oxidative damage.
Importantly, the translational potential of DHL-11 is underscored by its efficacy in patient-derived breast cancer organoids characterized by high IMPDH2 expression. These 3D organoid models recapitulate patient tumor architecture and heterogeneity, rendering them highly predictive for clinical outcomes. DHL-11 markedly suppressed the growth of these organoids, providing preclinical evidence supporting its development as a viable anti-TNBC agent.
In vivo validation was further achieved in TNBC xenograft models, where systemic administration of DHL-11 significantly inhibited tumor growth and metastasis. These animal studies not only confirmed the compound’s antitumor activity but also demonstrated an encouraging biosafety profile, with no significant adverse effects observed. This favorable therapeutic index enhances DHL-11’s appeal as a drug candidate worthy of further clinical investigation.
Collectively, these findings position DHL-11 as a pioneering IMPDH2 degrader with unique mechanisms disrupting tumor nucleotide metabolism and DNA repair pathways. This dual mechanism induces cytotoxicity in cancer cells exhibiting elevated IMPDH2 expression, particularly the notoriously treatment-resistant TNBC subtype. Such targeted biochemical interference may represent a new frontier in precision oncology.
This landmark study not only enriches the pharmacological landscape with a novel natural compound but also sets the stage for future research exploring prieurianin-type limonoids as a source of anticancer therapeutics. The compelling data encourage expansion into clinical trials, potentially offering renewed hope for patients battling triple-negative breast cancer, which has historically lacked effective targeted drugs.
The promising capacity for DHL-11 to selectively degrade IMPDH2 and induce lethal DNA damage suggests a broader application scope beyond TNBC, possibly extending to other malignancies reliant on guanine nucleotide biosynthesis. Continued exploration of this compound’s mechanism may unravel further insights into the intricate interplay between metabolic enzymes and DNA repair in cancer pathophysiology.
In essence, DHL-11 embodies a molecular breakthrough by leveraging targeted enzyme degradation and oxidative stress augmentation to undermine TNBC cell survival. This innovative approach exemplifies the fusion of natural product discovery and molecular oncology, underscoring the potential of plant-derived compounds in addressing formidable cancer subtypes like triple-negative breast cancer.
Subject of Research: Investigation of DHL-11, a prieurianin-type limonoid from Munronia henryi, as a targeted IMPDH2 degrader for the treatment of triple-negative breast cancer.
Article Title: DHL-11, a novel prieurianin-type limonoid isolated from Munronia henryi, targeting IMPDH2 to inhibit triple-negative breast cancer.
News Publication Date: Not explicitly provided (article in Acta Pharmaceutica Sinica B, Volume 16, Issue 1, 2026).
Web References:
DOI Link: http://dx.doi.org/10.1016/j.apsb.2025.10.031
Journal Site: https://www.sciencedirect.com/journal/acta-pharmaceutica-sinica-b
Keywords: Limonoids, DHL-11, Triple-negative breast cancer (TNBC), Reactive oxygen species (ROS), DNA damage, IMPDH2, Guanine synthesis, FANCI, Apoptosis, Cell cycle arrest, Metastasis, Enzyme degradation.
Tags: Acta Pharmaceutica Sinica B publicationalternative breast cancer therapiesDHL-11 limonoidIMPDH2 targeting in cancermetastatic cancer researchMunronia henryi extractnatural compounds in oncologynovel anticancer agentsprieurianin-type limonoidsTNBC therapeutic strategiestriple negative breast cancer treatmenttumor growth inhibition
