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The downregulation of ADH4 expression induces hepatocyte apoptosis, thereby contributing to liver fibrosis and the initiation of hepatocellular carcinoma (HCC). Moreover, sustained suppression of ADH4 in HCC cells disrupts retinoic acid synthesis, leading to reduced expression of the Wnt/β-catenin signaling inhibitor WIF-1 via RARs/RXRs-mediated mechanisms. This disruption fosters the upregulation of oncogenic regulators such as c-Myc and Cyclin D1, thereby accelerating HCC progression. Notably, the combination therapy involving all-trans retinoic acid (ATRA) and cisplatin exhibits a pronounced synergistic antitumor effect.
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Credit: Dr. Nan Wang
A research team from the Air Force Medical University in China has uncovered a critical mechanistic link between retinol metabolism and the progression of hepatocellular carcinoma (HCC). Published in Medcomm-Oncology, their study identifies alcohol dehydrogenase 4 (ADH4), the enzyme responsible for converting retinol (vitamin A) to its bioactive metabolite retinoic acid (RA), serves as a key suppressor of HCC.
While retinol metabolism has long been associated with liver physiology, its specific role in oncogenic regulation has remained poorly understood. By conducting analysis of HCC transcriptomic profiling, the researchers identified retinol metabolism as the most significantly dysregulated pathway in HCC tissues. They observed a marked downregulation of ADH4 expression in tumor tissues compared to adjacent cirrhotic regions, and low ADH4 levels were linked to poorer patient survival and higher recurrence rates, underscoring its potential as a prognostic biomarker.
Functional studies revealed that silencing ADH4 in HCC cell lines heightened proliferative activity and colony formation, while forced ADH4 expression in cells with low endogenous levels reversed these oncogenic traits. Mechanistic investigations further demonstrated that loss of ADH4 reduces intracellular RA concentrations, thereby impairing the activation of retinoid receptors (RAR/RXR). These nuclear receptors are known to counteract the Wnt/β-catenin signaling pathway, a frequently hyperactivated oncogenic cascade in HCC that drives unchecked cellular proliferation. Through this regulatory mechanism, ADH4-mediated RA production emerges as a critical metabolic checkpoint in hepatocarcinogenesis.
In vivo experiments showed that ADH4 overexpression significantly reduced tumor burden. Moreover, the combination of RA with cisplatin demonstrated synergistic anti-tumor efficacy, leading to greater reductions in tumor growth compared to either treatment alone. This combinatorial approach also improved survival rates without inducing significant systemic toxicity, addressing a major challenge associated with current HCC therapies.
Interestingly, the study also uncovered a dual role for ADH4: while its deficiency promotes HCC progression, its overexpression promotes liver fibrosis by inducing apoptosis in normal hepatocytes. This tissue-specific dichotomy highlights the complex interplay of retinol metabolism in hepatic homeostasis and cancer progression, emphasizing the need for therapeutic strategies that selectively target malignant cells while preserving normal liver function.
These findings suggest two promising translational applications: the use of ADH4 expression levels for prognostic stratification of HCC patients and the implementation of RA-based combination therapies to improve treatment outcomes. Future research should aim to validate these results in larger clinical cohorts and explore the immunomodulatory effects of RA within the tumor microenvironment to further refine therapeutic interventions.
See the article:
Alcohol dehydrogenase 4-mediated retinol metabolism inhibits hepatocellular carcinoma progression through inhibiting the Wnt/β-catenin pathway
Journal
MedComm – Oncology
DOI
10.1002/mog2.70021
Article Title
Alcohol Dehydrogenase 4-Mediated Retinol Metabolism Inhibits Hepatocellular Carcinoma Progression Through Inhibiting the Wnt/β-Catenin Pathway
Article Publication Date
24-Apr-2025
Media Contact
Chunhua Li
Sichuan International Medical Exchange and Promotion Association
Cell: 17738402936
Journal
MedComm – Oncology
DOI
10.1002/mog2.70021
Article Title
Alcohol Dehydrogenase 4-Mediated Retinol Metabolism Inhibits Hepatocellular Carcinoma Progression Through Inhibiting the Wnt/β-Catenin Pathway
Article Publication Date
24-Apr-2025
bu içeriği en az 2000 kelime olacak şekilde ve alt başlıklar ve madde içermiyecek şekilde ünlü bir science magazine için İngilizce olarak yeniden yaz. Teknik açıklamalar içersin ve viral olacak şekilde İngilizce yaz. Haber dışında başka bir şey içermesin. Haber içerisinde en az 12 paragraf ve her bir paragrafta da en az 50 kelime olsun. Cevapta sadece haber olsun. Ayrıca haberi yazdıktan sonra içerikten yararlanarak aşağıdaki başlıkların bilgisi var ise haberin altında doldur. Eğer yoksa bilgisi ilgili kısmı yazma.:
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Keywords
Tags: ADH4 expression and hepatocyte apoptosisAir Force Medical University liver researchATRA and cisplatin combination therapyhepatocellular carcinoma progression mechanismsliver cancer treatmentliver fibrosis and cancer initiationoncogenic regulators in hepatocellular carcinomaresearch advancements in liver cancer therapyretinoic acid metabolism in HCCsynergistic antitumor effectstherapeutic potential of retinoic acidWnt/β-catenin signaling in liver cancer
