Lactate Dehydrogenase and its clinical significance in pancreatic and thoracic cancers
- PMID: 36096316
- DOI: 10.1016/j.semcancer.2022.09.001
Lactate Dehydrogenase and its clinical significance in pancreatic and thoracic cancers
Abstract
The energy metabolism of tumor cells is considered one of the hallmarks of cancer because it is different from normal cells and mainly consists of aerobic glycolysis, fatty acid oxidation, and glutaminolysis. It is about one hundred years ago since Warburg observed that cancer cells prefer aerobic glycolysis even in normoxic conditions, favoring their high proliferation rate. A pivotal enzyme driving this phenomenon is lactate dehydrogenase (LDH), and this review describes prognostic and therapeutic opportunities associated with this enzyme, focussing on tumors with limited therapeutic strategies and life expectancy (i.e., pancreatic and thoracic cancers). Expression levels of LDH-A in pancreatic cancer tissues correlate with clinicopathological features: LDH-A is overexpressed during pancreatic carcinogenesis and showed significantly higher expression in more aggressive tumors. Similarly, LDH levels are a marker of negative prognosis in patients with both adenocarcinoma or squamous cell lung carcinoma, as well as in malignant pleural mesothelioma. Additionally, serum LDH levels may play a key role in the clinical management of these diseases because they are associated with tissue damage induced by tumor burden. Lastly, we discuss the promising results of strategies targeting LDH as a treatment strategy, reporting recent preclinical and translational studies supporting the use of LDH-inhibitors in combinations with current/novel chemotherapeutics that can synergistically target the oxygenated cells present in the tumor.
Keywords: Glycolysis; Lactate dehydrogenase; Pancreatic cancer Lung cancer; Tumor metabolism.
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest All the authors declare no conflicts of interest.
Similar articles
-
miR-16-5p regulates aerobic glycolysis and tumorigenesis of NSCLC cells via LDH-A/lactate/NF-κB signaling.Life Sci. 2022 Sep 1;304:120722. doi: 10.1016/j.lfs.2022.120722. Epub 2022 Jun 15. Life Sci. 2022. PMID: 35714705
-
Lactate dehydrogenase 5: an old friend and a new hope in the war on cancer.Cancer Lett. 2015 Mar 1;358(1):1-7. doi: 10.1016/j.canlet.2014.12.035. Epub 2014 Dec 17. Cancer Lett. 2015. PMID: 25528630 Review.
-
FOXM1 promotes the warburg effect and pancreatic cancer progression via transactivation of LDHA expression.Clin Cancer Res. 2014 May 15;20(10):2595-606. doi: 10.1158/1078-0432.CCR-13-2407. Epub 2014 Mar 14. Clin Cancer Res. 2014. PMID: 24634381 Free PMC article.
-
Relationships between LDH-A, lactate, and metastases in 4T1 breast tumors.Clin Cancer Res. 2013 Sep 15;19(18):5158-69. doi: 10.1158/1078-0432.CCR-12-3300. Epub 2013 Jul 5. Clin Cancer Res. 2013. PMID: 23833310 Free PMC article.
-
Lactate dehydrogenase A in cancer: a promising target for diagnosis and therapy.IUBMB Life. 2013 Nov;65(11):904-10. doi: 10.1002/iub.1216. Epub 2013 Nov 7. IUBMB Life. 2013. PMID: 24265197 Review.
Cited by
-
Role of Lactate Dehydrogenase as a Biomarker of Early Cardiac Remodeling: A Cross-Sectional Study.Cureus. 2024 Sep 7;16(9):e68906. doi: 10.7759/cureus.68906. eCollection 2024 Sep. Cureus. 2024. PMID: 39381455 Free PMC article.
-
Clonorchis sinensis infection contributes to hepatocellular carcinoma progression via enhancing angiogenesis.PLoS Negl Trop Dis. 2024 Nov 11;18(11):e0012638. doi: 10.1371/journal.pntd.0012638. eCollection 2024 Nov. PLoS Negl Trop Dis. 2024. PMID: 39527585 Free PMC article.
-
Energy metabolism in health and diseases.Signal Transduct Target Ther. 2025 Feb 18;10(1):69. doi: 10.1038/s41392-025-02141-x. Signal Transduct Target Ther. 2025. PMID: 39966374 Free PMC article. Review.
-
Identification of hub genes within the CCL18 signaling pathway in hepatocellular carcinoma through bioinformatics analysis.Front Oncol. 2024 Mar 6;14:1371990. doi: 10.3389/fonc.2024.1371990. eCollection 2024. Front Oncol. 2024. PMID: 38511143 Free PMC article.
-
Targeting metabolism by B-raf inhibitors and diclofenac restrains the viability of BRAF-mutated thyroid carcinomas with Hif-1α-mediated glycolytic phenotype.Br J Cancer. 2023 Aug;129(2):249-265. doi: 10.1038/s41416-023-02282-2. Epub 2023 May 17. Br J Cancer. 2023. PMID: 37198319 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous