Multiple splice variants of lactate dehydrogenase C selectively expressed in human cancer.

Détails

ID Serval
serval:BIB_4F0DA2E7DE97
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Multiple splice variants of lactate dehydrogenase C selectively expressed in human cancer.
Périodique
Cancer Research
Auteur⸱e⸱s
Koslowski M., Türeci O., Bell C., Krause P., Lehr H.A., Brunner J., Seitz G., Nestle F.O., Huber C., Sahin U.
ISSN
0008-5472 (Print)
ISSN-L
0008-5472
Statut éditorial
Publié
Date de publication
2002
Volume
62
Numéro
22
Pages
6750-6755
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Résumé
We applied a combined data mining and experimental validation Approach for the discovery of germ cell-specific genes aberrantly expressed in cancer. Six of 21 genes with confirmed germ cell specificity were detected in tumors, indicating that ectopic activation of testis-specific genes in cancer is a frequent phenomenon. Most surprisingly one of the genes represented lactate dehydrogenase C (LDHC), the germ cell-specific member of the lactate dehydrogenase family. LDHC escapes from transcriptional repression, resulting in significant expression levels in virtually all tumor types tested. Moreover, we discovered aberrant splicing of LDHC restricted to cancer cells, resulting in four novel tumor-specific variants displaying structural alterations of the catalytic domain. Expression of LDHC in tumors is neither mediated by gene promotor demethylation, as previously described for other germ cell-specific genes activated in cancer, nor induced by hypoxia as demonstrated for enzymes of the glycolytic pathway. LDHC represents the first lactate dehydrogenase isoform with restriction to tumor cells. In contrast to other LDH isoenzymes, LDHC has a preference for lactate as a substrate. Thus LDHC activation in cancer may provide a metabolic rescue pathway in tumor cells by exploiting lactate for ATP delivery.
Mots-clé
Alternative Splicing, Databases, Nucleic Acid, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Humans, Isoenzymes/biosynthesis, Isoenzymes/genetics, L-Lactate Dehydrogenase/biosynthesis, L-Lactate Dehydrogenase/genetics, Male, Neoplasms/enzymology, Neoplasms/genetics, Reverse Transcriptase Polymerase Chain Reaction, Testicular Neoplasms/enzymology, Testicular Neoplasms/genetics, Transcription, Genetic
Pubmed
Création de la notice
26/11/2011 14:04
Dernière modification de la notice
20/08/2019 14:04
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