Lactate dehydrogenase A, an unexplored target for cancer treatment (notice n° 177716)

détails MARC
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control field 20250112040730.0
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Robert, Jacques
Relator term author
245 00 - TITLE STATEMENT
Title Lactate dehydrogenase A, an unexplored target for cancer treatment
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2023.<br/>
500 ## - GENERAL NOTE
General note 49
520 ## - SUMMARY, ETC.
Summary, etc. Several recent studies have reported the association, for several types of cancers, between cancer aggressiveness and the expression of one of the enzymes responsible for the interconversion between pyruvate and lactate in the final stage of glycolysis—lactate dehydrogenase A (LDHA). LDHA favors the conversion of pyruvate to lactate, while lactate dehydrogenase B (LDHB) favors the opposite reaction. Several more or less specific LDHA inhibitors have been identified, but no clinical trial seems to have been undertaken to date. We carried out a preliminary study using The Cancer Genome Atlas (TCGA) database to analyze the association between the aggressiveness of the most lethal cancers and the level of expression of LDHA and LDHB genes (the criterion used to assess aggressiveness at the clinical level being overall survival of patients). A significant link between overall survival and a low level of expression of the LDHA gene was noted in pancreatic adenocarcinomas and glioblastomas, but not in bronchopulmonary carcinomas, adenocarcinomas or squamous cell carcinomas, nor in breast or colorectal cancers. Furthermore, high expression of the LDHB gene was associated with a favorable prognosis in patients with glioblastomas. Data in the literature, supported by our study, suggest that LDHA is a potential target for therapeutic development in oncology, at least for pancreatic cancer and glioblastoma, provided that the molecules chosen are sufficiently selective for LDHA.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element Cancer Genome Atlas (TCGA)
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element glioblastomas
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element pancreatic cancers
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element lactate dehydrogenases A and B
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element glioblastomas
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element lactate dehydrogenases A and B
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element in silico
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element research
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element Cancer Genome Atlas (TCGA)
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element pancreatic cancers
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Le Morvan, Valérie
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Fessart, Delphine
Relator term author
786 0# - DATA SOURCE ENTRY
Note Innovations & Thérapeutiques en Oncologie | Volume 9 | 5 | 2023-09-04 | p. 257-265 | 2431-3203
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/journal-innovations-et-therapeutiques-en-oncologie-2023-5-page-257?lang=en">https://shs.cairn.info/journal-innovations-et-therapeutiques-en-oncologie-2023-5-page-257?lang=en</a>

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