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dc.contributor.authorAntonia Garrido, María
dc.contributor.authorNavarro Ocón, Alba 
dc.contributor.authorRonco Díaz, Víctor
dc.contributor.authorOlea Serrano, Nicolás 
dc.date.accessioned2024-12-03T09:41:05Z
dc.date.available2024-12-03T09:41:05Z
dc.date.issued2024-11-28
dc.identifier.citationAntonia Garrido, M. et. al. Genes 2024, 15, 1542. [https://doi.org/10.3390/genes15121542]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/97640
dc.description.abstractMajor histocompatibility complex (MHC) class-I molecules (or Human Leucocyte Antigen class-I) play a key role in adaptive immunity against cancer. They present specific tumor neoantigens to cytotoxic T cells and provoke an antitumor cytotoxic response. The total or partial loss of HLA molecules can inhibit the immune system’s ability to detect and destroy cancer cells. Loss of heterozygosity (LOH) is a common irreversible genetic alteration that occurs in the great majority of human tumors, including breast cancer. LOH at chromosome 6, which involves HLA genes (LOH-HLA), leads to the loss of an HLA haplotype and is linked to cancer progression and a weak response to cancer immunotherapy. Therefore, the loss of genes or an entire chromosomal region which are critical for antigen presentation is of particular importance in the search for novel prognostic and clinical biomarkers in breast cancer. Here, we review the role of LOH-HLA in breast cancer, its contribution to an understanding of cancer immune escape and tumor progression, and discuss how it can be targeted in cancer therapy.es_ES
dc.description.sponsorshipAndalusian Government and co-funded by FEDER funds (B-CTS-410-UGR-20)es_ES
dc.description.sponsorshipMinistry of Science and Innovation (PID2020-115087GB-100)es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHLA class-Ies_ES
dc.subjectLOH HLAes_ES
dc.subjectcancer immune escapees_ES
dc.titleLoss of Heterozygosity (LOH) Affecting HLA Genes in Breast Cancer: Clinical Relevance and Therapeutic Opportunitieses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/genes15121542
dc.type.hasVersionVoRes_ES


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Atribución 4.0 Internacional
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