LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article ; Online: Sexual-biased necroinflammation is revealed as a predictor of bevacizumab benefit in Glioblastoma.

    Hiller-Vallina, Sara / Mondejar-Ruescas, Lucia / Caamaño-Moreno, Marta / Cómitre-Mariano, Blanca / Alcivar-López, Denisse / Sepulveda, Juan M / Hernández-Laín, Aurelio / Pérez-Núñez, Ángel / Segura-Collar, Berta / Gargini, Ricardo

    Neuro-oncology

    2024  

    Abstract: Background: Glioblastoma (GBM) is a highly malignant brain tumor that affects men more often than women. In addition, the former shows a poorer survival prognosis. To date the reason for this sex-specific aggressiveness remains unclear. Therefore, the ... ...

    Abstract Background: Glioblastoma (GBM) is a highly malignant brain tumor that affects men more often than women. In addition, the former shows a poorer survival prognosis. To date the reason for this sex-specific aggressiveness remains unclear. Therefore, the aim of this study is to investigate tumor processes that explain these sex differences.
    Methods: This was a retrospective study of GBM patients which was stratified according to sex. Cohort with 73 tumors were analyzed with immunohistochemistry, RNA-seq and RT-qPCR to characterize differences in vascular and immunological profiles. Transcriptomic profiling, GSEA and pathway enrichment analysis were used for discovery molecular pathways predominant in each group. We further investigated the therapeutic effect of Bevacizumab (VEGFA blocking antibody) in retrospective GBM cohort (36 tumors) based on sex differences.
    Results: We found that under hypoxic tumor conditions, two distinct tumor immuno-angiogenic ecosystems develop linked to sex differences and ESR1 expression are generated. One of these subgroups, which includes male patients with low ESR1 expression, is characterized by vascular fragility associated with the appearance of regions of necrosis and high inflammation (called necroinflamed tumors). This male-specific tumor subtype shows high inflammation related to MDSC infiltration. Using this stratification, we identified a possible group of patients who could respond to bevacizumab (BVZ) and revealed a genetic signature that may find clinical applications as a predictor of those who may benefit most from this treatment.
    Conclusions: This study provides a stratification based on the sexual differences in GBM, which associates the poor prognosis with the presence of immunosuppressive myeloid cells in the necrotic areas. This new stratification could change the current prognosis of GBM and identifies those who respond to BVZ treatment.
    Language English
    Publishing date 2024-02-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 2028601-6
    ISSN 1523-5866 ; 1522-8517
    ISSN (online) 1523-5866
    ISSN 1522-8517
    DOI 10.1093/neuonc/noae033
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Advanced immunotherapies for glioblastoma: tumor neoantigen vaccines in combination with immunomodulators.

    Segura-Collar, Berta / Hiller-Vallina, Sara / de Dios, Olaya / Caamaño-Moreno, Marta / Mondejar-Ruescas, Lucia / Sepulveda-Sanchez, Juan M / Gargini, Ricardo

    Acta neuropathologica communications

    2023  Volume 11, Issue 1, Page(s) 79

    Abstract: Glial-origin brain tumors, including glioblastomas (GBM), have one of the worst prognoses due to their rapid and fatal progression. From an oncological point of view, advances in complete surgical resection fail to eliminate the entire tumor and the ... ...

    Abstract Glial-origin brain tumors, including glioblastomas (GBM), have one of the worst prognoses due to their rapid and fatal progression. From an oncological point of view, advances in complete surgical resection fail to eliminate the entire tumor and the remaining cells allow a rapid recurrence, which does not respond to traditional therapeutic treatments. Here, we have reviewed new immunotherapy strategies in association with the knowledge of the immune micro-environment. To understand the best lines for the future, we address the advances in the design of neoantigen vaccines and possible new immune modulators. Recently, the efficacy and availability of vaccine development with different formulations, especially liposome plus mRNA vaccines, has been observed. We believe that the application of new strategies used with mRNA vaccines in combination with personalized medicine (guided by different omic's strategies) could give good results in glioma therapy. In addition, a large part of the possible advances in new immunotherapy strategies focused on GBM may be key improving current therapies of immune checkpoint inhibitors (ICI), given the fact that this type of tumor has been highly refractory to ICI.
    MeSH term(s) Humans ; Glioblastoma/pathology ; Cancer Vaccines/therapeutic use ; Immunologic Factors ; Glioma/drug therapy ; Immunotherapy/methods ; Brain Neoplasms/pathology ; Tumor Microenvironment
    Chemical Substances Cancer Vaccines ; Immunologic Factors
    Language English
    Publishing date 2023-05-10
    Publishing country England
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2715589-4
    ISSN 2051-5960 ; 2051-5960
    ISSN (online) 2051-5960
    ISSN 2051-5960
    DOI 10.1186/s40478-023-01569-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Correction to: Advanced immunotherapies for glioblastoma: tumor neoantigen vaccines in combination with immunomodulators.

    Segura-Collar, Berta / Hiller-Vallina, Sara / de Dios, Olaya / Caamaño-Moreno, Marta / Mondejar-Ruescas, Lucia / Sepulveda-Sanchez, Juan M / Gargini, Ricardo

    Acta neuropathologica communications

    2023  Volume 11, Issue 1, Page(s) 116

    Language English
    Publishing date 2023-07-12
    Publishing country England
    Document type Published Erratum
    ZDB-ID 2715589-4
    ISSN 2051-5960 ; 2051-5960
    ISSN (online) 2051-5960
    ISSN 2051-5960
    DOI 10.1186/s40478-023-01600-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top