Transcriptional landscape of the interaction of human Mesenchymal Stem Cells with Glioblastoma in bioprinted co-cultures DOI Creative Commons
Lisa Oliver,

Yuna Landais,

Catherine Gratas

и другие.

Stem Cell Research & Therapy, Год журнала: 2024, Номер 15(1)

Опубликована: Ноя. 14, 2024

The interaction between mesenchymal stem cells (MSC) and Glioblastoma (GBM), although potentially of the highest importance, is ill-understood. This due, in part, to lack relevant experimental models. similarity vitro situations vivo situation can be improved by 3D co-culture as it reproduces key cell–cell interactions tumor microenvironment (TME) cancer cells. MSC Can acquired characteristics associated fibroblasts (CAF) being cultured with conditioned medium from GBM cultures thus are called MSCCAF. We co Cultured MSCCAF patient derived a scaffold bioprinted model. studied response current therapy (e.g. Temozolomide + /Radiation) on bulk transcriptomic (RNA Seq) epigenetic (ATAC analyses modifications induced standard treatment scaffolds mono- or co-cultures ± analyzed. found that mitochondrial encoded OXPHOS genes overexpressed under these conditions modified both (chemotherapy radiation). have identified two new markers MSC/GBM interactions, one epigenetically regulated (i.e. TREM-1) an increased overall survival patients another implicated post-transcriptional regulation long non-coding RNA, miR3681HG), which reduced patients.

Язык: Английский

Recent Treatment Strategies and Molecular Pathways in Resistance Mechanisms of Antiangiogenic Therapies in Glioblastoma DOI Open Access
Md. Ataur Rahman,

Meser M. Ali

Cancers, Год журнала: 2024, Номер 16(17), С. 2975 - 2975

Опубликована: Авг. 27, 2024

Malignant gliomas present great difficulties in treatment, with little change over the past 30 years median survival time of 15 months. Current treatment options include surgery, radiotherapy (RT), and chemotherapy. New therapies aimed at suppressing formation new vasculature (antiangiogenic treatments) or destroying formed tumor (vascular disrupting agents) show promise. This study summarizes existing knowledge regarding processes by which glioblastoma (GBM) tumors acquire resistance to antiangiogenic treatments. The discussion encompasses activation redundant proangiogenic pathways, heightened cell invasion metastasis, induced hypoxia, creation vascular mimicry channels, regulation immune microenvironment. Subsequently, we explore potential strategies overcome this resistance, such as combining other methods, personalizing treatments for each patient, focusing on therapeutic targets, incorporating immunotherapy, utilizing drug delivery systems based nanoparticles. Additionally, would like discuss limitations methods future directions enhance beneficial effects patients GBM. Therefore, review aims research outcome GBM provide a more promising opportunity thoroughly exploring mechanisms investigating novel strategies.

Язык: Английский

Процитировано

9

The Role of the Dysregulation of circRNAs Expression in Glioblastoma Multiforme DOI
Yafei Wang, Ying Yu, Jiahua Yu

и другие.

Journal of Molecular Neuroscience, Год журнала: 2025, Номер 75(1)

Опубликована: Янв. 22, 2025

Язык: Английский

Процитировано

0

The Clinical Role of miRNAs in the Development and Treatment of Glioblastoma DOI Open Access
Samantha Epistolio, Paolo Spina, Ismail Zaed

и другие.

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(6), С. 2723 - 2723

Опубликована: Март 18, 2025

Glioblastoma multiforme (GBM) is the most common brain tumor and one of aggressive, with a median overall survival (OS) only 15–18 months. These characteristics make it necessary to identify new targets for improvement prognosis better prediction response therapies currently available GBM patients. One possible candidate target could be evaluation miRNAs. miRNAs are small non-coding RNAs that play important roles in post-transcriptional gene regulation. Due their functions, also control biological processes underlying development may considered clinical role. This narrative review introduces concept from molecular perspective then addresses specific described literature as relevant development, prognosis, patients affected by GBM.

Язык: Английский

Процитировано

0

Unraveling the noncoding RNA landscape in glioblastoma: from pathogenesis to precision therapeutics DOI

K. Sandhanam,

Tamilanban Thamaraikani

Naunyn-Schmiedeberg s Archives of Pharmacology, Год журнала: 2024, Номер 397(12), С. 9475 - 9502

Опубликована: Июль 15, 2024

Язык: Английский

Процитировано

3

Mesenchymal-Stem-Cell-Based Therapy against Gliomas DOI Creative Commons

Sisa M. Santillán-Guaján,

Mehdi Hayat Shahi, Javier S. Castresana

и другие.

Cells, Год журнала: 2024, Номер 13(7), С. 617 - 617

Опубликована: Апрель 2, 2024

Glioblastoma is the most aggressive, malignant, and lethal brain tumor of central nervous system. Its poor prognosis lies in its inefficient response to currently available treatments that consist surgical resection, radiotherapy, chemotherapy. Recently, use mesenchymal stem cells (MSCs) as a possible kind cell therapy against glioblastoma gaining great interest due their immunomodulatory properties, tropism, differentiation into other types. However, MSCs seem present both antitumor pro-tumor properties depending on tissue from which they come. In this work, possibility using deliver therapeutic genes, oncolytic viruses, miRNA presented, well strategies can improve efficacy glioblastoma, such CAR-T cells, nanoparticles, exosomes.

Язык: Английский

Процитировано

2

Exploring miRNA therapies and gut microbiome–enhanced CAR-T cells: advancing frontiers in glioblastoma stem cell targeting DOI

K. Sandhanam,

Tamilanban Thamaraikani,

Bedanta Bhattacharjee

и другие.

Naunyn-Schmiedeberg s Archives of Pharmacology, Год журнала: 2024, Номер unknown

Опубликована: Окт. 9, 2024

Язык: Английский

Процитировано

2

Transcriptional landscape of the interaction of human Mesenchymal Stem Cells with Glioblastoma in bioprinted co-cultures DOI Creative Commons
Lisa Oliver,

Yuna Landais,

Catherine Gratas

и другие.

Stem Cell Research & Therapy, Год журнала: 2024, Номер 15(1)

Опубликована: Ноя. 14, 2024

The interaction between mesenchymal stem cells (MSC) and Glioblastoma (GBM), although potentially of the highest importance, is ill-understood. This due, in part, to lack relevant experimental models. similarity vitro situations vivo situation can be improved by 3D co-culture as it reproduces key cell–cell interactions tumor microenvironment (TME) cancer cells. MSC Can acquired characteristics associated fibroblasts (CAF) being cultured with conditioned medium from GBM cultures thus are called MSCCAF. We co Cultured MSCCAF patient derived a scaffold bioprinted model. studied response current therapy (e.g. Temozolomide + /Radiation) on bulk transcriptomic (RNA Seq) epigenetic (ATAC analyses modifications induced standard treatment scaffolds mono- or co-cultures ± analyzed. found that mitochondrial encoded OXPHOS genes overexpressed under these conditions modified both (chemotherapy radiation). have identified two new markers MSC/GBM interactions, one epigenetically regulated (i.e. TREM-1) an increased overall survival patients another implicated post-transcriptional regulation long non-coding RNA, miR3681HG), which reduced patients.

Язык: Английский

Процитировано

0