Evidence map›Paper›PMID 39329940›Full record

ReviewCurrent issues in molecular biology2024

Glioblastoma Tumor Microenvironment: An Important Modulator for Tumoral Progression and Therapy Resistance.

Ligia Gabriela Tataranu, Serban Turliuc, Amira Kamel, Radu Eugen Rizea, Anica Dricu, Georgiana-Adeline Staicu, Stefania Carina Baloi, Silvia Mara Baez Rodriguez, Andrada Ioana Maria Manole

Abstract readReview
In one paragraph

Review in Current issues in molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ligia Gabriela TataranuNeurosurgical Department, University of Medicine and Pharmacy "Carol Davila", 020022 Bucharest, Romania.ORCID 0000-0001-6788-5833
Serban TurliucMedical Department, University of Medicine and Pharmacy "G. T. Popa", 700115 Iasi, Romania.ORCID 0009-0005-7695-0509
Amira KamelNeurosurgical Department, Clinical Emergency Hospital "Bagdasar-Arseni", 041915 Bucharest, Romania.ORCID 0009-0006-0739-3224
Radu Eugen RizeaNeurosurgical Department, University of Medicine and Pharmacy "Carol Davila", 020022 Bucharest, Romania.ORCID 0000-0002-3848-0893
Anica DricuBiochemistry Department, University of Medicine and Pharmacy, 200349 Craiova, Romania.ORCID 0000-0002-3039-857X
Georgiana-Adeline StaicuBiochemistry Department, University of Medicine and Pharmacy, 200349 Craiova, Romania.ORCID 0009-0003-7522-0702
Stefania Carina BaloiBiochemistry Department, University of Medicine and Pharmacy, 200349 Craiova, Romania.ORCID 0000-0002-3468-9649
Silvia Mara Baez RodriguezNeurosurgical Department, Clinical Emergency Hospital "Bagdasar-Arseni", 041915 Bucharest, Romania.
Andrada Ioana Maria ManoleNeurosurgical Department, Clinical Emergency Hospital "Bagdasar-Arseni", 041915 Bucharest, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The race to find an effective treatment for glioblastoma (GBM) remains a critical topic, because of its high aggressivity and impact on survival and the quality of life. Currently, due to GBM's high heterogeneity, the conventional treatment success rate and response to therapy are relatively low, with a median survival rate of less than 20 months. A new point of view can be provided by the comprehension of the tumor microenvironment (TME) in pursuance of the development of new therapeutic strategies to aim for a longer survival rate with an improved quality of life and longer disease-free interval (DFI). The main components of the GBM TME are represented by the extracellular matrix (ECM), glioma cells and glioma stem cells (GSCs), immune cells (microglia, macrophages, neutrophils, lymphocytes), neuronal cells, all of them having dynamic interactions and being able to influence the tumoral growth, progression, and drug resistance thus being a potential therapeutic target. This paper will review the latest research on the GBM TME and the potential therapeutic targets to form an up-to-date strategy.

Indexed as

extracellular matrixglioblastomamolecular diagnostictumor microenvironment

Identifiers

PMID39329940
PMCPMC11430601

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.