Evidence map›Paper›PMID 36654821›Full record

ReviewExploration of targeted anti-tumor therapy2022

New phase therapeutic pursuits for targeted drug delivery in glioblastoma multiforme.

Manisha Singh, Divya Jindal, Vinayak Agarwal, Deepanshi Pathak, Mansi Sharma, Pranav Pancham, Shalini Mani, Rachana

Open access · diamondAbstract readReview
In one paragraph

Review in Exploration of targeted anti-tumor therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 45% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 1 institution in 1 country.

Manisha SinghDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0002-0466-8986
Divya JindalDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0002-1041-8510
Vinayak AgarwalDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0001-6239-5077
Deepanshi PathakDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0002-9394-0135
Mansi SharmaDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0003-1720-8708
Pranav PanchamDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0003-4332-5350
Shalini ManiDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0003-2500-6962
RachanaDepartment of Biotechnology, Jaypee Institute of Information Technology (JIIT), Noida 201301, India.ORCID https://orcid.org/0000-0002-8686-0372
Jaypee Institute of Information Technology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is known as the most aggressive and prevalent brain tumor with a high mortality rate. It is reported in people who are as young as 10 years old to as old as over 70 years old, exhibiting inter and intra tumor heterogeneity. There are several genomic and proteomic investigations that have been performed to find the unexplored potential targets of the drug against GBM. Therefore, certain effective targets have been taken to further validate the studies embarking on the robustness in the field of medicinal chemistry followed by testing in clinical trials. Also, The Cancer Genome Atlas (TCGA) project has identified certain overexpressed targets involved in the pathogenesis of GBM in three major pathways, i.e., tumor protein 53 (p53), retinoblastoma (RB), and receptor tyrosine kinase (RTK)/rat sarcoma virus (Ras)/phosphoinositide 3-kinase (PI3K) pathways. This review focuses on the compilation of recent developments in the fight against GBM thus, directing future research into the elucidation of pathogenesis and potential cure for GBM. Also, it highlights the potential biomarkers that have undergone extensive research and have promising prognostic and predictive values. Additionally, this manuscript analyses the advent of gene therapy and immunotherapy, unlocking the way to consider treatment approaches other than, or in addition to, conventional chemo-radiation therapies. This review study encompasses all the relevant research studies associated with the pathophysiology, occurrence, diagnostic tools, and therapeutic intervention for GBM. It highlights the evolution of various therapeutic perspectives against GBM from the most conventional form of radiotherapy to the recent advancement of gene/cell/immune therapy. Further, the review focuses on various targeted therapies for GBM including chemotherapy sensitization, radiotherapy, nanoparticles based, immunotherapy, cell therapy, and gene therapy which would offer a comprehensive account for exploring several facets related to GBM prognostics.

Indexed as

gene therapyimmune therapyP53 pathwayreceptor tyrosine kinase (RTK)/rat sarcoma virus (Ras)/phosphoinositide 3-kinase (PI3K) pathwayretinoblastoma pathwaytheranostic biomarkers

Identifiers

PMID36654821
PMCPMC9834280
OpenAlexW4313360942

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.