Evidence map›Paper›PMID 27672311›Full record

ArticleDrug design, development and therapy

Understanding cytoskeleton regulators in glioblastoma multiforme for therapy design.

Samaneh Masoumi, Aditya Harisankar, Aileen Gracias, Fabian Bachinger, Temesgen Fufa, Gayathri Chandrasekar, Frank Gaunitz, Julian Walfridsson, Satish S Kitambi

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Systems biology-driven drug repurposing in glioblastomaResearch in pharmaceutical sciences · 2026
    Article
  2. Article
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  8. Review
  9. Article
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  11. Cancers · 2021
    Article
  12. Review
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  14. Article
  15. [MACF1 knockdown in glioblastoma multiforme cells increases temozolomide-induced cytotoxicity].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017
    Article
  16. Review
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 at 3 institutions in 3 countries.

Samaneh MasoumiDepartment of Microbiology Tumor and Cell Biology.
Aditya HarisankarCenter for Hematology and Regenerative Medicine, Department of Medicine.
Aileen GraciasDepartment of Neuroscience, Karolinska Institutet, Solna, Sweden.
Fabian BachingerDepartment of Microbiology Tumor and Cell Biology.
Temesgen FufaDepartment of Microbiology Tumor and Cell Biology; Department of Neurosurgery, University Hospital, Leipzig, Germany.
Gayathri ChandrasekarDepartment of Biosciences and Nutrition, Karolinska Institutet, Solna, Sweden.
Frank GaunitzDepartment of Neurosurgery, University Hospital, Leipzig, Germany.
Julian WalfridssonCenter for Hematology and Regenerative Medicine, Department of Medicine.
Satish S KitambiDepartment of Microbiology Tumor and Cell Biology.
Karolinska Institutet · SECenter for Neuroscience and Regenerative Medicine · USUniversity Hospital Leipzig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cellular cytoskeleton forms the primary basis through which a cell governs the changes in size, shape, migration, proliferation, and forms the primary means through which the cells respond to their environment. Indeed, cell and tissue morphologies are used routinely not only to grade tumors but also in various high-content screening methods with an aim to identify new small molecules with therapeutic potential. This study examines the expression of various cytoskeleton regulators in glioblastoma multiforme (GBM). GBM is a very aggressive disease with a low life expectancy even after chemo- and radiotherapy. Cancer cells of GBM are notorious for their invasiveness, ability to develop resistance to chemo- and radiotherapy, and to form secondary site tumors. This study aims to gain insight into cytoskeleton regulators in GBM cells and to understand the effect of various oncology drugs, including temozolomide, on cytoskeleton regulators. We compare the expression of various cytoskeleton regulators in GBM-derived tumor and normal tissue, CD133-postive and -negative cells from GBM and neural cells, and GBM stem-like and differentiated cells. In addition, the correlation between the expression of cytoskeleton regulators with the clinical outcome was examined to identify genes associated with longer patient survival. This was followed by a small molecule screening with US Food and Drug Administration (FDA)-approved oncology drugs, and its effect on cellular cytoskeleton was compared to treatment with temozolomide. This study identifies various groups of cytoskeletal regulators that have an important effect on patient survival and tumor development. Importantly, this work highlights the advantage of using cytoskeleton regulators as biomarkers for assessing prognosis and treatment design for GBM.

Indexed as

actinactomyosincytoskeletonGBMgliomamicrotubulesPhenotypic Drug Discoverytubulin

Identifiers

PMID27672311
PMCPMC5026218
OpenAlexW2518865156

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.