Evidence map›Paper›PMID 35534356›Full record

ReviewTrends in pharmacological sciences2022

Pharmacological targeting of the tumor-immune symbiosis in glioblastoma.

Lizhi Pang, Fatima Khan, Madeline Dunterman, Peiwen Chen

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Interactions between glioblastoma and myeloid cells.Frontiers in cell and developmental biology · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Epigenetic regulation of tumor immunity.The Journal of clinical investigation · 2024
    Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Lizhi PangDepartment of Neurological Surgery, Lou and Jean Malnati Brain Tumor Institute, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Fatima KhanDepartment of Neurological Surgery, Lou and Jean Malnati Brain Tumor Institute, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Madeline DuntermanDepartment of Neurological Surgery, Lou and Jean Malnati Brain Tumor Institute, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Peiwen ChenDepartment of Neurological Surgery, Lou and Jean Malnati Brain Tumor Institute, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA. Electronic address: peiwen.chen@northwestern.edu.
Northwestern University · US

Funding

Mechanism and therapeutic potential of microglia regulation in glioblastomaR01NS124594 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peiwen Chen · 2022 to 2026
$2.0M
Targeting macrophage reprogramming in glioblastomaR01NS127824 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peiwen Chen · 2023 to 2026
$1.6M
Mechanism and therapeutic potential of macrophage regulation in glioblastomaR00CA240896 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CHEN, PEIWEN · 2020 to 2022
$663k
NCI NIH HHS R00 CA240896NINDS NIH HHS R01 NS124594NINDS NIH HHS R01 NS127824
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common and highly lethal form of primary brain tumor in adults. The median survival of GBM patients is approximately 14-16 months despite multimodal therapies. Emerging evidence has substantiated the critical role of symbiotic interactions between GBM cells and noncancerous immune cells (e.g., myeloid cells and T cells) in regulating tumor progression and therapy resistance. Approaches to target the tumor-immune symbiosis have emerged as a promising therapeutic strategy for GBM. Here, we review the recent developments for pharmacological targeting of the GBM-immune symbiosis and highlight the role of such strategies to improve the effectiveness of immunotherapies in GBM.

Indexed as

Brain NeoplasmsGlioblastomaAdultCombined Modality TherapyHumansImmunotherapySymbiosisTumor Microenvironmentglioblastomaimmunotherapymacrophagesmicroglia, MDSCssymbiosis

Identifiers

PMID35534356
PMCPMC9288491
OpenAlexW4229333966

What OpenQuestion holds

Textmetadata
LicenceTDM
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.