Evidence map›Paper›PMID 36185622›Full record

ReviewJournal of oncology2022

Genomic and Epigenomic Features of Glioblastoma Multiforme and its Biomarkers.

Sarmad Sheraz Jadoon, Umair Ilyas, Hajra Zafar, Ana Cláudia Paiva-Santos, Saifullah Khan, Saeed Ahmad Khan, Tanzeel Ahmed, Yasir Rasool, Reem Altaf, Faisal Raza and 1 more

Abstract readReview
In one paragraph

Review in Journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Complex Diagnostic Challenges in Glioblastoma: The Role ofPharmaceuticals (Basel, Switzerland) · 2024
    Review
  7. Article
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

11 authors.

Sarmad Sheraz JadoonState Key Laboratory of Esophageal Cancer Prevention & Treatment, School of Pharmaceutical Sciences, Zhengzhou University, China.
Umair IlyasDepartment of Pharmacy Practice, Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Hajra ZafarSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.ORCID https://orcid.org/0000-0002-0606-5783
Ana Cláudia Paiva-SantosDepartment of Pharmaceutical Technology, Faculty of Pharmacy of the University of Coimbra, University of Coimbra, Azinhaga Sta. Comba, 3000-548 Coimbra, Portugal.
Saifullah KhanInstitute of Biotechnology and Microbiology, Bacha Khan University, Charsadda, Pakistan.
Saeed Ahmad KhanDepartment of Pharmacy, Kohat University of Science and Technology, Kohat, Pakistan.
Tanzeel AhmedBolan Medical Complex Hospital, Quetta, Pakistan.
Yasir RasoolAkhtar Saeed College of Pharmacy, Bahria Golf City, Rawalpindi, Pakistan.
Reem AltafDepartment of Pharmacy, Iqra University-Islamabad Campus, Islamabad, Pakistan.ORCID https://orcid.org/0000-0003-3850-4944
Faisal RazaSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.ORCID https://orcid.org/0000-0001-5569-3535
Muhammad AbbasDepartment of Pharmacy Practice, Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.ORCID https://orcid.org/0000-0002-4453-0981

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme is a serious and life-threatening tumor of central nervous system, characterized by aggressive behavior, poor prognosis, and low survival rate. Despite of the availability of aggressive antitumor therapeutic regimen for glioblastoma (radiotherapy followed by chemotherapeutic dose), recovery rate, and patients' survival ratio is attributed to the lack of selectivity of therapeutic drugs and less advancement in cancer therapeutics over last decade. Moreover, tools employed in conventional diagnosis of glioblastoma are more invasive and painful, making the process excruciating for the patients. These challenges urge for the need of novel biomarkers for diagnosis, prognosis, and prediction purpose with less invasiveness and more patient compliance. This article will explore the genetic biomarkers isocitrate dehydrogenase mutation, MGMT mutations, and EGFR that can be deployed as an analytical tool in diagnosis of disease and prognosis of a therapeutic course. The review also highlights the importance of employing novel microRNAs as prognostic biomarkers. Recent clinical advancements to treat GBM and to prevent relapse of the disease are also discussed in this article in the hope of finding a robust and effective method to treat GBM.

Identifiers

PMID36185622
PMCPMC9519330

What OpenQuestion holds

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Registered trials

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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.