Evidence map›Paper›PMID 36697401›Full record

ArticleNPJ genomic medicine2023

Transcriptomic analyses of patient peripheral blood with hemoglobin depletion reveal glioblastoma biomarkers.

Dan Qi, Yiqun Geng, Jacob Cardenas, Jinghua Gu, S Stephen Yi, Jason H Huang, Ekokobe Fonkem, Erxi Wu

Open access · goldAbstract read
In one paragraph

Article in NPJ genomic medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Dan Qi *Department of Neurosurgery and Neuroscience Institute, Baylor Scott & White Health, Temple, TX, 76508, USA.ORCID http://orcid.org/0000-0001-7015-1849
Yiqun Geng *Department of Neurosurgery and Neuroscience Institute, Baylor Scott & White Health, Temple, TX, 76508, USA.
Jacob CardenasBaylor Scott & White Research Institute, Dallas, TX, 75204, USA.
Jinghua GuBaylor Scott & White Research Institute, Dallas, TX, 75204, USA.
S Stephen YiInstitute for Cellular and Molecular Biology (ICMB), College of Natural Sciences, The University of Texas at Austin, Austin, TX, 78712, USA.
Jason H HuangDepartment of Neurosurgery and Neuroscience Institute, Baylor Scott & White Health, Temple, TX, 76508, USA. Jason.Huang@BSWHealth.org.ORCID http://orcid.org/0000-0002-4426-0168
Ekokobe FonkemDepartment of Neurosurgery and Neuroscience Institute, Baylor Scott & White Health, Temple, TX, 76508, USA. Ekokobe.Fonkem@BSWHealth.org.ORCID http://orcid.org/0000-0001-6382-8866
Erxi WuDepartment of Neurosurgery and Neuroscience Institute, Baylor Scott & White Health, Temple, TX, 76508, USA. Erxi.Wu@BSWHealth.org.ORCID http://orcid.org/0000-0002-1680-3639
Baylor Scott & White Health · USLivestrong Foundation · USShantou University · CNTemple College · US

Funding

Network-based Framework to Decode Novel Gain-of-Function Mutations and their Mechanistic Roles in General Human DiseasesR35GM133658 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI S. Stephen Yi · 2019 to 2026
$2.6M
NIGMS NIH HHS R35 GM133658
6 · The paper itself

Abstract

Peripheral blood is gaining prominence as a noninvasive alternative to tissue biopsy to develop biomarkers for glioblastoma (GBM); however, widely utilized blood-based biomarkers in clinical settings have not yet been identified due to the lack of a robust detection approach. Here, we describe the application of globin reduction in RNA sequencing of whole blood (i.e., WBGR) and perform transcriptomic analysis to identify GBM-associated transcriptomic changes. By using WBGR, we improved the detection sensitivity of informatic reads and identified differential gene expression in GBM blood. By analyzing tumor tissues, we identified transcriptomic traits of GBM blood. Further functional enrichment analyses retained the most changed genes in GBM. Subsequent validation elicited a 10-gene panel covering mRNA, long noncoding RNA, and microRNA (i.e., GBM-Dx panel) that has translational potential to aid in the early detection or clinical management of GBM. Here, we report an integrated approach, WBGR, with comprehensive analytic capacity for blood-based marker identification.

Identifiers

PMID36697401
PMCPMC9877004
OpenAlexW4317936732

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.