Evidence map›Paper›PMID 34908119›Full record

ArticleBioscience reports2022

Integrative analysis reveals methylenetetrahydrofolate dehydrogenase 1-like as an independent shared diagnostic and prognostic biomarker in five different human cancers.

Nuzhat Sial, Jalil Ur Rehman, Saba Saeed, Mukhtiar Ahmad, Yasir Hameed, Muhammad Atif, Abdul Rehman, Rizwan Asif, Hamad Ahmed, Muhammad Safdar Hussain and 3 more

Abstract read
In one paragraph

Article in Bioscience reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
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1 · What the graph read from it

What it found

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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

26 citing papers in PubMed.

  1. Article
  2. A five-gene mitochondria-associated prognostic signature for bladder cancer.International journal of clinical and experimental pathology · 2026
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

13 authors.

Nuzhat SialDepartment of Zoology, The Islamia University of Bahawalpur, Bahawalpur, Pakistan.
Jalil Ur RehmanDepartment of Eastern Medicine, Qarshi University, Lahore, Pakistan.
Saba SaeedDepartment of Zoology, University of the Punjab, Lahore, Pakistan.
Mukhtiar AhmadDepartment of Biochemistry and Biotechnology, The Islamia University of Bahawalpur, Bahawalpur, Pakistan.
Yasir HameedDepartment of Zoology, University of the Punjab, Lahore, Pakistan.ORCID 0000-0002-6378-1962
Muhammad AtifUniversity College of Conventional Medicine, The Islamia University of Bahawalpur, Bahawalpur, Pakistan.
Abdul RehmanDepartment of Eastern Medicine, Qarshi University, Lahore, Pakistan.
Rizwan AsifDepartment of Microbiology, Government College University Faisalabad, Faisalabad, Pakistan.
Hamad AhmedDepartment of Eastern Medicine, Government College University Faisalabad, Faisalabad, Pakistan.
Muhammad Safdar HussainDepartment of Biochemistry and Biotechnology, The Islamia University of Bahawalpur, Bahawalpur, Pakistan.
Muhammad Rashid KhanUniversity College of Eastern Medicine, The Islamia University of Bahawalpur, Bahawalpur, Pakistan.
Atifa AmbreenAllied Department, The Sahara College, Narowal, Pakistan.
Ayesha AmbreenAllied Department, The Sahara College, Narowal, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDefects in methylenetetrahydrofolate dehydrogenase 1-like (MTHFD1L) expression have earlier been examined in only a few human cancers.

objectivesMulti-omics profiling of MTHFD1L as a shared biomarker in distinct subtypes of human cancers.

methodsIn the current study, for the multi-omics analysis of MTHFD1L in 24 major subtypes of human cancers, a comprehensive in silico approach was adopted to mine different open access online databases including UALCAN, Kaplan-Meier (KM) plotter, LOGpc, GEPIA, Human Protein Atlas (HPA), Gene Expression across Normal and Tumor tissue (GENT2), MEXPRESS, cBioportal, STRING, DAVID, TIMER, and Comparative Toxicogenomics Database (CTD).

resultsWe noticed that the expression of MTHFD1L was significantly higher in all the analyzed 24 subtypes of human cancers as compared with the normal controls. Moreover, MTHDF1L overexpression was also found to be significantly associated with the reduced overall survival (OS) duration of Bladder urothelial cancer (BLCA), Head and neck cancer (HNSC), Kidney renal papillary cell carcinoma (KIRP), Lung adenocarcinoma (LUAD), and Uterine corpus endometrial carcinoma (UCEC). This implies that MTHFD1L plays a significant role in the development and progression of these cancers. We further noticed that MTHFD1L was also overexpressed in BLCA, HNSC, KIRP, LUAD, and UCEC patients of different clinicopathological features. Pathways enrichment analysis revealed the involvement of MTHFD1L-associated genes in five diverse pathways. We also explored few interesting correlations between MTHFD1L expression and its promoter methylation, genetic alterations, CNVs, and between CD8+ T immune cells level.

conclusionIn conclusion, our results elucidated that MTHFD1L can serve as a shared diagnostic and prognostic biomarker in BLCA, HNSC, KIRP, LUAD, and UCEC patients of different clinicopathological features.

Indexed as

AdultAgedAged, 80 and overAminohydrolasesBiomarkers, TumorDatabases, GeneticFemaleFormate-Tetrahydrofolate LigaseGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMaleMethylenetetrahydrofolate Dehydrogenase (NADP)Middle AgedMultienzyme ComplexesNeoplasmsAminohydrolasesBiomarkers, TumorFormate-Tetrahydrofolate Ligaseformyl-methenyl-methylenetetrahydrofolate synthetaseMethylenetetrahydrofolate Dehydrogenase (NADP)Multienzyme ComplexesBiomarkerCancerExpression variationsMTHFD1L

Identifiers

PMID34908119
PMCPMC8738869

What Socratic holds

Textmetadata
LicenceCC BY
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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.