Evidence map›Paper›PMID 35135596›Full record

ArticleJournal of ovarian research2022

Up-regulation of MTHFD2 is associated with clinicopathological characteristics and poor survival in ovarian cancer, possibly by regulating MOB1A signaling.

Xiangrong Cui, Huancheng Su, Jiaolin Yang, Xueqing Wu, Kai Huo, Xuan Jing, Sanyuan Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. MTHFD2: a promising metabolic checkpoint for diseases.Journal of translational medicine · 2026
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  9. Common Variants in One-Carbon Metabolism Genes (International journal of molecular sciences · 2023
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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

7 authors at 1 institution in 1 country.

Xiangrong Cui *Reproductive Medicine Center, The affiliated Children's Hospital of Shanxi Medical University, Children's Hospital of Shanxi, Women Health Center of Shanxi, Taiyuan, 030001, China.
Huancheng Su *Gynaecology and Obstetrics Department, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Jiaolin YangGynaecology and Obstetrics Department, First Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Xueqing WuReproductive Medicine Center, The affiliated Children's Hospital of Shanxi Medical University, Children's Hospital of Shanxi, Women Health Center of Shanxi, Taiyuan, 030001, China.
Kai HuoBreast Surgery Department, Tumor Hospital of Shanxi, Affiliated of Shanxi Medical University, Taiyuan, 030000, China.
Xuan JingGynaecology and Obstetrics Department, First Hospital of Shanxi Medical University, Taiyuan, 030001, China. jx05070103@163.com.
Sanyuan ZhangClinical Laboratory, The Affiliated People's Hospital of Shanxi Medical University, Taiyuan, 030001, China. zhangsanyuanshanxi@163.com.
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMTHFD2 is a folate-coupled metabolic enzyme, which has been proved to participant in the metabolic reprogramming and tumor cell-sustaining proliferative capacity. However, the function of MTHFD2 in the development of ovarian cancer and its potential molecular mechanisms is still unclear. MATERIALS AND

methodsThe expression, various mutations, prognosis, and related network signaling pathways of MTHFD2 were analyzed using bioinformatics-related websites, including Oncomine, GEPIA, UCSC, cBioPortal, KM Plotter, TISIDB and TIMER. The prognostic value of MTHFD2 expression was validated by our own ovarian cancer samples using RT-qPCR. The migration ad invasion of ovarian cancer cells were further analyzed by CCK-8 and transwell assay. The Western-blot assay was performed to explore the protein levels of MTHFD2 and MOB1A.

resultsWe obtained the following important results. (1) MTHFD2 expression was markedly up-regulated in ovarian cancer than normal samples. (2) Among patients with ovarian cancer, those with higher MTHFD2 expression was associated with lower survival rate. (3) The major mutation type of MTHFD2 in ovarian cancer samples was missense mutation. (4) MTHFD2 knockdown inhibited proliferation, migration, invasion, as well as the expression of MOB1A in vitro.

conclusionMTHFD2, as a NAD + -dependent enzyme, accelerated tumor progression by up-regulating MBO1A, suggesting that this protein may be an independent prognostic factor and a potential therapeutic target for future ovarian cancer treatments.

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAminohydrolasesCell Line, TumorCell MovementCell ProliferationComputational BiologyDatabases, GeneticFemaleGene ExpressionGene Knockdown TechniquesHumansLymphocytes, Tumor-InfiltratingMethylenetetrahydrofolate Dehydrogenase (NADP)Middle AgedAdaptor Proteins, Signal TransducingAminohydrolasesMethylenetetrahydrofolate Dehydrogenase (NADP)MOB1A protein, humanMTHFD2 protein, humanMultifunctional EnzymesMOB1AMTHFD2Ovarian cancerPrognosis

Identifiers

PMID35135596
PMCPMC8827288
OpenAlexW4210940912

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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.