Evidence map›Paper›PMID 33311447›Full record

ArticleCell death & disease2020

SEMG1/2 augment energy metabolism of tumor cells.

Oleg Shuvalov, Alyona Kizenko, Alexey Petukhov, Olga Fedorova, Alexandra Daks, Andrew Bottrill, Anastasiya V Snezhkina, Anna V Kudryavtseva, Nikolai Barlev

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Age-Associated Proteomic Changes in Human Spermatozoa.International journal of molecular sciences · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Phytochemicals Target Multiple Metabolic Pathways in Cancer.Antioxidants (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Article
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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

9 authors at 5 institutions in 2 countries.

Oleg ShuvalovInstitute of Cytology RAS, St-Petersburg, Russia.
Alyona KizenkoInstitute of Cytology RAS, St-Petersburg, Russia.
Alexey PetukhovInstitute of Cytology RAS, St-Petersburg, Russia.
Olga FedorovaInstitute of Cytology RAS, St-Petersburg, Russia.
Alexandra DaksInstitute of Cytology RAS, St-Petersburg, Russia.
Andrew BottrillUniversity of Leicester, Leicester, UK.ORCID 0000-0002-5182-3643
Anastasiya V SnezhkinaEngelhardt Institute of Molecular Biology, Moscow, Russia.
Anna V KudryavtsevaEngelhardt Institute of Molecular Biology, Moscow, Russia.
Nikolai BarlevInstitute of Cytology RAS, St-Petersburg, Russia. nick.a.barlev@gmail.com.
Institute of Cytology · RUEngelhardt Institute of Molecular Biology · RUFederal Almazov North-West Medical Research Centre · RUMoscow Institute of Physics and Technology · RUUniversity of Leicester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SEMG1 and SEMG2 genes belong to the family of cancer-testis antigens (CTAs), whose expression normally is restricted to male germ cells but is often restored in various malignancies. High levels of SEMG1 and SEMG2 expression are detected in prostate, renal, and lung cancer as well as hemoblastosis. However, the functional importance of both SEMGs proteins in human neoplasms is still largely unknown. In this study, by using a combination of the bioinformatics and various cellular and molecular assays, we have demonstrated that SEMG1 and SEMG2 are frequently expressed in lung cancer clinical samples and cancer cell lines of different origins and are negatively associated with the survival rate of cancer patients. Using the pull-down assay followed by LC-MS/MS mass-spectrometry, we have identified 119 proteins associated with SEMG1 and SEMG2. Among the SEMGs interacting proteins we noticed two critical glycolytic enzymes-pyruvate kinase M2 (PKM2) and lactate dehydrogenase A (LDHA). Importantly, we showed that SEMGs increased the protein level and activity of both PKM2 and LDHA. Further, both SEMGs increased the membrane mitochondrial potential (MMP), glycolysis, respiration, and ROS production in several cancer cell lines. Taken together, these data provide first evidence that SEMGs can up-regulate the energy metabolism of cancer cells, exemplifying their oncogenic features.

Indexed as

Energy MetabolismCarrier ProteinsCell Line, TumorCell RespirationGene Expression Regulation, NeoplasticGlycolysisHEK293 CellsHumansLactate Dehydrogenase 5Lung NeoplasmsMembrane Potential, MitochondrialMembrane ProteinsModels, BiologicalNeoplasmsProtein BindingReactive Oxygen SpeciesCarrier ProteinsLactate Dehydrogenase 5Membrane ProteinsReactive Oxygen SpeciesRNA, MessengerSeminal Vesicle Secretory Proteinsseminal vesicle-specific antigenThyroid Hormone-Binding ProteinsThyroid Hormones

Identifiers

PMID33311447
PMCPMC7733513
OpenAlexW3110926740

What OpenQuestion holds

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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 OpenQuestion graph.