Evidence map›Paper›PMID 34833123›Full record

ArticleLife (Basel, Switzerland)2021

Role of PTEN, PI3K, and mTOR in Triple-Negative Breast Cancer.

Mirjana Prvanović, Milica Nedeljković, Nasta Tanić, Tijana Tomić, Tanja Terzić, Zorka Milovanović, Zlatko Maksimović, Nikola Tanić

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 40 citations in OpenAlex.

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  7. [HDAC2-mediated H3K27 acetylation promotes the proliferation and migration of hepatocellular carcinoma cells].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article
  8. Review
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  11. Divide and Conquer-Targeted Therapy for Triple-Negative Breast Cancer.International journal of molecular sciences · 2025
    Review
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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 3 institutions in 2 countries.

Mirjana PrvanovićInstitute of Pathology, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Milica NedeljkovićDepartment of Experimental Oncology, Institute of Oncology and Radiology of Serbia, 11000 Belgrade, Serbia.ORCID 0000-0003-0153-3901
Nasta TanićDepartment of Radiobiology and Molecular Genetics, Institute of Nuclear Sciences "Vinča", National Institute of Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
Tijana TomićDepartment of Radiobiology and Molecular Genetics, Institute of Nuclear Sciences "Vinča", National Institute of Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-2111-8687
Tanja TerzićInstitute of Pathology, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Zorka MilovanovićDepartment of Pathology, Institute of Oncology and Radiology of Serbia, 11000 Belgrade, Serbia.
Zlatko MaksimovićPublic Health Institution Hospital "Sveti Vracevi", 76300 Bijeljina, Republika Srpska, Bosnia and Herzegovina.
Nikola TanićDepartment of Neurobiology, Institute for Biological Research "Siniša Stanković", National Institute of Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
University of Belgrade · RSOncology Institute of Vojvodina · RSUniversity Sinergija · BA

Funding

Ministry of Education, Science and Technological Development, Republic of Serbia III41031the Ministry of Education, Science and Technological Development, Republic of Serbia ON173049
6 · The paper itself

Abstract

Breast cancer is the most commonly occurring malignancy and the leading cause of cancer-related death in women. Triple-negative breast cancer (TNBC) is the most aggressive subtype and is associated with high recurrence rates, high incidence of distant metastases, and poor overall survival. The aim of this study was to investigate the PI3K/PTEN/Akt/mTOR pathway as one of the most frequently deregulated pathways in cancer. We aimed to explore the impact of PI3K and mTOR oncogenes as well as the PTEN tumor suppressor on TNBC clinical behavior, prognosis, and multidrug resistance (MDR), using immunohistochemistry and copy number analysis by quantitative real-time PCR. Our results revealed that loss of PTEN and high expression of PI3K and mTOR proteins are associated with poor outcome of TNBC patients. PTEN deletions appeared as a major cause of reduced or absent PTEN expression in TNBC. Importantly, homozygous deletions of PTEN (and not hemizygous deletions) are a potential molecular marker of metastasis formation and good predictors of TNBC outcome. In conclusion, we believe that concurrent examination of PTEN/PI3K/mTOR protein expression may be more useful in predicting TNBC clinical course than the analysis of single protein expression. Specifically, our results showed that PTEN-reduced/PI3K-high/mTOR-high expression constitutes a 'high risk' profile of TNBC.

Indexed as

ABCB1ABCC1ABCG2gene deletionsmTORmultidrug resistancePI3Kprotein expressionPTENtriple-negative breast cancer

Identifiers

PMID34833123
PMCPMC8621563
OpenAlexW3211607321

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.