Evidence map›Paper›PMID 41226334›Full record

ArticleInternational journal of molecular sciences2025

Transcription Factor EB (TFEB) Expression and Localization in the Third-Trimester Placenta.

Cinzia Giacometti, Alessandro Ambrosi, Serena Cavaliere, Anna Caliò, Daniele Mautone, Guido Martignoni

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Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Cinzia GiacomettiPathology Unit, Pederzoli Hospital, Peschiera del Garda, 37019 Verona, Italy.ORCID 0000-0002-5313-0971
Alessandro AmbrosiIRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milano, Italy.ORCID 0000-0003-1976-5663
Serena CavaliereGynecology & Obstetrics Unit, Pederzoli Hospital, Peschiera del Garda, 37019 Verona, Italy.
Anna CaliòPathology Unit, Department of Diagnostic and Public Health, University of Verona, 37126 Verona, Italy.
Daniele MautoneGynecology & Obstetrics Unit, Pederzoli Hospital, Peschiera del Garda, 37019 Verona, Italy.
Guido MartignoniPathology Unit, Pederzoli Hospital, Peschiera del Garda, 37019 Verona, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factor EB (TFEB) is expressed at high levels in the trophoblast cells of the placenta, where it plays a critical role in regulating normal vascularization. Preeclampsia (PE) is a severe complication of pregnancy with a high incidence of maternal and fetal morbidity and mortality. Gestational diabetes (GD) is a metabolic disease that can affect placental villous maturation and villous vascularity. We analyzed the expression of three different antibodies: TFEB from Invitrogen (TFEB-INV), which detects endogenous levels of TFEB only when phosphorylated at Ser211; TFEB from Bethyl Labs (TFEB-B), which recognizes and binds E-box sequences; and TFEB from Santa Cruz (C-6) (TFEB-SC), which is specifically used for epitope mapping between 440 and 470. We evaluated the presence/absence of TFEB in six placental districts: syncytiotrophoblast (STB), cytotrophoblast (CTB), extravillous trophoblast (EVT), syncytial knots, stem villi vessels, and villous capillaries. TFEB-B was significantly expressed in the stem villi vessels, STB, and villi vessels of GD cases. The lack of TFEB expression in late-onset PE appears to corroborate the role of TFEB in vascular remodeling during placental development. The positive results in STB and vessels in GD cases, regardless of the histological diagnosis, may suggest that the expression of TFEB mitigates hypoxic injury via the Akt/mTOR pathway.

Indexed as

Basic Helix-Loop-Helix Leucine Zipper Transcription FactorsPlacentaPregnancy Trimester, ThirdAdultDiabetes, GestationalFemaleHumansPre-EclampsiaPregnancyTrophoblastsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsTFEB protein, humangestational diabetesimmunohistochemistrypreeclampsiaTFEB

Identifiers

PMID41226334
PMCPMC12608947

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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.