Evidence map›Paper›PMID 35898402›Full record

ArticleFrontiers in cell and developmental biology2022

ZIP11 Regulates Nuclear Zinc Homeostasis in HeLa Cells and Is Required for Proliferation and Establishment of the Carcinogenic Phenotype.

Monserrat Olea-Flores, Julia Kan, Alyssa Carlson, Sabriya A Syed, Cat McCann, Varsha Mondal, Cecily Szady, Heather M Ricker, Amy McQueen, Juan G Navea and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  15. Cell Immortality:Life (Basel, Switzerland) · 2024
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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

12 authors at 4 institutions in 1 country.

Monserrat Olea-FloresDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Julia KanDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Alyssa CarlsonDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Sabriya A SyedDepartment of Biochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, Worcester, MA, United States.
Cat McCannDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Varsha MondalDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Cecily SzadyDepartment of Chemistry, Skidmore College, Saratoga Springs, NY, United States.
Heather M RickerDepartment of Chemistry, Skidmore College, Saratoga Springs, NY, United States.
Amy McQueenDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Juan G NaveaDepartment of Chemistry, Skidmore College, Saratoga Springs, NY, United States.
Leslie A CaromileDepartment of Cell Biology, Center for Vascular Biology, UCONN Health-Center, Farmington, CT, United States.
Teresita Padilla-BenavidesDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT, United States.
Wesleyan University · USSkidmore College · USUniversity of Massachusetts Chan Medical School · USUConn Health · US

Funding

Mechanisms of Cu-binding factors to promote myogenic gene expressionR01AR077578 · NIAMS · WESLEYAN UNIVERSITY · PI Teresita Del Nino Jesus Padilla-Benavides · 2021 to 2026
$2.1M
NIAMS NIH HHS R01 AR077578
6 · The paper itself

Abstract

Zinc (Zn) is an essential trace element that plays a key role in several biological processes, including transcription, signaling, and catalysis. A subcellular network of transporters ensures adequate distribution of Zn to facilitate homeostasis. Among these are a family of importers, the Zrt/Irt-like proteins (ZIP), which consists of 14 members (ZIP1-ZIP14) that mobilize Zn from the extracellular domain and organelles into the cytosol. Expression of these transporters varies among tissues and during developmental stages, and their distribution at various cellular locations is essential for defining the net cellular Zn transport. Normally, the ion is bound to proteins or sequestered in organelles and vesicles. However, though research has focused on Zn internalization in mammalian cells, little is known about Zn mobilization within organelles, including within the nuclei under both normal and pathological conditions. Analyses from stomach and colon tissues isolated from mouse suggested that ZIP11 is the only ZIP transporter localized to the nucleus of mammalian cells, yet no clear cellular role has been attributed to this protein. We hypothesized that ZIP11 is essential to maintaining nuclear Zn homeostasis in mammalian cells. To test this, we utilized HeLa cells, as research in humans correlated elevated expression of ZIP11 with poor prognosis in cervical cancer patients. We stably knocked down ZIP11 in HeLa cancer cells and investigated the effect of Zn dysregulation

Indexed as

cell cyclecervical cancer cellsgene expressionMTF1senescencezinc transportZIP11

Identifiers

PMID35898402
PMCPMC9309433
OpenAlexW4285004631

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LicenceCC BY
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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.