Evidence map›Paper›PMID 32944394›Full record

ReviewCancer biology & medicine2020

Zinc dysregulation in cancers and its potential as a therapeutic target.

Jie Wang, Huanhuan Zhao, Zhelong Xu, Xinxin Cheng

Open access · goldAbstract readReview
In one paragraph

Review in Cancer biology & medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 2 pooled it
8.2field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 2 syntheses or guidelines pooled it, 120 citations in OpenAlex.

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  12. Identification of novel molecular subtypes in ovarian cancerThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
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19 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Jie WangDepartment of Physiology and Pathophysiology, Tianjin Medical University, Tianjin 300070, China.
Huanhuan ZhaoDepartment of Physiology and Pathophysiology, Tianjin Medical University, Tianjin 300070, China.
Zhelong XuDepartment of Physiology and Pathophysiology, Tianjin Medical University, Tianjin 300070, China.
Xinxin ChengDepartment of Physiology and Pathophysiology, Tianjin Medical University, Tianjin 300070, China.ORCID 0000-0001-6485-8960
Tianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zinc is an essential element and serves as a structural or catalytic component in many proteins. Two families of transporters are involved in maintaining cellular zinc homeostasis: the ZIP (SLC39A) family that facilitates zinc influx into the cytoplasm, and the ZnT (SLC30A) family that facilitates zinc efflux from the cytoplasm. Zinc dyshomeostasis caused by the dysfunction of zinc transporters can contribute to the initiation or progression of various cancers, including prostate cancer, breast cancer, and pancreatic cancer. In addition, intracellular zinc fluctuations lead to the disturbance of certain signaling pathways involved in the malignant properties of cancer cells. This review briefly summarizes our current understanding of zinc dyshomeostasis in cancer, and discusses the potential roles of zinc or zinc transporters in cancer therapy.

Indexed as

Carrier ProteinsCytoplasmHomeostasisHumansNeoplasmsRepressor ProteinsSignal TransductionZincCarrier ProteinsRepressor ProteinsZGPAT protein, humanZinczinc-binding proteinCancercancer therapyzinc homeostasiszinc transporter

Identifiers

PMID32944394
PMCPMC7476080
OpenAlexW3087583416

What OpenQuestion holds

Textmetadata
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.