Evidence map›Paper›PMID 40520016›Full record

ArticleInternational journal of biological sciences2025

Mechanistic role of metal-responsive transcription factor-1 (MTF1) in cadmium-induced prostate carcinogenesis.

Balaji Chandrasekaran, Bhawna Tyagi, Ashish Tyagi, Vaibhav Shukla, Mollie Schatz, Thulasidharan Nair Devanarayanan, Neha Tyagi, Chendil Damodaran

Abstract read
In one paragraph

Article in International journal of biological sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Balaji ChandrasekaranCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Bhawna TyagiCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Ashish TyagiCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Vaibhav ShuklaCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Mollie SchatzCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Thulasidharan Nair DevanarayananCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Neha TyagiCollege of Pharmacy, Texas A&M University, College Station, TX, USA.
Chendil DamodaranCollege of Pharmacy, Texas A&M University, College Station, TX, USA.

Funding

Cell Survival Advantage in Cadmium Induced CarcinogenesisR01ES030019 · NIEHS · UNIVERSITY OF LOUISVILLE · PI DAMODARAN, CHENDIL · 2019 to 2025
$2.3M
Elucidating the molecular signaling of Cadmium CarcinogenesisR01ES033657 · NIEHS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI Chendil Damodaran · 2022 to 2026
$2.0M
NIEHS NIH HHS R01 ES030019NIEHS NIH HHS R01 ES033657
6 · The paper itself

Abstract

Our previous report emphasized that chronic exposure to cadmium (10 µM) over one year led to the transformation of benign prostatic hyperplasia (BPH1) cells into malignancy through the ZIC2 signaling pathway (cerebellar zinc pathway). However, the upstream mechanisms that trigger this transformation have yet to be fully elucidated. The present study suggests that cadmium exposure induces metal regulatory element-binding transcription factor-1 (MTF1), which activates ZIC2 in BPH1 cells. Interestingly, knocking out ZIC2 expression did not affect MTF1 levels, indicating that MTF1 acts upstream of the ZIC2 signaling pathway. To further investigate the MTF-1/ZIC2 relationship, we overexpressed MTF-1 in untransformed BPH1 cells leading to the induction of ZIC2 along with other stem cell markers, such as ALDH1A1, Nanog, and CD44. This overexpression also facilitated spheroid formation. Conversely, silencing MTF1 expression in transformed cells inhibited spheroid formation and also reduced survival rate. It diminished the expression of stem cell and epithelial-to-mesenchymal transition markers and tumor growth in nude mice. Transcriptomic analysis of MTF1 silenced xenograft tumors confirmed these findings. Using CRISPR-Cas9 to knock out ZIC2 also prevented tumor formation in nude mice. These results emphasize the critical role of MTF1 in the oncogenic process and its involvement in the ZIC2-mediated transformation associated with Cd-induced malignant changes.

Indexed as

CadmiumCarcinogenesisDNA-Binding ProteinsProstatic NeoplasmsTranscription FactorsAnimalsEpithelial-Mesenchymal TransitionHumansMaleMiceMice, NudeSignal TransductionTranscription Factor MTF-1CadmiumDNA-Binding ProteinsTranscription Factor MTF-1Transcription FactorsBPH1cadmiummetalMTF1transformation.ZIC2

Identifiers

PMID40520016
PMCPMC12160861

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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.