Evidence map›Paper›PMID 40621755›Full record

ArticleCurrent drug targets2025

GSTP1, PRDX2 and NFE2L2: Potential Markers for Primary Stage Breast Cancer.

Syeda Abiha Zehra Jaffari, Fatima Haider, Nida Syed, Amber Ilyas, Farha Idrees, Alex von Kriegsheim, Roopesh Krishnankutty, Syeda Nuzhat Nawab, Zehra Hashim

Abstract read
PubMed Publisher
In one paragraph

Article in Current drug targets, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Syeda Abiha Zehra JaffariDr. Zafar H. Zaidi Center for Proteomics, University of Karachi, Karachi, 75270, Pakistan.ORCID 0000-0003-1080-6721
Fatima HaiderDr. Zafar H. Zaidi Center for Proteomics, University of Karachi, Karachi, 75270, Pakistan.
Nida SyedDr. Zafar H. Zaidi Center for Proteomics, University of Karachi, Karachi, 75270, Pakistan.ORCID 0000-0003-2213-2648
Amber IlyasDr. Zafar H. Zaidi Center for Proteomics, University of Karachi, Karachi, 75270, Pakistan.ORCID 0000-0002-2994-3884
Farha IdreesDr. Ziauddin Hospital, Karachi, 74700, Pakistan.ORCID 0000-0003-1892-0457
Alex von KriegsheimInstitute of Genetics and Cancer, The University of Edinburgh, Crewe Road South, Edinburgh EH4 2XR, UK.ORCID 0000-0002-4952-8573
Roopesh KrishnankuttyInstitute of Genetics and Cancer, The University of Edinburgh, Crewe Road South, Edinburgh EH4 2XR, UK.ORCID 0000-0002-1496-6135
Syeda Nuzhat NawabThe Karachi Institute of Biotechnology and Genetic Engineering (KIBGE), University of Karachi, Karachi, 75270, Pakistan.ORCID 0000-0002-4828-3287
Zehra HashimDr. Zafar H. Zaidi Center for Proteomics, University of Karachi, Karachi, 75270, Pakistan.ORCID 0000-0001-6750-093X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBreast cancer incidence and mortality have continued to rise over the past few decades. Despite advancements made in clinical research, the most imperative feature of breast cancer management is the diagnosis at the earliest stages. The current focus of the study is to identify and quantify differentially expressed oxidative stress-related proteins as putative early- stage markers for breast cancer.

methodsNormal and cancerous breast tissue samples (n = 40) were collected after approval from the institutional bioethics committee (IBC) and with patient's consent. A label-free proteomic approach was used to quantify oxidative stress-related proteins. Gene expression of GSTP1, PRDX2, HSP90, NFE2L2, and miR-365a was quantified using RT-qPCR in all samples. Protein expression of PRDX2 and GSTP1 was further analyzed using immunohistochemistry.

resultsThe protein and gene expression of PRDX2, GSTP1, and HSP90 were significantly upregulated (p < 0.05) in cancerous samples as compared to normal. However, gene and protein expression of the transcription factor NFE2L2 was significantly downregulated (p < 0.05) in diseased samples. OncomiR-365a was also significantly upregulated (p < 0.05) in cancerous samples. Immunohistochemical analysis also confirmed the upregulated expression of GSTP1 and PRDX2 in cancer tissues. DISCUSSION: Our study provides insight into the significant role of GSTP1, PRDX2, and NFE2L2 in the pathophysiology of the disease as early-stage breast cancer markers. It is suggested that altered expression of these key proteins could play a protective role in reducing the damage.

conclusionIt can be concluded that GSTP1, PRDX2, and NFE2L2 may serve as predictive early- stage markers for diagnosis and potential therapeutic targets for breast cancer.

Indexed as

Biomarkers, TumorBreast NeoplasmsGlutathione S-Transferase piNF-E2-Related Factor 2PeroxiredoxinsAdultAgedFemaleGene Expression Regulation, NeoplasticHSP90 Heat-Shock ProteinsHumansMicroRNAsMiddle AgedNeoplasm StagingOxidative StressProteomicsBiomarkers, TumorGlutathione S-Transferase piGSTP1 protein, humanHSP90 Heat-Shock ProteinsMicroRNAsNFE2L2 protein, humanNF-E2-Related Factor 2PeroxiredoxinsPRDX2 protein, humanBreast cancerearly stage markersGSTP1NFE2L2.oxidative stressPRDX2

Identifiers

PMID40621755

What OpenQuestion holds

Textmetadata
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.