Evidence map›Paper›PMID 41723216›Full record

ArticleScientific reports2026

EGFR and AR expression and co-expression in Indian triple-negative breast cancer with patient outcome association.

Pooja Vaid, Anirudha Puntambekar, Pranali Kanse, Shweta Kadu, Piyush Agrawal, Aditi Khatpe, Rituja Banale, Ruhi Reddy, Devaki A Kelkar, Sridhar Hannenhalli and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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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

13 authors.

Pooja VaidCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Anirudha PuntambekarSahyadri Hospitals PVT Ltd, Pune, India.
Pranali KanseCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Shweta KaduCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Piyush AgrawalDivision of Medical Research, SRM Medical College Hospital & Research Centre, SRMIST, Kattankulathur, Chennai, India.
Aditi KhatpeCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Rituja BanaleCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Ruhi ReddyCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Devaki A KelkarCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Sridhar HannenhalliCancer Data Science Laboratory, Center for Cancer Research, NCI, NIH, Bethesda, USA.
L S ShashidharaCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Chaitanyanand KoppikerCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India.
Madhura KulkarniCentre for Translational Cancer Research: a joint initiative of Indian Institute of Science Education and Research (IISER) Pune and Prashanti Cancer Care Mission (PCCM) Pune, Pune, India. madhura.kulkarni@prashanticancercare.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple negative breast cancer (TNBC) is a highly heterogeneous disease lacking established molecular targets. Its incidence is notably higher in Indian women compared to Western populations. To characterize molecular diversity within Indian TNBCs, we analyzed 93 tumor samples for the expression of EGFR, CK5/6, and androgen receptor (AR) and examined their association with clinicopathological parameters and patient outcomes. EGFR expression was detected in 65% of tumors and AR in 38%. EGFR-positive tumors were of higher grade and had a significant association with vimentin positivity and were associated with a trend toward shorter disease-free survival (DFS). AR-positive tumors exhibited lower vimentin expression, suggesting a less mesenchymal phenotype, but paradoxically showed a trend toward poorer survival. Approximately 25% of the tumors displayed co-expression of EGFR and AR at the tissue level, and 15% contained EGFR-positive, AR-positive, double-positive tumor cells, as detected by multiplex immunofluorescence. Patients harboring such double-positive cells showed a trend towards poorer DFS. Single-cell RNA-sequencing data from independent TNBC cohorts confirmed the presence of EGFR + AR+ tumor cells at lower frequencies (0.8-5%). These findings suggest that EGFR-AR co-expression in TNBC tumors is defined as an exploratory group with potential therapeutic implications to combat the increased risk of recurrence. Our results underscore the importance of population-specific molecular profiling in TNBC and suggest that dual targeting of the EGFR and AR pathways may be a promising direction for clinical research in Indian breast cancer patients.

Indexed as

ErbB ReceptorsReceptors, AndrogenTriple Negative Breast NeoplasmsAdultAgedBiomarkers, TumorDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansIndiaMiddle AgedPrognosisAR protein, humanBiomarkers, TumorEGFR protein, humanErbB ReceptorsReceptors, AndrogenARBasal TNBCco-expression of EGFR and AREGFRMolecular profile

Identifiers

PMID41723216
PMCPMC13043925

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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.