Evidence map›Paper›PMID 42421143›Full record

ReviewBreast cancer research : BCR2026

Postpartum breast cancer as a distinct oncologic entity: linking physiological tissue remodelling to tumor biology and clinical translation.

Vidya P Nimbalkar, Snijesh V P, Akash Dash, Meenakshi Jothikumar, Anjaney J Pandey, P S Hari, Aruna Korlimarla, Sabarinathan Radhakrishanan, Jyothi S Prabhu

Abstract readReview
In one paragraph

Review in Breast cancer research : BCR, 2026. 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.

Vidya P NimbalkarDivision of Molecular Medicine, St. John's Research Institute, St. John's Medical College, Bangalore, Karnataka, India.
Snijesh V PDivision of Molecular Medicine, St. John's Research Institute, St. John's Medical College, Bangalore, Karnataka, India.
Akash DashDivision of Molecular Medicine, St. John's Research Institute, St. John's Medical College, Bangalore, Karnataka, India.
Meenakshi JothikumarDivision of Molecular Medicine, St. John's Research Institute, St. John's Medical College, Bangalore, Karnataka, India.
Anjaney J PandeyNational Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, Karnataka, India.
P S HariDepartment of Molecular Oncology, Sri Shankara National Center for Cancer Prevention and Research, Sri Shankara Cancer Foundation, Bangalore, India.
Aruna KorlimarlaDepartment of Molecular Oncology, Sri Shankara National Center for Cancer Prevention and Research, Sri Shankara Cancer Foundation, Bangalore, India.
Sabarinathan RadhakrishananNational Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, Karnataka, India.
Jyothi S PrabhuDivision of Molecular Medicine, St. John's Research Institute, St. John's Medical College, Bangalore, Karnataka, India. jyothi@sjri.res.in.ORCID http://orcid.org/0000-0002-2269-3704

Funding

Integrated Networks of Scholars in Global Health Research Training (INSIGHT) Program D43TW012274 · FIC · UNIVERSITY OF MARYLAND BALTIMORE · PI Olakunle Alonge, Jessica Griffin Burke · 2022 to 2026
$6.5M
FIC NIH HHS D43 TW012274FIC NIH HHS D43TW012274Indian Council of Medical Research IIRPIG-2024-01-00934
6 · The paper itself

Abstract

Postpartum breast cancer (PPBC), defined as breast cancer diagnosed within 10 years after childbirth, is increasingly recognized as a biologically distinct and clinically aggressive subtype affecting young women worldwide. The postpartum mammary gland undergoes extensive remodelling during involution, characterized by inflammation, extracellular matrix reorganization, and immune suppression, collectively creating a tumor-promoting microenvironment. Recent studies have revealed unique molecular features of PPBC, including alterations in immune composition, stromal activation, and selective pathway enrichment that distinguish it from breast cancers in nulliparous or age-matched parous women. While estrogen signalling remains an important regulatory axis during the postpartum period, its interplay with involution-associated processes and tumor behaviour requires further elucidation. In this review, we summarize current advances in understanding PPBC biology, highlight emerging biomarkers, and discuss evolving therapeutic considerations relevant to this high-risk population. We also provide an overview of ongoing clinical investigations, such as aspirin-based anti-inflammatory trials aimed at targeting postpartum-specific mechanisms that may contribute to tumor initiation or progression. Together, these insights emphasize the need for dedicated translational research and tailored clinical strategies to improve early detection, risk stratification, and outcomes for women diagnosed with PPBC.

Indexed as

Breast NeoplasmsPostpartum PeriodBiomarkers, TumorFemaleHumansTranslational Research, BiomedicalTumor MicroenvironmentBiomarkers, TumorEstrogen signalingExtracellular matrix remodellingImmune infiltrationMammary gland involutionPostpartum breast cancerTherapeutics

Identifiers

PMID42421143
PMCPMC13628952

What OpenQuestion holds

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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.