Evidence map›Paper›PMID 40622584›Full record

ReviewJournal of mammary gland biology and neoplasia2025

Intraductal Injection of Adenoviruses to Perform Lineage Tracing in the Mammary Gland.

Xueqing Chen, Sen Han, Dongyi Zhao, Zhe Li

Abstract readReview
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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.

Xueqing ChenDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Sen HanDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Dongyi ZhaoDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Zhe LiDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA. zhli@bwh.harvard.edu.ORCID 0000-0002-3434-0885

Funding

Mechanism of LSD1 in breast cancer metastasis suppressionR01CA248306 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI LI, ZHE · 2021 to 2025
$1.9M
Interplay of mammary luminal cells and environmental factors in establishing p53-deficient premalignant fieldR01CA222560 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI LI, ZHE · 2018 to 2022
$1.9M
DNA damage-related stemness program during BRCA1 breast cancer initiationR01CA295752 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Zhe Li · 2025 to 2026
$1.1M
CRISPR/Cas9-based lineage tracing for fate mapping of cancer cells and stem cellsR21CA205825 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI LI, ZHE · 2016 to 2017
$420k
Development of a clinically relevant mouse model of ER+ breast cancerR21CA256468 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI LI, ZHE · 2021 to 2022
$414k
Harvard Stem Cell Institute SG-0062-10NCI NIH HHS R01 CA222560NCI NIH HHS R01 CA248306NCI NIH HHS R01 CA295752NCI NIH HHS R21 CA205825NCI NIH HHS R21 CA256468U.S. Department of Defense W81XWH-15-1-0100
6 · The paper itself

Abstract

Lineage tracing is a fundamental tool in developmental biology and cancer research, providing critical insights into cell fate decisions, tissue homeostasis and tumor initiation. The mammary gland is a highly dynamic organ with a complex cellular hierarchy, making it an ideal system for lineage-tracing studies. Classic approaches, such as tamoxifen-inducible CreER/loxP recombination, have significantly advanced our understanding of mammary epithelial cell (MEC) differentiation, homeostasis, and transformation. However, these methods have limitations, including potential effects of tamoxifen on estrogen signaling, low mammary gland specificity, and the requirement for transgenic model creation and mouse breeding. Adenovirus-Cre (Ad-Cre)-based lineage tracing has emerged as a powerful alternative, enabling rapid and organ-specific recombination. This review provides a comprehensive evaluation of the Ad-Cre approach in mammary gland biology, comparing its efficiency, specificity, and technical advantages over the CreER-based method. We discuss applications of Ad-Cre intraductal injection-based lineage tracing in mapping MEC fates, identifying the cellular origins of breast cancer, and modeling tumor progression. Additionally, we highlight its ability to induce genetic marking at a clonal level, facilitating precise investigations into MEC plasticity and tumor cell heterogeneity. Despite its advantages, Ad-Cre lineage tracing also presents challenges, such as low cell-targeting efficiency and potential effect on the mammary gland immune microenvironment. Future advancements, including the integration of CRISPR-based barcoding, may further enhance its utility for high-resolution fate mapping. By summarizing recent advancements and comparative analyses, this review underscores the significance of Ad-Cre lineage tracing as a versatile and powerful tool in mammary gland biology and breast cancer research.

Indexed as

AdenoviridaeBreast NeoplasmsCell LineageMammary Glands, AnimalMammary Glands, HumanAnimalsCell DifferentiationEpithelial CellsFemaleHumansIntegrasesMiceIntegrasesAdenovirusBreast cancerCell-of-originCellular OriginIntraductal InjectionMammary Epithelial CellMammary GlandPulse-chase Lineage Tracing

Identifiers

PMID40622584
PMCPMC12234609

What OpenQuestion holds

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LicenceCC BY
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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.