Evidence map›Paper›PMID 41085554›Full record

ReviewMolecular cancer research : MCR2025

MDSCs in Breast Cancer: Metastasis, Lipid Metabolism, and Therapeutics.

Ukjin Kim, Rumela Chakrabarti

Abstract readReview
In one paragraph

Review in Molecular cancer research : MCR, 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. Review
  3. 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

2 authors.

Ukjin KimDepartment of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-2974-0710
Rumela ChakrabartiDepartment of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0001-7720-9660

Funding

Deciphering the function of DNp63 and MDSCs in tumor promotion and metastasis of TNBCsR01CA237243 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CHAKRABARTI, RUMELA · 2019 to 2023
$1.8M
American Cancer Society (ACS) ACS-CSCC-Team-23-978452-01-CSCCAmerican Cancer Society (ACS) RSG DDC-133604Breast Cancer Research Foundation (BCRF) SPEC-23-024NCI NIH HHS R01 CA237243
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSC) are one of the major contributors to the immunosuppressive microenvironment of breast cancer. MDSCs have unique mechanisms for each breast cancer metastasis site, and lipid metabolism acts as an energy source necessary to perform the role of MDSCs. In addition, MDSCs show different characteristics depending on the breast cancer subtype. Currently, there is no clear understanding of MDSCs tailored to subtypes and metastatic sites in breast cancer. In this study, we reviewed the biology and function of MDSCs revealed in breast cancer, focusing on metastasis and lipid metabolism, and discussed treatments targeting MDSCs. Understanding MDSC properties and functions by breast cancer subtype and metastatic niche will be a prerequisite for taking the next step in subdividing patients with breast cancer and providing customized treatment.

Indexed as

Breast NeoplasmsLipid MetabolismMyeloid-Derived Suppressor CellsAnimalsFemaleHumansNeoplasm MetastasisTumor Microenvironment

Identifiers

PMID41085554
PMCPMC12742582

What OpenQuestion holds

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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.