Evidence map›Paper›PMID 38715072›Full record

ReviewMolecular cancer2024

Modulation of the tumor microenvironment and mechanism of immunotherapy-based drug resistance in breast cancer.

Moumita Kundu, Ramesh Butti, Venketesh K Panda, Diksha Malhotra, Sumit Das, Tandrima Mitra, Prachi Kapse, Suresh W Gosavi, Gopal C Kundu

Abstract readReview
In one paragraph

Review in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed, 2 pooled it
–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

172 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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112 more citing papers are in PubMed but not listed here.

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.

Moumita KunduSchool of Biotechnology, KIIT Deemed to be University, Bhubaneswar, 751024, India.
Ramesh ButtiDepartment of Internal Medicine, Division of Hematology and Oncology, University of Texas Southwestern Medical Center, Dallas, TX, 75235, USA.
Venketesh K Panda *School of Biotechnology, KIIT Deemed to be University, Bhubaneswar, 751024, India.
Diksha Malhotra *School of Biotechnology, KIIT Deemed to be University, Bhubaneswar, 751024, India.
Sumit DasNational Centre for Cell Sciences, Savitribai Phule Pune University Campus, Pune, 411007, India.
Tandrima MitraSchool of Biotechnology, KIIT Deemed to be University, Bhubaneswar, 751024, India.
Prachi KapseSchool of Basic Medical Sciences, Savitribai Phule Pune University, Pune, 411007, India.
Suresh W GosaviSchool of Basic Medical Sciences, Savitribai Phule Pune University, Pune, 411007, India.
Gopal C KunduSchool of Biotechnology, KIIT Deemed to be University, Bhubaneswar, 751024, India. gopalc.kundu@kiit.ac.in.ORCID 0000-0003-3534-4033

Funding

DBT-BUILDER Program, Govt. of India BT/INF/22/SP42155/2021Department of Biotechnology (DBT) Program, Govt of India Project/Grant No. BT/PR-32388/TRM/120/242/2019DST INSPIRE Fellowship Program DST/INSPIRE Fellowship/2021/IF210059Science and Engineering Research Board (SERB) Program, Govt. of India Project/Grant No. JCB/2023/000011
6 · The paper itself

Abstract

Breast cancer, the most frequent female malignancy, is often curable when detected at an early stage. The treatment of metastatic breast cancer is more challenging and may be unresponsive to conventional therapy. Immunotherapy is crucial for treating metastatic breast cancer, but its resistance is a major limitation. The tumor microenvironment (TME) is vital in modulating the immunotherapy response. Various tumor microenvironmental components, such as cancer-associated fibroblasts (CAFs), tumor-associated macrophages (TAMs), and myeloid-derived suppressor cells (MDSCs), are involved in TME modulation to cause immunotherapy resistance. This review highlights the role of stromal cells in modulating the breast tumor microenvironment, including the involvement of CAF-TAM interaction, alteration of tumor metabolism leading to immunotherapy failure, and other latest strategies, including high throughput genomic screening, single-cell and spatial omics techniques for identifying tumor immune genes regulating immunotherapy response. This review emphasizes the therapeutic approach to overcome breast cancer immune resistance through CAF reprogramming, modulation of TAM polarization, tumor metabolism, and genomic alterations.

Indexed as

Breast NeoplasmsDrug Resistance, NeoplasmImmunotherapyTumor MicroenvironmentCancer-Associated FibroblastsFemaleHumansTumor-Associated MacrophagesBreast cancerCancer-associated fibroblastImmune resistanceTherapeutic approachTumor-associated macrophageTumor microenvironment

Identifiers

PMID38715072
PMCPMC11075356

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.