Evidence map›Paper›PMID 38383522›Full record

ArticleNature communications2024

Converging and evolving immuno-genomic routes toward immune escape in breast cancer.

Juan Blanco-Heredia, Carla Anjos Souza, Juan L Trincado, Maria Gonzalez-Cao, Samuel Gonçalves-Ribeiro, Sara Ruiz Gil, Dmytro Pravdyvets, Samandhy Cedeño, Maurizio Callari, Antonio Marra and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. CD4Science advances · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. 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

23 authors at 9 institutions in 4 countries.

Juan Blanco-Heredia *IrsiCaixa, Germans Trias i Pujol University Hospital, Badalona, Spain.ORCID 0000-0001-9526-7450
Carla Anjos Souza *IrsiCaixa, Germans Trias i Pujol University Hospital, Badalona, Spain.ORCID 0000-0003-0671-7275
Juan L Trincado *Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.ORCID 0000-0001-5363-3774
Maria Gonzalez-CaoDexeus Institute of Oncology, Quironsalud Group, Barcelona, Spain.ORCID 0000-0003-3791-540X
Samuel Gonçalves-RibeiroVall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron University Hospital, Barcelona, Spain.ORCID 0000-0002-0261-3965
Sara Ruiz GilCentro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.
Dmytro PravdyvetsOmniscope, Barcelona, Spain.
Samandhy CedeñoIrsiCaixa, Germans Trias i Pujol University Hospital, Badalona, Spain.ORCID 0000-0001-8312-0208
Maurizio CallariCancer Research UK Cambridge Institute, Robinson Way, Cambridge, UK.ORCID 0000-0001-5239-0918
Antonio MarraDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Andrea M GazzoDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Britta WeigeltDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0001-9927-1270
Fresia ParejaDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0003-3748-8049
Theodore VougiouklakisDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Achim A JungbluthDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Rafael RosellDexeus Institute of Oncology, Quironsalud Group, Barcelona, Spain.ORCID 0000-0003-0817-3400
Christian BranderIrsiCaixa, Germans Trias i Pujol University Hospital, Badalona, Spain.ORCID 0000-0002-0548-5778
Francesc TresserraDexeus Institute of Oncology, Quironsalud Group, Barcelona, Spain.
Jorge S Reis-FilhoDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0003-2969-3173
Daniel Guimarães Tiezzi *Department of Gynecology and Obstetrics - Breast Disease Division and Laboratory for Translational Data Science, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Brazil.ORCID 0000-0002-2660-0093
Nuria de la IglesiaIrsiCaixa, Germans Trias i Pujol University Hospital, Badalona, Spain.ORCID 0000-0002-1083-7715
Holger HeynCentro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.ORCID 0000-0002-3276-1889
Leticia De Mattos-ArrudaIrsiCaixa, Germans Trias i Pujol University Hospital, Badalona, Spain. ldmarruda@gmail.com.ORCID 0000-0002-4992-3645
Memorial Sloan Kettering Cancer Center · USIrsiCaixa · ESCentro Nacional de Análisis Genómico · ESCancer Research UK Cambridge Center · GBInstitut d'Investigació en Ciències de la Salut Germans Trias i Pujol · ESJosep Carreras Leukaemia Research Institute · ESUniversidade de São Paulo · BRUniversitat de Vic - Universitat Central de Catalunya · ESVall d'Hebron Hospital Universitari · ES

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Targeting Polθ to Overcome PARP Inhibitor Resistance in Homologous Recombination Deficient Breast CancerP50CA247749 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Simon N. Powell · 2020 to 2026
$16.3M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA247749
6 · The paper itself

Abstract

The interactions between tumor and immune cells along the course of breast cancer progression remain largely unknown. Here, we extensively characterize multiple sequential and parallel multiregion tumor and blood specimens of an index patient and a cohort of metastatic triple-negative breast cancers. We demonstrate that a continuous increase in tumor genomic heterogeneity and distinct molecular clocks correlated with resistance to treatment, eventually allowing tumors to escape from immune control. TCR repertoire loses diversity over time, leading to convergent evolution as breast cancer progresses. Although mixed populations of effector memory and cytotoxic single T cells coexist in the peripheral blood, defects in the antigen presentation machinery coupled with subdued T cell recruitment into metastases are observed, indicating a potent immune avoidance microenvironment not compatible with an effective antitumor response in lethal metastatic disease. Our results demonstrate that the immune responses against cancer are not static, but rather follow dynamic processes that match cancer genomic progression, illustrating the complex nature of tumor and immune cell interactions.

Indexed as

Breast NeoplasmsTriple Negative Breast NeoplasmsFemaleGenomicsHumansTumor Microenvironment

Identifiers

PMID38383522
PMCPMC10882008
OpenAlexW4391997442

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.