Evidence map›Paper›PMID 38254917›Full record

ArticleGenes2023

The Mutational Spectrum of Pre- and Post-Neoadjuvant Chemotherapy Triple-Negative Breast Cancers.

Adriana Aguilar-Mahecha, Najmeh Alirezaie, Josiane Lafleur, Eric Bareke, Ewa Przybytkowski, Cathy Lan, Luca Cavallone, Myriam Salem, Manuela Pelmus, Olga Aleynikova and 10 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

20 authors at 5 institutions in 2 countries.

Adriana Aguilar-MahechaCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Najmeh AlirezaieDepartment of Human Genetics, McGill University, Montreal, QC H3A 1A4, Canada.
Josiane LafleurCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Eric BarekeDepartment of Human Genetics, McGill University, Montreal, QC H3A 1A4, Canada.
Ewa PrzybytkowskiCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Cathy LanCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Luca CavalloneCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Myriam SalemCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Manuela PelmusDepartment of Pathology, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Olga AleynikovaDepartment of Pathology, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Celia GreenwoodLady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.ORCID 0000-0002-2427-5696
Amanda LovatoLady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Cristiano FerrarioDepartment of Oncology, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Jean-François BoileauDepartment of Oncology, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Catalin MihalcioiuMcGill University Health Center, Montreal, QC H3A 3J1, Canada.
Josée-Anne RoyHôpital du Sacré-Cœur de Montréal, Montreal, QC H4J 1C5, Canada.
Elizabeth MarcusCook County Hospital, Chicago, IL 60612, USA.
Federico DiscepolaDepartment of Radiology, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Jacek MajewskiDepartment of Human Genetics, McGill University, Montreal, QC H3A 1A4, Canada.
Mark BasikCancer Genomics and Translational Research Laboratory, Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.ORCID 0000-0002-2633-5410
Jewish General Hospital · CAMcGill University · CAMcGill University Health Centre · CAHôpital du Sacré-Cœur de Montréal · CAJohn H. Stroger, Jr. Hospital of Cook County · US

Funding

Genome Quebec, Jewish General Hospital Foundation and McGill University N/a
6 · The paper itself

Abstract

The response of triple-negative breast cancer (TNBC) patients to pre-operative (neoadjuvant chemotherapy) is a critical factor of their outcome. To determine the effects of chemotherapy on the tumor genome and to identify mutations associated with chemoresistance and sensitivity, we performed whole exome sequencing on pre/post-chemotherapy tumors and matched lymphocytes from 26 patients. We observed great inter-tumoral heterogeneity with no gene mutated recurrently in more than four tumors besides TP53. Although the degree of response to chemotherapy in residual tumors was associated with more subclonal changes during chemotherapy, there was minimal evolution between pre/post-tumors. Indeed, gene sets enriched for mutations in pre- and post-chemotherapy tumors were very similar and reflected genes involved in the biological process of neurogenesis. Somatically mutated genes present in chemosensitive tumors included COL1A2, PRMD15, APOBEC3B, PALB2 and histone protein encoding genes, while BRCA1, ATR, ARID1A, XRCC3 and genes encoding for tubulin-associated proteins were present in the chemoresistant tumors. We also found that the mutational spectrum of post-chemotherapy tumors was more reflective of matching metastatic tumor biopsies than pre-chemotherapy samples. These findings support a portrait of modest ongoing genomic instability with respect to single-nucleotide variants induced by or selected for by chemotherapy in TNBCs.

Indexed as

Triple Negative Breast NeoplasmsCytidine DeaminaseGenomic InstabilityHistonesHumansMinor Histocompatibility AntigensMutationNeoadjuvant TherapyAPOBEC3B protein, humanCytidine DeaminaseHistonesMinor Histocompatibility Antigenschemoresistancechemotherapyexome sequencinggenomicsmutationstriple-negative breast cancer

Identifiers

PMID38254917
PMCPMC10815241
OpenAlexW4390174665

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.