Evidence map›Paper›PMID 34524579›Full record

ReviewCancer metastasis reviews2022

MicroRNAs as a clue to overcome breast cancer treatment resistance.

Iris Garrido-Cano, Birlipta Pattanayak, Anna Adam-Artigues, Ana Lameirinhas, Sandra Torres-Ruiz, Eduardo Tormo, Raimundo Cervera, Pilar Eroles

Abstract readReview
In one paragraph

Review in Cancer metastasis reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Loss of miR-122 promotes cell migration and poor prognosis in triple-negative breast cancer treated by neoadjuvant chemotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  2. Article
  3. Review
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  6. MicroRNAs as Endocrine Modulators of Breast Cancer.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Article
  9. Review
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  19. miRNA therapeutics in precision oncology: a natural premium to nurture.Exploration of targeted anti-tumor therapy · 2022
    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

8 authors.

Iris Garrido-Cano *INCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Birlipta Pattanayak *INCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Anna Adam-ArtiguesINCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Ana LameirinhasINCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Sandra Torres-RuizINCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Eduardo TormoINCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Raimundo CerveraINCLIVA Biomedical Research Institute, 46010, Valencia, Spain.
Pilar ErolesINCLIVA Biomedical Research Institute, 46010, Valencia, Spain. pilar.eroles@uv.es.ORCID 0000-0003-2708-6206

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most frequent cancer in women worldwide. Despite the improvement in diagnosis and treatments, the rates of cancer relapse and resistance to therapies remain higher than desirable. Alterations in microRNAs have been linked to changes in critical processes related to cancer development and progression. Their involvement in resistance or sensitivity to breast cancer treatments has been documented by different in vivo and in vitro experiments. The most significant microRNAs implicated in modulating resistance to breast cancer therapies are summarized in this review. Resistance to therapy has been linked to cellular processes such as cell cycle, apoptosis, epithelial-to-mesenchymal transition, stemness phenotype, or receptor signaling pathways, and the role of microRNAs in their regulation has already been described. The modulation of specific microRNAs may modify treatment response and improve survival rates and cancer patients' quality of life. As a result, a greater understanding of microRNAs, their targets, and the signaling pathways through which they act is needed. This information could be useful to design new therapeutic strategies, to reduce resistance to the available treatments, and to open the door to possible new clinical approaches.

Indexed as

Breast NeoplasmsMicroRNAsDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansQuality of LifeMicroRNAsBreastCancerMicroRNAsResistance

Identifiers

PMID34524579
PMCPMC8924146

What OpenQuestion holds

Textmetadata
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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.