Evidence map›Paper›PMID 27822407›Full record

ReviewAmerican journal of cancer research2016

Exosomes-mediate microRNAs transfer in breast cancer chemoresistance regulation.

Juliana Carvalho Santos, Marcelo Lima Ribeiro, Luis Otávio Sarian, Manoela Marques Ortega, Sophie Françoise Derchain

Open access · greenAbstract readReview
In one paragraph

Review in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
19.4field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Article
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  9. Review
  10. Review
  11. Novel exosomal miR-46146 transfer oxaliplatin chemoresistance in colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Article
  12. Article
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  14. Article
  15. Article
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  17. Article
  18. Extracellular Vesicles: New Players in Lymphomas.International journal of molecular sciences · 2018
    Review
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Juliana Carvalho SantosWomen's Health Hospital "Prof Dr José Aristodemo Pinotti" (CAISM), State University of Campinas (UNICAMP) Campinas, SP, Brazil.
Marcelo Lima RibeiroClinical Pharmacology and Gastroenterology Unit, São Francisco University, São Francisco University Bragança Paulista, SP, Brazil.
Luis Otávio SarianWomen's Health Hospital "Prof Dr José Aristodemo Pinotti" (CAISM), State University of Campinas (UNICAMP) Campinas, SP, Brazil.
Manoela Marques OrtegaClinical Pharmacology and Gastroenterology Unit, São Francisco University, São Francisco University Bragança Paulista, SP, Brazil.
Sophie Françoise DerchainWomen's Health Hospital "Prof Dr José Aristodemo Pinotti" (CAISM), State University of Campinas (UNICAMP) Campinas, SP, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade São Francisco · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common and fatal type of cancer in women worldwide due to the metastatic process and resistance to treatment. Despite advances in molecular knowledge, little is known regarding resistance to chemotherapy. One highlighted aspect is the DNA damage response (DDR) pathway that is activated upon genotoxic damage, controlling the cell cycle arrest or DNA repair activation. Recently, studies have showed that cancer stem cells (CSCs) could promote chemoresistance through DDR pathway. Furthermore, it is known that the epithelial-mesenchymal transition (EMT) can generate cells with CSCs characteristics and therefore regulate the chemoresistance process. The exosomes are microvesicles filled with RNAs, proteins and microRNAs (miRNAs) that can be released by many cell types, including tumor cells and CSCs. The exosomes content may be cell-to-cell transferable and it could control a wide range of pathways during tumor development and metastasis. A big challenge for modern medicine is to determine the reasons why patients do not respond to chemotherapy treatments and also guide the most appropriate therapy for each one. Considering that the CSCs are able to stimulate the formation of a more aggressive tumor phenotype with migration and metastasis ability, resistance to treatment and disease recurrence, as well as few studies capable to determine clearly the interaction of breast CSCs with its microenvironment, the present review summarize the possibility that exosomes-mediate miRNAs transfer and regulate chemoresistance in breast tumor cells and CSCs, to clarify the complexity of breast cancer progression and therapy.

Indexed as

Breast cancerchemoresistanceexosomesmicroRNAs

Identifiers

PMID27822407
PMCPMC5088281
OpenAlexW2565113067

What OpenQuestion holds

Textmetadata
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.