Evidence map›Paper›PMID 26181203›Full record

ArticleCell death & disease2015

miR-205-5p-mediated downregulation of ErbB/HER receptors in breast cancer stem cells results in targeted therapy resistance.

A De Cola, S Volpe, M C Budani, M Ferracin, R Lattanzio, A Turdo, D D'Agostino, E Capone, G Stassi, M Todaro and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

55 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. The mechanism of ncRNA in trastuzumab resistance in HER2-positive tumors.Medical oncology (Northwood, London, England) · 2025
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  11. Landscape of NcRNAs involved in drug resistance of breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
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  13. Article
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  19. Article
  20. miR-205 in Breast Cancer: State of the Art.International journal of molecular sciences · 2020
    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

16 authors at 3 institutions in 1 country.

A De ColaDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
S VolpeDepartment of Surgical and Oncological Sciences, University of Palermo, Palermo, Italy.
M C BudaniDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
M FerracinDepartment of Morphology, Surgery and Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.ORCID 0000000215956887
R LattanzioDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
A TurdoDepartment of Surgical and Oncological Sciences, University of Palermo, Palermo, Italy.
D D'AgostinoDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
E CaponeDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
G StassiDepartment of Surgical and Oncological Sciences, University of Palermo, Palermo, Italy.
M TodaroDepartment of Surgical and Oncological Sciences, University of Palermo, Palermo, Italy.
C Di IlioDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
G Sala1] Department of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy [2] Mediapharma s.r.l., Via dei Vestini, Chieti, Italy.
M PiantelliDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
M NegriniDepartment of Morphology, Surgery and Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.
A VeroneseDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
V De LaurenziDepartment of Experimental and Clinical Sciences, Aging Research Center (Ce.S.I.), University G. D'Annunzio, Chieti-Pescara, Italy.
University of Chieti-Pescara · ITUniversity of Palermo · ITUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ErbB tyrosine kinase receptor family has been shown to have an important role in tumorigenesis, and the expression of its receptor members is frequently deregulated in many types of solid tumors. Various drugs targeting these receptors have been approved for cancer treatment. Particularly, in breast cancer, anti-Her2/EGFR molecules represent the standard therapy for Her2-positive malignancies. However, in a number of cases, the tumor relapses or progresses thus suggesting that not all cancer cells have been targeted. One possibility is that a subset of cells capable of regenerating the tumor, such as cancer stem cells (CSCs), may not respond to these therapeutic agents. Accumulating evidences indicate that miR-205-5p is significantly downregulated in breast tumors compared with normal breast tissue and acts as a tumor suppressor directly targeting oncogenes such as Zeb1 and ErbB3. In this study, we report that miR-205-5p is highly expressed in BCSCs and represses directly ERBB2 and indirectly EGFR leading to resistance to targeted therapy. Furthermore, we show that miR-205-5p directly regulates the expression of p63 which is in turn involved in the EGFR expression suggesting a miR-205/p63/EGFR regulation.

Indexed as

Breast NeoplasmsCell Line, TumorCell ProliferationDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHumansLapatinibMicroRNAsMolecular Targeted TherapyNeoplasm Recurrence, LocalNeoplastic Stem CellsQuinazolinesTranscription FactorsEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsLapatinibMicroRNAsMIR205, humanQuinazolinesTP63 protein, humanTranscription FactorsTrastuzumabTumor Suppressor Proteins

Identifiers

PMID26181203
PMCPMC4650737
OpenAlexW906179597

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.