Evidence map›Paper›PMID 23584479›Full record

ArticleOncogene2014

Gain-of-function mutant p53 downregulates miR-223 contributing to chemoresistance of cultured tumor cells.

S Masciarelli, G Fontemaggi, S Di Agostino, S Donzelli, E Carcarino, S Strano, G Blandino

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

85 citing papers in PubMed, 1 synthesis or guideline pooled it, 153 citations in OpenAlex.

  1. Targeting p53 pathways: mechanisms, structures, and advances in therapy.Signal transduction and targeted therapy · 2023
    Pooled it
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  14. Anticancer Therapeutic Strategies Targeting p53 Aggregation.International journal of molecular sciences · 2022
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25 more citing papers are in PubMed but not listed here.

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

7 authors.

S MasciarelliTranslational Oncogenomic Unit, Regina Elena National Cancer Institute, Rome, Italy.
G FontemaggiTranslational Oncogenomic Unit, Regina Elena National Cancer Institute, Rome, Italy.
S Di AgostinoTranslational Oncogenomic Unit, Regina Elena National Cancer Institute, Rome, Italy.
S DonzelliTranslational Oncogenomic Unit, Regina Elena National Cancer Institute, Rome, Italy.
E CarcarinoTranslational Oncogenomic Unit, Regina Elena National Cancer Institute, Rome, Italy.
S StranoChemoprevention Unit, Regina Elena National Cancer Institute, Rome, Italy.
G BlandinoTranslational Oncogenomic Unit, Regina Elena National Cancer Institute, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutant p53 proteins are expressed at high frequency in human tumors and are associated with poor clinical prognosis and resistance to chemotherapeutic treatments. Here we show that mutant p53 proteins downregulate micro-RNA (miR)-223 expression in breast and colon cancer cell lines. Mutant p53 binds the miR-223 promoter and reduces its transcriptional activity. This requires the transcriptional repressor ZEB-1. We found that miR-223 exogenous expression sensitizes breast and colon cancer cell lines expressing mutant p53 to treatment with DNA-damaging drugs. Among the putative miR-223 targets, we focused on stathmin-1 (STMN-1), an oncoprotein known to confer resistance to chemotherapeutic drugs associated with poor clinical prognosis. Mutant p53 silencing or miR-223 exogenous expression lowers the levels of STMN-1 and knockdown of STMN-1 by small interfering RNA increases cell death of mutant p53-expressing cell lines. On the basis of these findings, we propose that one of the pathways affected by mutant p53 to increase cellular resistance to chemotherapeutic agents involves miR-223 downregulation and the consequent upregulation of STMN-1.

Indexed as

MutationAntineoplastic AgentsCell Line, TumorDown-RegulationDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansMicroRNAsStathminTumor Suppressor Protein p53Antineoplastic AgentsMicroRNAsMIR223, humanStathminSTMN1 protein, humanTumor Suppressor Protein p53

Identifiers

PMID23584479
OpenAlexW2034330475

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.