Evidence map›Paper›PMID 33322132›Full record

ReviewCancers2020

Modulating the Crosstalk between the Tumor and the Microenvironment Using SiRNA: A Flexible Strategy for Breast Cancer Treatment.

Giuseppina Roscigno, Iolanda Scognamiglio, Francesco Ingenito, Rosario Vincenzo Chianese, Francesco Palma, Alan Chan, Gerolama Condorelli

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
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  5. Nanoparticles in Medicine: Current Status in Cancer Treatment.International journal of molecular sciences · 2023
    Review
  6. Article
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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 at 2 institutions in 2 countries.

Giuseppina RoscignoPercuros BV, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Iolanda ScognamiglioDepartment of Molecular Medicine and Medical Biotechnology, "Federico II" University of Naples, Via Pansini 5, 80131 Naples, Italy.
Francesco IngenitoPercuros BV, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Rosario Vincenzo ChianeseDepartment of Molecular Medicine and Medical Biotechnology, "Federico II" University of Naples, Via Pansini 5, 80131 Naples, Italy.
Francesco PalmaPercuros BV, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Alan ChanPercuros BV, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Gerolama CondorelliDepartment of Molecular Medicine and Medical Biotechnology, "Federico II" University of Naples, Via Pansini 5, 80131 Naples, Italy.
University of Naples Federico II · ITPercuros (Netherlands) · NL

Funding

Associazione Italiana per la Ricerca sul Cancro IG 2013 N.14046Associazione Italiana per la Ricerca sul Cancro IG 2016 N. 8473CAST 857894cONCReTE 872391IF_MSCA 895151PAVE 861190POR Campania "SATIN" FESR 2014-2020PRISAR2 872860
6 · The paper itself

Abstract

Tumorigenesis is a complex and multistep process in which sequential mutations in oncogenes and tumor-suppressor genes result in enhanced proliferation and apoptosis escape. Over the past decades, several studies have provided evidence that tumors are more than merely a mass of malignant cancer cells, with the tumor microenvironment (TME) also contributing to cancer progression. For this reason, the focus of cancer research in recent years has shifted from the malignant cancer cell itself to the TME and its interactions. Since the TME actively participates in tumor progression, therapeutic strategies targeting it have created great interest. In this context, much attention has been paid to the potential application of small interfering RNA (siRNA), a class of non-coding RNA that has the ability to downregulate the expression of target genes in a sequence-specific way. This is paving the way for a novel therapeutic approach for the treatment of several diseases, including cancer. In this review, we describe recent efforts in developing siRNA therapeutics for the treatment of breast cancer, with particular emphasis on TME regulation. We focus on studies that adapt siRNA design to reprogram/re-educate the TME and eradicate the interplay between cancer cells and TME.

Indexed as

breast cancercancer therapysiRNATME

Identifiers

PMID33322132
PMCPMC7763441
OpenAlexW3112310105

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.