Evidence map›Paper›PMID 38664697›Full record

ArticleStem cell research & therapy2024

Synergistic effect of human uterine cervical mesenchymal stem cell secretome and paclitaxel on triple negative breast cancer.

Noemi Eiro, Maria Fraile, Sara Escudero-Cernuda, Juan Sendon-Lago, Luis O Gonzalez, Maria Luisa Fernandez-Sánchez, Francisco J Vizoso

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Mesenchymal Stem Cells and Their Derived Products in Ageing and Diseases.International journal of molecular sciences · 2024
    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

7 authors at 3 institutions in 1 country.

Noemi EiroResearch Unit, Hospital de Jove Foundation, Gijón, Spain. noemi.eiro@hospitaldejove.com.ORCID 0000-0001-5840-4807
Maria FraileResearch Unit, Hospital de Jove Foundation, Gijón, Spain.
Sara Escudero-CernudaDepartment of Physical and Analytical Chemistry, University of Oviedo, Oviedo, Spain.
Juan Sendon-LagoExperimental Biomedicine Centre (CEBEGA), University of Santiago de Compostela, Santiago de Compostela, Spain.
Luis O GonzalezResearch Unit, Hospital de Jove Foundation, Gijón, Spain.
Maria Luisa Fernandez-SánchezDepartment of Physical and Analytical Chemistry, University of Oviedo, Oviedo, Spain.
Francisco J VizosoResearch Unit, Hospital de Jove Foundation, Gijón, Spain. investigacion@hospitaldejove.com.ORCID 0000-0002-2827-5511
Fundación Hospital de Jove · ESUniversidad de Oviedo · ESUniversidade de Santiago de Compostela · ES

Funding

Gobierno del Principado de Asturias GRUPIN IDI 2021/000081Gobierno del Principado de Asturias PA-21-PF-BP20-067Instituto de Salud Carlos III PI17/02236Instituto de Salud Carlos III PI20/01122Ministerio de Ciencia e Innovación PID2022-142323NB-I00
6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is the most lethal subtype of breast cancer and, despite its adverse effects, chemotherapy is the standard systemic treatment option for TNBC. Since, it is of utmost importance to consider the combination of different agents to achieve greater efficacy and curability potential, MSC secretome is a possible innovative alternative.

methodsIn the present study, we proposed to investigate the anti-tumor effect of the combination of a chemical agent (paclitaxel) with a complex biological product, secretome derived from human Uterine Cervical Stem cells (CM-hUCESC) in TNBC.

resultsThe combination of paclitaxel and CM-hUCESC decreased cell proliferation and invasiveness of tumor cells and induced apoptosis in vitro (MDA-MB-231 and/or primary tumor cells). The anti-tumor effect was confirmed in a mouse tumor xenograft model showing that the combination of both products has a significant effect in reducing tumor growth. Also, pre-conditioning hUCESC with a sub-lethal dose of paclitaxel enhances the effect of its secretome and in combination with paclitaxel reduced significantly tumor growth and even allows to diminish the dose of paclitaxel in vivo. This effect is in part due to the action of extracellular vesicles (EVs) derived from CM-hUCESC and soluble factors, such as TIMP-1 and - 2.

conclusionsIn conclusion, our data demonstrate the synergistic effect of the combination of CM-hUCESC with paclitaxel on TNBC and opens an opportunity to reduce the dose of the chemotherapeutic agents, which may decrease chemotherapy-related toxicity.

Indexed as

Cell ProliferationMesenchymal Stem CellsPaclitaxelSecretomeTriple Negative Breast NeoplasmsAnimalsApoptosisCell Line, TumorCervix UteriFemaleHumansMiceXenograft Model Antitumor AssaysPaclitaxelBreast cancerChemotherapyConditioned mediumhUCESCMesenchymal stem cellsSecretome

Identifiers

PMID38664697
PMCPMC11044487
OpenAlexW4395465378

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.