Evidence map›Paper›PMID 30192811›Full record

ArticlePloS one2018

Adipose-derived stem cell-mediated paclitaxel delivery inhibits breast cancer growth.

Maria Giovanna Scioli, Simona Artuso, Carmen D'Angelo, Manuela Porru, Federico D'Amico, Alessandra Bielli, Pietro Gentile, Valerio Cervelli, Carlo Leonetti, Augusto Orlandi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Breast fat grafting and cancer: a systematic review of the science behind enhancements and concerns.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2024
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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

10 authors at 2 institutions in 2 countries.

Maria Giovanna ScioliAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Simona ArtusoSAFU, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Carmen D'AngeloUnit of Oncogenomics and Epigenetics, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Manuela PorruSAFU, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Federico D'AmicoAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.ORCID 0000-0001-7825-4922
Alessandra BielliAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Pietro GentilePlastic and Reconstructive Surgery, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Valerio CervelliPlastic and Reconstructive Surgery, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Carlo LeonettiSAFU, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Augusto OrlandiAnatomic Pathology, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.ORCID 0000-0001-7202-5854
University of Rome Tor Vergata · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer represents the main malignancy in women and autologous fat grafting is a diffuse procedure in the management of post-surgical breast defects causing patients' psychosocial problems, with high costs for the public health. Recently, beneficial effects of fat grafting during post-surgical breast reconstruction have been amplified from the enrichment with human adipose-derived stem cells (ASCs) present in the stromal vascular fraction (SVF) of adult adipose tissue isolated during intraoperatory procedures. The major concern about the ASC enrichment during post-surgery breast reconstruction depends on their potential ability to release growth factors and hormones that can promote proliferation of residual or quiescent cancer cells, with the risk of de novo cancer development or recurrence. The recent description that adult stem cells primed in vitro may be vehicle for anti-cancer drug delivery offers a new vision concerning the role of ASCs in breast reconstruction after cancer surgery. Paclitaxel (PTX) is a chemotherapeutic agent acting as a microtubule-stabilizing drug inhibiting cancer cell mitotic activity. We optimized PTX loading and release in cultured ASCs and then analyzed the effects of PTX-loaded ASCs and their conditioned medium on CG5 breast cancer survival, proliferation and apoptosis in vitro, and inCG5 xenograft in vivo. We documented that ASCs can uptake and release PTX in vitro, with slight cytotoxic effects. Interestingly, PTX-loaded ASCs in co-culture, as well as conditioned medium alone, inhibited CG5 cell proliferation and survival in vitro and xenograft tumor growth in vivo. The antitumor effect of PTX-loaded ASCs may offer a new perspective concerning the use of ASCs during breast reconstruction becoming an additional local preventive chemotherapeutic agent against tumor recurrence. However, further experiments in vitro and in vivo are needed to collect more evidence confirming the efficacy and safety in cancer patients.

Indexed as

Xenograft Model Antitumor AssaysAdipose TissueAnimalsAntineoplastic Agents, PhytogenicApoptosisBreast NeoplasmsCell ProliferationCells, CulturedCulture Media, ConditionedFemaleHumansMCF-7 CellsMice, NudePaclitaxelStem CellsTumor BurdenAntineoplastic Agents, PhytogenicCulture Media, ConditionedPaclitaxel

Identifiers

PMID30192811
PMCPMC6128546
OpenAlexW2892141339

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.