Evidence map›Paper›PMID 29072369›Full record

ReviewStem cells translational medicine2017

Concise Review: Cancer Cells, Cancer Stem Cells, and Mesenchymal Stem Cells: Influence in Cancer Development.

Federica Papaccio, Francesca Paino, Tarik Regad, Gianpaolo Papaccio, Vincenzo Desiderio, Virginia Tirino

Open access · goldAbstract readReview
In one paragraph

Review in Stem cells translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 182 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
182citing papers in PubMed, 1 pooled it
14.7field-weighted citation impact, top 1% 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

182 citing papers in PubMed, 1 synthesis or guideline pooled it, 289 citations in OpenAlex.

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122 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

6 authors at 2 institutions in 2 countries.

Federica PapaccioDipartimento Medico-Chirurgico di Internistica Clinica e Sperimentale "F. Magrassi", Università degli Studi della Campania 'L. Vanvitelli', Naples, Italy.
Francesca PainoDipartimento di Medicina Sperimentale, Sezione di Sezione di Biotecnologie, Istologia Medica e Biologia Molecolare, Università degli Studi della Campania 'L. Vanvitelli', Naples, Italy.
Tarik RegadThe John van Geest Cancer Research Centre, School of Science and Technology, Nottingham Trent University, Nottingham, United Kingdom.
Gianpaolo PapaccioDipartimento di Medicina Sperimentale, Sezione di Sezione di Biotecnologie, Istologia Medica e Biologia Molecolare, Università degli Studi della Campania 'L. Vanvitelli', Naples, Italy.ORCID 0000-0002-4014-5306
Vincenzo DesiderioDipartimento di Medicina Sperimentale, Sezione di Sezione di Biotecnologie, Istologia Medica e Biologia Molecolare, Università degli Studi della Campania 'L. Vanvitelli', Naples, Italy.
Virginia TirinoDipartimento di Medicina Sperimentale, Sezione di Sezione di Biotecnologie, Istologia Medica e Biologia Molecolare, Università degli Studi della Campania 'L. Vanvitelli', Naples, Italy.
University of Campania "Luigi Vanvitelli" · ITNottingham Trent University · GB

Funding

DNA SAMPLE ANALYSIS27307C2007 · NIEHS · PI LEHMAN, TERESA · 2007 to 2007
$74k
NIEHS NIH HHS 27307C2007
6 · The paper itself

Abstract

Tumors are composed of different types of cancer cells that contribute to tumor heterogeneity. Among these populations of cells, cancer stem cells (CSCs) play an important role in cancer initiation and progression. Like their stem cells counterpart, CSCs are also characterized by self-renewal and the capacity to differentiate. A particular population of CSCs is constituted by mesenchymal stem cells (MSCs) that differentiate into cells of mesodermal characteristics. Several studies have reported the potential pro-or anti-tumorigenic influence of MSCs on tumor initiation and progression. In fact, MSCs are recruited to the site of wound healing to repair damaged tissues, an event that is also associated with tumorigenesis. In other cases, resident or migrating MSCs can favor tumor angiogenesis and increase tumor aggressiveness. This interplay between MSCs and cancer cells is fundamental for cancerogenesis, progression, and metastasis. Therefore, an interesting topic is the relationship between cancer cells, CSCs, and MSCs, since contrasting reports about their respective influences have been reported. In this review, we discuss recent findings related to conflicting results on the influence of normal and CSCs in cancer development. The understanding of the role of MSCs in cancer is also important in cancer management. Stem Cells Translational Medicine 2017;6:2115-2125.

Indexed as

AnimalsCarcinogenesisHumansMesenchymal Stem CellsNeoplasmsNeoplastic Stem CellsTumor MicroenvironmentCancer progressionDrug resistanceEpithelial to mesenchymal transitionMesenchymal stem cellsMicroenvironment

Identifiers

PMID29072369
PMCPMC5702541
OpenAlexW2767025366

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.