Evidence map›Paper›PMID 27721239›Full record

ArticleThe Journal of clinical investigation2016

Epithelial-to-mesenchymal transition confers pericyte properties on cancer cells.

Anitha K Shenoy, Yue Jin, Huacheng Luo, Ming Tang, Christine Pampo, Rong Shao, Dietmar W Siemann, Lizi Wu, Coy D Heldermon, Brian K Law and 2 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

59 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

12 authors.

Anitha K Shenoy
Yue Jin
Huacheng Luo
Ming Tang
Christine Pampo
Rong Shao
Dietmar W Siemann
Lizi Wu
Coy D Heldermon
Brian K Law
Lung-Ji Chang
Jianrong Lu

Funding

Signaling and Targeting of CRTC1-MAML2 Fusion Oncoprotein in Salivary Gland TumorR01DE023641 · NIDCR · UNIVERSITY OF FLORIDA · PI Lizi Wu · 2014 to 2026
$3.3M
A novel noncoding RNA and human lung cancers with inactivated LKB1 signalingR21CA187730 · NCI · UNIVERSITY OF FLORIDA · PI WU, LIZI · 2015 to 2016
$349k
NCI NIH HHS R21 CA187730NIDCR NIH HHS R01 DE023641
6 · The paper itself

Abstract

Carcinoma cells can acquire increased motility and invasiveness through epithelial-to-mesenchymal transition (EMT). However, the significance of EMT in cancer metastasis has been controversial, and the exact fates and functions of EMT cancer cells in vivo remain inadequately understood. Here, we tracked epithelial cancer cells that underwent inducible or spontaneous EMT in various tumor transplantation models. Unlike epithelial cells, the majority of EMT cancer cells were specifically located in the perivascular space and closely associated with blood vessels. EMT markedly activated multiple pericyte markers in carcinoma cells, in particular PDGFR-β and N-cadherin, which enabled EMT cells to be chemoattracted towards and physically interact with endothelium. In tumor xenografts generated from carcinoma cells that were prone to spontaneous EMT, a substantial fraction of the pericytes associated with tumor vasculature were derived from EMT cancer cells. Depletion of such EMT cells in transplanted tumors diminished pericyte coverage, impaired vascular integrity, and attenuated tumor growth. These findings suggest that EMT confers key pericyte attributes on cancer cells. The resulting EMT cells phenotypically and functionally resemble pericytes and are indispensable for vascular stabilization and sustained tumor growth. This study thus proposes a previously unrecognized role for EMT in cancer.

Indexed as

Epithelial-Mesenchymal TransitionA549 CellsAnimalsAntigens, CDBiomarkers, TumorCadherinsHumansMCF-7 CellsMiceNeoplasm ProteinsNeoplasmsNeovascularization, PathologicPericytesReceptor, Platelet-Derived Growth Factor betaAntigens, CDBiomarkers, TumorCadherinsCDH2 protein, humanCdh2 protein, mouseNeoplasm ProteinsPDGFRB protein, humanReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID27721239
PMCPMC5096906

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.