Evidence map›Paper›PMID 22264789›Full record

ArticleCancer cell2012

Pericyte depletion results in hypoxia-associated epithelial-to-mesenchymal transition and metastasis mediated by met signaling pathway.

Vesselina G Cooke, Valerie S LeBleu, Doruk Keskin, Zainab Khan, Joyce T O'Connell, Yingqi Teng, Michael B Duncan, Liang Xie, Genta Maeda, Sylvia Vong and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 286 papers.

0numbers the graph read from it
0cells of the map it votes in
286citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

286 citing papers in PubMed, 16 citations in OpenAlex.

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  4. Mechanisms of Pericyte-Mediated Cancer Metastasis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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226 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 2 countries.

Vesselina G CookeDivision of Matrix Biology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.
Valerie S LeBleu
Doruk Keskin
Zainab Khan
Joyce T O'Connell
Yingqi Teng
Michael B Duncan
Liang Xie
Genta Maeda
Sylvia Vong
Hikaru Sugimoto
Rafael M Rocha
Aline Damascena
Ricardo R Brentani
Raghu Kalluri
Beth Israel Deaconess Medical Center · USAC Camargo Hospital · BR

Funding

Training Program in Cardiovascular ResearchT32HL007374 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI MITTLEMAN, MURRAY A · 1985 to 2019
$7.9M
Stromal Regulation of Bone MetastasisU54CA163191 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU · 2011 to 2015
$4.8M
RESEARCH TRAINING IN GASTROENTEROLOGYT32DK007760 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KELLY, CIARAN P · 1999 to 2019
$4.6M
TYPE IV COLLAGEN IN ALPORT SYNDROME PATHOGENESISR01DK055001 · NIDDK · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU · 1999 to 2014
$4.3M
Role of Fibroblasts, Myeloid Cells and Matrix in PDACU01CA151925 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU, MOSES, HAROLD L · 2010 to 2014
$3.2M
TRAINING PROGRAM IN CANCER BIOLOGYT32CA081156 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BALK, STEVEN P. · 2000 to 2011
$2.9M
Epigenetic Modifications in Renal FibrogenesisR01DK081576 · NIDDK · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU · 2009 to 2013
$1.8M
Targeting Pericytes in CancerR01CA155370 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU · 2011 to 2015
$1.7M
Role of Fibroblasts in CancerR01CA125550 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KALLURI, RAGHU · 2008 to 2010
$1.1M
Role of NG2 in diabetic nephropathyF32DK082119 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI COOKE, VESSELINA G · 2008 to 2010
$149k
NCI NIH HHS 5T32CA081156-08NCI NIH HHS CA125550NCI NIH HHS CA151925NCI NIH HHS CA155370NCI NIH HHS CA163191NCI NIH HHS R01 CA125550NCI NIH HHS R01 CA155370NCI NIH HHS T32 CA081156NCI NIH HHS U01 CA151925NHLBI NIH HHS 5T32HL007374-30NHLBI NIH HHS T32 HL007374NIDDK NIH HHS 2T32DK007760-11NIDDK NIH HHS 5F32DK082119-02NIDDK NIH HHS DK55001NIDDK NIH HHS DK81576NIDDK NIH HHS F32 DK082119NIDDK NIH HHS R01 DK055001NIDDK NIH HHS R01 DK081576NIDDK NIH HHS T32 DK007760
6 · The paper itself

Abstract

The functional role of pericytes in cancer progression remains unknown. Clinical studies suggest that low numbers of vessel-associated pericytes correlated with a drop in overall survival of patients with invasive breast cancer. Using genetic mouse models or pharmacological inhibitors, pericyte depletion suppressed tumor growth but enhanced metastasis. Pericyte depletion was further associated with increased hypoxia, epithelial-to-mesenchymal transition (EMT), and Met receptor activation. Silencing of Twist or use of a Met inhibitor suppressed hypoxia and EMT/Met-driven metastasis. In addition, poor pericyte coverage coupled with high Met expression in cancer cells speculates the worst prognosis for patients with invasive breast cancer. Collectively, our study suggests that pericytes within the primary tumor microenvironment likely serve as important gatekeepers against cancer progression and metastasis.

Indexed as

Epithelial-Mesenchymal TransitionNeoplasm MetastasisAnimalsAntineoplastic AgentsBenzamidesBenzenesulfonatesBreast NeoplasmsCell HypoxiaCell Line, TumorCrizotinibFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitImatinib MesylateIndolesMiceAntineoplastic AgentsBenzamidesBenzenesulfonatesCrizotinibHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitImatinib MesylateIndolesNiacinamidePhenylurea CompoundsPiperazinesPiperidinesProtein Kinase InhibitorsProto-Oncogene Proteins c-metPyrazolesPyridinesPyrimidinesPyrrolesSorafenibSunitinib

Identifiers

PMID22264789
PMCPMC3999522
OpenAlexW1562355542

What OpenQuestion holds

Textmetadata
LicenceTDM
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.