Evidence map›Paper›PMID 21637948›Full record

ReviewCellular and molecular life sciences : CMLS2011

Vimentin in cancer and its potential as a molecular target for cancer therapy.

Arun Satelli, Shulin Li

Registry-linked trialAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04549584 (Neoadjuvant Chemotherapy Response in Metaplastic Carcinoma of Triple Negative Breast Cancer), which is not on this map. Cited by 853 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
853citing papers in PubMed, 2 pooled it
25.0field-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.

NCT04549584 terminatednot on this mapstarted 2020, after this paper: background citation

Neoadjuvant Chemotherapy Response in Metaplastic Carcinoma of Triple Negative Breast Cancer

Typeobservational_patient_registrySponsorSeoul National University HospitalRan2020 to 2020Enrolled3ConditionsMetaplastic Breast CarcinomaArmsVimentin/pan CK stain
3 · Its place in the literature

Who cites it

853 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,569 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Type III intermediate filaments as novel CoAlation targets.Redox report : communications in free radical research · 2026
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  7. Beyond the Needle: Is Liquid Biopsy the Future of Veterinary Medicine?International journal of molecular sciences · 2026
    Review
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793 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

2 authors at 1 institution in 1 country.

Arun SatelliDepartment of Pediatrics, Unit 853, The University of Texas MD Anderson Cancer Center, 1515 Holocombe Blvd, Houston, TX 77030, USA.
Shulin Li
The University of Texas MD Anderson Cancer Center · US

Funding

Gene-Product Auto-Targeting to Tumor VesselsR01CA120895 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2007 to 2025
$4.8M
Elimination of residual malignancy by programmed systemic cytokine gene therapyR01CA098928 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2002 to 2013
$3.0M
IL12 Gene Therapy For Enhancing Therapeutic Efficacy of Bleomycin Against Oral TuR01CA142855 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2010 to 2014
$1.6M
Elimination of residual malignancy by programmed systemic cytokine gene therapyR56CA098928 · NCI · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI LI, SHULIN · 2008 to 2008
$148k
NCI NIH HHS R01 CA098928NCI NIH HHS R01 CA120895NCI NIH HHS R01CA120895NCI NIH HHS R01 CA142855
6 · The paper itself

Abstract

Vimentin, a major constituent of the intermediate filament family of proteins, is ubiquitously expressed in normal mesenchymal cells and is known to maintain cellular integrity and provide resistance against stress. Vimentin is overexpressed in various epithelial cancers, including prostate cancer, gastrointestinal tumors, tumors of the central nervous system, breast cancer, malignant melanoma, and lung cancer. Vimentin's overexpression in cancer correlates well with accelerated tumor growth, invasion, and poor prognosis; however, the role of vimentin in cancer progression remains obscure. In recent years, vimentin has been recognized as a marker for epithelial-mesenchymal transition (EMT). Although EMT is associated with several tumorigenic events, vimentin's role in the underlying events mediating these processes remains unknown. By virtue of its overexpression in cancer and its association with tumor growth and metastasis, vimentin serves as an attractive potential target for cancer therapy; however, more research would be crucial to evaluate its specific role in cancer. Our recent discovery of a vimentin-binding mini-peptide has generated further impetus for vimentin-targeted tumor-specific therapy. Furthermore, research directed toward elucidating the role of vimentin in various signaling pathways would reveal new approaches for the development of therapeutic agents. This review summarizes the expression and functions of vimentin in various types of cancer and suggests some directions toward future cancer therapy utilizing vimentin as a potential molecular target.

Indexed as

Drug Delivery SystemsEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansModels, BiologicalNeoplasmsSignal TransductionVimentinVimentin

Identifiers

PMID21637948
PMCPMC3162105
OpenAlexW1995097523

What OpenQuestion holds

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Registered trials

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.