Evidence map›Paper›PMID 21838596›Full record

ReviewExpert opinion on therapeutic targets2011

Integrin α3β1 as a breast cancer target.

Sita Subbaram, C Michael Dipersio

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.1field-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

43 citing papers in PubMed, 68 citations in OpenAlex.

  1. Integrin α3Cancer pathogenesis and therapy · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. The epidermal integrin-mediated secretome regulates the skin microenvironment during tumorigenesis and repair.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Review
  8. Review
  9. Article
  10. Integrins in cancer stem cells.Frontiers in cell and developmental biology · 2024
    Review
  11. Integrin α3 promotes TScience immunology · 2023
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

2 authors at 1 institution in 1 country.

Sita SubbaramAlbany Medical College, Center for Cell Biology & Cancer Research, Albany, NY 12208, USA.
C Michael Dipersio
Albany Medical Center Hospital · US

Funding

Regulation of MMP-9 mRNA stability and tumor growth by alpha3 beta1 integrinR01CA129637 · NCI · ALBANY MEDICAL COLLEGE · PI DIPERSIO, C. MICHAEL · 2008 to 2020
$3.3M
Concerted role for integrin alpha3beta1 and TGFb signaling in cancer progressionF32CA153976 · NCI · ALBANY MEDICAL COLLEGE · PI SUBBARAM, SITA · 2010 to 2013
$160k
NCI NIH HHS F32 CA153976NCI NIH HHS IF32CA153976NCI NIH HHS R01 CA129637NCI NIH HHS R01CA129637
6 · The paper itself

Abstract

introductionIntegrin receptors for cell adhesion to the extracellular matrix have important roles in all stages of cancer progression and metastasis. Since the integrin family was discovered in the early 1980's, many studies have identified critical adhesion and signaling functions for integrins expressed on tumor cells, endothelial cells and other cell types of the tumor microenvironment, in controlling proliferation, survival, migration and angiogenesis. In recent years, the laminin-binding integrin α3β1 has emerged as a potentially promising anti-cancer target on breast cancer cells. AREAS COVERED: Studies from the past decade that implicate integrins as promising anti-cancer targets and the development of integrin antagonists as anti-cancer therapeutics. Recent preclinical studies that have identified the laminin-binding integrin α3β1 as an appealing anti-cancer target and the knowledge gaps that must be closed to fully exploit this integrin as a therapeutic target for breast cancer. EXPERT OPINION: Although the tumor-promoting functions of α3β1 implicate this integrin as a promising therapeutic target on breast cancer cells, successful exploitation of this integrin as an anti-cancer target will require a better understanding of the molecular mechanisms whereby it regulates specific tumor cell behaviors and the identification of the most appropriate α3β1 functions to antagonize on breast cancer cells.

Indexed as

Breast NeoplasmsFemaleHumansIntegrin alpha3beta1Neovascularization, PathologicSignal TransductionIntegrin alpha3beta1

Identifiers

PMID21838596
PMCPMC3212412
OpenAlexW2108395670

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.