Evidence map›Paper›PMID 22194601›Full record

ArticleThe Journal of biological chemistry2012

Loss of Hypermethylated in Cancer 1 (HIC1) in breast cancer cells contributes to stress-induced migration and invasion through β-2 adrenergic receptor (ADRB2) misregulation.

Gaylor Boulay, Nicolas Malaquin, Ingrid Loison, Bénédicte Foveau, Capucine Van Rechem, Brian R Rood, Albin Pourtier, Dominique Leprince

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Transcription Factor E2F1 Regulates the Expression of ADRB2.International journal of analytical chemistry · 2023
    Article
  3. Article
  4. Article
  5. Network Pharmacology-Based Analysis of the Effects ofEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Downregulation of hypermethylated in cancer-1 byCancer cell international · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. BTG2 inhibits the proliferation, invasion, and apoptosis of MDA-MB-231 triple-negative breast cancer cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
  19. Article
  20. Signification of Hypermethylated in Cancer 1 (HIC1) as Tumor Suppressor Gene in Tumor Progression.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2012
    Article
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

8 authors at 4 institutions in 2 countries.

Gaylor BoulayCNRS UMR 8161, CNRS-Université de Lille 1-Institut Pasteur de Lille, Lille 59021, France.
Nicolas Malaquin
Ingrid Loison
Bénédicte Foveau
Capucine Van Rechem
Brian R Rood
Albin Pourtier
Dominique Leprince
Institut de Biologie de Lille · FRUniversité de Lille · FRCentre National de la Recherche Scientifique · FRGeorge Washington University · US

Funding

Creation of a PDGF-C Autocrine Loop by HIC1 InactivationK08NS051477 · NINDS · CHILDREN'S NATIONAL MEDICAL CENTER · PI ROOD, BRIAN R · 2007 to 2011
$729k
NINDS NIH HHS 1K08NS051477NINDS NIH HHS K08 NS051477
6 · The paper itself

Abstract

The transcriptional repressor HIC1 (Hypermethylated in Cancer 1) is a tumor suppressor gene inactivated in many human cancers including breast carcinomas. In this study, we show that HIC1 is a direct transcriptional repressor of β-2 adrenergic receptor (ADRB2). Through promoter luciferase activity, chromatin immunoprecipitation (ChIP) and sequential ChIP experiments, we demonstrate that ADRB2 is a direct target gene of HIC1, endogenously in WI-38 cells and following HIC1 re-expression in breast cancer cells. Agonist-mediated stimulation of ADRB2 increases the migration and invasion of highly malignant MDA-MB-231 breast cancer cells but these effects are abolished following HIC1 re-expression or specific down-regulation of ADRB2 by siRNA treatment. Our results suggest that early inactivation of HIC1 in breast carcinomas could predispose to stress-induced metastasis through up-regulation of the β-2 adrenergic receptor.

Indexed as

Cell MovementStress, PhysiologicalBreast NeoplasmsCell AdhesionCell Line, TumorFemaleFibroblastsHumansKruppel-Like Transcription FactorsNeoplasm InvasivenessNeoplasm MetastasisReceptors, Adrenergic, beta-2RNA InterferenceRNA, Small InterferingADRB2 protein, humanHIC1 protein, humanKruppel-Like Transcription FactorsReceptors, Adrenergic, beta-2RNA, Small Interfering

Identifiers

PMID22194601
PMCPMC3285317
OpenAlexW1995333768

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.