Evidence map›Paper›PMID 17188427›Full record

ReviewCancer letters2007

Tumor-suppressive activity of retinoic acid receptor-beta in cancer.

Xiao-Chun Xu

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Exploring the nexus of nuclear receptors in hematological malignancies.Cellular and molecular life sciences : CMLS · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Targeting the Retinoic Acid Pathway to Eradicate Cancer Stem Cells.International journal of molecular sciences · 2023
    Review
  14. Demystifying the Functional Role of Nuclear Receptors in Esophageal Cancer.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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

1 author at 1 institution in 1 country.

Xiao-Chun XuDepartment of Clinical Cancer Prevention, Unit 1360, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA. xxumdanderson.org
The University of Texas MD Anderson Cancer Center · US

Funding

Targeting RAR-beta2-led Gene Pathway in Prevention of Esophageal CancerR01CA117895 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI XU, XIAOCHUN · 2007 to 2010
$971k
RETINOID/RETINOID RECEPTOR IN ESOPHAGUS CANCER RESPONSER29CA074835 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI XU, XIAOCHUN · 1998 to 2002
$310k
To identify tobacco carcinogen-binding DNA as biomarkerR21CA102265 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI XU, XIAOCHUN · 2005 to 2006
$267k
NCI NIH HHS R01 CA117895NCI NIH HHS R21 CA10226NCI NIH HHS R21 CA102265NCI NIH HHS R29 CA074835NCI NIH HHS R29 CA74835
6 · The paper itself

Abstract

Retinoids, a group of structural and functional analogs of vitamin A, are known to regulate a large number of essential biological processes and to suppress carcinogenesis. The effects of retinoids are mainly mediated by nuclear retinoid receptors, which include retinoic acid receptors (RARs) and retinoid X receptors (RXRs). Each receptor has three subtypes (alpha, beta, and gamma) and each subtype has different isoforms. Retinoic acid receptor-beta (RAR-beta) has four isoforms that have different affinities to retinoids and different biological functions. Loss of expression of RAR-beta(2) during cancer development is associated with tumorigenesis and retinoid resistance; induction of its expression, on the other hand, can suppress carcinogenesis. Expression of another isoform, RAR-beta(4), is increased in various types of cancer. RAR-beta(4) transgenic mice develop hyperplasia and neoplasia in various tissues, and induction of RAR-beta(4) expression increases the growth of tumor cells that do not express RAR-beta(2). Future studies will focus on molecular pathways involving RAR-beta(2) and the role of RAR-beta(4) in cancer development.

Indexed as

Base SequenceBiomarkersForecastingHumansMolecular Sequence DataNeoplasmsProtein IsoformsReceptors, Retinoic AcidBiomarkersProtein IsoformsReceptors, Retinoic Acidretinoic acid receptor beta

Identifiers

PMID17188427
PMCPMC2562790
OpenAlexW2122808667

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.