Evidence map›Paper›PMID 19432890›Full record

ReviewCancer science2009

Reviewing the current classification of inhibitor of growth family proteins.

Motoko Unoki, Kensuke Kumamoto, Seiichi Takenoshita, Curtis C Harris

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.2field-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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. AnPeerJ · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. ING5 inhibits epithelial-mesenchymal transition in breast cancer by suppressing PI3K/Akt pathway.International journal of clinical and experimental medicine · 2015
    Article
  19. Truncation of inhibitor of growth family protein 5 effectively induces senescence, but not apoptosis in human tongue squamous cell carcinoma cell line.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  20. 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

4 authors at 3 institutions in 2 countries.

Motoko UnokiLaboratory for Biomarker, The Institute of Physical and Chemical Research, RIKEN, Tokyo, Japan.
Kensuke Kumamoto
Seiichi Takenoshita
Curtis C Harris
Fukushima Medical University · JPNational Cancer Institute · USRIKEN · JP

Funding

p53 Tumor Suppressor PathwayZIABC005795 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 2009 to 2012
$3.0M
p53 Tumor Suppressor PathwayZ01BC005795 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 1996 to 2008
$2.3M
Inhibitor of Normal Growth (ING)ZIABC010875 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 2009 to 2011
$2.1M
Inhibitor of Normal Growth (ING)Z01BC010875 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 2008 to 2008
$649k
Intramural NIH HHS Z01 BC005795Intramural NIH HHS Z01 BC010875
6 · The paper itself

Abstract

Inhibitor of growth (ING) family proteins have been defined as candidate tumor suppressors for more than a decade. Recent emerging results using siRNA and knockout mice are expanding the previous understanding of this protein family. The results of ING1 knockout mouse experiments revealed that ING1 has a protective effect on apoptosis. Our recent results showed that ING2 is overexpressed in colorectal cancer, and induces colon cancer cell invasion through an MMP13-dependent pathway. Knockdown of ING2 by siRNA induces premature senescence in normal human fibroblast cells, and apoptosis or cell cycle arrest in various adherent cancer cells. Taken together, these results suggest that ING2 may also have roles in cancer progression and/or malignant transformation under some conditions. Additionally, knockdown of ING4 and ING5 by siRNA shows an inhibitory effect on the transition from G(2)/M to G(1) phase and DNA replication, respectively, suggesting that these proteins may play roles during cell proliferation in some context. ING family proteins may play dual roles, similar to transforming growth factor-beta, which has tumor suppressor-like functions in normal epithelium and also oncogenic functions in invasive metastatic cancers. In the present article, we briefly review ING history and propose a possible interpretation of discrepancies between past and recent data.

Indexed as

AnimalsDNA ReplicationHumansMiceModels, BiologicalNuclear ProteinsOncogene ProteinsRNA, Small InterferingSignal TransductionTumor Suppressor ProteinsNuclear ProteinsOncogene ProteinsRNA, Small InterferingTumor Suppressor Proteins

Identifiers

PMID19432890
PMCPMC2790152
OpenAlexW2011890675

What OpenQuestion holds

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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.