Evidence map›Paper›PMID 18428028›Full record

ArticleGrowth factors (Chur, Switzerland)2008

Precursor IGF-II (proIGF-II) and mature IGF-II (mIGF-II) induce Bcl-2 And Bcl-X L expression through different signaling pathways in breast cancer cells.

S Kalla Singh, D Moretta, F Almaguel, M De León, Daisy D De León

Abstract read
In one paragraph

Article in Growth factors (Chur, Switzerland), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Differential insulin-like growth factor II (IGF-II) expression: A potential role for breast cancer survival disparity.Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society · 2010
    Article
  13. IGF and insulin receptor signaling in breast cancer.Journal of mammary gland biology and neoplasia · 2008
    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

5 authors at 1 institution in 1 country.

S Kalla SinghCenter for Health Disparities and Molecular Medicine, Loma Linda University, Loma Linda, California 92350, USA.
D Moretta
F Almaguel
M De León
Daisy D De León
Loma Linda University · US

Funding

NIH-LLU Initiative for Maximizing Student DiversityR25GM060507 · NIGMS · LOMA LINDA UNIVERSITY · PI DE LEON, MARINO · 2001 to 2022
$11.3M
The role of imidazoline receptor in type-2 diabetesP20MD001632 · NIMHD · LOMA LINDA UNIVERSITY · PI DE LEON, DAISY D. · 2005 to 2009
$8.0M
Research Training/Education CoreP20MD006988 · NIMHD · LOMA LINDA UNIVERSITY · PI CASIANO, CARLOS A. · 2012 to 2016
$6.2M
NIGMS NIH HHS 5R25GM060507NIGMS NIH HHS R25 GM060507NIMHD NIH HHS 5P20 MD001632NIMHD NIH HHS P20 MD001632NIMHD NIH HHS P20 MD006988
6 · The paper itself

Abstract

IGF-II plays a crucial role in fetal and cancer development by signaling through the IGF-I receptor. We have shown that inhibition of IGF-II by resveratrol (RSV) induced apoptosis and that proIGF-II (highly expressed in cancer) was more potent than mIGF-II in inhibiting this effect. Thus, we hypothesized that IGF-II differentially regulates the signaling cascade of the IGF-I receptor to stimulate the anti-apoptotic proteins Bcl-2 and Bcl-X(L) to prevent apoptosis. RSV treatment to breast cancer cells inhibited Bcl-2 and Bcl-X(L) expression and induced mitochondrial membrane depolarization. ProIGF-II was more potent than mIGF-II in: (1) activating the PI3/Akt pathway, (2) regulating Bcl-2 and Bcl-X(L) expression, and (3) inducing phosphorylation/nuclear translocation of Cyclic AMP-responsive element binding protein. Furthermore, IGF-II differentially regulated the intracellular translocation of Bcl-2 and Bcl-X(L), a critical process in breast cancer progression to hormone-independence. Our study provides a novel mechanism of how proIGF-II promotes progression and chemoresistance in breast cancer development.

Indexed as

Antineoplastic Agents, Phytogenicbcl-X ProteinBreast NeoplasmsCell Line, TumorCell SurvivalCytochromes cEnzyme InhibitorsGene Expression Regulation, NeoplasticHumansInsulin-Like Growth Factor IIIntracellular Signaling Peptides and ProteinsMitochondrial MembranesPhosphorylationProtein TransportProto-Oncogene Proteins c-bcl-2ResveratrolAntineoplastic Agents, PhytogenicBCL2L1 protein, humanbcl-X ProteinCytochromes cEnzyme InhibitorsInsulin-Like Growth Factor IIIntracellular Signaling Peptides and ProteinsProto-Oncogene Proteins c-bcl-2ResveratrolRNA, MessengerRNA, Small InterferingStilbenes

Identifiers

PMID18428028
PMCPMC2774405
OpenAlexW1992420244

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.