Evidence map›Paper›PMID 25255861›Full record

ArticleBMC cancer2014

Enhanced down-regulation of ALCAM/CD166 in African-American Breast Cancer.

Fang Tan, Marina Mosunjac, Amy L Adams, Beverly Adade, Oleyad Taye, Yijuan Hu, Monica Rizzo, Solomon F Ofori-Acquah

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. ALCAM is indirectly modulated by miR-125b in MCF7 cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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 3 institutions in 1 country.

Fang Tan
Marina Mosunjac
Amy L Adams
Beverly Adade
Oleyad Taye
Yijuan Hu
Monica Rizzo
Solomon F Ofori-AcquahAflac Cancer Center and Blood Disorders Service, Department of Pediatrics, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA 30322, USA. sfo2@pitt.edu.
Emory University · USCenter for Cancer and Blood Disorders · USGrady Memorial Hospital · US

Funding

The Impact of Family Labor Market Status on Access to Health CareP20MD002314 · NIMHD · UNIVERSITY OF SOUTH ALABAMA · PI CROOK, ERROL D · 2007 to 2016
$12.9M
Role of CD166/ALCAM in Lung Endothelial Barrier FunctionR01HL077769 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI OFORI-ACQUAH, SOLOMON FIIFI · 2004 to 2007
$1.1M
NHLBI NIH HHS R01 HL077769NHLBI NIH HHS R01HL077769NIMHD NIH HHS P20 MD002314NIMHD NIH HHS P20MD002314
6 · The paper itself

Abstract

backgroundVariation in tumor biology in African-American (AA) and Caucasian (CAU) women with breast cancer is poorly defined. Activated leukocyte cell adhesion molecule (ALCAM) is a bad prognostic factor of breast cancer yet it has never being studied in the AA population. We tested the hypothesis that ALCAM expression would be markedly lower in cases of AA breast cancer when compared to CAU.

methodsCases of breast cancer among AA (n = 78) and CAU (n = 95) women were studied. Immunohistochemical staining was used to semi-quantitatively score ALCAM expression in tumor and adjacent non-tumor breast tissues. Clinico-pathological characteristics including histological type, histological grade, tumor size, lymph node metastasis, estrogen receptor (ER), progesterone receptor (PR), and HER2-neu status were abstracted, and their association with ALCAM expression tested.

resultsUnivariate analysis revealed that the level of ALCAM expression at intercellular junctions of primary tumors correlates with histological grade (AA; p = 0.04, CUA; p = 0.02), ER status (AA; p = 0.0004, CAU; p = 0.0015), PR status (AA; p = 0.002, CUA p = 0.034) and triple-negative tumor status (AA; p = 0.0002, CAU; p = 0.0006,) in both ethnic groups. Multivariate analysis demonstrated that ethnicity contribute significantly to ALCAM expression after accounting for basal-like subtype, age, histological grade, tumor size, and lymph node status. Compared to CAU tumors, the AA are 4 times more likely to have low ALCAM expression (p = 0.003).

conclusionsMarkedly low expression of ALCAM at sites of cell-cell contact in primary breast cancer tumors regardless of differentiation, size and lymph node involvement may contribute to the more aggressive phenotype of breast cancer among AA women.

Indexed as

Down-RegulationActivated-Leukocyte Cell Adhesion MoleculeAntigens, CDBlack or African AmericanBreast NeoplasmsCarcinoma, Ductal, BreastCell Adhesion Molecules, NeuronalErb-b2 Receptor Tyrosine KinasesFemaleFetal ProteinsGene ExpressionHumansLymphatic MetastasisMiddle AgedPhenotypeReceptors, EstrogenActivated-Leukocyte Cell Adhesion MoleculeALCAM protein, humanAntigens, CDCell Adhesion Molecules, NeuronalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFetal ProteinsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID25255861
PMCPMC4190464
OpenAlexW1985679384

What OpenQuestion holds

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LicenceCC BY
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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.