Evidence map›Paper›PMID 23404580›Full record

ArticleOncology reports2013

Genomic and phenotypic profiles of two Brazilian breast cancer cell lines derived from primary human tumors.

Natássia C R Corrêa, Hellen Kuasne, Jerusa A Q A Faria, Ciça C S Seixas, Iria G D Santos, Francine B Abreu, Suely Nonogaki, Rafael M Rocha, Gerluza Aparecida Borges Silva, Helenice Gobbi and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Voltage-gated NaPflugers Archiv : European journal of physiology · 2025
    Article
  2. Article
  3. Article
  4. 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

13 authors at 3 institutions in 1 country.

Natássia C R CorrêaDepartment of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Hellen Kuasne
Jerusa A Q A Faria
Ciça C S Seixas
Iria G D Santos
Francine B Abreu
Suely Nonogaki
Rafael M Rocha
Gerluza Aparecida Borges Silva
Helenice Gobbi
Silvia R Rogatto
Alfredo M Goes
Dawidson A Gomes
Universidade Federal de Minas Gerais · BRAC Camargo Hospital · BRUniversidade Estadual de Londrina · BR

Funding

Trafficking of the EGF receptor to the nucleus: Mechanisms and EffectsR03TW008709 · FIC · YALE UNIVERSITY · PI NATHANSON, MICHAEL H · 2012 to 2014
$230k
FIC NIH HHS 1R03TW008709FIC NIH HHS R03 TW008709
6 · The paper itself

Abstract

Breast cancer is the most common type of cancer among women worldwide. Research using breast cancer cell lines derived from primary tumors may provide valuable additional knowledge regarding this type of cancer. Therefore, the aim of this study was to investigate the phenotypic profiles of MACL-1 and MGSO-3, the only Brazilian breast cancer cell lines available for comparative studies. We evaluated the presence of hormone receptors, proliferation, differentiation and stem cell markers, using immunohistochemical staining of the primary tumor, cultured cells and xenografts implanted in immunodeficient mice. We also investigated the ability of the cell lines to form colonies and copy number alterations by array comparative genomic hybridization. Histopathological analysis showed that the invasive primary tumor from which the MACL-1 cell line was derived, was a luminal A subtype carcinoma, while the ductal carcinoma in situ (DCIS) that gave rise to the MGSO-3 cell line was a HER2 subtype tumor, both showing different proliferation levels. The cell lines and the tumor xenografts in mice preserved their high proliferative potential, but did not maintain the expression of the other markers assessed. This shift in expression may be due to the selection of an 'establishment' phenotype in vitro. Whole-genome DNA evaluation showed a large amount of copy number alterations (CNAs) in the two cell lines. These findings render MACL-1 and MGSO-3 the first characterized Brazilian breast cancer cell lines to be potentially used for comparative research.

Indexed as

Cell ProliferationAnimalsBrazilBreast NeoplasmsCell Line, TumorComparative Genomic HybridizationErb-b2 Receptor Tyrosine KinasesFemaleHumansMiceXenograft Model Antitumor AssaysERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID23404580
PMCPMC3621816
OpenAlexW2104694219

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.