Evidence map›Paper›PMID 31691056›Full record

ArticleMolecular biology reports2019

CCL5 protein level: influence on breast cancer staging and lymph nodes commitment.

Daniela Rudgeri Derossi, Marla Karine Amarante, Roberta Losi Guembarovski, Carlos Eduardo Coral de Oliveira, Karen Mayumi Suzuki, Maria Angelica Ehara Watanabe, Ilce Mara de Syllos Cólus

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Relationship ofJournal of clinical medicine · 2023
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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

7 authors at 1 institution in 1 country.

Daniela Rudgeri DerossiDepartment of Pathology, Clinical Analysis and Toxicology, Londrina State University, Londrina, PR, Brazil.
Marla Karine AmaranteLaboratory of DNA Polymorphisms and Immunology, Department of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, PR, Brazil. marlakarineuel@gmail.com.ORCID http://orcid.org/0000-0001-8218-8518
Roberta Losi GuembarovskiDepartment of Biology, Biological Sciences Center, Londrina State University, Londrina, PR, Brazil.
Carlos Eduardo Coral de OliveiraLaboratory of DNA Polymorphisms and Immunology, Department of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, PR, Brazil.
Karen Mayumi SuzukiDepartment of Biology, Biological Sciences Center, Londrina State University, Londrina, PR, Brazil.
Maria Angelica Ehara WatanabeLaboratory of DNA Polymorphisms and Immunology, Department of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, PR, Brazil.
Ilce Mara de Syllos CólusDepartment of Biology, Biological Sciences Center, Londrina State University, Londrina, PR, Brazil.
Universidade Estadual de Londrina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many tumor cells express chemokines and chemokine receptors, and these molecules can contribute to distinct modes of metastasis processes. It is known that they play a crucial role in breast cancer (BC) tumorigenesis and progression. Considering this, it was investigated a possible role for C-Chemokine receptor type 5(CCR5) polymorphism (rs333/delta32) by conventional polymerase chain reaction (PCR) and CCL5 (C-C motif chemokine ligand 5) protein level by immunosorbent assay (ELISA) in 47 BC patients (resulting in 47 tumoral tissue samples and 47 adjacent normal tissue samples). There was a significant difference between CCL5 level in tumoral and adjacent normal tissues for the same BC patients (p < 0.0001). A significant association was also found for CCL5 level in relation to lymph nodes commitment (p = 0.03). Likewise, there was a significant difference in CCL5 level from tumor tissue of stage III in relation to stage I (p < 0.02). On the other hand, it was verified that CCR5-delta32 polymorphism presented no significant association in relation to CCL5 protein level. Considering the present findings, we suggest that CCL5 may be involved in BC staging and metastasis process.

Indexed as

BiomarkersBreast NeoplasmsChemokine CCL5FemaleHumansImmunohistochemistryLymphatic MetastasisMiddle AgedNeoplasm StagingPrognosisBiomarkersCCL5 protein, humanChemokine CCL5Breast cancerCCL5CCR5ELISAPolymorphismTumoral stages

Identifiers

PMID31691056
OpenAlexW2983967358

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.