Evidence map›Paper›PMID 29926386›Full record

ArticleMolecular biology reports2018

CXCL12 chemokine and CXCR4 receptor: association with susceptibility and prognostic markers in triple negative breast cancer.

Alda Losi Guembarovski, Roberta Losi Guembarovski, Bruna Karina Banin Hirata, Glauco Akelinghton Freire Vitiello, Karen Mayumi Suzuki, Mayara Tiemi Enokida, Maria Angelica Ehara Watanabe, Edna Maria Vissoci Reiche

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In one paragraph

Article in Molecular biology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 27% 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, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  3. Research process of PET tracers for neuroendocrine tumors diagnosis.American journal of nuclear medicine and molecular imaging · 2025
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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 1 institution in 1 country.

Alda Losi GuembarovskiDepartment of Pathology, Clinical and Toxicological Analyses, Health Sciences Center, Londrina State University, Londrina, Parana, Brazil.
Roberta Losi GuembarovskiDepartment of General Biology, Biological Sciences Center, Londrina State University, Londrina, Parana, Brazil. rolosi@uol.com.br.
Bruna Karina Banin HirataDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Parana, Brazil.
Glauco Akelinghton Freire VitielloDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Parana, Brazil.
Karen Mayumi SuzukiDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Parana, Brazil.
Mayara Tiemi EnokidaDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Parana, Brazil.
Maria Angelica Ehara WatanabeDepartment of Pathological Sciences, Biological Sciences Center, Londrina State University, Londrina, Parana, Brazil.ORCID http://orcid.org/0000-0003-1789-8200
Edna Maria Vissoci ReicheDepartment of Pathology, Clinical and Toxicological Analyses, Health Sciences Center, Londrina State University, Londrina, Parana, Brazil.
Universidade Estadual de Londrina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CXCL12/CXCR4 signaling has been implicated in breast carcinogenesis, and genetic polymorphisms in these molecules have been associated with different types of cancer. The present study analyzed genetic polymorphisms in CXCL12 (rs1801157, G > A) and CXCR4 (rs2228014, C > T) and CXCR4 immunostaining in tumor tissues from patients with triple negative breast cancer (TNBC) aiming to evaluate their possible role in its' susceptibility and prognosis. Genetic polymorphisms were analyzed in 59 TNBC patients and 150 control women; age-adjusted logistic regression showed no association when variants were considered in isolation; however, a statistically significant interaction was noted for heterozygosis for both allelic variants increasing the odds for TNBC (CXCL12-GA by CXCR4-CT: OR 7.23; 95% CI 1.15-45.41; p = 0.035). CXCL12 polymorphism was correlated negatively with proliferation index (Ki67) (Tau-b = - 0.406; p = 0.006). CXCR4 immunostaining was evaluated in 37 TNBC patients (22 with paired tumor-normal adjacent tissue). CXCR4 was detected more intensely in cell cytoplasm than in membrane, and was more expressed in tumor than in normal adjacent tissues, although not statistically significant. CXCR4 expression on the membrane of tumor cells was correlated positively with histopathological grade (Tau-b = 0.271; p = 0.036) and negatively with lymph node metastasis (Tau-b = - 0.478; p = 0.036). The present study indicates that CXCL12 and CXCR4 polymorphisms and CXCR4 immunostaining might have susceptibility and prognostic roles in TNBC pathogenesis.

Indexed as

AdultAgedAllelesBiomarkers, TumorChemokine CXCL12FemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansLymphatic MetastasisMiddle AgedPolymorphism, GeneticPolymorphism, Single NucleotidePrognosisReceptors, CXCR4Biomarkers, TumorChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanReceptors, CXCR4CXCL12CXCR4Genetic polymorphismImmunohistochemistryPrognosisTriple-negative breast cancer

Identifiers

PMID29926386
OpenAlexW2809176496

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Registered trials

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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.