Evidence map›Paper›PMID 33671956›Full record

ArticleInternational journal of molecular sciences2021

Stromal CCL5 Promotes Breast Cancer Progression by Interacting with CCR3 in Tumor Cells.

Mio Yamaguchi, Kiyoshi Takagi, Koki Narita, Yasuhiro Miki, Yoshiaki Onodera, Minoru Miyashita, Hironobu Sasano, Takashi Suzuki

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

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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.

Mio YamaguchiDepartment of Pathology and Histotechnology, Graduate School of Medicine, Tohoku University, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan.ORCID 0000-0002-4276-5445
Kiyoshi TakagiDepartment of Pathology and Histotechnology, Graduate School of Medicine, Tohoku University, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan.
Koki NaritaDepartment of Pathology and Histotechnology, Graduate School of Medicine, Tohoku University, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan.
Yasuhiro MikiDepartment of Disaster Obstetrics and Gynecology, International Research Institute of Disaster Science, Tohoku University, Sendai 980-8574, Miyagi, Japan.ORCID 0000-0003-3618-5652
Yoshiaki OnoderaDepartment of Anatomic Pathology, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Miyagi, Japan.
Minoru MiyashitaDepartment of Breast and Endocrine Surgical Oncology, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Miyagi, Japan.ORCID 0000-0002-4151-8725
Hironobu SasanoDepartment of Anatomic Pathology, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Miyagi, Japan.
Takashi SuzukiDepartment of Pathology and Histotechnology, Graduate School of Medicine, Tohoku University, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Miyagi, Japan.
Tohoku University · JP

Funding

Japan Society for the Promotion of Science 19K07410Japan Society for the Promotion of Science 19K09065
6 · The paper itself

Abstract

Chemokines secreted from stromal cells have important roles for interactions with carcinoma cells and regulating tumor progression. C-C motif chemokine ligand (CCL) 5 is expressed in various types of stromal cells and associated with tumor progression, interacting with C-C chemokine receptor (CCR) 1, 3 and 5 expressed in tumor cells. However, the expression on CCL5 and its receptors have so far not been well-examined in human breast carcinoma tissues. We therefore immunolocalized CCL5, as well as CCR1, 3 and 5, in 111 human breast carcinoma tissues and correlated them with clinicopathological characteristics. Stromal CCL5 immunoreactivity was significantly correlated with the aggressive phenotype of breast carcinomas. Importantly, this tendency was observed especially in the CCR3-positive group. Furthermore, the risk of recurrence was significantly higher in the patients with breast carcinomas positive for CCL5 and CCR3 but negative for CCR1 and CCR5, as compared with other patients. In summary, the CCL5-CCR3 axis might contribute to a worse prognosis in breast cancer patients, and these findings will contribute to a better understanding of the significance of the CCL5/CCRs axis in breast carcinoma microenvironment.

Indexed as

Disease ProgressionSignal TransductionAdultAgedAged, 80 and overBreast NeoplasmsChemokine CCL5Disease-Free SurvivalFemaleFollow-Up StudiesHumansImmunohistochemistryMiddle AgedNeoplasm Recurrence, LocalParacrine CommunicationPrognosisCCL5 protein, humanCCR1 protein, humanCCR3 protein, humanCCR5 protein, humanChemokine CCL5Receptors, CCR1Receptors, CCR3Receptors, CCR5breast carcinomachemokineimmunohistochemistryprognosistumor microenvironment

Identifiers

PMID33671956
PMCPMC7919043
OpenAlexW3132656131

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.