Evidence map›Paper›PMID 35133060›Full record

ArticleCancer science2022

CXCL12 promotes CCR7 ligand-mediated breast cancer cell invasion and migration toward lymphatic vessels.

Haruko Hayasaka, Junichi Yoshida, Yasutaka Kuroda, Akihiro Nishiguchi, Michiya Matsusaki, Kei Kishimoto, Hitoshi Nishimura, Mari Okada, Yuki Shimomura, Daichi Kobayashi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. 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
3.3field-weighted citation impact, top 6% 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, 31 citations in OpenAlex.

  1. Review
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  9. Neuronal guidance behaviours: the primary cilium perspective.Frontiers in cell and developmental biology · 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

14 authors at 7 institutions in 2 countries.

Haruko HayasakaFaculty of Science & Engineering, Department of Science, Graduate School of Science and Engineering, Kindai University, Higashiosaka, Japan.ORCID https://orcid.org/0000-0003-1694-9248
Junichi YoshidaDepartment of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita, Japan.
Yasutaka KurodaDepartment of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita, Japan.ORCID https://orcid.org/0000-0003-0796-4331
Akihiro NishiguchiDepartment of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Japan.
Michiya MatsusakiDepartment of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Japan.
Kei KishimotoFaculty of Science & Engineering, Department of Science, Graduate School of Science and Engineering, Kindai University, Higashiosaka, Japan.
Hitoshi NishimuraFaculty of Science & Engineering, Department of Science, Graduate School of Science and Engineering, Kindai University, Higashiosaka, Japan.
Mari OkadaDepartment of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita, Japan.
Yuki ShimomuraDepartment of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita, Japan.
Daichi KobayashiNiigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.ORCID https://orcid.org/0000-0003-0389-0240
Yoshihito ShimazuDepartment of Life and Food Science, School of Life and Environmental Science, Azabu University, Sagamihara, Japan.
Yuji TayaLife Dentistry at Tokyo, The Nippon Dental University, Chiyoda-ku, Japan.
Mitsuru AkashiDepartment of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Japan.
Masayuki MiyasakaDepartment of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita, Japan.
The University of Osaka · JPKindai University · JPOsaka Gakuin University · JPAzabu University · JPNiigata University · JPNippon Dental University · JPUniversity of Turku · FI

Funding

Ministry of Education, Culture, Sports, Science and Technology 19K07278
6 · The paper itself

Abstract

Chemokines are a family of cytokines that mediate leukocyte trafficking and are involved in tumor cell migration, growth, and progression. Although there is emerging evidence that multiple chemokines are expressed in tumor tissues and that each chemokine induces receptor-mediated signaling, their collaboration to regulate tumor invasion and lymph node metastasis has not been fully elucidated. In this study, we examined the effect of CXCL12 on the CCR7-dependent signaling in MDA-MB-231 human breast cancer cells to determine the role of CXCL12 and CCR7 ligand chemokines in breast cancer metastasis to lymph nodes. CXCL12 enhanced the CCR7-dependent in vitro chemotaxis and cell invasion into collagen gels at suboptimal concentrations of CCL21. CXCL12 promoted CCR7 homodimer formation, ligand binding, CCR7 accumulation into membrane ruffles, and cell response at lower concentrations of CCL19. Immunohistochemistry of MDA-MB-231-derived xenograft tumors revealed that CXCL12 is primarily located in the pericellular matrix surrounding tumor cells, whereas the CCR7 ligand, CCL21, mainly associates with LYVE-1

Indexed as

Breast NeoplasmsCell MovementChemokine CXCL12Lymphatic VesselsReceptors, CCR7Cell Line, TumorChemokine CCL21FemaleHumansLigandsLymphatic MetastasisNeoplasm InvasivenessReceptors, CXCR4CCR7 protein, humanChemokine CCL21Chemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanLigandsReceptors, CCR7Receptors, CXCR4breast cancerchemokineinvasionlymph nodemetastasis

Identifiers

PMID35133060
PMCPMC8990860
OpenAlexW4210829015

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.