Evidence map›Paper›PMID 25655677›Full record

ArticleBMC cancer2015

Trogocytosis-mediated expression of HER2 on immune cells may be associated with a pathological complete response to trastuzumab-based primary systemic therapy in HER2-overexpressing breast cancer patients.

Eiji Suzuki, Tatsuki R Kataoka, Masahiro Hirata, Kosuke Kawaguchi, Mariko Nishie, Hironori Haga, Masakazu Toi

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 25 citations in OpenAlex.

  1. Immune surveillance interrupted: how cancer exploits trogocytosis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  2. Trogocytosis in cancer immunity and cellular immunotherapy: mechanisms, therapeutic challenges, and translational opportunities.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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  11. The Biological Significance of Trogocytosis.Results and problems in cell differentiation · 2024
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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

7 authors at 1 institution in 1 country.

Eiji SuzukiDepartment of Breast Surgery, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. eijis@kuhp.kyoto-u.ac.jp.
Tatsuki R KataokaDepartment of Diagnostic Pathology, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. trkata@kuhp.kyoto-u.ac.jp.
Masahiro HirataDepartment of Diagnostic Pathology, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. hiratama@kuhp.kyoto-u.ac.jp.
Kosuke KawaguchiDepartment of Breast Surgery, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. kkosuke@kuhp.kyoto-u.ac.jp.
Mariko NishieDepartment of Breast Surgery, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. nishie@kuhp.kyoto-u.ac.jp.
Hironori HagaDepartment of Diagnostic Pathology, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. haga@kuhp.kyoto-u.ac.jp.
Masakazu ToiDepartment of Breast Surgery, Kyoto University Hospital, 54 Shogoin kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. toi@kuhp.kyoto-u.ac.jp.
Kyoto University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrogocytosis is defined as the transfer of cell-surface membrane proteins and membrane patches from one cell to another through contact. It is reported that human epidermal growth factor receptor 2 (HER2) could be transferred from cancer cells to monocytes via trogocytosis; however, the clinical significance of this is unknown. The aim of this study is to demonstrate the presence and evaluate the clinical significance of HER2(+) tumor-infiltrated immune cells (arising through HER2 trogocytosis) in HER2-overexpressing (HER2+) breast cancer patients receiving trastuzumab-based primary systemic therapy (PST).

methodsTo assess the trogocytosis of HER2 from cancer cells to immune cells, and to evaluate the up- and down-regulation of HER2 on immune and cancer cells, peripheral blood mononuclear cells from healthy volunteers and breast cancer patients were co-cultured with HER2+ and HER2-negative breast cancer cell lines with and without trastuzumab, respectively. The correlation between HER2 expression on tumor-infiltrated immune cells and a pathological complete response (pCR) in HER2+ breast cancer patients treated with trastuzumab-based PST was analyzed.

resultsHER2 was transferred from HER2+ breast cancer cells to monocytes and natural killer cells by trogocytosis. Trastuzumab-mediated trogocytosed-HER2(+) effector cells exhibited greater CD107a expression than non-HER2-trogocytosed effector cells. In breast cancer patients, HER2 expression on tumor-infiltrated immune cells in treatment naïve HER2+ tumors was associated with a pCR to trastuzumab-based PST.

conclusionsHER2-trogocytosis is visible evidence of tumor microenvironment interaction between cancer cells and immune cells. Given that effective contact between these cells is critical for immune destruction of target cancer cells, this interaction is of great significance. It is possible that HER2 trogocytosis could be used as a predictive biomarker for trastuzumab-based PST efficacy in HER2(+) breast cancer patients.

Indexed as

Gene ExpressionAntibody-Dependent Cell CytotoxicityAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBreast NeoplasmsCD56 AntigenCell Line, TumorCell MembraneErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunophenotypingLeukocytes, MononuclearLipopolysaccharide ReceptorsLysosomal-Associated Membrane Protein 1Protein BiosynthesisBiomarkers, TumorCD56 AntigenErb-b2 Receptor Tyrosine KinasesLipopolysaccharide ReceptorsLysosomal-Associated Membrane Protein 1Trastuzumab

Identifiers

PMID25655677
PMCPMC4329225
OpenAlexW1982169105

What OpenQuestion holds

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LicenceCC BY
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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.