Evidence map›Paper›PMID 32907912›Full record

ArticleJournal of clinical pathology2021

Prognostic values of L-type amino acid transporter 1 and CD98hc expression in breast cancer.

Masaaki Ichinoe, Tetuo Mikami, Nobuyuki Yanagisawa, Tsutomu Yoshida, Kiyomi Hana, Hitoshi Endou, Isao Okayasu, Norihiko Sengoku, Hideaki Ogata, Makoto Saegusa and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Comprehensive Characterization of LAT1 Cholesterol-Binding Sites.Journal of chemical theory and computation · 2024
    Article
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  10. Review
  11. Article
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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

12 authors at 3 institutions in 1 country.

Masaaki IchinoeDepartment of Pathology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan hanabi@med.kitasato-u.ac.jp.ORCID http://orcid.org/0000-0002-4622-0565
Tetuo MikamiDepartment of Pathology, Toho University School of Medicine, Ota-ku, Tokyo, Japan.
Nobuyuki YanagisawaDepartment of Pathology, St. Marianna University School of Medicine Yokohama-City Seibu Hospital, Yokohama, Kanagawa, Japan.
Tsutomu YoshidaDepartment of Pathology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kiyomi HanaJ-Pharma Co., Ltd, Yokohma, Kanagawa, Japan.
Hitoshi EndouJ-Pharma Co., Ltd, Yokohma, Kanagawa, Japan.
Isao OkayasuDepartment of Pathology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Norihiko SengokuDepartment of Breast and Thyroid Surgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Hideaki OgataDepartment of Surgery, Toho University Omori Medical Center, Ota-ku, Tokyo, Japan.
Makoto SaegusaDepartment of Pathology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kazutoshi ShibuyaDepartment of Surgical Pathology, Toho University School of Medicine, Ota-ku, Tokyo, Japan.
Yoshiki MurakumoDepartment of Pathology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Kitasato University · JPToho University · JPSt. Marianna University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsL-type amino acid transporter 1 (LAT1) is a major Na

methodsLAT1 and CD98hc expression was immunohistochemically assessed in 280 invasive breast cancers and analysed for association with clinicopathological features.

resultsHigh levels of LAT1 and CD98hc were observed in triple-negative breast cancers (TNBCs) possessing negative immunoreactivity with oestrogen receptor, progesterone receptor and human epidermal growth factor receptor 2, compared with non-TNBCs (NTNBCs), and were associated with lymph-node metastasis and higher nuclear grade. The high-LAT1-expression group showed a poor prognosis in NTNBC and TNBC, however, high-CD98hc-expression group showed a poor prognosis only in NTNBC. LAT1 and CD98hc expression could be the prognostic factors in univariate analyses, but not in multivariate analyses. Further, we found that invasive tumour components showed higher LAT1 and CD98hc expression than non-invasive tumour components.

conclusionsLAT1 and CD98hc may possess prognostic values in invasive breast cancer. LAT1 may be linked with cancer cell activities and disease progression in breast cancer.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBreast NeoplasmsDisease ProgressionFemaleFusion Regulatory Protein 1, Heavy ChainHumansLarge Neutral Amino Acid-Transporter 1Middle AgedPrognosisBiomarkers, TumorFusion Regulatory Protein 1, Heavy ChainLarge Neutral Amino Acid-Transporter 1SLC3A2 protein, humanSLC7A5 protein, humanbreast cancerbreast pathologyhistopathology

Identifiers

PMID32907912
PMCPMC8380907
OpenAlexW3084322596

What OpenQuestion holds

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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.