Evidence map›Paper›PMID 35336794›Full record

ArticleBiology2022

Extracellular Release of HMGB1 as an Early Potential Biomarker for the Therapeutic Response in a Xenograft Model of Boron Neutron Capture Therapy.

Shoji Imamichi, Lichao Chen, Tasuku Ito, Ying Tong, Takae Onodera, Yuka Sasaki, Satoshi Nakamura, PierLuigi Mauri, Yu Sanada, Hiroshi Igaki and 5 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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  10. Role of HMGB1 in Cutaneous Melanoma: State of the Art.International journal of molecular sciences · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 2 countries.

Shoji ImamichiDepartment of Molecular and Genomic Biomedicine, School of Biomedical Sciences, Nagasaki University Graduate, Nagasaki 852-8523, Japan.ORCID 0000-0003-4131-6258
Lichao ChenDepartment of Molecular and Genomic Biomedicine, School of Biomedical Sciences, Nagasaki University Graduate, Nagasaki 852-8523, Japan.
Tasuku ItoLab of Collaborative Research, Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
Ying TongDepartment of Molecular and Genomic Biomedicine, School of Biomedical Sciences, Nagasaki University Graduate, Nagasaki 852-8523, Japan.
Takae OnoderaDepartment of Molecular and Genomic Biomedicine, School of Biomedical Sciences, Nagasaki University Graduate, Nagasaki 852-8523, Japan.
Yuka SasakiDepartment of Molecular and Genomic Biomedicine, School of Biomedical Sciences, Nagasaki University Graduate, Nagasaki 852-8523, Japan.
Satoshi NakamuraDivision of BNCT, EPOC, National Cancer Center, Tokyo 104-0045, Japan.
PierLuigi MauriClinical Proteomics Laboratory, Institute of Biomedical Technologies, National Research Council, 93-20054 Milan, Italy.ORCID 0000-0003-4364-0393
Yu SanadaInstitute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori 590-0494, Japan.
Hiroshi IgakiDivision of BNCT, EPOC, National Cancer Center, Tokyo 104-0045, Japan.
Yasufumi MurakamiDepartment of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Tokyo 125-8585, Japan.
Minoru SuzukiInstitute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori 590-0494, Japan.ORCID 0000-0002-5421-9417
Jun ItamiDivision of BNCT, EPOC, National Cancer Center, Tokyo 104-0045, Japan.ORCID 0000-0003-1579-7406
Shinichiro MasunagaInstitute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori 590-0494, Japan.
Mitsuko MasutaniDepartment of Molecular and Genomic Biomedicine, School of Biomedical Sciences, Nagasaki University Graduate, Nagasaki 852-8523, Japan.
Japan Radioisotope Association · JPKyoto University · JPTokyo National Hospital · JPNagasaki University · JPTokyo University of Science · JPInstitute of Biomedical Technologies · IT

Funding

Cancer Intelligence Care Systems, Inc. (MM)JSPS Grant-in-Aid for Scientific Research 17K15814 (SI) and 18H02693 (MM)National Cancer Center Research and Development Fund H26-A-18, H29-A-8
6 · The paper itself

Abstract

Boron neutron capture therapy (BNCT) is a non-invasive therapeutic technique for treating malignant tumors, however, methods to evaluate its therapeutic efficacy and adverse reactions are lacking. High mobility group box 1 (HMGB1) is an inflammatory molecule released during cell death. Therefore, we aimed to investigate HMGB1 as a biomarker for BNCT response, by examining the early responses of tumor cells to

Indexed as

10B-boronophenylalanine (BPA)boron neutron capture reaction (BNCR)boron neutron capture therapy (BNCT)high mobility group box 1 (HMGB1)

Identifiers

PMID35336794
PMCPMC8945761
OpenAlexW4220686460

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.