Evidence map›Paper›PMID 38665698›Full record

ArticleBiomaterials research2024

Targeting Heme Oxygenase 2 (HO2) with TiNIR, a Theragnostic Approach for Managing Metastatic Non-Small Cell Lung Cancer.

Seul-Ki Mun, Hyun Bo Sim, Jae-Hyuk Lee, Hyeongyeong Kim, Dae-Han Park, Yong-An Lee, Ji Yeon Han, Yu-Jeong Choi, Jun Sang Son, Jeongwon Park and 6 more

Open access · goldAbstract read
In one paragraph

Article in Biomaterials research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Therapeutic Effects ofCurrent issues in molecular biology · 2025
    Article
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

16 authors at 1 institution in 1 country.

Seul-Ki MunDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Hyun Bo SimDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Jae-Hyuk LeeGwangju Center, Korea Basic Science Institute (KBSI), Gwangju 61751, Republic of Korea.
Hyeongyeong KimDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Dae-Han ParkDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Yong-An LeeGenome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), 60 Biopolis Street, Genome, Singapore 138672, Republic of Singapore.
Ji Yeon HanDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Yu-Jeong ChoiDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Jun Sang SonDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Jeongwon ParkGwangju Center, Korea Basic Science Institute (KBSI), Gwangju 61751, Republic of Korea.
Tae-Hwan LimCollege of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Suncheon 57922, Republic of Korea.
Sung-Tae YeeCollege of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Suncheon 57922, Republic of Korea.
Young-Tae ChangSchool of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.
Seongsoo LeeGwangju Center, Korea Basic Science Institute (KBSI), Gwangju 61751, Republic of Korea.
Dong-Jo ChangCollege of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Suncheon 57922, Republic of Korea.
Jong-Jin KimDepartment of Biomedical Science, Sunchon National University, Suncheon 57922, Republic of Korea.
Government of the Republic of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite notable advancements in cancer therapeutics, metastasis remains a primary obstacle impeding a successful prognosis. Our prior study has identified heme oxygenase 2 (HO2) as a promising therapeutic biomarker for the aggressive subsets within tumor. This study aims to systematically evaluate HO2 as a therapeutic target of cancer, with a specific emphasis on its efficacy in addressing cancer metastasis. Through targeted inhibition of HO2 by TiNIR (tumor-initiating cell probe with near infrared), we observed a marked increase in reactive oxygen species. This, in turn, orchestrated the modulation of AKT and cJUN activation, culminating in a substantial attenuation of both proliferation and migration within a metastatic cancer cell model. Furthermore, in a mouse model, clear inhibition of cancer metastasis was unequivocally demonstrated with an HO2 inhibitor administration. These findings underscore the therapeutic promise of targeting HO2 as a strategic intervention to impede cancer metastasis, enhancing the effectiveness of cancer treatments.

Identifiers

PMID38665698
PMCPMC11045274
OpenAlexW4393929868

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.