Evidence map›Paper›PMID 37649051›Full record

ArticleMolecular cancer2023

BNIP3 as a potential biomarker for the identification of prognosis and diagnosis in solid tumours.

Qin Yu, Wenhao Fu, Yutang Fu, Wenjing Ye, Huiqiong Yan, Zecheng Yu, Ruirui Li, Yili Cai, Yuxin Chen, Lingyun Wang and 7 more

Open access · goldAbstract readLetter
In one paragraph

Article in Molecular cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  9. Frontiers in pharmacology · 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

17 authors at 2 institutions in 1 country.

Qin Yu *School of Information Engineering, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Wenhao Fu *School of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Yutang Fu *School of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Wenjing Ye *School of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Huiqiong Yan *Center of Laboratory Animal, Hangzhou Medical College, Hangzhou, 310013, Zhejiang, China.
Zecheng YuSchool of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Ruirui LiSchool of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Yili CaiSchool of Clinical Medicine, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Yuxin ChenSchool of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Lingyun WangSchool of Medical Laboratory and Biological Engineering, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Xianqiao WeiSchool of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Yangkun ChenSchool of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Yuheng ZhangSchool of Medical Imaging, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Huazhong YingCenter of Laboratory Animal, Hangzhou Medical College, Hangzhou, 310013, Zhejiang, China.
Furong TangThe Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, China. furong.tang@hotmail.com.
Fangwei DaiCenter of Laboratory Animal, Hangzhou Medical College, Hangzhou, 310013, Zhejiang, China. fangweidai@163.com.
Wei HanCenter of Laboratory Animal, Hangzhou Medical College, Hangzhou, 310013, Zhejiang, China. hanwei3612@163.com.
Hangzhou Medical College · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTraditional radiotherapy and chemotherapy have been intensively studied for their role in the treatment of tumours. However, these therapies often cause side effects for patients, which calls for the development of novel treatment options for tumours. B-cell lymphoma-2 (Bcl-2)/adenovirus E1B 19 kDa-interacting protein 3 (BNIP3) reportedly apoptosis-inducing effects in tumour cells and is associated with the progression and treatment of multiple tumours. Nevertheless, little is known about its potential role in tumour diagnosis and targeted therapy.

findingsThe results of the study demonstrated that the interaction of BNIP3 with HDAC1 may affect the progression of breast invasive cancer (BRCA), sarcoma (SARC), kidney renal clear cell carcinoma (KIRC), and low-grade glioma (LGG). BNIP3 seemed to exert its effects in BRCA and SARC primarily through gene silencing and integrator complex, and in KIRC and LGG, mainly by affecting olfactory function, suggesting that targeted therapy can be developed based on the above signalling pathway and downstream molecules.

interpretationBNIP3 has emerged as a promising therapeutic and diagnostic target for BRCA, SARC, KIRC, and LGG, providing new insights into tumour molecular therapies in the clinic.

Indexed as

Breast NeoplasmsCarcinoma, Renal CellGliomaKidney NeoplasmsSarcomaBiomarkersFemaleHumansMembrane ProteinsPrognosisProto-Oncogene ProteinsBiomarkersBNIP3 protein, humanMembrane ProteinsProto-Oncogene ProteinsBNIP3DiagnosisImmune infiltrationPan-cancer analysisPrognostic biomarker

Identifiers

PMID37649051
PMCPMC10466744
OpenAlexW4386289901

What OpenQuestion holds

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LicenceCC BY
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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.