Evidence map›Paper›PMID 42621017›Full record

ArticleSmart molecules : open access2026

Rational design of a lipophilic β-galactosidase-responsive near-infrared probe for in vivo imaging of cellular senescence.

Jiani Huang, Feiyi Chu, Bin Feng, Lin Chen, Peili Cen, Jing Wang, Ying Qu, Lu Hong, Fei Wu, Huanfeng Tian and 6 more

Abstract read
In one paragraph

Article in Smart molecules : open access, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jiani HuangDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.ORCID https://orcid.org/0009-0004-5581-325X
Feiyi ChuXiangya School of Pharmaceutical Sciences Central South University Changsha China.
Bin FengXiangya School of Pharmaceutical Sciences Central South University Changsha China.
Lin ChenDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.
Peili CenDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.ORCID https://orcid.org/0000-0003-1497-2209
Jing WangDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.ORCID https://orcid.org/0000-0001-9761-9915
Ying QuDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.
Lu HongDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.
Fei WuDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.
Huanfeng TianXiangya School of Pharmaceutical Sciences Central South University Changsha China.
Yanpeng FangXiangya School of Pharmaceutical Sciences Central South University Changsha China.
Yuanjie ChenDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.
Mei TianHuman Phenome Institute Fudan University Shanghai China.ORCID https://orcid.org/0000-0002-1587-2114
Wenbin ZengXiangya School of Pharmaceutical Sciences Central South University Changsha China.ORCID https://orcid.org/0000-0001-8314-9174
Hong ZhangDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.ORCID https://orcid.org/0000-0002-4084-5150
Yan ZhongDepartment of Nuclear Medicine Zhejiang Cancer Hospital Hangzhou Institute of Medicine Chinese Academy of Sciences Hangzhou Zhejiang China.ORCID https://orcid.org/0009-0001-2288-8034

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Senescence-associated β-galactosidase (SA-β-gal) is a key biomarker of cellular senescence and has been demonstrated to be a major driver of various age-related diseases and tumor resistance. However, noninvasive in vivo imaging of SA-β-gal remains challenging due to the poor membrane permeability of existing probes, their reliance on intratumoral injection, and limited blood-brain barrier (BBB) permeability. This study reports a novel, rationally designed near-infrared (NIR) fluorescent probe,

Indexed as

blood‐brain barrierbrain agingcellular senescencenear‐infrared fluorescent probestumor senescenceβ‐galactosidase

Identifiers

PMID42621017
PMCPMC13487403

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.