Evidence map›Paper›PMID 41147157›Full record

ArticleChembiochem : a European journal of chemical biology2025

Characterization of BRCA1-Associated Protein-1 (BAP1) Aggregation Properties Induced by Cancer-Associated Mutations.

Li-Ching Hsiao, Sarita Puri, Manoj Kumar Sriramoju, Yong-Sheng Wang, Tian-Neng Lee, Lily Hui-Ching Wang, Shang-Te Danny Hsu

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Li-Ching HsiaoInstitute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.
Sarita PuriInstitute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.ORCID https://orcid.org/0000-0002-0896-9460
Manoj Kumar SriramojuInstitute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.
Yong-Sheng WangInstitute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.ORCID https://orcid.org/0000-0002-4868-4507
Tian-Neng LeeInstitute of Molecular and Cellular Biology, National Tsing Hua University, Hsinchu, 300044, Taiwan.
Lily Hui-Ching WangInstitute of Molecular and Cellular Biology, National Tsing Hua University, Hsinchu, 300044, Taiwan.ORCID https://orcid.org/0000-0003-0659-0139
Shang-Te Danny HsuInstitute of Biological Chemistry, Academia Sinica, Taipei, 11529, Taiwan.ORCID https://orcid.org/0000-0002-7231-0185

Funding

Academia Sinica Infectious Disease Research Supporting Grants AS-IDR-111-03, AS-IDR-114-S01Academia Sinica Investigator Award AS-IV-114-L04National Science and Technology Council 109-2811-M-001-605National Science and Technology Council 110-2113-M-001-050-MY3National Science and Technology Council 113-2123-M-001-010National Science and Technology Council 113-2811-M-001-110National Science and Technology Council 114-2123-M-001-008National Science and Technology Council 114-2124-M-007-008National Science and Technology Council 114-2311-B-007 -006National Science and Technology Council 114-2811-M-001-106
6 · The paper itself

Abstract

BRCA1-associated protein-1 (BAP1) is a tumor suppressor protein that regulates DNA transcription through its deubiquitinase activity. Cancer-associated missense mutations within its ubiquitin C-terminal hydrolase (UCH) domain result in structural destabilization and aggregation, contributing to various malignancies such as malignant mesothelioma and uveal melanoma. In this study, we investigated the aggregation mechanisms of highly destabilized BAP1-UCH variants, including N78S, C91W, F81V, and G128R, using Thioflavin T (ThT) binding assays and AmyloFit analysis. Our results reveal that all BAP1-UCH variants follow a secondary nucleation-dominated aggregation model, exhibiting strong concentration dependence and significantly higher aggregation rates, which may be responsible for their impaired nuclear import, leading to increased cytosolic retention. These findings provide critical insights into how specific mutations in BAP1 drive aggregation and compromise its tumor-suppressing functions inside the nucleus, thereby contributing to cancer progression.

Indexed as

NeoplasmsTumor Suppressor ProteinsUbiquitin ThiolesteraseBenzothiazolesHumansMutationProtein AggregatesBAP1 protein, humanBenzothiazolesProtein AggregatesTumor Suppressor ProteinsUbiquitin Thiolesteraseaggregation kineticsBRCA1‐associated protein‐1cancer disease

Identifiers

PMID41147157
PMCPMC12666247

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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.