Evidence map›Paper›PMID 40640803›Full record

ArticleCell communication and signaling : CCS2025

NASP implication in the androgen receptor associated with castration resistance in prostate cancer.

Yun Feng, Jin Sun, Xuan Kang, Yining Wang, Kai Liu, Wenfei Wang, Chen Wang, Yabin Li, Qian Zhao, Kaile Li and 2 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. 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
–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

1 citing paper in PubMed.

  1. 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

12 authors.

Yun Feng *Research Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Jin Sun *Research Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Xuan KangTeaching Laboratory Center, School of Medicine, Tongji University, Shanghai, China.
Yining WangResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Kai LiuResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Wenfei WangResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Chen WangResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Yabin LiResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Qian ZhaoResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Kaile LiResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Fang-Lin SunResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China. sfl@tongji.edu.cn.
Jianfeng ChangResearch Center for Translational Medicine at East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China. jfchang@tongji.edu.cn.

Funding

National Natural Science Foundation of China 81972743National Natural Science Foundation of China 82273146the Ministry of Science and Technology of China 2017YFA0103301the Postdoctoral Fellowship Program of CPSF GZC20241067
6 · The paper itself

Abstract

Uncovering the mechanisms underlying tumor malignancy is extremely important for cancer treatment and management. In this study, using a pairwise cell model, LNCaP and its castration-resistant derivative C42B, we analyze the function of enhanced NASP protein in castration resistance. The data show that the expression of androgen receptor-targeted genes was obviously affected by NASP knockdown in C42B cells, and nearly 20% of the differential genes were AR dependent. ATAC-seq analysis revealed that NASP knockdown in C42B cells comprehensively increased chromatin accessibility, and disorders at AR occupancy regions were more prominent. Castration-induced genes, especially androgen-independent AR target genes, were enriched in the downregulated gene group. Further analysis of high-order chromatin interactions revealed that NASP knockdown in C42B led to frequent changes in multiple layers, including the compartment A/B transition, TAD boundary distance and chromatin loop, and AR-binding regions especially underwent more extensive reconstruction. Finally, we found that the recovery of the histone H3 pool in C42B can actually recall H3 back to the previous regions with both H3 and AR loss induced by NASP knockdown, but AR rebinding to the corresponding sites is obviously inhibited and lagging. These data indicate that NASP plays a fundamental role in guarding proper and fine mechanisms of AR in prostate cancer promotion and malignancy.

Indexed as

Nuclear ProteinsProstatic Neoplasms, Castration-ResistantReceptors, AndrogenCell Line, TumorChromatinGene Expression Regulation, NeoplasticGene Knockdown TechniquesHistonesHumansMaleAR protein, humanChromatinHistonesNuclear ProteinsReceptors, AndrogenAndrogen receptorEMTEpigenetic landscapeHistone turnoverNASPProstate cancer

Identifiers

PMID40640803
PMCPMC12243143

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.