Evidence map›Paper›PMID 35091679›Full record

ArticleOncogene2022

TRIM32 promotes radioresistance by disrupting TC45-STAT3 interaction in triple-negative breast cancer.

Yan Ma, Haibo Zhang, Cheng Chen, Lixin Liu, Ting Ding, Ying Wang, Dachang Ma, Xiaoling Ling, Xiaohua Chen, Jianping Li and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

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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

15 authors at 5 institutions in 1 country.

Yan Ma *Department of Radiation Oncology, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China.
Haibo Zhang *Oncology center, Department of Radiation Oncology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, 310014, P.R. China.
Cheng Chen *Department of Breast Surgery, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China.
Lixin Liu *Department of thoracic surgery, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China.
Ting Ding *Department of endocrinology, Yiyang Central Hospital, Yiyang, Hunan, 413000, P.R. China.
Ying WangOncology center, Department of Radiation Oncology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, 310014, P.R. China.
Dachang MaDepartment of Breast Surgery, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China.
Xiaoling LingDepartment of Oncology, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China.
Xiaohua ChenDepartment of Radiation Oncology, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China.
Jianping LiShanghai Bioegene Co.,Ltd, Shanghai, 200003, P.R. China.
Guansheng
ZhongDepartment of Breast Surgery, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310003, P.R. China.
Guoqing RuDepartment of Pathology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Zhejiang, 310014, P.R. China.
Lei ZhangDepartment of Radiation Oncology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, P.R. China. hrbmuzl@126.com.
Jianming TangDepartment of Radiation Oncology, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P.R. China. 15900792812@163.com.ORCID http://orcid.org/0000-0003-3738-9761
First Hospital of Lanzhou University · CNZhejiang Provincial People's Hospital · CNShanghai Jiao Tong University · CNYichang Central People's Hospital · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radioresistance is common in the treatment of triple-negative breast cancer (TNBC), but the molecular mechanisms involved remain unclear. Herein, we reveal that tripartite motif-containing protein 32 (TRIM32) is upregulated in TNBC and is negatively associated with survival of TNBC patients. Radiotherapy resulted in enhanced expression of TRIM32, whereas TRIM32 depletion reduced TNBC radioresistance in vitro and in vivo. Mechanistically, radiotherapy promoted the association between TRIM32 and nuclear STAT3, which suppressed TC45-induced dephosphorylation of STAT3, resulting in increased STAT3 transcriptional activation and TNBC radioresistance. Finally, we demonstrated that TRIM32 and STAT3 phosphorylation are co-expressed in TNBC tissues. Moreover, high expression of TRIM32 and STAT3 phosphorylation is positively linked to poor prognosis of TNBC patients. Our study demonstrates that TRIM32 is a novel target for predicting radioresistance in TNBC patients.

Indexed as

Triple Negative Breast NeoplasmsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansSTAT3 Transcription FactorTranscriptional ActivationTranscription FactorsTripartite Motif ProteinsUbiquitin-Protein LigasesSTAT3 protein, humanSTAT3 Transcription FactorTranscription FactorsTRIM32 protein, humanTripartite Motif ProteinsUbiquitin-Protein Ligases

Identifiers

PMID35091679
OpenAlexW4210494582

What OpenQuestion holds

Textmetadata
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.