Evidence map›Paper›PMID 35414770›Full record

ArticleInternational journal of biological sciences2022

USF1-ATRAP-PBX3 Axis Promote Breast Cancer Glycolysis and Malignant Phenotype by Activating AKT/mTOR Signaling.

Dandan Wang, Xiaoying Jin, Mengxia Lei, Ying Jiang, Yali Liu, Fei Yu, Yan Guo, Bing Han, Yue Yang, Weiling Sun and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 22 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 4 institutions in 1 country.

Dandan WangDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Xiaoying JinDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Mengxia LeiDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Ying JiangDepartment of Biochemistry and Molecular Biology, Mudanjiang Medical University, 3 Tongxiang Street, Mudanjang 157011, China.
Yali LiuDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Fei YuDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Yan GuoDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Bing HanDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Yue YangHeilongjiang Academy of Medical Sciences, Harbin Medical University, 157 Baojian Road, Harbin 150081, China.
Weiling SunDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Ying LiuDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Guangchun ZengDepartment of Pathology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Feng LiuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Jing HuDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Xuesong ChenDepartment of Breast Medical Oncology, Harbin Medical University Cancer Hospital, 150 Haping Road, Harbin 150040, China.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CNHeilongjiang Academy of Sciences · CNMudanjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiotensin II type 1 receptor-associated protein (ATRAP) is widely expressed in different tissues and organs, although its mechanistic role in breast cancer remains unclear. Here, we show that ATRAP is highly expressed in breast cancer tissues. Its aberrant upregulation promotes breast cancer aggressiveness and is positively correlated with poor prognosis. Functional assays revealed that ATRAP participates in promoting cell growth, metastasis, and aerobic glycolysis, while microarray analysis showed that ATRAP can activate the AKT/mTOR signaling pathway in cancer progression. In addition, ATRAP was revealed to direct Ubiquitin-specific protease 14 (USP14)-mediated deubiquitination and stabilization of Pre-B cell leukemia homeobox 3 (PBX3). Importantly, ATRAP is a direct target of Upstream stimulatory factor 1 (USF1), and that ATRAP overexpression reverses the inhibitory effects of USF1 knockdown. Our study demonstrates the broad contribution of the USF1/ATRAP/PBX3 axis to breast cancer progression and provides a strong potential therapeutic target.

Indexed as

Breast NeoplasmsProto-Oncogene Proteins c-aktAdaptor Proteins, Signal TransducingFemaleGlycolysisHomeodomain ProteinsHumansPhenotypeProto-Oncogene ProteinsReceptor, Angiotensin, Type 1Signal TransductionTOR Serine-Threonine KinasesUbiquitin ThiolesteraseUpstream Stimulatory FactorsAdaptor Proteins, Signal TransducingAGTRAP protein, humanHomeodomain ProteinsMTOR protein, humanproto-oncogene protein Pbx3Proto-Oncogene ProteinsProto-Oncogene Proteins c-aktReceptor, Angiotensin, Type 1TOR Serine-Threonine KinasesUbiquitin ThiolesteraseUpstream Stimulatory FactorsUSF1 protein, humanUSP14 protein, humanAKT/mTOR signalingATRAP, Glycolytic metabolismBreast cancerUbiquitination

Identifiers

PMID35414770
PMCPMC8990462
OpenAlexW4225931506

What Socratic holds

Textmetadata
LicenceCC BY
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.