Evidence map›Paper›PMID 36088429›Full record

ArticleJournal of ovarian research2022

UBE2T regulates epithelial-mesenchymal transition through the PI3K-AKT pathway and plays a carcinogenic role in ovarian cancer.

Ping Cui, Hao Li, Can Wang, Yuan Liu, Mengjun Zhang, Yue Yin, Zhenxing Sun, Yiru Wang, Xiuwei Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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  6. Processed Products ofAnti-cancer agents in medicinal chemistry · 2025
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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

9 authors at 2 institutions in 1 country.

Ping CuiDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Hao LiDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Can WangDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Yuan LiuDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Mengjun ZhangDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Yue YinDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Zhenxing SunDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Yiru WangDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China.
Xiuwei ChenDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Heilongjiang, 150040, Harbin, China. chenxiuwei1023@163.com.
Third Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CN

Funding

National Natural Science Foundation of China 81772274
6 · The paper itself

Abstract

backgroundUbiquitin-binding enzyme E2T (UBE2T), a member of the E2 family of the ubiquitin-proteasome pathway, is associated with tumorigenesis of varioustumours; however, its role and mechanism in ovarian cancer remain unclear.

resultsOur study revealed that UBE2T is highly expressed in ovarian cancer; this high expression was closely related to poor prognosis. Immunohistochemistry was used to validate the high expression of UBE2T in ovarian cancer. This is the first study to demonstrate that UBE2T expression is higher in ovarian cancer with BRCA mutation. Moreover, we demonstrated that UBE2T gene silencing significantly inhibited ovarian cancer cell proliferation and invasion. The epithelial-mesenchymal transition (EMT) of ovarian cancer cells and phosphatidylinositol 3 kinase/protein kinase B (PI3K-AKT) pathway were significantly inhibited. Adding the mechanistic target of rapamycin activator MHY1485 activated the PI3K-AKT pathway and significantly restored the proliferative and invasive ability of ovarian cancer cells. Furthermore, a tumorigenesis experiment in nude mice revealed that tumour growth on mice body surface and tumour tissue EMT were significantly inhibited after UBE2T gene silencing.

conclusionsThis study demonstrated that UBE2T regulates EMT via the PI3K-AKT pathway and plays a carcinogenic role in ovarian cancer. Moreover, UBE2T may interact with BRCA to affect ovarian cancer occurrence and development. Hence, UBE2T may be a valuable novel biomarker for the early diagnosis and prognosis and treatment of ovarian cancer. Further, UBE2T inhibition may be effective for treating ovarian cancer.

Indexed as

Ovarian NeoplasmsAnimalsCarcinogenesisCarcinogensCarcinoma, Ovarian EpithelialCell Line, TumorEpithelial-Mesenchymal TransitionFemaleHumansMiceMice, NudePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktUbiquitin-Conjugating EnzymesUbiquitinsCarcinogensPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktUBE2T protein, humanUbiquitin-Conjugating EnzymesUbiquitinsEpithelial–mesenchymal transitionOvarian cancerTumorigenesisUbiquitin-binding enzyme E2T

Identifiers

PMID36088429
PMCPMC9464398
OpenAlexW4295450562

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LicenceCC BY
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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.