Evidence map›Paper›PMID 27833130›Full record

ArticleScientific reports2016

Protein tyrosine phosphatase PTPN3 promotes drug resistance and stem cell-like characteristics in ovarian cancer.

Shuqin Li, Jian Cao, Wei Zhang, Fan Zhang, Guantai Ni, Qian Luo, Man Wang, Xiang Tao, Hongping Xia

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. 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
1.4field-weighted citation impact, top 17% 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, 25 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

9 authors at 5 institutions in 1 country.

Shuqin LiDepartment of Gynecology and Obstetrics, Yijishan Hospital of Wannan Medical College, Wuhu, China.
Jian CaoDepartment of Gynecology and Obstetrics, Nanjing Maternal and Children Care Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Wei ZhangDepartment of Pathology, Yijishan Hospital of Wannan Medical College, Wuhu, China.
Fan ZhangDepartment of Pathology, Yijishan Hospital of Wannan Medical College, Wuhu, China.
Guantai NiDepartment of Gynecology and Obstetrics, Yijishan Hospital of Wannan Medical College, Wuhu, China.
Qian LuoDepartment of Gynecology and Obstetrics, Yijishan Hospital of Wannan Medical College, Wuhu, China.
Man WangDepartment of Gynecology and Obstetrics, Xiaogan Central Hospital, Xiaogan, China.
Xiang TaoDepartment of Pathology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Hongping XiaDepartment of Pathology, Yijishan Hospital of Wannan Medical College, Wuhu, China.
Wannan Medical College · CNFirst Affiliated Hospital of Wannan Medical College · CNNanjing Medical University · CNObstetrics and Gynecology Hospital of Fudan University · CNThe Central Hospital of Xiao gan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current standard treatment for ovarian cancer is aggressive surgery followed by platinum-based combination chemotherapy. Recurrence and chemotherapeutic drug resistance are the two main factors that account for the high mortality of most ovarian cancers. Liposomal doxorubicin is primarily used for the treatment of ovarian cancer when the disease has progressed after platinum-based chemotherapy. However, relatively little is known about the genomic changes that contribute to both cisplatin and doxorubicin resistance in high-grade serous ovarian cancer (HGSC) under the selective pressure of chemotherapy. Here, we found that protein tyrosine phosphatase PTPN3 gene expression was substantially increased in both cisplatin and doxorubicin-resistant ovarian cancer cells. Silencing of PTPN3 restored sensitivity to cisplatin and doxorubicin in resistant ovarian cancer cells. Down-regulation of PTPN3 also inhibited cell cycle progression, migration, stemness in vitro and the tumorigenicity of resistant ovarian cancer cells in vivo. Meanwhile, the expression of PTPN3 was found to be regulated by miR-199 in resistant ovarian cancer cells. These findings suggest that PTPN3 promotes tumorigenicity, stemness and drug resistance in ovarian cancer, and thus is a potential therapeutic target for the treatment of ovarian cancer.

Indexed as

Drug Resistance, Neoplasm3' Untranslated RegionsAnimalsAntibiotics, AntineoplasticBase SequenceBinding SitesCarcinogenesisCell Line, TumorCell MovementCell ProliferationCisplatinDoxorubicinFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumans3' Untranslated RegionsAntibiotics, AntineoplasticCisplatinDoxorubicinMicroRNAsmirn199 microRNA, humanProtein Tyrosine Phosphatase, Non-Receptor Type 3PTPN3 protein, human

Identifiers

PMID27833130
PMCPMC5105059
OpenAlexW2550426731

What OpenQuestion holds

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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.