Evidence map›Paper›PMID 31938273›Full record

ArticleInternational journal of clinical and experimental pathology2018

Overexpression of Polo-like kinase1 (PLK1) in chondrosarcoma and its implications for cancer progression.

Kelu Li, Hongmei Ma, Xiuyan Zheng, Yali Hu, Yue Wang, Kunpeng Zhang, Jiahan Chen, Yan Qi, Jinfang Jiang, Lijuan Pang and 4 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 92% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

14 authors at 3 institutions in 2 countries.

Kelu LiDepartment of Pathology, First Affiliated Hospital, Shihezi University Shihezi, China.
Hongmei MaKey Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathology, School of Medicine, Shihezi University, Ministry of Education of China Shihezi, China.
Xiuyan ZhengKey Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathology, School of Medicine, Shihezi University, Ministry of Education of China Shihezi, China.
Yali HuKey Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathology, School of Medicine, Shihezi University, Ministry of Education of China Shihezi, China.
Yue WangKey Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathology, School of Medicine, Shihezi University, Ministry of Education of China Shihezi, China.
Kunpeng ZhangKey Laboratory of Xinjiang Endemic and Ethnic Diseases, Department of Pathology, School of Medicine, Shihezi University, Ministry of Education of China Shihezi, China.
Jiahan ChenSchool of Medicine, Shihezi University Shihezi, China.
Yan QiDepartment of Pathology, First Affiliated Hospital, Shihezi University Shihezi, China.
Jinfang JiangDepartment of Pathology, First Affiliated Hospital, Shihezi University Shihezi, China.
Lijuan PangDepartment of Pathology, First Affiliated Hospital, Shihezi University Shihezi, China.
Lin TaoDepartment of Pathology, First Affiliated Hospital, Shihezi University Shihezi, China.
Wenyi GuAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland Brisbane, Australia.
Feng LiDepartment of Pathology, Beijing Chaoyang Hospital, Capital Medical University Beijing, China.
Hong ZouDepartment of Pathology, First Affiliated Hospital, Shihezi University Shihezi, China.
Beijing Chao-Yang Hospital · CNShihezi University · CNUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polo-like kinase1 (PLK1) is a new therapeutic target for osteosarcoma with good application prospects. Whether PLK1 is highly expressed in chondrosarcoma and whether PLK1 can be a potential therapeutic target for chondrosarcoma are worth exploring. However, PLK1 expression in chondrosarcoma is scarcely investigated. Therefore, we collected 11 cases of chondrosarcoma and 26 cases of osteochondroma with complete clinical pathological data and used immunohistochemical staining to detect the expression of PLK1 in chondrosarcoma and osteochondroma and then studied its significance and relationship with clinical pathological parameters. Our results showed that the positive expression rate of PLK1 in chondrosarcoma tissue (90.91%, 10/11) was significantly higher than the rate of osteochondroma tissues (53.85%, 14/26) (P<0.05). The expression of PLK1 enhanced gradually with the increase in histological grade (P<0.05). PLK1 was highly expressed in chondrosarcoma, and the high expression of PLK1 might be involved in cartilage tumor malignant progression.

Indexed as

chondrosarcomaimmunohistochemistryosteochondromaPLK1

Identifiers

PMID31938273
PMCPMC6958127
OpenAlexW2804031180

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.