Evidence map›Paper›PMID 36900292›Full record

ArticleCancers2023

KIF2C Facilitates Tumor Growth and Metastasis in Pancreatic Ductal Adenocarcinoma.

Xing Huang, Feng Zhao, Quan Wu, Zitong Wang, Haiyue Ren, Qiqi Zhang, Zhe Wang, Jin Xu

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In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Pan-cancer analysis of telomere maintenance mechanisms.The Journal of biological chemistry · 2024
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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

8 authors.

Xing HuangDepartment of General Surgery, Shengjing Hospital, China Medical University, Shenyang 110004, China.
Feng ZhaoDepartment of Stem Cells and Regenerative Medicine, China Medical University, Shenyang 110122, China.
Quan WuDepartment of Pathology, Shengjing Hospital, China Medical University, Shenyang 110004, China.
Zitong WangDepartment of Pathology, Shengjing Hospital, China Medical University, Shenyang 110004, China.ORCID 0000-0003-4103-6336
Haiyue RenDepartment of Pathology, Shengjing Hospital, China Medical University, Shenyang 110004, China.
Qiqi ZhangDepartment of Pathology, Shengjing Hospital, China Medical University, Shenyang 110004, China.
Zhe WangDepartment of Pathology, Shengjing Hospital, China Medical University, Shenyang 110004, China.
Jin XuDepartment of General Surgery, Shengjing Hospital, China Medical University, Shenyang 110004, China.

Funding

National Natural Science Foundation of China 81601692the Technology Research from the Department of Education of Liaoning Province JCZR2020013
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal cancer with a poor prognosis. For PDAC, an increase in the survival time of patients and a reduction mortality have not yet successfully been achieved. In many research works, Kinesin family member 2C (KIF2C) is highly expressed in several tumors. Nevertheless, the role of KIF2C in pancreatic cancer is unknown. In this study, we found that KIF2C expression is significantly upregulated in human PDAC tissues and cell lines such as ASPC-1 and MIA-PaCa2. Moreover, KIF2C upregulation is associated with a poor prognosis when combining the expression of KIF2C with clinical information. Through cell functional assays and the construction of animal models, we showed that KIF2C promotes PDAC cell proliferation, migration, invasion, and metastasis, both in vitro and in vivo. Finally, the results of sequencing showed that the overexpression of KIF2C causes a decrease in some proinflammatory factors and chemokines. The cell cycle detection indicated that the pancreatic cancer cells in the overexpressed group had abnormal proliferation in the G2 and S phases. These results revealed the potential of KIF2C as a therapeutic target for the treatment of PDAC.

Indexed as

cell cycleinvasionKIF2CmigrationPDACprognosisproliferation

Identifiers

PMID36900292
PMCPMC10000478

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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.