Evidence map›Paper›PMID 29524043›Full record

ArticleInternational urology and nephrology2018

Chemokine CXCL3 mediates prostate cancer cells proliferation, migration and gene expression changes in an autocrine/paracrine fashion.

Hua Xin, Yu Cao, Ming-Liang Shao, Wei Zhang, Chun-Bin Zhang, Jing-Tao Wang, Li-Chun Liang, Wen-Wu Shao, Ya-Ling Qi, Yue Li and 6 more

Abstract read
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In one paragraph

Article in International urology and nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 45 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

16 authors at 4 institutions in 1 country.

Hua XinDepartment of Laboratory Medicine, The First Affiliated Hospital, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Yu CaoDepartment of Laboratory Medicine, The First Affiliated Hospital, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Ming-Liang ShaoDepartment of Interventional Medicine, The Fifth Hospital, Shijiazhuang, 050000, Hebei, China.
Wei ZhangDepartment of Interventional Medicine, The Fifth Hospital, Shijiazhuang, 050000, Hebei, China.
Chun-Bin ZhangDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Jing-Tao WangDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Li-Chun LiangDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Wen-Wu ShaoDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Ya-Ling QiDepartment of Histology and Embryology, Hainan Medical College, Haikou, 571199, Hainan, China.
Yue LiDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Ze-Yu ZhangDepartment of Laboratory Medicine, The First Affiliated Hospital, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Zhe YangDepartment of Laboratory Medicine, The First Affiliated Hospital, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Yu-Hong SunDepartment of Laboratory Medicine, The First Affiliated Hospital, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Peng-Xia ZhangDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China.
Lin-Lin JiaDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China. zhangshurui175@163.com.
Wei-Qun WangDepartment of Physiology, Jiamusi University, Jiamusi, 154002, Heilongjiang, China. wangweiqun1974@163.com.ORCID http://orcid.org/0000-0002-9238-3517
Jiamusi University · CNFirst Affiliated Hospital of Jiamusi University · CNFifth Hospital of Shijiazhuang · CNHainan Medical College Hospital · CN

Funding

Graduate Student Science and Technology Innovation Project of Jiamusi University LZR2015_011Innovation and entrepreneurship training program for college students of Heilongjiang Province 201710222003Key Research Program of Jiamusi University 12Z1201504National Nature Science Foundation of China 81272854Nature Science Foundation of Heilongjiang Province H201362President Innovation and Entrepreneurship Foundation of Jiamusi University xzyf2017-30Science and Technology Innovation Team Building Project of Department of Education of Heilongjiang Province cxtd-2016-03
6 · The paper itself

Abstract

introductionWe have previously indicated that CXCL3 was upregulated in the tissues of prostate cancer, and exogenous administration of CXCL3 played a predominant role in the tumorigenicity of prostate cancer cells. In the present study, we further explored the role and the underlying mechanism of CXCL3 overexpression in the oncogenic potential of prostate cancer in an autocrine/paracrine fashion.

methodsCXCL3-overexpressing prostate cancer cell line PC-3 and immortalized prostate stromal cell line WPMY-1 were established by gene transfection. CCK-8, transwell assays and growth of tumor xenografts were conducted to characterize the effects of CXCL3 on PC-3 cells' proliferation and migration. Western blotting was conducted to test whether CXCL3 could affect the expression of tumorigenesis-associated genes.

resultsThe results showed that CXCL3 overexpression in PC-3 cells and the PC-3 cells treated with the supernatants of CXCL3-transfected WPMY-1 cells stimulated the proliferation and migration of PC-3 cells in vitro and in a nude mouse xenograft model. Western blotting revealed higher levels of p-ERK, Akt and Bcl-2 and lower levels of Bax in the tumor xenografts transplanted with CXCL3-transfected PC-3 cells. Moreover, the tumor xenografts derived from the PC-3 cells treated with supernatants of CXCL3-transfected WPMY-1 cells showed higher expression of ERK, Akt and Bcl-2 and lower expression of Bax.

conclusionsThese findings suggest that CXCL3 autocrine/paracrine pathways are involved in the development of prostate cancer by regulating the expression of the target genes that are related to the progression of malignancies.

Indexed as

Cell MovementCell ProliferationAnimalsAutocrine Communicationbcl-2-Associated X ProteinCell Line, TumorChemokines, CXCExtracellular Signal-Regulated MAP KinasesGene ExpressionHumansMaleMiceMice, NudeNeoplasm TransplantationParacrine CommunicationPhosphorylationBAX protein, humanbcl-2-Associated X ProteinChemokines, CXCCXCL3 protein, humanExtracellular Signal-Regulated MAP KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2RNA, MessengerAutocrineChemokinesCXCL3ParacrineProstate cancer

Identifiers

PMID29524043
OpenAlexW2793015008

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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.