Evidence map›Paper›PMID 31731888›Full record

ArticleCell cycle (Georgetown, Tex.)2019

C-X-C chemokine receptor 2 correlates with unfavorable prognosis and facilitates malignant cell activities via activating JAK2/STAT3 pathway in non-small cell lung cancer.

Lin Wei, Yugang Liu, Yuefeng Ma, Chao Ding, Huijun Zhang, Zhenghui Lu, Zhenning Gu, Changsheng Zhu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. NFATC3 enhances osteosarcoma progression by increasing PD-L1 and CXCL2 levels.Medical oncology (Northwood, London, England) · 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

8 authors at 2 institutions in 1 country.

Lin WeiDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Yugang LiuDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Yuefeng MaDepartment of Thoracic Surgery, The Second Affiliated Hospital, Medical College of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Chao DingDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Huijun ZhangDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Zhenghui LuDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Zhenning GuDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Changsheng ZhuDepartment of Thoracic Surgery, Xi'an Chest Hospital,Xi'an, Shaanxi, China.
Xi'an Chest Hospital · CNSecond Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate the correlation of C-X-C chemokine receptor 2 (CXCR2) with clinicopathological characteristics and survival in non-small cell lung cancer (NSCLC) patients and further explore its effect on proliferation, apoptosis, invasion, stemness, chemosensitivity as well as JAK2/STAT3 pathway in NSCLC cells. The expression of CXCR2 in tumor tissues and adjacent tissues from 340 NSCLC patients received surgery was detected by immunohistochemistry. CXCR2 overexpression and knockdown were constructed through plasmid transfection and the effect of CXCR2 dysregulation on cell proliferation, apoptosis, invasion, stemness, chemosensitivity as well as its regulatory effect on JAK2/STAT signaling pathway was assessed in NCI-H1437 cells and NCI-H1299 cells. CXCR2 expression was higher in tumor tissues than that in paired adjacent tissues, and it was correlated with poor pathological differentiation, greater tumor size, lymph node metastasis, higher TNM stage and poor survival in NSCLC patients.

Indexed as

A549 CellsAgedApoptosisCarcinoma, Non-Small-Cell LungCell MovementCell ProliferationCisplatinDeoxycytidineDrug Resistance, NeoplasmFemaleGemcitabineGene Expression Regulation, NeoplasticHumansJanus Kinase 2MaleMiddle AgedCisplatinCXCR2 protein, humanDeoxycytidineGemcitabineJAK2 protein, humanJanus Kinase 2Receptors, Interleukin-8BSTAT3 protein, humanSTAT3 Transcription FactorC-X-C chemokine receptor 2JAK2/STAT3 pathwaynon-small cell lung cancer

Identifiers

PMID31731888
PMCPMC6927725
OpenAlexW2983347510

What OpenQuestion holds

Textmetadata
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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.