Evidence map›Paper›PMID 30899375›Full record

ArticleAmerican journal of translational research2019

CCL2-CCL5/CCR4 contributed to radiation-induced epithelial-mesenchymal transition of HPAEpiC cells via the ERK signaling pathways.

Yazhen Zhong, Zechen Lin, Jinhua Lu, Xianlei Lin, Wei Xu, Nan Wang, Siyu Huang, Yuanyuan Wang, Yuan Zhu, Zhu Chen and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. 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 18% 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, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The roles of CC chemokines in response to radiation.Radiation oncology (London, England) · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

11 authors at 2 institutions in 1 country.

Yazhen ZhongOncology Department, Hangzhou Hospital of Traditional Chinese Medicine, GuangXing Hospital Affiliated to Zhejiang Chinese Medical University Hangzhou, China.
Zechen LinFourth Clinical Medical College, Hangzhou Cancer Hospital Hangzhou, China.
Jinhua LuDepartment of Oncology Comprehensive Treatment, Hangzhou Cancer Hospital Hangzhou, China.
Xianlei LinOncology Department, Hangzhou Hospital of Traditional Chinese Medicine, GuangXing Hospital Affiliated to Zhejiang Chinese Medical University Hangzhou, China.
Wei XuDepartment of Integrated Chinese and Western Medicine, Hangzhou Cancer Hospital, Hangzhou Hospital Affiliated to Nanjing Medical University Hangzhou, China.
Nan WangThe First People's Hospital of Xiaoshan Hangzhou Hangzhou, China.
Siyu HuangFourth Clinical Medical College, Hangzhou Cancer Hospital Hangzhou, China.
Yuanyuan WangFourth Clinical Medical College, Hangzhou Cancer Hospital Hangzhou, China.
Yuan ZhuFourth Clinical Medical College, Hangzhou Cancer Hospital Hangzhou, China.
Zhu ChenDepartment of Oncology Comprehensive Treatment, Hangzhou Cancer Hospital Hangzhou, China.
Shengyou LinOncology Department, Hangzhou Hospital of Traditional Chinese Medicine, GuangXing Hospital Affiliated to Zhejiang Chinese Medical University Hangzhou, China.
Zhejiang Chinese Medical University · CNHangzhou Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiation-induced lung toxicity, including radiation pneumonitis and pulmonary fibrosis, often occurs in patients receiving radiation therapy. Epithelial-mesenchymal transition (EMT) of alveolar epithelial cells (AECs) plays critical roles in radiation-induced lung toxicity. In the present study, RNA sequencing was applied to examine the whole transcriptomes of human pulmonary AEC cells (HPAEpiC) with or without radiation treatment. We found that cytokine, chemokine and cell adhesion signaling pathways were enriched in radiation-treated cells. CCL2 (C-C Motif Chemokine Ligand 2), CCL5 and CCR4 (C-C Motif Chemokine Receptor 4) were among the top enriched genes in chemokine signaling pathway. The upregulation of CCL2, CCL5 and CCR4 in response to irradiation was confirmed at both mRNA and protein levels by real-time PCR, western blotting and enzyme-linked immunosorbent assay analyses. Ophiopogonin B, a bioactive ingredient of Radix

Indexed as

alveolar epithelial cellsChemokinesEMTophiopogonin B

Identifiers

PMID30899375
PMCPMC6413271
OpenAlexW2982512663

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.