Evidence map›Paper›PMID 31396319›Full record

ArticleAmerican journal of translational research2019

Interleukin-22 secreted by cancer-associated fibroblasts regulates the proliferation and metastasis of lung cancer cells via the PI3K-Akt-mTOR signaling pathway.

Hongbo Li, Quan Zhang, Qi Wu, Yayun Cui, Hong Zhu, Mingming Fang, Xifa Zhou, Zhiqiang Sun, Jingping Yu

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 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 53 citations in OpenAlex.

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  9. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 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

9 authors at 6 institutions in 1 country.

Hongbo LiDepartment of Radiotherapy, Changzhou Tumor Hospital, Soochow University Changzhou, China.
Quan ZhangDepartment of Radiotherapy, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University Huai'an, China.
Qi WuDepartment of Histology and Embryology, Heze Medical College Heze, China.
Yayun CuiDepartment of Radiotherapy, Anhui Provincial Hospital Hefei, China.
Hong ZhuDepartment of Radiotherapy, Minhang Branch of Cancer Hospital of Fudan University Shanghai, China.
Mingming FangDepartment of Radiotherapy, Changzhou Tumor Hospital, Soochow University Changzhou, China.
Xifa ZhouDepartment of Radiotherapy, Changzhou Tumor Hospital, Soochow University Changzhou, China.
Zhiqiang SunDepartment of Radiotherapy, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University Changzhou, China.
Jingping YuDepartment of Radiotherapy, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University Changzhou, China.
Soochow University · CNChangzhou No.2 People's Hospital · CNAnhui Provincial Hospital · CNFudan University Shanghai Cancer Center · CNHeze Medical College · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is one of the most common human cancers and is the leading cause of cancer-related mortality. Previous studies have suggested that IL-22 might promote the survival of human lung cancer cells. However, the source of IL-22 and the regulatory mechanism of lung cancer cell proliferation remain unclear. In this study, we found that the expression of IL-22 was upregulated in non-small-cell lung cancer (NSCLC) tumor specimens, as revealed by RT-qPCR analysis. Furthermore, IL-22 was profoundly elevated in cell cultures of primary cancer-associated fibroblasts (CAFs) compared to the levels in cell cultures of normal fibroblasts. Moreover, treatment with the supernatant of CAF cell cultures significantly increased the proliferation, migration and invasion of A549 and H1650 cells but reduced apoptosis via the activation of PI3K-Akt-mTOR signaling, and the application of an anti-IL-22 antibody can partially block the effects induced by the CAF cell culture supernatant. Finally, we also identified a panel of critical genes with differential expression between A549 cells treated with and without IL-22. In summary, our results demonstrate a novel regulatory function of IL-22 secreted by CAFs in NSCLC and provide a potential therapeutic target for treating lung cancer.

Indexed as

Interleukin-22lung cancerPI3K-Akt-mTORproliferation

Identifiers

PMID31396319
PMCPMC6684901
OpenAlexW2991555977

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.